Computer Futures - London & S.E(Permanent and Contract)
Swindon, Wiltshire
Position: Contract Manufacturing Engineer Location: Swindon - onsite Duration: 3 months - possibility for extension Start Date: February Rate: up to £55ph Inside IR35 - negotiable dependent upon experience Our client is a leading innovator in advanced manufacturing, dedicated to creating high-quality, reliable products within a highly regulated industry. Their commitment to excellence and innovation has established us as a trusted name in the industry. Project Overview: You will play a pivotal role in the scoping, implementation, and integration of worker guidance systems, including smart torque tooling, within our production cells. Your work will ensure ergonomic and efficient use by operators, ultimately enhancing our manufacturing processes. Key Responsibilities: * Scope all equipment required for the worker guidance systems across the entire manufacturing shop floor. * Develop comprehensive business cases for the proposed systems. * Create detailed process plans for the implementation of worker guidance systems. * Install pre-purchased worker guidance systems, including smart tooling. * Contribute to other continuous improvement projects. Essential Skills/Experience: * Proven experience in creating detailed work instructions. * Hands-on experience with smart torque tooling. * Background in Process, Industrial, or Manufacturing Engineering. Desirable Skills: * Experience with worker guidance systems. * Ability to program smart torque tooling. Why Join Us? * Be a part of an innovative team committed to excellence. * Work on exciting projects with cutting-edge technology. * Opportunity to contribute to significant continuous improvement initiatives. If you have the expertise and passion to drive manufacturing excellence, we want to hear from you. Apply Today! To find out more about SThree, please visit our website SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom| Partnership Number | OC387148 England and Wales
21/01/2025
Project-based
Position: Contract Manufacturing Engineer Location: Swindon - onsite Duration: 3 months - possibility for extension Start Date: February Rate: up to £55ph Inside IR35 - negotiable dependent upon experience Our client is a leading innovator in advanced manufacturing, dedicated to creating high-quality, reliable products within a highly regulated industry. Their commitment to excellence and innovation has established us as a trusted name in the industry. Project Overview: You will play a pivotal role in the scoping, implementation, and integration of worker guidance systems, including smart torque tooling, within our production cells. Your work will ensure ergonomic and efficient use by operators, ultimately enhancing our manufacturing processes. Key Responsibilities: * Scope all equipment required for the worker guidance systems across the entire manufacturing shop floor. * Develop comprehensive business cases for the proposed systems. * Create detailed process plans for the implementation of worker guidance systems. * Install pre-purchased worker guidance systems, including smart tooling. * Contribute to other continuous improvement projects. Essential Skills/Experience: * Proven experience in creating detailed work instructions. * Hands-on experience with smart torque tooling. * Background in Process, Industrial, or Manufacturing Engineering. Desirable Skills: * Experience with worker guidance systems. * Ability to program smart torque tooling. Why Join Us? * Be a part of an innovative team committed to excellence. * Work on exciting projects with cutting-edge technology. * Opportunity to contribute to significant continuous improvement initiatives. If you have the expertise and passion to drive manufacturing excellence, we want to hear from you. Apply Today! To find out more about SThree, please visit our website SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom| Partnership Number | OC387148 England and Wales
Process Engineer - Plymouth We are seeking an experienced Process Engineer to join a highly technical and fast-paced manufacturing environment. This role is ideal for a hands-on professional with strong problem-solving skills and a passion for driving continuous improvement in production processes. Key Responsibilities Investigate and resolve production losses related to breakdowns, waste, and speed. Implement basic maintenance processes for designated product lines. Drive center-lining activities to sustain optimal line performance. Lead quality improvement initiatives to align with company metrics. Requirements HNC or Degree in Engineering, Mechatronics, or a similar field. 5+ years of technical or manufacturing experience, preferably with high-speed automated assembly and packaging equipment. Strong troubleshooting and problem-solving abilities. If you have the skills and experience to excel in this role, we'd love to hear from you. Click Apply Today! This is an equal opportunity role, and we welcome applications from all qualified candidates.
21/01/2025
Full time
Process Engineer - Plymouth We are seeking an experienced Process Engineer to join a highly technical and fast-paced manufacturing environment. This role is ideal for a hands-on professional with strong problem-solving skills and a passion for driving continuous improvement in production processes. Key Responsibilities Investigate and resolve production losses related to breakdowns, waste, and speed. Implement basic maintenance processes for designated product lines. Drive center-lining activities to sustain optimal line performance. Lead quality improvement initiatives to align with company metrics. Requirements HNC or Degree in Engineering, Mechatronics, or a similar field. 5+ years of technical or manufacturing experience, preferably with high-speed automated assembly and packaging equipment. Strong troubleshooting and problem-solving abilities. If you have the skills and experience to excel in this role, we'd love to hear from you. Click Apply Today! This is an equal opportunity role, and we welcome applications from all qualified candidates.
Manufacturing Project & Improvement Manager vacancy for a globally operating Zurich based company in the pharmaceutical sector . Description: The Process Support/Business Analyst will play a crucial role in supporting the CAPEX Operational Readiness project. This role involves collaborating with various stakeholders, including engineering partners, validation, and maintenance teams, to ensure the successful integration of systems and processes. The analyst will be responsible for documenting requirements, analysing data, and providing insights to drive project milestones. Key responsibilities include: Your experience/knowledge: . Supporting the project lead and integration leads in achieving project milestones . Facilitating communication between project teams to ensure seamless knowledge transfer . Analyzing project data to identify inefficiencies and propose improvements . Ensuring alignment of stakeholder expectations and project objectives . Coordinating with external project support to ensure timely completion of tasks Knowledge The ideal candidate should possess the following knowledge and skills: . Strong understanding of engineering design tools (Autodesk CC, Aveva, etc.) . Experience in project management and process improvement methodologies . Excellent documentation and data analysis skills . Knowledge of standardization practices for data exchange (eg, DEXPI) . Strong problem-solving skills and attention to detail . Proficiency in using project management tools and software . Good knowledge of CAE tools (preferably COMOS) . Knowledge of SAP maintenance structure . Excellent communication skills (English) Your soft skills: Analytical spirit and sense of detail Able to manage priorities in fast paced environment Strength of proposal and able to challenge the status quo Flexibility and agility Autonomy and ability to take initiatives in line with the site priorities Proactivity in personal development Location: Zurich, Switzerland Sector: Pharmaceutical Start: 01/03/2025 Duration: 12 MM+ Ref .Nr.: BH22518 Take the next step and send us your resume along with a daytime phone number where we can reach you. Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens as well as current work-permit holders for Switzerland. Ukrainian refugees are warmly welcomed, we will support you all the way. We welcome applications from individuals of all genders, age groups, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. Therefore, there is no requirement to provide gender information or a photo in your application. As per client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore potential solutions with our end client.
20/01/2025
Project-based
Manufacturing Project & Improvement Manager vacancy for a globally operating Zurich based company in the pharmaceutical sector . Description: The Process Support/Business Analyst will play a crucial role in supporting the CAPEX Operational Readiness project. This role involves collaborating with various stakeholders, including engineering partners, validation, and maintenance teams, to ensure the successful integration of systems and processes. The analyst will be responsible for documenting requirements, analysing data, and providing insights to drive project milestones. Key responsibilities include: Your experience/knowledge: . Supporting the project lead and integration leads in achieving project milestones . Facilitating communication between project teams to ensure seamless knowledge transfer . Analyzing project data to identify inefficiencies and propose improvements . Ensuring alignment of stakeholder expectations and project objectives . Coordinating with external project support to ensure timely completion of tasks Knowledge The ideal candidate should possess the following knowledge and skills: . Strong understanding of engineering design tools (Autodesk CC, Aveva, etc.) . Experience in project management and process improvement methodologies . Excellent documentation and data analysis skills . Knowledge of standardization practices for data exchange (eg, DEXPI) . Strong problem-solving skills and attention to detail . Proficiency in using project management tools and software . Good knowledge of CAE tools (preferably COMOS) . Knowledge of SAP maintenance structure . Excellent communication skills (English) Your soft skills: Analytical spirit and sense of detail Able to manage priorities in fast paced environment Strength of proposal and able to challenge the status quo Flexibility and agility Autonomy and ability to take initiatives in line with the site priorities Proactivity in personal development Location: Zurich, Switzerland Sector: Pharmaceutical Start: 01/03/2025 Duration: 12 MM+ Ref .Nr.: BH22518 Take the next step and send us your resume along with a daytime phone number where we can reach you. Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens as well as current work-permit holders for Switzerland. Ukrainian refugees are warmly welcomed, we will support you all the way. We welcome applications from individuals of all genders, age groups, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. Therefore, there is no requirement to provide gender information or a photo in your application. As per client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore potential solutions with our end client.
ECS Resource Group Limited
Skelmersdale, Lancashire
Electrical Maintenance Technician Permanent Salary Range: Up to £45,140 including shift allowance Location: Skelmersdale I am working with one of the world's largest and most well known & respected manufacturing companies with a fantastic reputation globally for innovation and quality. They have an exciting opportunity to join their team in Skelmersdale as Maintenance Technician on a full time, permanent basis Responsibilities Tracking and reporting of process improvement results Improving the overall reliability and performance of plant, personnel and production equipment and processes Ensuring production targets are met, optimising output & minimising defects Providing production line support in line with company goals and objectives Preventive maintenance Equipment breakdown repairs Establishing process conditions In-line quality checks Process monitoring and controlling according to Statistical Process Control (SPC) method Analysing data to fault find and developing prioritised improvement plans for the platform Maintaining and developing the delivery of finished products in line with cost, quality and production schedule requirements Prioritizing and promoting Health and Safety awareness Training and mentoring staff in an approachable and constructive manner Fostering and developing excellent relationships with key business stakeholders Gathering & sharing best practice, both within the business and world class manufacturing sites Experience Required First accomplished technical production support experience. Electrical, mechanical, pneumatic, servo controls PLC fault finding (Omron preferred) Experience of robotics (ABB preferred), including experience of automated assembly production lines Experience of vision systems Ability to read electrical/mechanical drawings Ability to follow SOP's and training processes Ability and willingness to work a night shift if required Qualifications Electrical - 18th Edition ECS Recruitment Group Ltd is acting as an Employment Agency in relation to this vacancy.
20/01/2025
Full time
Electrical Maintenance Technician Permanent Salary Range: Up to £45,140 including shift allowance Location: Skelmersdale I am working with one of the world's largest and most well known & respected manufacturing companies with a fantastic reputation globally for innovation and quality. They have an exciting opportunity to join their team in Skelmersdale as Maintenance Technician on a full time, permanent basis Responsibilities Tracking and reporting of process improvement results Improving the overall reliability and performance of plant, personnel and production equipment and processes Ensuring production targets are met, optimising output & minimising defects Providing production line support in line with company goals and objectives Preventive maintenance Equipment breakdown repairs Establishing process conditions In-line quality checks Process monitoring and controlling according to Statistical Process Control (SPC) method Analysing data to fault find and developing prioritised improvement plans for the platform Maintaining and developing the delivery of finished products in line with cost, quality and production schedule requirements Prioritizing and promoting Health and Safety awareness Training and mentoring staff in an approachable and constructive manner Fostering and developing excellent relationships with key business stakeholders Gathering & sharing best practice, both within the business and world class manufacturing sites Experience Required First accomplished technical production support experience. Electrical, mechanical, pneumatic, servo controls PLC fault finding (Omron preferred) Experience of robotics (ABB preferred), including experience of automated assembly production lines Experience of vision systems Ability to read electrical/mechanical drawings Ability to follow SOP's and training processes Ability and willingness to work a night shift if required Qualifications Electrical - 18th Edition ECS Recruitment Group Ltd is acting as an Employment Agency in relation to this vacancy.
Produktionsexperte an der Fertigspritzenlinie (m/w/d) - GMP / Produktion / Schichtmodell/Pharma /Deutsch Projekt: Für unseren Kunden, ein grosses Pharmaunternehmen mit Sitz in Kaiseraugst suchen wir einen Produktionsexperte an der Fertigspritzenlinie (m/w/d) Hintergrund: Der moderne Produktionsbetrieb für Parenteralia in Kaiseraugst (PKau) ist verantwortlich für die Herstellung steriler Arzneimittel und beliefert den Markt mit biopharmazeutischen Arzneimittelprodukten. Unter Einhaltung von GMP-Vorschriften werden an der Fertigspritzen-Linie vorgefertigte Lösungen aseptisch in einem Isolator abgefüllt und anschliessend in-line mittels einer automatischen Inspektionsmaschine optisch kontrolliert. Die Linie arbeitet fünf Tage die Woche im Dreischichtbetrieb. Der oder die perfekte Kandidat:in hat eine Ausbildung in der Produktion in der Pharmabranche innerhalb eines GMP-Umfeldes, mind. 2 Jahre Berufserfahrung im Produktionsumfeld und idealerweise Erfahrungen in der Herstellung steriler Arzneimittel. Hauptaufgaben und Verantwortungsbereiche: Identifikation und Abrechnung von Materialien In Prozess - Kontrollen, Funktionskontrollen und Musterzüge Sicherstellung der Verfügbarkeit von Formatteilen, Packmitteln und Verbrauchsmaterialien am Einsatzort (GMP, Qualität, Sicherheit) Bearbeitung von Produktionsaufträgen Bedienen der Produktions- und Inspektionsanlagen und der dazugehörenden EDV Systeme Bestücken der Produktions- und Inspektionsanlagen mit Material Ausräumen und Reinigung der Produktions- und Inspektionsanlagen Entsorgen des Abfalls an den Produktions- und Inspektionsanlagen Koordinieren und Durchführung der Umrüstaktivitäten in Zusammenarbeit mit der Technik Korrekte und zeitgerechte Dokumentation gem. gültiger GMP Vorschriften Melden von fehlerhaften Zuständen bei verwendetem Equipment oder Materialien Unterstützung bei der Störungsbehebung, Instandhaltung sowie Meldung an Support bei Störungen Must Haves: Abgeschlossene Berufsausbildung im Pharmaumfeld oder Ausbildung mit zusätzlicher relevanter Arbeitserfahrung Mind. 2-3 Berufserfahrung im Produktionsumfeld in der Anlagenbedienung, vorzugsweise in der Pharmabranche Erfahrung im GMP-Umfeld Gute EDV-Kenntnisse mit gängigen Programmen (Microsoft Office, G-Suite) Sehr gute Deutschkenntnisse in Wort und Schrift Gutes technisches Verständnis im Umgang mit Produktionsanlagen und Freude an praktischen Arbeiten Bereitschaft im 5-Schichtmodus zu arbeiten (24 7) Selbständigkeit als auch ein hohes Maß an Teamfähigkeit Qualitätsbewusstsein, Flexibilität Nice to have: Erfahrung in der Herstellung steriler Arzneimittel Referenz Nr.: 923949TP Rolle: Produktionsexperte an der Fertigspritzenlinie (m/w/d) Industrie: Pharma Arbeitsort: Kaiseraugst Pensum: 100% Start: 01.03.2025 Dauer: 12 Bewerbungsfrist : 24.01.2025 Sollte diese Position Ihr Interesse geweckt haben, senden Sie uns bitte Ihr komplettes Dossier zu. Über uns : ITech Consult ist ein nach ISO 9001:2015 zertifiziertes Schweizer Unternehmen mit Niederlassungen in Deutschland und Irland. ITech Consult ist spezialisiert auf die Vermittlung von hochqualifizierten Kandidaten für den Personalverleih in den Bereichen, IT, Life Science & Engineering. Wir bieten Personalverleih & Payroll Dienstleistungen an. Für unsere Kandidaten ist dies kostenlos, auch bei Payroll berechnen wir Ihnen keine zusätzlichen Geb
20/01/2025
Project-based
Produktionsexperte an der Fertigspritzenlinie (m/w/d) - GMP / Produktion / Schichtmodell/Pharma /Deutsch Projekt: Für unseren Kunden, ein grosses Pharmaunternehmen mit Sitz in Kaiseraugst suchen wir einen Produktionsexperte an der Fertigspritzenlinie (m/w/d) Hintergrund: Der moderne Produktionsbetrieb für Parenteralia in Kaiseraugst (PKau) ist verantwortlich für die Herstellung steriler Arzneimittel und beliefert den Markt mit biopharmazeutischen Arzneimittelprodukten. Unter Einhaltung von GMP-Vorschriften werden an der Fertigspritzen-Linie vorgefertigte Lösungen aseptisch in einem Isolator abgefüllt und anschliessend in-line mittels einer automatischen Inspektionsmaschine optisch kontrolliert. Die Linie arbeitet fünf Tage die Woche im Dreischichtbetrieb. Der oder die perfekte Kandidat:in hat eine Ausbildung in der Produktion in der Pharmabranche innerhalb eines GMP-Umfeldes, mind. 2 Jahre Berufserfahrung im Produktionsumfeld und idealerweise Erfahrungen in der Herstellung steriler Arzneimittel. Hauptaufgaben und Verantwortungsbereiche: Identifikation und Abrechnung von Materialien In Prozess - Kontrollen, Funktionskontrollen und Musterzüge Sicherstellung der Verfügbarkeit von Formatteilen, Packmitteln und Verbrauchsmaterialien am Einsatzort (GMP, Qualität, Sicherheit) Bearbeitung von Produktionsaufträgen Bedienen der Produktions- und Inspektionsanlagen und der dazugehörenden EDV Systeme Bestücken der Produktions- und Inspektionsanlagen mit Material Ausräumen und Reinigung der Produktions- und Inspektionsanlagen Entsorgen des Abfalls an den Produktions- und Inspektionsanlagen Koordinieren und Durchführung der Umrüstaktivitäten in Zusammenarbeit mit der Technik Korrekte und zeitgerechte Dokumentation gem. gültiger GMP Vorschriften Melden von fehlerhaften Zuständen bei verwendetem Equipment oder Materialien Unterstützung bei der Störungsbehebung, Instandhaltung sowie Meldung an Support bei Störungen Must Haves: Abgeschlossene Berufsausbildung im Pharmaumfeld oder Ausbildung mit zusätzlicher relevanter Arbeitserfahrung Mind. 2-3 Berufserfahrung im Produktionsumfeld in der Anlagenbedienung, vorzugsweise in der Pharmabranche Erfahrung im GMP-Umfeld Gute EDV-Kenntnisse mit gängigen Programmen (Microsoft Office, G-Suite) Sehr gute Deutschkenntnisse in Wort und Schrift Gutes technisches Verständnis im Umgang mit Produktionsanlagen und Freude an praktischen Arbeiten Bereitschaft im 5-Schichtmodus zu arbeiten (24 7) Selbständigkeit als auch ein hohes Maß an Teamfähigkeit Qualitätsbewusstsein, Flexibilität Nice to have: Erfahrung in der Herstellung steriler Arzneimittel Referenz Nr.: 923949TP Rolle: Produktionsexperte an der Fertigspritzenlinie (m/w/d) Industrie: Pharma Arbeitsort: Kaiseraugst Pensum: 100% Start: 01.03.2025 Dauer: 12 Bewerbungsfrist : 24.01.2025 Sollte diese Position Ihr Interesse geweckt haben, senden Sie uns bitte Ihr komplettes Dossier zu. Über uns : ITech Consult ist ein nach ISO 9001:2015 zertifiziertes Schweizer Unternehmen mit Niederlassungen in Deutschland und Irland. ITech Consult ist spezialisiert auf die Vermittlung von hochqualifizierten Kandidaten für den Personalverleih in den Bereichen, IT, Life Science & Engineering. Wir bieten Personalverleih & Payroll Dienstleistungen an. Für unsere Kandidaten ist dies kostenlos, auch bei Payroll berechnen wir Ihnen keine zusätzlichen Geb
Manufacturing Engineer - Pharma vacancy for a globally operating Neuchatel based company in the pharmaceutical sector . Description: Within the Manufacturing department, reporting to Deviation Manager, the primary mission for the Manufacturing Engineer is to support the manufacturing operations to meet their goals in terms of quality and productivity. He/she specifically provides technical expertise needed to investigate deviations related to the manufacturing process and acts as a catalyst for continuous improvement. Main responsibilities are problem solving, creation of added value, standardization and improvement of manufacturing processes. Your tasks: While this is a day-time job, must be able to work on occasions in controlled environments requiring special gowning. Will be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet and body Lean/Six Sigma Certification(s) highly desirable Manufacturing Engineer may be requested to manage deviation and provide technical expertise on subjects out of his/her own field of expertise to back-up Manufacturing Engineers from other sub-groups (PUT) Deviation management Initiate and manage deviations within the framework of production events and within quality systems in a timely manner Perform evaluations related to impact on concerned equipment/product/material with the support of relevant Subject Matter Experts (SME) Perform investigations of low, moderate and high complexity/severity using root cause analysis tools (eg DMAIC, Is/Is Not, Cause & Effect Diagram, 5M, Contradiction Matrix, etc.) Lead multi-disciplinary investigation teams and associated workshops as appropriate Perform interview in the frame of deviation related to human factors Collect/compile data and write investigation summary reports Define robust corrective and preventive actions Identify relevant criteria to monitor efficacy of CAPA and ensure follow-up until closure of the record Technical expertise on manufacturing processes relevant to sub-group (PUT) Your experience/knowledge: Bachelor/Master in Engineering and 3-5 years of experience within a biotech/pharmaceutical manufacturing environment (Process Operations or Quality) Technical knowledge of the biotechnological processes (USP and/or DSP) Ideally demonstrated experience in "deviation" management including use of Six Sigma tools (eg DMAIC, Is/Is Not, Cause & Effect Diagram, 5M, Contradiction Matrix, etc.) Experience of Quality/Compliance requirements within cGMP manufacturing environment Experience in computerized/automated/QMS systems (ex: Trackwise, ERP, Veeva Vault) Master MS Office suite (Word, Excel, PowerPoint, Visio) MiniTab or other statistics software is a plus Proficiency in a cGMP environment Strong knowledge in detailed manufacturing operations (eg engineering designs, automated documentation) and biotechnological processes (USP, DSP and/or FF). Experience in "deviation" management including use of Six Sigma tools Ability to think and act cross-functionally, interacting with various SME Written and oral proficiency in French and English Your soft skills: Analytical spirit and sense of detail Able to manage priorities in fast paced environment Strength of proposal and able to challenge the status quo Flexibility and agility Autonomy and ability to take initiatives in line with the site priorities Proactivity in personal development Location: Neuchatel, Switzerland Sector: Pharmaceutical Start: 02/2025 Duration: 05MM+ Ref .Nr.: BH22512 Take the next step and send us your resume along with a daytime phone number where we can reach you. Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens as well as current work-permit holders for Switzerland. Ukrainian refugees are warmly welcomed, we will support you all the way. We welcome applications from individuals of all genders, age groups, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. Therefore, there is no requirement to provide gender information or a photo in your application. As per client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore potential solutions with our end client.
17/01/2025
Project-based
Manufacturing Engineer - Pharma vacancy for a globally operating Neuchatel based company in the pharmaceutical sector . Description: Within the Manufacturing department, reporting to Deviation Manager, the primary mission for the Manufacturing Engineer is to support the manufacturing operations to meet their goals in terms of quality and productivity. He/she specifically provides technical expertise needed to investigate deviations related to the manufacturing process and acts as a catalyst for continuous improvement. Main responsibilities are problem solving, creation of added value, standardization and improvement of manufacturing processes. Your tasks: While this is a day-time job, must be able to work on occasions in controlled environments requiring special gowning. Will be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet and body Lean/Six Sigma Certification(s) highly desirable Manufacturing Engineer may be requested to manage deviation and provide technical expertise on subjects out of his/her own field of expertise to back-up Manufacturing Engineers from other sub-groups (PUT) Deviation management Initiate and manage deviations within the framework of production events and within quality systems in a timely manner Perform evaluations related to impact on concerned equipment/product/material with the support of relevant Subject Matter Experts (SME) Perform investigations of low, moderate and high complexity/severity using root cause analysis tools (eg DMAIC, Is/Is Not, Cause & Effect Diagram, 5M, Contradiction Matrix, etc.) Lead multi-disciplinary investigation teams and associated workshops as appropriate Perform interview in the frame of deviation related to human factors Collect/compile data and write investigation summary reports Define robust corrective and preventive actions Identify relevant criteria to monitor efficacy of CAPA and ensure follow-up until closure of the record Technical expertise on manufacturing processes relevant to sub-group (PUT) Your experience/knowledge: Bachelor/Master in Engineering and 3-5 years of experience within a biotech/pharmaceutical manufacturing environment (Process Operations or Quality) Technical knowledge of the biotechnological processes (USP and/or DSP) Ideally demonstrated experience in "deviation" management including use of Six Sigma tools (eg DMAIC, Is/Is Not, Cause & Effect Diagram, 5M, Contradiction Matrix, etc.) Experience of Quality/Compliance requirements within cGMP manufacturing environment Experience in computerized/automated/QMS systems (ex: Trackwise, ERP, Veeva Vault) Master MS Office suite (Word, Excel, PowerPoint, Visio) MiniTab or other statistics software is a plus Proficiency in a cGMP environment Strong knowledge in detailed manufacturing operations (eg engineering designs, automated documentation) and biotechnological processes (USP, DSP and/or FF). Experience in "deviation" management including use of Six Sigma tools Ability to think and act cross-functionally, interacting with various SME Written and oral proficiency in French and English Your soft skills: Analytical spirit and sense of detail Able to manage priorities in fast paced environment Strength of proposal and able to challenge the status quo Flexibility and agility Autonomy and ability to take initiatives in line with the site priorities Proactivity in personal development Location: Neuchatel, Switzerland Sector: Pharmaceutical Start: 02/2025 Duration: 05MM+ Ref .Nr.: BH22512 Take the next step and send us your resume along with a daytime phone number where we can reach you. Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens as well as current work-permit holders for Switzerland. Ukrainian refugees are warmly welcomed, we will support you all the way. We welcome applications from individuals of all genders, age groups, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. Therefore, there is no requirement to provide gender information or a photo in your application. As per client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore potential solutions with our end client.
Produktions Experte (m/w/d) im Wertstrom Solids Finished Good - GMP/Verpackung/MES/SAP eWM/Schichtmodell/Deutsch Projekt: Für unseren Kunden, ein grosses Pharmaunternehmen mit Sitz in Basel suchen wir einen Produktions Experte (m/w/d) im Wertstrom Solids Finished Good . Hintergrund: Als Produktions Experte (m/w/d) bist du ein fester Bestandteil des Verpackungsteams und damit für die Bedienung der Produktionsanlagen sowie für die korrekte Durchführung von Auftrags- und Chargenwechsel zuständig, um eine GMP- und SHE (Safety, Health & Environment) gerechte Produktion zu gewährleisten. Du trägst mittels organisatorischer und technischer Verbesserungen zur Optimierung der Produktionsabläufe und zur Erhöhung der Anlagenverfügbarkeit bei. Du berichtest direkt an die Leiter der Prozess-Einheit VS-Solids Kaiseraugst. Der/die perfekte Kandidat/in: Der/die perfekte/r Kandidat/in: bringt mindestens 3 Jahre relevante Berufserfahrung mit und verfügt über eine abgeschlossene Berufsausbildung im technischen Bereich. Ausserdem besitzt der Kandidat eine hohe Lernbereitschaft für den Einsatz in verschiedenen Bereichen und Technologien, sowie Routinierter Umgang mit produktionsrelevanten Systemen. Hohe Teamfähigkeit und Bereitschaft in einem selbstorganisierten Team zu arbeiten, sowie entsprechend Verantwortung zu übernehmen sind Fähigkeiten die der Kandidat mitbringen sollte. Hauptaufgaben und Verantwortungsbereiche: * Selbstständige Durchführung der Verpackungstätigkeiten gemäss geltender GMP-Vorschriften inkl. Identifikation und Abrechnung von Materialien, Durchführen von In-Prozess-Kontrollen und Musterzügen, Warentransport und -entsorgung Mitarbeit in der Routineproduktion als Produktions Experte (Anlagenbediener) Selbstständige Bedienung der Produktionsanlagen und der dazugehörenden EDV-Systeme Selbständige Dokumentation sämtlicher GMP-relevanter Arbeiten und Störungen (SAP, MES, OEE) und umgehende Meldung von festgestellten Abweichungen und fehlerhaften Zuständen Sicherstellung der Verfügbarkeit von Formatteilen, Packmitteln und Verbrauchsmaterialien am Einsatzort Bewertung und Bearbeitung von Alarmen und Störungen inklusive Kommentierung dieser im OEE-Tool Ausräumen und reinigen der Produktionsanlagen Entsorgung des Abfalls Abarbeitung der Produktionsaufträge in den entsprechenden EDV-Systemen (Abrechnen der Produktionsaufträge, Bedienung des Linienleitstandes) Koordination und Durchführung der Umrüst Aktivitäten in Zusammenarbeit mit der Technik und den Linienmonteuren Aktive Mitarbeit bei der Einführung, Optimierung und Anwendung von LPS (Lean Production System) Methoden Sicherstellung der Einhaltung aller Sicherheitsvorschriften Sicherstellung der Produktion nach schriftlichen Vorgaben in qualitativer und quantitativer Hinsicht Must Haves: . Abgeschlossene Berufsausbildung im Bereich der Mechanik, Lebensmittelindustrie oder Pharmazie Min. 3 Jahre Berufserfahrung in der pharmazeutischen Industrie (GMP), idealerweise in den Bereichen der Verpackung Routinierter Umgang mit produktionsrelevanten Systemen (MES, SAP eWM), sowie generell mit MS Office bzw. G-Suite Hohe Lernbereitschaft für den Einsatz in verschiedenen Bereichen und Technologien (Polyvalenz) Hohe Teamfähigkeit und Bereitschaft in einem selbstorganisierten Team zu arbeiten, sowie entsprechend Verantwortung zu übernehmen Bereitschaft und Flexibilität zur Schichtarbeit Freude am Arbeiten in einem dynamischen Umfeld Strukturierte, eigenverantwortliche und selbständige Arbeitsweise Gutes Prozess- und technisches Verständnis Sehr gute Deutschkenntnisse (Wort und Schrift) Nice to have: Englischkenntnisse Referenz Nr.: 923697TP Rolle: Produktions Experte (m/w/d) im Wertstrom Solids Finished Good Industrie: Pharma Arbeitsort: Kaiseraugst Pensum: 80-100% Arbeitszeiten (Regulär, flexibel, Schichtbetrieb): 3-Schicht, 5 Tage, varriert 2-Schicht auch möglich Start: ASAP Dauer: 12 Bewerbungsfrist : 22.01.2025 Sollte diese Position Ihr Interesse geweckt haben, senden Sie uns bitte Ihr komplettes Dossier via dem Link in dieser Anzeige zu. Über uns : ITech Consult ist ein nach ISO 9001:2015 zertifiziertes Schweizer Unternehmen mit Niederlassungen in Deutschland und Irland. ITech Consult ist spezialisiert auf die Vermittlung von hochqualifizierten Kandidaten für den Personalverleih in den Bereichen, IT, Life Science & Engineering. Wir bieten Personalverleih & Payroll Dienstleistungen an. Für unsere Kandidaten ist dies kostenlos, auch bei Payroll berechnen wir Ihnen kein zusätzlichen Gebühren.
16/01/2025
Project-based
Produktions Experte (m/w/d) im Wertstrom Solids Finished Good - GMP/Verpackung/MES/SAP eWM/Schichtmodell/Deutsch Projekt: Für unseren Kunden, ein grosses Pharmaunternehmen mit Sitz in Basel suchen wir einen Produktions Experte (m/w/d) im Wertstrom Solids Finished Good . Hintergrund: Als Produktions Experte (m/w/d) bist du ein fester Bestandteil des Verpackungsteams und damit für die Bedienung der Produktionsanlagen sowie für die korrekte Durchführung von Auftrags- und Chargenwechsel zuständig, um eine GMP- und SHE (Safety, Health & Environment) gerechte Produktion zu gewährleisten. Du trägst mittels organisatorischer und technischer Verbesserungen zur Optimierung der Produktionsabläufe und zur Erhöhung der Anlagenverfügbarkeit bei. Du berichtest direkt an die Leiter der Prozess-Einheit VS-Solids Kaiseraugst. Der/die perfekte Kandidat/in: Der/die perfekte/r Kandidat/in: bringt mindestens 3 Jahre relevante Berufserfahrung mit und verfügt über eine abgeschlossene Berufsausbildung im technischen Bereich. Ausserdem besitzt der Kandidat eine hohe Lernbereitschaft für den Einsatz in verschiedenen Bereichen und Technologien, sowie Routinierter Umgang mit produktionsrelevanten Systemen. Hohe Teamfähigkeit und Bereitschaft in einem selbstorganisierten Team zu arbeiten, sowie entsprechend Verantwortung zu übernehmen sind Fähigkeiten die der Kandidat mitbringen sollte. Hauptaufgaben und Verantwortungsbereiche: * Selbstständige Durchführung der Verpackungstätigkeiten gemäss geltender GMP-Vorschriften inkl. Identifikation und Abrechnung von Materialien, Durchführen von In-Prozess-Kontrollen und Musterzügen, Warentransport und -entsorgung Mitarbeit in der Routineproduktion als Produktions Experte (Anlagenbediener) Selbstständige Bedienung der Produktionsanlagen und der dazugehörenden EDV-Systeme Selbständige Dokumentation sämtlicher GMP-relevanter Arbeiten und Störungen (SAP, MES, OEE) und umgehende Meldung von festgestellten Abweichungen und fehlerhaften Zuständen Sicherstellung der Verfügbarkeit von Formatteilen, Packmitteln und Verbrauchsmaterialien am Einsatzort Bewertung und Bearbeitung von Alarmen und Störungen inklusive Kommentierung dieser im OEE-Tool Ausräumen und reinigen der Produktionsanlagen Entsorgung des Abfalls Abarbeitung der Produktionsaufträge in den entsprechenden EDV-Systemen (Abrechnen der Produktionsaufträge, Bedienung des Linienleitstandes) Koordination und Durchführung der Umrüst Aktivitäten in Zusammenarbeit mit der Technik und den Linienmonteuren Aktive Mitarbeit bei der Einführung, Optimierung und Anwendung von LPS (Lean Production System) Methoden Sicherstellung der Einhaltung aller Sicherheitsvorschriften Sicherstellung der Produktion nach schriftlichen Vorgaben in qualitativer und quantitativer Hinsicht Must Haves: . Abgeschlossene Berufsausbildung im Bereich der Mechanik, Lebensmittelindustrie oder Pharmazie Min. 3 Jahre Berufserfahrung in der pharmazeutischen Industrie (GMP), idealerweise in den Bereichen der Verpackung Routinierter Umgang mit produktionsrelevanten Systemen (MES, SAP eWM), sowie generell mit MS Office bzw. G-Suite Hohe Lernbereitschaft für den Einsatz in verschiedenen Bereichen und Technologien (Polyvalenz) Hohe Teamfähigkeit und Bereitschaft in einem selbstorganisierten Team zu arbeiten, sowie entsprechend Verantwortung zu übernehmen Bereitschaft und Flexibilität zur Schichtarbeit Freude am Arbeiten in einem dynamischen Umfeld Strukturierte, eigenverantwortliche und selbständige Arbeitsweise Gutes Prozess- und technisches Verständnis Sehr gute Deutschkenntnisse (Wort und Schrift) Nice to have: Englischkenntnisse Referenz Nr.: 923697TP Rolle: Produktions Experte (m/w/d) im Wertstrom Solids Finished Good Industrie: Pharma Arbeitsort: Kaiseraugst Pensum: 80-100% Arbeitszeiten (Regulär, flexibel, Schichtbetrieb): 3-Schicht, 5 Tage, varriert 2-Schicht auch möglich Start: ASAP Dauer: 12 Bewerbungsfrist : 22.01.2025 Sollte diese Position Ihr Interesse geweckt haben, senden Sie uns bitte Ihr komplettes Dossier via dem Link in dieser Anzeige zu. Über uns : ITech Consult ist ein nach ISO 9001:2015 zertifiziertes Schweizer Unternehmen mit Niederlassungen in Deutschland und Irland. ITech Consult ist spezialisiert auf die Vermittlung von hochqualifizierten Kandidaten für den Personalverleih in den Bereichen, IT, Life Science & Engineering. Wir bieten Personalverleih & Payroll Dienstleistungen an. Für unsere Kandidaten ist dies kostenlos, auch bei Payroll berechnen wir Ihnen kein zusätzlichen Gebühren.
Role: Experienced Manufacturing Engineer/Production Engineer Location: Exeter (onsite) Salary: £ competitive Who would this role suit? This role would suit a production or planning manager with planning and organisational skills to become a team lead. OR someone with the production and manufacturing experience. Your Role The position entails working within the Services Division of our Production department and leading a small team to resolve technical problems, selecting the best manufacturing processes and suppliers and working closely with the design team to make improvements for future manufacturing. Overall purpose of your role is to oversee the design and implementation of production processes to ensure a high-level of manufacturing for the business. You are responsible for improving efficiency and quality of the production processes to produce a better product, at a lower cost. This is a highly interactive role internally and externally, and developing strong, supportive working relationships will be key for the success of this role and your department. Day-to-day Responsibilities: Analysing and planning workflow, space requirements and equipment placement to maximise manufacturing efficiency. Ensuring all asset and component builds for the Services division are successfully manufactured on time and within budget. Evaluate and review work instructions for manufacturing to ensure they are accurate and easy to follow. Responsible for identifying internal training that is required for the team. Ensure the company is not reliant on key suppliers wherever possible, by investigating other suppliers regularly and visiting their facility for due diligence. Planning, prioritising and scheduling of production activity, including workload forecasting to ensure the delivery of quality products, on time and on budget. Stock management of the controlled storeroom. Responsible for all assembly and testing activity in the Services manufacturing area. Management of suppliers to ensure we are provided with quality materials at a fair price by implementing a fair quoting process. Onboarding of new suppliers. Keeping the workshop safe, tidy and organised. Manufacturing processes such as assembly and component marking. Writing prototype assembly and test instructions. Resolve technical problems when they arise and feedback to engineering suggested improvements for the design in the future. Evaluating quality control processes and making recommendations for improvements. Analysing and reporting on production processes, methods, schedules, downtime, availability of machines and waste management. Ensuring that the organisation's manufacturing processes comply with relevant policies and government laws and regulations. Analysing and planning workflow, space requirements and equipment placement to maximise manufacturing efficiency. Coordinating maintenance and repair services to keep production equipment operational and reduce department downtime. Ensure the team follow the manufacturer's procedures and instructions while operating the equipment. Overseeing the work of technicians Experience, knowledge and skills Essential skills: 5+ years of experience as a Manufacturing Engineer. Experience in an engineering supervisory role, preferably within a similarly regulated industry. Engineering Degree: in systems engineering, mechanical engineering, manufacturing engineering, electrical or industrial engineering. Demonstrable experience in leading and motivating different technical teams. In-depth knowledge of manufacturing production and processes. Experience of successfully managing and completing complex projects. Experience in successful operating ERP & MRP systems. Desirable skills: Experience in the use of 3D printers. Knowledge of engineering science. Master's degree in manufacturing engineering. Experience in operating and/or implementing six sigma manufacturing and lean manufacturing processes. Experience in implementing MRP systems. Personal Attributes: Ability to motivate and lead a team. Ability to work unsupervised. Ability to work on your own initiative and to think on your feet when things to go exactly to plan. Self-motivated. Ability to deliver within agreed timeframes but also have a passion to improve these lead times. Ability to work accurately and under time pressure due to production needs. Safety mindset. Passion for efficiency and process improvement. Enjoy developing and training people. Enjoy sharing best practices across the business. Benefits: Free parking Life insurance On-site parking How to apply? Please send a CV to (see below) People Source Consulting Ltd is acting as an Employment Agency in relation to this vacancy. People Source specialise in technology recruitment across niche markets including Information Technology, Digital TV, Digital Marketing, Project and Programme Management, SAP, Digital and Consumer Electronics, Air Traffic Management, Management Consultancy, Business Intelligence, Manufacturing, Telecoms, Public Sector, Healthcare, Finance and Oil & Gas.
15/01/2025
Full time
Role: Experienced Manufacturing Engineer/Production Engineer Location: Exeter (onsite) Salary: £ competitive Who would this role suit? This role would suit a production or planning manager with planning and organisational skills to become a team lead. OR someone with the production and manufacturing experience. Your Role The position entails working within the Services Division of our Production department and leading a small team to resolve technical problems, selecting the best manufacturing processes and suppliers and working closely with the design team to make improvements for future manufacturing. Overall purpose of your role is to oversee the design and implementation of production processes to ensure a high-level of manufacturing for the business. You are responsible for improving efficiency and quality of the production processes to produce a better product, at a lower cost. This is a highly interactive role internally and externally, and developing strong, supportive working relationships will be key for the success of this role and your department. Day-to-day Responsibilities: Analysing and planning workflow, space requirements and equipment placement to maximise manufacturing efficiency. Ensuring all asset and component builds for the Services division are successfully manufactured on time and within budget. Evaluate and review work instructions for manufacturing to ensure they are accurate and easy to follow. Responsible for identifying internal training that is required for the team. Ensure the company is not reliant on key suppliers wherever possible, by investigating other suppliers regularly and visiting their facility for due diligence. Planning, prioritising and scheduling of production activity, including workload forecasting to ensure the delivery of quality products, on time and on budget. Stock management of the controlled storeroom. Responsible for all assembly and testing activity in the Services manufacturing area. Management of suppliers to ensure we are provided with quality materials at a fair price by implementing a fair quoting process. Onboarding of new suppliers. Keeping the workshop safe, tidy and organised. Manufacturing processes such as assembly and component marking. Writing prototype assembly and test instructions. Resolve technical problems when they arise and feedback to engineering suggested improvements for the design in the future. Evaluating quality control processes and making recommendations for improvements. Analysing and reporting on production processes, methods, schedules, downtime, availability of machines and waste management. Ensuring that the organisation's manufacturing processes comply with relevant policies and government laws and regulations. Analysing and planning workflow, space requirements and equipment placement to maximise manufacturing efficiency. Coordinating maintenance and repair services to keep production equipment operational and reduce department downtime. Ensure the team follow the manufacturer's procedures and instructions while operating the equipment. Overseeing the work of technicians Experience, knowledge and skills Essential skills: 5+ years of experience as a Manufacturing Engineer. Experience in an engineering supervisory role, preferably within a similarly regulated industry. Engineering Degree: in systems engineering, mechanical engineering, manufacturing engineering, electrical or industrial engineering. Demonstrable experience in leading and motivating different technical teams. In-depth knowledge of manufacturing production and processes. Experience of successfully managing and completing complex projects. Experience in successful operating ERP & MRP systems. Desirable skills: Experience in the use of 3D printers. Knowledge of engineering science. Master's degree in manufacturing engineering. Experience in operating and/or implementing six sigma manufacturing and lean manufacturing processes. Experience in implementing MRP systems. Personal Attributes: Ability to motivate and lead a team. Ability to work unsupervised. Ability to work on your own initiative and to think on your feet when things to go exactly to plan. Self-motivated. Ability to deliver within agreed timeframes but also have a passion to improve these lead times. Ability to work accurately and under time pressure due to production needs. Safety mindset. Passion for efficiency and process improvement. Enjoy developing and training people. Enjoy sharing best practices across the business. Benefits: Free parking Life insurance On-site parking How to apply? Please send a CV to (see below) People Source Consulting Ltd is acting as an Employment Agency in relation to this vacancy. People Source specialise in technology recruitment across niche markets including Information Technology, Digital TV, Digital Marketing, Project and Programme Management, SAP, Digital and Consumer Electronics, Air Traffic Management, Management Consultancy, Business Intelligence, Manufacturing, Telecoms, Public Sector, Healthcare, Finance and Oil & Gas.
Our client is an established pharmaceutical company engaged in the development, manufacture, marketing and distribution of generic medicines in the UK and Europe. They offer a wide range of high-quality medicines to the healthcare sector, that optimises cost efficiency whilst ensuring reliable supply. They are now looking to hire a Site Head of Quality Assurance for their site in the North East. The Site Head of Quality Assurance will lead the designated site in terms of compliance, including in the areas of: QA, QC, GMP, GDP, QP activities and RP activities. Responsibilities: Establish clear and compliant GMP/GDP standards for all site activities Align with the broader organisation, to ensure organisation has uniform high standards Share best practices, for the benefit of the organisation in relation to QA Establish a clear site-level governance process, feeding the organisation committee Deliver clear and concise scorecards, on a weekly basis, in conjunction with the Site Director, including status and progress The Head of Quality Assurance will deliver a weekly report, in conjunction with the Site Director, communicating areas of challenge, delivery and risk Escalate issues of significance, in a timely manner at site level and beyond Lead and demonstrate a continuous improvement mindset (eg lean, six sigma etc.) Plan to have a deputy, capable of supporting operations, including when senior staff are absent or unavailable Lead on Governance, Quality and H&S and Environmental matters The Head of Quality Assurance will implement independent audit systems for internal audits of relevant departments Risk governance processes, looking at understanding and proactively managing site risk Establish/Improve on metrics, to demonstrate and understand changes in the performance of the site, in terms of Compliance Duties: Lead the site Compliance Council process Lead regulatory inspections, linked to GMDP, H&S etc. Deputise for the Site Director on matters associated with Ethics and Compliance Build a relationship with the regulators that impact the site eg MHRA etc. Support the building of a high-capability and high-delivery team, linked compliance, with the Company HR team Lead site recall activities, as required Manage DMRC communication, as required Qualifications/Skills: Ideally Degree level education or track record in a similar position Solid Dose and Generic Pharmaceuticals Quality Assurance Management Ideally QP status although this isn't a deal breaker To find out more about Real, please visit our website Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office |8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales
15/01/2025
Full time
Our client is an established pharmaceutical company engaged in the development, manufacture, marketing and distribution of generic medicines in the UK and Europe. They offer a wide range of high-quality medicines to the healthcare sector, that optimises cost efficiency whilst ensuring reliable supply. They are now looking to hire a Site Head of Quality Assurance for their site in the North East. The Site Head of Quality Assurance will lead the designated site in terms of compliance, including in the areas of: QA, QC, GMP, GDP, QP activities and RP activities. Responsibilities: Establish clear and compliant GMP/GDP standards for all site activities Align with the broader organisation, to ensure organisation has uniform high standards Share best practices, for the benefit of the organisation in relation to QA Establish a clear site-level governance process, feeding the organisation committee Deliver clear and concise scorecards, on a weekly basis, in conjunction with the Site Director, including status and progress The Head of Quality Assurance will deliver a weekly report, in conjunction with the Site Director, communicating areas of challenge, delivery and risk Escalate issues of significance, in a timely manner at site level and beyond Lead and demonstrate a continuous improvement mindset (eg lean, six sigma etc.) Plan to have a deputy, capable of supporting operations, including when senior staff are absent or unavailable Lead on Governance, Quality and H&S and Environmental matters The Head of Quality Assurance will implement independent audit systems for internal audits of relevant departments Risk governance processes, looking at understanding and proactively managing site risk Establish/Improve on metrics, to demonstrate and understand changes in the performance of the site, in terms of Compliance Duties: Lead the site Compliance Council process Lead regulatory inspections, linked to GMDP, H&S etc. Deputise for the Site Director on matters associated with Ethics and Compliance Build a relationship with the regulators that impact the site eg MHRA etc. Support the building of a high-capability and high-delivery team, linked compliance, with the Company HR team Lead site recall activities, as required Manage DMRC communication, as required Qualifications/Skills: Ideally Degree level education or track record in a similar position Solid Dose and Generic Pharmaceuticals Quality Assurance Management Ideally QP status although this isn't a deal breaker To find out more about Real, please visit our website Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office |8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales
