Role Overview We are currently looking for a Manufacturing Scientist to join a growing Biotechnology company based in South West London. You will working in a state of the art laboratory and collaborating with the Manufacturing Development team and Research Teams to deliver quality standards and products. Duties and Responsibilities You will be responsible for manufacturing DNA for clients. You will use a wide range of molecular biology techniques such as analysis of DNA and proteins and PCR. You will work in a GMP regulated environment and use aseptic techniques. As the Manufacturing Scientist, you will be responsible for running batches and managing weekly manufacturing duties and projects. Experience and Education BSc or MSc in a relevant scientific discipline such as, but not limited to, Biotechnology, Molecular Biology or Biochemistry. Proven industry experience working in a GMP laboratory. Quality Control experience would be highly beneficial to your application. Proven experience using molecular biology techniques such as DNA and Protein analysis is essential to your application. Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | London, United Kingdom | Partnership Number | OC387148 England and Wales
24/11/2020
Full time
Role Overview We are currently looking for a Manufacturing Scientist to join a growing Biotechnology company based in South West London. You will working in a state of the art laboratory and collaborating with the Manufacturing Development team and Research Teams to deliver quality standards and products. Duties and Responsibilities You will be responsible for manufacturing DNA for clients. You will use a wide range of molecular biology techniques such as analysis of DNA and proteins and PCR. You will work in a GMP regulated environment and use aseptic techniques. As the Manufacturing Scientist, you will be responsible for running batches and managing weekly manufacturing duties and projects. Experience and Education BSc or MSc in a relevant scientific discipline such as, but not limited to, Biotechnology, Molecular Biology or Biochemistry. Proven industry experience working in a GMP laboratory. Quality Control experience would be highly beneficial to your application. Proven experience using molecular biology techniques such as DNA and Protein analysis is essential to your application. Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | London, United Kingdom | Partnership Number | OC387148 England and Wales
Job Title : Quality Compliance Manager Location: Mulhuddart, Dublin 15 Benefits: Excellent salary and benefits, including pension, healthcare and yearly bonus. 12 month fixed term contract for Maternity leave. Client: My client one of the worlds leading global manufacturers in the design and production on technologically advanced, high-quality, integrated containment and delivery systems for injectable medicines. Job Overview: Responsible for compliance with the quality and regulatory requirements for combination medicinal and device products assembled and packed. Responsible for upgrading and maintaining of quality systems to meet the requirements Manage the Quality Compliance team, 1:1 meetings and Training & Development Plan for Reports Provide regulatory guidance to the business Liaise with Customers and regulatory agencies Supply Chain QA responsible for the review and approval of all Suppliers Develop reports/presentations on the status of the compliance program for senior management team and the wider West Pharmaceutical Services colleagues. Embed QMS management principles in the organisation & drive continuous improvement Work closely with the NPI and Operations Department Requirements: Degree programme in either pharmacy, chemistry, biology, microbiology or equivalent with at least 5 years in a Medical Device/Pharmaceutical environment Experience in setting up and maintaining a QMS which meets the legislative requirement of human medicines and medical devices in the EU and USA and the ISO13485 standard. Experience of hosting regulatory audits from either the European or US authorities. For more infor on this position forward your updated CV of contact me directly to organise a consultation. Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy| Registered office | London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales
24/11/2020
Job Title : Quality Compliance Manager Location: Mulhuddart, Dublin 15 Benefits: Excellent salary and benefits, including pension, healthcare and yearly bonus. 12 month fixed term contract for Maternity leave. Client: My client one of the worlds leading global manufacturers in the design and production on technologically advanced, high-quality, integrated containment and delivery systems for injectable medicines. Job Overview: Responsible for compliance with the quality and regulatory requirements for combination medicinal and device products assembled and packed. Responsible for upgrading and maintaining of quality systems to meet the requirements Manage the Quality Compliance team, 1:1 meetings and Training & Development Plan for Reports Provide regulatory guidance to the business Liaise with Customers and regulatory agencies Supply Chain QA responsible for the review and approval of all Suppliers Develop reports/presentations on the status of the compliance program for senior management team and the wider West Pharmaceutical Services colleagues. Embed QMS management principles in the organisation & drive continuous improvement Work closely with the NPI and Operations Department Requirements: Degree programme in either pharmacy, chemistry, biology, microbiology or equivalent with at least 5 years in a Medical Device/Pharmaceutical environment Experience in setting up and maintaining a QMS which meets the legislative requirement of human medicines and medical devices in the EU and USA and the ISO13485 standard. Experience of hosting regulatory audits from either the European or US authorities. For more infor on this position forward your updated CV of contact me directly to organise a consultation. Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy| Registered office | London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales
Autostream Global have a project with a Global customer in Uppsala and they are about to install three machines on site and the client needs help with the installation, commissioning and IQ/OQ validation of the line. There are three machines from three suppliers - a Sienader standalone inspection machine, an autoclave sterilization and a micron assembly machine for labelling. Downstream is a form filled seal machine that puts the cartridge into a blister with other components which is then covered with a Tyvek lid. A SCADA Alan Bradley system is used. Some additional info; Accommodation and expenses are paid for- flights, accommodation and day allowance for food in this Will return people home for Xmas and will allow travel home during the project but not every week December start - right up to end of March Hands on roll needed for them with expertise SCADA Allan Bradley -Rockwell knowledge
24/11/2020
Project-based
Autostream Global have a project with a Global customer in Uppsala and they are about to install three machines on site and the client needs help with the installation, commissioning and IQ/OQ validation of the line. There are three machines from three suppliers - a Sienader standalone inspection machine, an autoclave sterilization and a micron assembly machine for labelling. Downstream is a form filled seal machine that puts the cartridge into a blister with other components which is then covered with a Tyvek lid. A SCADA Alan Bradley system is used. Some additional info; Accommodation and expenses are paid for- flights, accommodation and day allowance for food in this Will return people home for Xmas and will allow travel home during the project but not every week December start - right up to end of March Hands on roll needed for them with expertise SCADA Allan Bradley -Rockwell knowledge
The Warehouse Associate may perform a variety of tasks in picking, packing and shipping. The ideal candidate must be able to work in various departments and adapt quickly to a rapidly changing work load to support business needs. Responsibilities Maintain high quality customer service by efficiently, accurately and quickly selecting orders Maintain a safe and clean work environment in assigned work area, the facility and on company property Cross train, to meet workload needs and maintain company needs Stocks primary item locations to effectively eliminate highlighting items for backorders Responsible for confirming orders are correct in a timely manner Conducts physical inventories as required Ensure items being packaged are not damaged or broken Weigh, measure and calculate package sizes as needed Meet and maintain company productivity and quality standards Able to work mandatory overtime as needed to complete customer orders Accurately pick orders for shipment Label and mark containers Work effectively to have all customer orders packed for shipment Communicate and cooperate with management and co-workers Support periods of increased business by working overtime, weekends and various schedules as needed Completes all documents fully, neatly and accurately Performs various tasks as directed by management Qualifications Minimum 1-3 years' experience in a picking/packing environment High school diploma or equivalent Adheres to all safety guidelines Strong attention to detail Ability to follow directions Excellent communication skills Good organizational and time management skills Able to work as a team Basic computer knowledge Able to read and perform simple math quickly and accurately Regularly lift and move objects up to 50 pounds Must be capable of standing and walking for extended periods of time Must be able to walk, stoop, kneel, bend, crouch and climb ladders Flexible start time between 8:30am and 10:00am Monday through Friday Must be flexible and able to change work hours
24/11/2020
Project-based
The Warehouse Associate may perform a variety of tasks in picking, packing and shipping. The ideal candidate must be able to work in various departments and adapt quickly to a rapidly changing work load to support business needs. Responsibilities Maintain high quality customer service by efficiently, accurately and quickly selecting orders Maintain a safe and clean work environment in assigned work area, the facility and on company property Cross train, to meet workload needs and maintain company needs Stocks primary item locations to effectively eliminate highlighting items for backorders Responsible for confirming orders are correct in a timely manner Conducts physical inventories as required Ensure items being packaged are not damaged or broken Weigh, measure and calculate package sizes as needed Meet and maintain company productivity and quality standards Able to work mandatory overtime as needed to complete customer orders Accurately pick orders for shipment Label and mark containers Work effectively to have all customer orders packed for shipment Communicate and cooperate with management and co-workers Support periods of increased business by working overtime, weekends and various schedules as needed Completes all documents fully, neatly and accurately Performs various tasks as directed by management Qualifications Minimum 1-3 years' experience in a picking/packing environment High school diploma or equivalent Adheres to all safety guidelines Strong attention to detail Ability to follow directions Excellent communication skills Good organizational and time management skills Able to work as a team Basic computer knowledge Able to read and perform simple math quickly and accurately Regularly lift and move objects up to 50 pounds Must be capable of standing and walking for extended periods of time Must be able to walk, stoop, kneel, bend, crouch and climb ladders Flexible start time between 8:30am and 10:00am Monday through Friday Must be flexible and able to change work hours
The Warehouse Associate may perform a variety of tasks in receiving, picking, packing, replenishment and shipping. The ideal candidate must be able to work in various departments and adapt quickly to a rapidly changing work load to support business needs. This is a 2nd shift position. Responsibilities Maintain high quality customer service by efficiently, accurately and quickly selecting orders Maintain a safe and clean work environment in assigned work area, the facility and on company property Cross train, to meet workload needs and maintain company needs Handles incoming shipments and verifies that quality and quantity are correct Receives and unloads merchandise and checks for damaged goods Stocks primary item locations to effectively eliminate highlighting items for backorders Responsible for confirming orders are correct in a timely manner Conducts physical inventories as required Ensure items being packaged are not damaged or broken Weigh, measure and calculate package sizes as needed Meet and maintain company productivity and quality standards Able to work mandatory overtime as needed to complete customer orders Accurately pick orders for shipment Label and mark containers Work effectively to have all customer orders packed for shipment Communicate and cooperate with management and co-workers Completes all documents fully, neatly and accurately Performs various tasks as directed by management Qualifications Minimum 1-3 years' experience in a picking/packing environment High school diploma or equivalent Adheres to all safety guidelines Strong attention to detail Ability to follow directions Excellent communication skills Good organizational and time management skills Able to work as a team Basic computer knowledge Able to read and perform simple math quickly and accurately Regularly lift and move objects up to 50 pounds Must be capable of standing and walking for extended periods of time Must be able to walk, stoop, kneel, bend, crouch and climb ladders Must be flexible and able to change work hours
24/11/2020
Project-based
The Warehouse Associate may perform a variety of tasks in receiving, picking, packing, replenishment and shipping. The ideal candidate must be able to work in various departments and adapt quickly to a rapidly changing work load to support business needs. This is a 2nd shift position. Responsibilities Maintain high quality customer service by efficiently, accurately and quickly selecting orders Maintain a safe and clean work environment in assigned work area, the facility and on company property Cross train, to meet workload needs and maintain company needs Handles incoming shipments and verifies that quality and quantity are correct Receives and unloads merchandise and checks for damaged goods Stocks primary item locations to effectively eliminate highlighting items for backorders Responsible for confirming orders are correct in a timely manner Conducts physical inventories as required Ensure items being packaged are not damaged or broken Weigh, measure and calculate package sizes as needed Meet and maintain company productivity and quality standards Able to work mandatory overtime as needed to complete customer orders Accurately pick orders for shipment Label and mark containers Work effectively to have all customer orders packed for shipment Communicate and cooperate with management and co-workers Completes all documents fully, neatly and accurately Performs various tasks as directed by management Qualifications Minimum 1-3 years' experience in a picking/packing environment High school diploma or equivalent Adheres to all safety guidelines Strong attention to detail Ability to follow directions Excellent communication skills Good organizational and time management skills Able to work as a team Basic computer knowledge Able to read and perform simple math quickly and accurately Regularly lift and move objects up to 50 pounds Must be capable of standing and walking for extended periods of time Must be able to walk, stoop, kneel, bend, crouch and climb ladders Must be flexible and able to change work hours
Global Enterprise Partners is looking for an SAP PP Consultant to join an S4HANA roll-out in few European locations. This is an opportunity for a long term assignment. We are looking for creative people with high work ethic. There will be a high expectation to travel according to the needs of the project but in the near and perhaps far future the work will be remote due to Covid-19. Please read the job requirements carefully and submit your resume if there is a match. A European passport or residence permit is mandatory! Skills: SAP PP Manufacturing experience is a must Automotive experience is a big plus 1+ full S4HANA life cycle implementation is a must Excellent communication skills English speaking Project info Start: 01/12/2020 Duration: at least 1 year Location: Poland, Denmark and Hungary Rate: competitive
24/11/2020
Project-based
Global Enterprise Partners is looking for an SAP PP Consultant to join an S4HANA roll-out in few European locations. This is an opportunity for a long term assignment. We are looking for creative people with high work ethic. There will be a high expectation to travel according to the needs of the project but in the near and perhaps far future the work will be remote due to Covid-19. Please read the job requirements carefully and submit your resume if there is a match. A European passport or residence permit is mandatory! Skills: SAP PP Manufacturing experience is a must Automotive experience is a big plus 1+ full S4HANA life cycle implementation is a must Excellent communication skills English speaking Project info Start: 01/12/2020 Duration: at least 1 year Location: Poland, Denmark and Hungary Rate: competitive
Experis IT
Newcastle Upon Tyne, Tyne And Wear, United Kingdom
Job Title: Manufacturing Operator Number of contractors required: 8 Duration of assignment: 01/12/2020 - 28/02/2021 Role Summary: To work on shift within manufacturing operational environment which specialises in assembling and testing flexible oil pipes. Key Activities: To Ensure any tooling/equipment used on shop floor is returned to required location once finished with To carry out duties in-line with required company 5S standards (visual display/tidiness) To carry any duties requested by on shift supervisor/lead operator to support assembly and testing operations To carry out duties in-line with HSE regulations To follow SOIs and Risk Assessments for end fitting assembly and reel to reel operations Essential responsibilities: Follow HSE regulations whilst on-site Ensure all tooling is returned to dedicated storage locations when finished on operations Completed any requests from stores/warehouse for items when required and deliver to shop floor Desired characteristics: Experience in manufacturing Forklift Trucks Lifting/Slinging Crane Operations Hand Power Tools Understanding of Assembly drawings HSE foundations 5S/Lean Quality Management Systems Additional Information Shift Work: Continental Shift Pattern 12 hrs: 7am - 7pm and 7 pm to 7am Pattern consists of Week 1: Mon-Tue Dayshift: off Wed/Thur: Days Fri/Say/Sun Week 2: Off Mon/Tues: days wed/Thurs Off Fri/Sat/Sun Week 3 and Week 4: same working days as Week 1 and 2 but nightshift as opposed to days
22/11/2020
Project-based
Job Title: Manufacturing Operator Number of contractors required: 8 Duration of assignment: 01/12/2020 - 28/02/2021 Role Summary: To work on shift within manufacturing operational environment which specialises in assembling and testing flexible oil pipes. Key Activities: To Ensure any tooling/equipment used on shop floor is returned to required location once finished with To carry out duties in-line with required company 5S standards (visual display/tidiness) To carry any duties requested by on shift supervisor/lead operator to support assembly and testing operations To carry out duties in-line with HSE regulations To follow SOIs and Risk Assessments for end fitting assembly and reel to reel operations Essential responsibilities: Follow HSE regulations whilst on-site Ensure all tooling is returned to dedicated storage locations when finished on operations Completed any requests from stores/warehouse for items when required and deliver to shop floor Desired characteristics: Experience in manufacturing Forklift Trucks Lifting/Slinging Crane Operations Hand Power Tools Understanding of Assembly drawings HSE foundations 5S/Lean Quality Management Systems Additional Information Shift Work: Continental Shift Pattern 12 hrs: 7am - 7pm and 7 pm to 7am Pattern consists of Week 1: Mon-Tue Dayshift: off Wed/Thur: Days Fri/Say/Sun Week 2: Off Mon/Tues: days wed/Thurs Off Fri/Sat/Sun Week 3 and Week 4: same working days as Week 1 and 2 but nightshift as opposed to days
Operator Sensorproduktion für den GMP-Bereich (m/w/d) - GMP/Reagents/ Produktion/Schicht/Deutsch Projekt: Wir suchen für unseren Kunden Roche Diagnostics AG in Rotkreuz versierte Operator Sensorproduktion für den GmP Bereich (m/w/d) Hintergrund: Die Abteilung BGE Sensor & Reagent Operations ist zuständig für die Produktion von Dickschichtsensoren und der Herstellung von Blutgas Analyse Sensoren unter Reinraumbedingungen. Aufgrund der geplanten Beschaffung zukunftsorientierter Maschinen, nach Industrie 4.0 Standard, wird im Team Unterstützung benötigt. Als motivierter Allrounder mit Faszination für moderne Produktionstechnologien erwartet Sie ein interessantes Arbeitsumfeld zusammen mit einem dynamischen Team, DASS im 3 - Schichtbetrieb arbeitet. Wir suchen eine flexible Persönlichkeit mit guter Auffassungsgabe für ein langfristiges Engagement! Hauptaufgaben: * Bedienen, Einrichten und Beobachten von Halb- und vollautomatischen Maschinen . Störungsbehebung und Wartungsarbeiten an den zugeteilten Anlagen . Produzieren, Protokollieren und Überwachen der einzelnen Prozessschritte nach Industrie 4.0 Standard . Anpassung der Produktionspläne . Erstellen von Dispensierlösungen und Pasten zur Produktion . Durchführen von In-Prozesskontrollen (IPC) . Auffälligkeiten und Abweichungen aufnehmen und gegebenenfalls Massnahmen einleiten . Arbeiten unter Einhaltung der Hygienevorschriften und sicherstellen, DASS die entsprechenden Arbeitsbedingungen gewahrt bleiben . Permanente Optimierung des Arbeitsablaufs zu Qualitäts- und Effizienzsteigerung . SAP geführte Materialverwaltung und Dokumentation (Inventur, Verschrottung, Buchungen) . Bereitschaft nach intensiver Einarbeitung als Springer zu unterstützen . Durchführen der täglichen Reinigungsmassnahmen nach GMP Vorschrift . Einhalten der GMP Richtlichtlinien in allen Arbeitsschritten Must Haves: * Abgeschlossene Berufsausbildung oder mehrjährige Produktionskenntnisse von Vorteil . Selbständiges Arbeiten gewohnt, teamfähig, kreativ und lösungsorientiert . Bereitschaft 3 - Schicht Rotierend (5 Tage Woche) zu arbeiten . Deutsch in Wort und Schrift (C1) erforderlich Nice to Haves: * Roche Erfahrung . Erfahrung mit Diagnostiksystemen . Erfahrung in einem Produktionsumfeld . Erfahrung in einem regulierten Umfeld Referenz-Nr.: 919767SGR Rolle: Operator Sensorproduktion für den GMP-Bereich Industrie: Pharma Arbeitsort: Rotkreuz Pensum: 100% Start: ASAP Dauer: 12++ Should you find yourself suitable for this position then please send us your complete CV using the link in this advert. About us: ITech Consult is a certified ISO 9001:2015 Swiss company with offices also located in Germany and Ireland. ITech Consult is specialised in delivering IT and Life Science candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed.
22/11/2020
Project-based
Operator Sensorproduktion für den GMP-Bereich (m/w/d) - GMP/Reagents/ Produktion/Schicht/Deutsch Projekt: Wir suchen für unseren Kunden Roche Diagnostics AG in Rotkreuz versierte Operator Sensorproduktion für den GmP Bereich (m/w/d) Hintergrund: Die Abteilung BGE Sensor & Reagent Operations ist zuständig für die Produktion von Dickschichtsensoren und der Herstellung von Blutgas Analyse Sensoren unter Reinraumbedingungen. Aufgrund der geplanten Beschaffung zukunftsorientierter Maschinen, nach Industrie 4.0 Standard, wird im Team Unterstützung benötigt. Als motivierter Allrounder mit Faszination für moderne Produktionstechnologien erwartet Sie ein interessantes Arbeitsumfeld zusammen mit einem dynamischen Team, DASS im 3 - Schichtbetrieb arbeitet. Wir suchen eine flexible Persönlichkeit mit guter Auffassungsgabe für ein langfristiges Engagement! Hauptaufgaben: * Bedienen, Einrichten und Beobachten von Halb- und vollautomatischen Maschinen . Störungsbehebung und Wartungsarbeiten an den zugeteilten Anlagen . Produzieren, Protokollieren und Überwachen der einzelnen Prozessschritte nach Industrie 4.0 Standard . Anpassung der Produktionspläne . Erstellen von Dispensierlösungen und Pasten zur Produktion . Durchführen von In-Prozesskontrollen (IPC) . Auffälligkeiten und Abweichungen aufnehmen und gegebenenfalls Massnahmen einleiten . Arbeiten unter Einhaltung der Hygienevorschriften und sicherstellen, DASS die entsprechenden Arbeitsbedingungen gewahrt bleiben . Permanente Optimierung des Arbeitsablaufs zu Qualitäts- und Effizienzsteigerung . SAP geführte Materialverwaltung und Dokumentation (Inventur, Verschrottung, Buchungen) . Bereitschaft nach intensiver Einarbeitung als Springer zu unterstützen . Durchführen der täglichen Reinigungsmassnahmen nach GMP Vorschrift . Einhalten der GMP Richtlichtlinien in allen Arbeitsschritten Must Haves: * Abgeschlossene Berufsausbildung oder mehrjährige Produktionskenntnisse von Vorteil . Selbständiges Arbeiten gewohnt, teamfähig, kreativ und lösungsorientiert . Bereitschaft 3 - Schicht Rotierend (5 Tage Woche) zu arbeiten . Deutsch in Wort und Schrift (C1) erforderlich Nice to Haves: * Roche Erfahrung . Erfahrung mit Diagnostiksystemen . Erfahrung in einem Produktionsumfeld . Erfahrung in einem regulierten Umfeld Referenz-Nr.: 919767SGR Rolle: Operator Sensorproduktion für den GMP-Bereich Industrie: Pharma Arbeitsort: Rotkreuz Pensum: 100% Start: ASAP Dauer: 12++ Should you find yourself suitable for this position then please send us your complete CV using the link in this advert. About us: ITech Consult is a certified ISO 9001:2015 Swiss company with offices also located in Germany and Ireland. ITech Consult is specialised in delivering IT and Life Science candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed.
Change Manager - Techniker/GxP/ Change Management/ISO13485/Deutsch Projekt: Für unseren Kunden, Roche Diagnostics in Rotkreuz suchen wir einen Change Manager. Hintergrund : Die Teams des Production Engineerings sind für die Umsetzung und die Koordination von technischen Änderungsanfragen verantwortlich. Damit Änderungen reibungslos umgesetzt werden können, müssen die einzelnen Schritte der Änderung geplant werden, das Risiko der Änderung abgeschätzt und begründet werden, Tasks den jeweiligen Stakeholdern zugewiesen werden wie auch die Änderung verifiziert/validiert werden. Hauptaufgaben: Change Management: * Verantwortlich für Planung, Koordination und Umsetzung von Änderungen in Absprache mit dem Product Leader und/oder Team Leader . Durchführung von zugewiesenen Abschlussreviews von Änderungen Produkt: * Teilnahme an regelmässigen Planungs-/Statusmeetings in Absprache mit dem Product Leader . Technische Beurteilung von Änderungsanträgen . Technische Beurteilung der Verwendung von Komponenten und Baugruppen bei Transportschäden . Verfügt über vertieftes Wissen von den zugewiesenen Produkten . Erstellung und Pflege von Vorgabe- und Nachweisdokumente zur Produkt Herstellung . Erstellung und Pflege von Arbeitsplänen, Materialstammdaten und Stücklisten . Durchführung von Vorgabe- und Nachweisdokumenten-Trainings zur Produkt Herstellung sowie Erstellung und Koordination vom entsprechenden Trainingsnachweis . Mitarbeit bei der Erstellung und Überarbeitung von technischen Lieferbedingungen . Unterstützung des Technical Supplier Management und der Produktion bei Fehlerbeseitigungs- bzw. Korrekturmassnahmen . Mitarbeit bei der Definierung und Beschaffung oder Änderung von Betriebs- und Hilfsmittel Nebenaufgaben: Qualitätsmanagement: * CAPA Aktivitäten unterstützen und zugewiesene Tasks in der geforderten Qualität und Frist abarbeiten . Trägt für alle ihm übertragenen Aufgaben die Verantwortung der qualitativ korrekten und zielgerichteten Ausführung unter Einhaltung der terminlichen Vorgaben. . Einhaltung der gültigen Regularien, insbesondere hinsichtlich Arbeitssicherheit, GxP und ISO 13485 . Fachliche Prüfung von Verifizierungs-/Validierungsdokumentation . Pflege der Wissensdatenbank Wiki . Teilnahme an regelmässigem Teammeetings KVP/TOPinOPS (Kontinuierlicher Verbesserungsprozess): . Technische Unterstützung von definierten Verbesserungsmassnahmen und Dokumentation im Change Management . Einbringen von Ideen zur Verbesserung von Effizienz, Sicherheit, Ergonomie im gesamten Areitsumfeld . Permanente Optimierung der Arbeitsabläufe und Prozesse zur Qualitäts- und Effizienzsteigerung . Aktive Unterstützung in der Umsetzung von Verbesserungsmassnahmen . Projektmitarbeit gemäss Zuteilung Must Haves: * Mindestens HF Abschluss oder vergleichbare technische Aus/Weiterbildung (z.b. Montagetechniker oder Elektronikausbildung mit Weiterbildung Prozessfachmann und zwingend Office Erfahrung) . Mindestens 2 Jahre Erfahrung im Change Management/Projektmanagement in der Medizinaltechnik . Mindestens 3 Jahre Erfahrung im GMP Umfeld in der Medizinaltechnik (ISO 13458, FDA 21, CFR 820) . Gute Anwenderkenntnisse der gängigen Windows und Google Applikationen . Vertiefte Anwenderkenntnisse im SAP oder vergleichbarem ERP System . Deutsch und Englisch fließend in Wort und Schrift (Dokumentation) . Teamfähig, selbständig und zuverlässig Nice to Haves: . Roche Erfahrung Reference No.: 919741SGR Role: Change Manager Industry: Pharma Location: Rotkreuz Workload: 100% Start: 16.12.2020 Duration: 12++ Should you find yourself suitable for this position then please send us your complete CV using the link in this advert. About us: ITech Consult is a certified ISO 9001:2015 Swiss company with offices also located in Germany and Ireland. ITech Consult is specialised in delivering IT and Life Science candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed.
22/11/2020
Project-based
Change Manager - Techniker/GxP/ Change Management/ISO13485/Deutsch Projekt: Für unseren Kunden, Roche Diagnostics in Rotkreuz suchen wir einen Change Manager. Hintergrund : Die Teams des Production Engineerings sind für die Umsetzung und die Koordination von technischen Änderungsanfragen verantwortlich. Damit Änderungen reibungslos umgesetzt werden können, müssen die einzelnen Schritte der Änderung geplant werden, das Risiko der Änderung abgeschätzt und begründet werden, Tasks den jeweiligen Stakeholdern zugewiesen werden wie auch die Änderung verifiziert/validiert werden. Hauptaufgaben: Change Management: * Verantwortlich für Planung, Koordination und Umsetzung von Änderungen in Absprache mit dem Product Leader und/oder Team Leader . Durchführung von zugewiesenen Abschlussreviews von Änderungen Produkt: * Teilnahme an regelmässigen Planungs-/Statusmeetings in Absprache mit dem Product Leader . Technische Beurteilung von Änderungsanträgen . Technische Beurteilung der Verwendung von Komponenten und Baugruppen bei Transportschäden . Verfügt über vertieftes Wissen von den zugewiesenen Produkten . Erstellung und Pflege von Vorgabe- und Nachweisdokumente zur Produkt Herstellung . Erstellung und Pflege von Arbeitsplänen, Materialstammdaten und Stücklisten . Durchführung von Vorgabe- und Nachweisdokumenten-Trainings zur Produkt Herstellung sowie Erstellung und Koordination vom entsprechenden Trainingsnachweis . Mitarbeit bei der Erstellung und Überarbeitung von technischen Lieferbedingungen . Unterstützung des Technical Supplier Management und der Produktion bei Fehlerbeseitigungs- bzw. Korrekturmassnahmen . Mitarbeit bei der Definierung und Beschaffung oder Änderung von Betriebs- und Hilfsmittel Nebenaufgaben: Qualitätsmanagement: * CAPA Aktivitäten unterstützen und zugewiesene Tasks in der geforderten Qualität und Frist abarbeiten . Trägt für alle ihm übertragenen Aufgaben die Verantwortung der qualitativ korrekten und zielgerichteten Ausführung unter Einhaltung der terminlichen Vorgaben. . Einhaltung der gültigen Regularien, insbesondere hinsichtlich Arbeitssicherheit, GxP und ISO 13485 . Fachliche Prüfung von Verifizierungs-/Validierungsdokumentation . Pflege der Wissensdatenbank Wiki . Teilnahme an regelmässigem Teammeetings KVP/TOPinOPS (Kontinuierlicher Verbesserungsprozess): . Technische Unterstützung von definierten Verbesserungsmassnahmen und Dokumentation im Change Management . Einbringen von Ideen zur Verbesserung von Effizienz, Sicherheit, Ergonomie im gesamten Areitsumfeld . Permanente Optimierung der Arbeitsabläufe und Prozesse zur Qualitäts- und Effizienzsteigerung . Aktive Unterstützung in der Umsetzung von Verbesserungsmassnahmen . Projektmitarbeit gemäss Zuteilung Must Haves: * Mindestens HF Abschluss oder vergleichbare technische Aus/Weiterbildung (z.b. Montagetechniker oder Elektronikausbildung mit Weiterbildung Prozessfachmann und zwingend Office Erfahrung) . Mindestens 2 Jahre Erfahrung im Change Management/Projektmanagement in der Medizinaltechnik . Mindestens 3 Jahre Erfahrung im GMP Umfeld in der Medizinaltechnik (ISO 13458, FDA 21, CFR 820) . Gute Anwenderkenntnisse der gängigen Windows und Google Applikationen . Vertiefte Anwenderkenntnisse im SAP oder vergleichbarem ERP System . Deutsch und Englisch fließend in Wort und Schrift (Dokumentation) . Teamfähig, selbständig und zuverlässig Nice to Haves: . Roche Erfahrung Reference No.: 919741SGR Role: Change Manager Industry: Pharma Location: Rotkreuz Workload: 100% Start: 16.12.2020 Duration: 12++ Should you find yourself suitable for this position then please send us your complete CV using the link in this advert. About us: ITech Consult is a certified ISO 9001:2015 Swiss company with offices also located in Germany and Ireland. ITech Consult is specialised in delivering IT and Life Science candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed.
Huxley Banking & Financial Services
Oxfordshire, United Kingdom
*This is a permanent position* We have a unique opportunity for a Test Engineer to join a world-leader in the design and manufacture of consumer products at their base in Oxfordshire. Reporting to the Head of Engineering, you will be responsible for leading and developing the test function within the engineering department including - technical leadership, resource allocation and providing test verification & validation support to NPD and the wider business on components, systems and full product assemblies. As test engineer you'll be responsible for the following; Develop in-house test facility, equipment and procedures to enable in-house design verification and validation, and performance testing of full product assemblies in accordance with industry requirements. Identifying means for verification of requirements Create and modify technical documentation (eg test processes, procedures and reports). Contribute to design reviews and assist programme reviews Plan and execute test plans Participation in cross-functional teams and support problem solving and corrective action activities to resolve design issues, ATP failures and customer returns/failures. To apply for this role you must have the following experience: Test & development engineering background Some project management/leadership experience Technical background in mechanical engineering would be advantageous Knowledge of design for manufacture and assembly This position would provide a competitive basic salary which is completely dependent on experience level, plus a competitive benefits package. If you would be interested in this opportunity or would like more information then please reply with a copy of your latest CV. To find out more about Huxley Engineering, please visit our website Huxley Engineering, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy
22/11/2020
Full time
*This is a permanent position* We have a unique opportunity for a Test Engineer to join a world-leader in the design and manufacture of consumer products at their base in Oxfordshire. Reporting to the Head of Engineering, you will be responsible for leading and developing the test function within the engineering department including - technical leadership, resource allocation and providing test verification & validation support to NPD and the wider business on components, systems and full product assemblies. As test engineer you'll be responsible for the following; Develop in-house test facility, equipment and procedures to enable in-house design verification and validation, and performance testing of full product assemblies in accordance with industry requirements. Identifying means for verification of requirements Create and modify technical documentation (eg test processes, procedures and reports). Contribute to design reviews and assist programme reviews Plan and execute test plans Participation in cross-functional teams and support problem solving and corrective action activities to resolve design issues, ATP failures and customer returns/failures. To apply for this role you must have the following experience: Test & development engineering background Some project management/leadership experience Technical background in mechanical engineering would be advantageous Knowledge of design for manufacture and assembly This position would provide a competitive basic salary which is completely dependent on experience level, plus a competitive benefits package. If you would be interested in this opportunity or would like more information then please reply with a copy of your latest CV. To find out more about Huxley Engineering, please visit our website Huxley Engineering, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy
Huxley Banking & Financial Services
Oxfordshire, United Kingdom
*This is a permanent position* We have a unique opportunity for a Test Engineer to join a world-leader in the design and manufacture of consumer products at their base in Oxfordshire. Reporting to the Head of Engineering, you will be responsible for leading and developing the test function within the engineering department including - technical leadership, resource allocation and providing test verification & validation support to NPD and the wider business on components, systems and full product assemblies. As test engineer you'll be responsible for the following; Develop in-house test facility, equipment and procedures to enable in-house design verification and validation, and performance testing of full product assemblies in accordance with industry requirements. Identifying means for verification of requirements Create and modify technical documentation (eg test processes, procedures and reports). Contribute to design reviews and assist programme reviews Plan and execute test plans Participation in cross-functional teams and support problem solving and corrective action activities to resolve design issues, ATP failures and customer returns/failures. To apply for this role you must have the following experience: Test & development engineering background Some project management/leadership experience Technical background in mechanical engineering would be advantageous Knowledge of design for manufacture and assembly This position would provide a competitive basic salary which is completely dependent on experience level, plus a competitive benefits package. If you would be interested in this opportunity or would like more information then please reply with a copy of your latest CV. To find out more about Huxley Engineering, please visit our website Huxley Engineering, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy
22/11/2020
Full time
*This is a permanent position* We have a unique opportunity for a Test Engineer to join a world-leader in the design and manufacture of consumer products at their base in Oxfordshire. Reporting to the Head of Engineering, you will be responsible for leading and developing the test function within the engineering department including - technical leadership, resource allocation and providing test verification & validation support to NPD and the wider business on components, systems and full product assemblies. As test engineer you'll be responsible for the following; Develop in-house test facility, equipment and procedures to enable in-house design verification and validation, and performance testing of full product assemblies in accordance with industry requirements. Identifying means for verification of requirements Create and modify technical documentation (eg test processes, procedures and reports). Contribute to design reviews and assist programme reviews Plan and execute test plans Participation in cross-functional teams and support problem solving and corrective action activities to resolve design issues, ATP failures and customer returns/failures. To apply for this role you must have the following experience: Test & development engineering background Some project management/leadership experience Technical background in mechanical engineering would be advantageous Knowledge of design for manufacture and assembly This position would provide a competitive basic salary which is completely dependent on experience level, plus a competitive benefits package. If you would be interested in this opportunity or would like more information then please reply with a copy of your latest CV. To find out more about Huxley Engineering, please visit our website Huxley Engineering, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy
Speditionskaufmann/Zolldeklarant Import (m/w/d) - Speditionskaufmann/Zolldeklarant/ MS Office / SAP /Englisch Projekt: Für unseren Kunden Roche Diagnostics in Rotkreuz, suchen wir einen Speditionskaufmann/Zolldeklarant Import (m/w/d) Hintergrund : Die Import/Export & Customs Abteilung, als Teil von Instrumentation Operations der Roche Diagnostics International AG in Rotkreuz, ist für die Abwicklung eingehender und ausgehender Waren am Standort verantwortlich. Des Weiteren sorgt sie dafür, DASS Gesetze und Richtlinien gegenüber den Behörden eingehalten werden und die internen Compliance Anforderungen sichergestellt sind. Ferner unterstützt das Team interne Stellen bei Import-, Export-, Zoll-, Transport- und Aussenhandelsfragen. Hauptaufgaben Veranlagung von Einfuhrzollanmeldungen im e-dec * Abwicklung von Transitdokumenten im NCTS * Begleitung und Mitwirkung bei Warenkontrollen (Beschau) durch Zollbehörden * Organisation und Überwachung von Verzollungs- und Transportaufträgen * Prüfung und Freigabe von Transport- und Verzollungsdienstleistungen * Korrespondenz und Kommunikation mit Zollbehörden, Lieferanten, Speditionen und internen Stellen * Überwachung und Sicherstellung der internen Richtlinien und Compliance gegenüber Behörden Berufliche Anforderungen: * Abgeschlossene Ausbildung oder adäquate Weiterbildung als Speditionskaufmann/Zolldeklarant * Mindestens 3 Jahre Erfahrung in der Zollabwicklung Schweiz und internationale Spedition * Breites Fachwissen im Speditionswesen und Zollrecht * Sehr gute PC-Kenntnisse (MS Office, SAP von Vorteil) * Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift Persönliche Anforderungen: * Hohes Durchsetzungsvermögen, Kommunikations- und Verhandlungsgeschick . Flexibilität und Freude an teamorientierter Zusammenarbeit . Pflichtbewusste und selbständige Arbeitsweise Reference No.: 919834SGR Role: Speditionskaufmann/Zolldeklarant Import Industry: Pharma Location: Rotkreuz Workload: 100% Start: 04.01.2021 Duration: 12++ Should you find yourself suitable for this position then please send us your complete CV using the link in this advert. About us: ITech Consult is a certified ISO 9001:2015 Swiss company with offices also located in Germany and Ireland. ITech Consult is specialised in delivering IT and Life Science candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed.
22/11/2020
Project-based
Speditionskaufmann/Zolldeklarant Import (m/w/d) - Speditionskaufmann/Zolldeklarant/ MS Office / SAP /Englisch Projekt: Für unseren Kunden Roche Diagnostics in Rotkreuz, suchen wir einen Speditionskaufmann/Zolldeklarant Import (m/w/d) Hintergrund : Die Import/Export & Customs Abteilung, als Teil von Instrumentation Operations der Roche Diagnostics International AG in Rotkreuz, ist für die Abwicklung eingehender und ausgehender Waren am Standort verantwortlich. Des Weiteren sorgt sie dafür, DASS Gesetze und Richtlinien gegenüber den Behörden eingehalten werden und die internen Compliance Anforderungen sichergestellt sind. Ferner unterstützt das Team interne Stellen bei Import-, Export-, Zoll-, Transport- und Aussenhandelsfragen. Hauptaufgaben Veranlagung von Einfuhrzollanmeldungen im e-dec * Abwicklung von Transitdokumenten im NCTS * Begleitung und Mitwirkung bei Warenkontrollen (Beschau) durch Zollbehörden * Organisation und Überwachung von Verzollungs- und Transportaufträgen * Prüfung und Freigabe von Transport- und Verzollungsdienstleistungen * Korrespondenz und Kommunikation mit Zollbehörden, Lieferanten, Speditionen und internen Stellen * Überwachung und Sicherstellung der internen Richtlinien und Compliance gegenüber Behörden Berufliche Anforderungen: * Abgeschlossene Ausbildung oder adäquate Weiterbildung als Speditionskaufmann/Zolldeklarant * Mindestens 3 Jahre Erfahrung in der Zollabwicklung Schweiz und internationale Spedition * Breites Fachwissen im Speditionswesen und Zollrecht * Sehr gute PC-Kenntnisse (MS Office, SAP von Vorteil) * Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift Persönliche Anforderungen: * Hohes Durchsetzungsvermögen, Kommunikations- und Verhandlungsgeschick . Flexibilität und Freude an teamorientierter Zusammenarbeit . Pflichtbewusste und selbständige Arbeitsweise Reference No.: 919834SGR Role: Speditionskaufmann/Zolldeklarant Import Industry: Pharma Location: Rotkreuz Workload: 100% Start: 04.01.2021 Duration: 12++ Should you find yourself suitable for this position then please send us your complete CV using the link in this advert. About us: ITech Consult is a certified ISO 9001:2015 Swiss company with offices also located in Germany and Ireland. ITech Consult is specialised in delivering IT and Life Science candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed.
The Organisation An ambitious VC backed start up seeking to hire a Procurement Manager to build their sourcing strategy and develop relationships with all new/existing manufacturers, suppliers, and co-packers The Role Development of the sourcing strategy for the business - working closely with the Founders and Innovation team Build and manage great relationships with all manufacturers, suppliers and co-packing partners to ensure the brand continues to create world-class products Identify and onboard new manufacturers, suppliers and co-packing partners with a focus on capability and quality Management of negotiations with all partners with a focus on high quality at a good price Work closely with the Innovation/NPD team Work with partners to ensure continuous quality management and improvement Ensuring the brands' innovation is protected The Candidate A degree or master's qualification in Supply Chain, Business or another strategically focused subject is ideal 3-5 years+ experience in hands-on procurement, relationship building and negotiation Experience of working with 3rd party manufacturers, suppliers and copackers wthin the FMCG industry is a must Experience with IP contract development is a must An understanding of pricing and costing strategies within manufacturing Able to work at a strategic level but also happy to get their hands dirty in a fast-growth startup environment
22/11/2020
Full time
The Organisation An ambitious VC backed start up seeking to hire a Procurement Manager to build their sourcing strategy and develop relationships with all new/existing manufacturers, suppliers, and co-packers The Role Development of the sourcing strategy for the business - working closely with the Founders and Innovation team Build and manage great relationships with all manufacturers, suppliers and co-packing partners to ensure the brand continues to create world-class products Identify and onboard new manufacturers, suppliers and co-packing partners with a focus on capability and quality Management of negotiations with all partners with a focus on high quality at a good price Work closely with the Innovation/NPD team Work with partners to ensure continuous quality management and improvement Ensuring the brands' innovation is protected The Candidate A degree or master's qualification in Supply Chain, Business or another strategically focused subject is ideal 3-5 years+ experience in hands-on procurement, relationship building and negotiation Experience of working with 3rd party manufacturers, suppliers and copackers wthin the FMCG industry is a must Experience with IP contract development is a must An understanding of pricing and costing strategies within manufacturing Able to work at a strategic level but also happy to get their hands dirty in a fast-growth startup environment
Daca doresti sa lucrezi intr-un mediu de lucru placut cu posibilitatea de dezvoltare, te asteptam alaturi de noi! Angajam pizzer program full time! Va rugam sa ne trimiteti CV-ul dumneavoastra pe adresa de email sau sa ne contactati la numarul de telefon 0722546868
18/09/2020
Full time
Daca doresti sa lucrezi intr-un mediu de lucru placut cu posibilitatea de dezvoltare, te asteptam alaturi de noi! Angajam pizzer program full time! Va rugam sa ne trimiteti CV-ul dumneavoastra pe adresa de email sau sa ne contactati la numarul de telefon 0722546868
Job role: Automation/Manufacturing Engineer (PLC/Scada experience) Location: Cork, Ireland Job type: Permanent Key responsibilities: Support design, buy-off, installation and validation of automated production lines. Process Characterization/Optimization (DFMEA's, PFMEA's DOE's etc.). Testing of control panels and automation systems including FAT and SAT Lead systematic technical root cause investigations. Support production line ramp to achieve mature production targets. Drive continuous improvement projects. Manage assigned project budgets; liaise with Customers, contractors as required. Support technical training. Support all company safety and quality programs and initiatives. Ensure ongoing compliance with GMP in all practices, recording of events and processes. Ensure compliance with all learnings from all GMP training events. Other responsibilities may be assigned from time to time as needed, based on the evolution of the company and the requirements of the department/position. The ideal candidate will have: 3-6 years' experience in a manufacturing environment (high volume automated assembly experience would be an advantage as would medical device manufacturing experience). Travel as necessary to support equipment buy-offs and training at vendor/customer sites. Level 7 bachelor's degree in one of the following Software/Automation/Electrical/Electronic/Mechatronic Engineering. PLC Programming/Debugging Previous experience with PLC bus systems (Profinet/Profibus/CAN bus/Modbus etc, working with Allen Bradley, Siemens, ABB) PC Hardware/Programming (Visual Basic, vision system, etc) Vision Systems development (preferably Cognex Vision systems) Experience and good understanding of IP industrial networking and system communications. SCADA systems application/development Along with: Ability to work in a team environment Excellent organization, communication, computer and presentation skills Systematic troubleshooting skills Strong leadership of technical issue resolution Lean Six Sigma skills an advantage Provide innovative solutions to complex problems Good data analysis skills. Proficient in MS Office applications, MS Project CAD experience desirable.
25/06/2020
Full time
Job role: Automation/Manufacturing Engineer (PLC/Scada experience) Location: Cork, Ireland Job type: Permanent Key responsibilities: Support design, buy-off, installation and validation of automated production lines. Process Characterization/Optimization (DFMEA's, PFMEA's DOE's etc.). Testing of control panels and automation systems including FAT and SAT Lead systematic technical root cause investigations. Support production line ramp to achieve mature production targets. Drive continuous improvement projects. Manage assigned project budgets; liaise with Customers, contractors as required. Support technical training. Support all company safety and quality programs and initiatives. Ensure ongoing compliance with GMP in all practices, recording of events and processes. Ensure compliance with all learnings from all GMP training events. Other responsibilities may be assigned from time to time as needed, based on the evolution of the company and the requirements of the department/position. The ideal candidate will have: 3-6 years' experience in a manufacturing environment (high volume automated assembly experience would be an advantage as would medical device manufacturing experience). Travel as necessary to support equipment buy-offs and training at vendor/customer sites. Level 7 bachelor's degree in one of the following Software/Automation/Electrical/Electronic/Mechatronic Engineering. PLC Programming/Debugging Previous experience with PLC bus systems (Profinet/Profibus/CAN bus/Modbus etc, working with Allen Bradley, Siemens, ABB) PC Hardware/Programming (Visual Basic, vision system, etc) Vision Systems development (preferably Cognex Vision systems) Experience and good understanding of IP industrial networking and system communications. SCADA systems application/development Along with: Ability to work in a team environment Excellent organization, communication, computer and presentation skills Systematic troubleshooting skills Strong leadership of technical issue resolution Lean Six Sigma skills an advantage Provide innovative solutions to complex problems Good data analysis skills. Proficient in MS Office applications, MS Project CAD experience desirable.
Patrician Training srl
23 August, Constanța County, România
Fabrica de peste si fructe de mare cauta echipa pentru curatare, eviscerare, congelare si ambalare.
Locatie : 23 August, jud. Constanta Program : 7:30-16:30 Salariu + bonusuri + decontare transport
punem la dispozitie si cazare
25/06/2020
Full time
Fabrica de peste si fructe de mare cauta echipa pentru curatare, eviscerare, congelare si ambalare.
Locatie : 23 August, jud. Constanta Program : 7:30-16:30 Salariu + bonusuri + decontare transport
punem la dispozitie si cazare
DORN COLOR, west-side color card manufacturer has an immediate need for a Print Manager. Primary role is to effectively manage the pre-press and press departments for continuous improvement of productivity and quality while building a strong team that aligns with Dorn's cultural values. Preferred Experience : Knowledge and experience with multicolor offset printing process/industry. Source, negotiate, purchase, coordinate and expedite print, printing paper, and other outside materials for all color projects. Ability to lead and develop the graphic services and print team. Insure that Graphic Services is effectively integrated with Project Management and meeting the scheduling needs for the overall manufacturing process. Maintain a clean, organized and safe work area. Proficient with MS Excel and Word. Experience with InDesign, Photoshop, Illustrator and Fiji XMF software is a plus. Qualified candidates should send resume to Tom in Human Resources at (see below)
20/06/2020
Full time
DORN COLOR, west-side color card manufacturer has an immediate need for a Print Manager. Primary role is to effectively manage the pre-press and press departments for continuous improvement of productivity and quality while building a strong team that aligns with Dorn's cultural values. Preferred Experience : Knowledge and experience with multicolor offset printing process/industry. Source, negotiate, purchase, coordinate and expedite print, printing paper, and other outside materials for all color projects. Ability to lead and develop the graphic services and print team. Insure that Graphic Services is effectively integrated with Project Management and meeting the scheduling needs for the overall manufacturing process. Maintain a clean, organized and safe work area. Proficient with MS Excel and Word. Experience with InDesign, Photoshop, Illustrator and Fiji XMF software is a plus. Qualified candidates should send resume to Tom in Human Resources at (see below)
GRAPHIC SERVICES MANAGER DORN COLOR, westside color card manufacturer has an immediate need for a Graphic Services Manager. Primary role is to effectively manage the pre-press and press departments for continuous improvement of productivity and quality while building a strong team that aligns with Dorn's cultural values. Preferred Experience : Knowledge of multicolor offset printing process/industry. Source, negotiate, purchase, coordinate and expedite print, printing paper, and other outside materials for all color projects. Ability to lead and develop the graphic services and print team. Insure that Graphic Services is effectively integrated with Project Management and meeting the scheduling needs for the overall manufacturing process. Maintain a clean, organized and safe work area. InDesign, Photoshop, Illustrator, Excel and Word. Fiji XMF is a plus. Qualified candidates should send resume to Tom in Human Resources at (see below)
20/06/2020
Full time
GRAPHIC SERVICES MANAGER DORN COLOR, westside color card manufacturer has an immediate need for a Graphic Services Manager. Primary role is to effectively manage the pre-press and press departments for continuous improvement of productivity and quality while building a strong team that aligns with Dorn's cultural values. Preferred Experience : Knowledge of multicolor offset printing process/industry. Source, negotiate, purchase, coordinate and expedite print, printing paper, and other outside materials for all color projects. Ability to lead and develop the graphic services and print team. Insure that Graphic Services is effectively integrated with Project Management and meeting the scheduling needs for the overall manufacturing process. Maintain a clean, organized and safe work area. InDesign, Photoshop, Illustrator, Excel and Word. Fiji XMF is a plus. Qualified candidates should send resume to Tom in Human Resources at (see below)
The ECS Group Limited
Loughborough, Leicestershire, United Kingdom
I have an exciting opportunity to work for a global manufacturing company as a Site services Leader on site in Loughborough. If you have an excellent eye for detail, fantastic communication skills and a strong background in handling legal documentation, managing various service providers (pest control, canteen services, waste management) then this could be the perfect opportunity for to take your career to the next level. Key Responsibilities * Responsibility and coordination of all the legal Document processes and files * Coordination of all site training management process and SOP Management process * Scheduling insurance inspections * Monitoring the site CAPA scorecard * Managing and maintaining the contracts of waste management, pest control and catering service providers Experience & Qualification required * Workplace legislation (eg Asbestos, legionella, pressure systems, LOLER etc) * Experience in a GMP and Engineering environment * Facility management and contractor control * Health and safety stands * Engineering and manufacturing standards ECS Recruitment Group Ltd is acting as an Employment Agency in relation to this vacancy.
19/06/2020
Full time
I have an exciting opportunity to work for a global manufacturing company as a Site services Leader on site in Loughborough. If you have an excellent eye for detail, fantastic communication skills and a strong background in handling legal documentation, managing various service providers (pest control, canteen services, waste management) then this could be the perfect opportunity for to take your career to the next level. Key Responsibilities * Responsibility and coordination of all the legal Document processes and files * Coordination of all site training management process and SOP Management process * Scheduling insurance inspections * Monitoring the site CAPA scorecard * Managing and maintaining the contracts of waste management, pest control and catering service providers Experience & Qualification required * Workplace legislation (eg Asbestos, legionella, pressure systems, LOLER etc) * Experience in a GMP and Engineering environment * Facility management and contractor control * Health and safety stands * Engineering and manufacturing standards ECS Recruitment Group Ltd is acting as an Employment Agency in relation to this vacancy.
