Job title: Buyer Location: Crewe/Hybrid Duration: Until 31/07/2025 Adecco is an employment consultancy. We put expertise, energy, and enthusiasm into improving everyone's chance of being part of the workplace. We respect and appreciate people of all ethnicities, generations, religious beliefs, sexual orientations, gender identities, and more. We do this by showcasing their talents, skills, and unique experience in an inclusive environment that helps them thrive. The role: The purpose of this role is to ensure the efficient handling of back orders, supplier management, and order processing to meet customer needs and maintain smooth operations. The candidate will play a crucial role in coordinating with departments, managing supplier relationships, and performing general purchasing tasks to ensure timely delivery and value for money. Responsibilities: Handling Back Orders : Coordinating with departments to fulfil customer needs when parts are not readily available. Supplier Management : Preparing presentations for the sourcing committee to ensure value for money and due diligence. Order Processing : Raising orders and checking supply routes, prices, and minimum order quantities (MOQs). General Purchasing Tasks : Routine tasks typical for a buyer, including liaising with suppliers and ensuring timely delivery of parts. Requirements: Technical Skills : Proficiency in Excel and SAP, along with general computer literacy. Communication Skills : Strong verbal and written communication skills are essential, as the role involves interacting with a global supply base. Industry Knowledge : Preference for candidates with experience in the metals industry or interior components, though other industries like transportation or aerospace are also considered. Candidates will ideally show evidence of the above in their CV in order to be considered. Please be advised if you haven't heard from us within 48 hours then unfortunately your application has not been successful on this occasion, we may however keep your details on file for any suitable future vacancies and contact you accordingly.
04/04/2025
Project-based
Job title: Buyer Location: Crewe/Hybrid Duration: Until 31/07/2025 Adecco is an employment consultancy. We put expertise, energy, and enthusiasm into improving everyone's chance of being part of the workplace. We respect and appreciate people of all ethnicities, generations, religious beliefs, sexual orientations, gender identities, and more. We do this by showcasing their talents, skills, and unique experience in an inclusive environment that helps them thrive. The role: The purpose of this role is to ensure the efficient handling of back orders, supplier management, and order processing to meet customer needs and maintain smooth operations. The candidate will play a crucial role in coordinating with departments, managing supplier relationships, and performing general purchasing tasks to ensure timely delivery and value for money. Responsibilities: Handling Back Orders : Coordinating with departments to fulfil customer needs when parts are not readily available. Supplier Management : Preparing presentations for the sourcing committee to ensure value for money and due diligence. Order Processing : Raising orders and checking supply routes, prices, and minimum order quantities (MOQs). General Purchasing Tasks : Routine tasks typical for a buyer, including liaising with suppliers and ensuring timely delivery of parts. Requirements: Technical Skills : Proficiency in Excel and SAP, along with general computer literacy. Communication Skills : Strong verbal and written communication skills are essential, as the role involves interacting with a global supply base. Industry Knowledge : Preference for candidates with experience in the metals industry or interior components, though other industries like transportation or aerospace are also considered. Candidates will ideally show evidence of the above in their CV in order to be considered. Please be advised if you haven't heard from us within 48 hours then unfortunately your application has not been successful on this occasion, we may however keep your details on file for any suitable future vacancies and contact you accordingly.
* Supply Chain Engagement Lead - Berkshire.* For our international client, RED is currently looking for a Supply Chain Engagement Lead to join an ongoing project. The consultant is expected to start in June 2025 for a 12-month contract. The project is based in Berkshire, UK and involves working remotely with 3 days on-site, please note these are not fixed days. Desired skills: Previous Customer Engagement Management experience (ie led projects to enhance customer value and retention, focusing on improving the customer journey and aligning service offerings with priority customers needs) Experience in optimising supply chain processes, particularly in order and claims management, to better serve customers Any Automation experience, including experience with tools like Co-Pilot and Power Automate to automate processes, reporting, and non-value activities Any experience with Customer Segmentation & Value ServiceProjects Excellent English - written and communication skills If you are interested in this position, please apply or send your updated CV to (see below) for immediate consideration.
04/04/2025
Project-based
* Supply Chain Engagement Lead - Berkshire.* For our international client, RED is currently looking for a Supply Chain Engagement Lead to join an ongoing project. The consultant is expected to start in June 2025 for a 12-month contract. The project is based in Berkshire, UK and involves working remotely with 3 days on-site, please note these are not fixed days. Desired skills: Previous Customer Engagement Management experience (ie led projects to enhance customer value and retention, focusing on improving the customer journey and aligning service offerings with priority customers needs) Experience in optimising supply chain processes, particularly in order and claims management, to better serve customers Any Automation experience, including experience with tools like Co-Pilot and Power Automate to automate processes, reporting, and non-value activities Any experience with Customer Segmentation & Value ServiceProjects Excellent English - written and communication skills If you are interested in this position, please apply or send your updated CV to (see below) for immediate consideration.
Our client is one of the world's leading manufacturers of medical devices with a presence in over 100 countries. They have a permanent opportunity for a Senior Scientist - Biocompatibility with a particular focus on Biological Evaluation. In this role, you will be responsible for generating, maintaining, and updating Biological Evaluation Reports (BERs) per EU MDR requirements. Responsibilities: Compile and deliver biocompatibility assessments and biocompatibility evaluation plans Generation and maintenance of Biological Evaluation Reports to meet EU MDR regulations Perform and assist with risk assessments and gap analysis of external standards, regulatory requirements, and guidance documents Collaborate with cross-functional teams to support projects requiring biocompatibility evaluation Keep abreast of regulatory requirements including monitoring EU MDR, FDA and other agency regulations and international standards Prepare or collaborate in the preparation of toxicological safety assessments including materials, chemicals, technologies and processes or finished products Work within multi-disciplinary teams (notably R&D, HS&E, Import/Export, Supply Chain and RA/QA) Ensure due process is followed under R&D Policies Support the creation and development of the strategy for biological/toxicological evaluation (including testing requirements) for materials and finished products Provide technical support and coaching for members of R&D, regulatory or any other relevant department Provide consultancy on technical issues both within R&D and other stakeholders. Qualifications: Either a BSc in a biological science (Pharmacology, Biology, Physiology, Biochemistry or similar) or related discipline (MSc in Toxicology or any work-related experience in toxicology a bonus) Industrial experience within the chemical area (Medical device/pharmaceutical preferred) Direct experience working with ISO 10993 Success in leading change in particular for the implementation of ISO 10993 standards 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
04/04/2025
Full time
Our client is one of the world's leading manufacturers of medical devices with a presence in over 100 countries. They have a permanent opportunity for a Senior Scientist - Biocompatibility with a particular focus on Biological Evaluation. In this role, you will be responsible for generating, maintaining, and updating Biological Evaluation Reports (BERs) per EU MDR requirements. Responsibilities: Compile and deliver biocompatibility assessments and biocompatibility evaluation plans Generation and maintenance of Biological Evaluation Reports to meet EU MDR regulations Perform and assist with risk assessments and gap analysis of external standards, regulatory requirements, and guidance documents Collaborate with cross-functional teams to support projects requiring biocompatibility evaluation Keep abreast of regulatory requirements including monitoring EU MDR, FDA and other agency regulations and international standards Prepare or collaborate in the preparation of toxicological safety assessments including materials, chemicals, technologies and processes or finished products Work within multi-disciplinary teams (notably R&D, HS&E, Import/Export, Supply Chain and RA/QA) Ensure due process is followed under R&D Policies Support the creation and development of the strategy for biological/toxicological evaluation (including testing requirements) for materials and finished products Provide technical support and coaching for members of R&D, regulatory or any other relevant department Provide consultancy on technical issues both within R&D and other stakeholders. Qualifications: Either a BSc in a biological science (Pharmacology, Biology, Physiology, Biochemistry or similar) or related discipline (MSc in Toxicology or any work-related experience in toxicology a bonus) Industrial experience within the chemical area (Medical device/pharmaceutical preferred) Direct experience working with ISO 10993 Success in leading change in particular for the implementation of ISO 10993 standards 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
We're looking for a Senior Regulatory Affairs Specialist for a fast growing med tech company based Cork (Ireland). The successful candidate will collaborate with cross-functional teams to facilitate regulatory approvals, manage submissions, and maintain compliance with evolving regulatory requirements. This position offers an excellent compensation package and potentially hybrid working. Responsibilities Regulatory Strategy Development: Formulate and execute strategies for product registration, approval, and compliance Daily Regulatory Management: Oversee day-to-day regulatory activities and manage multiple projects related to regulatory compliance Submission Management: Prepare, maintain, review, and submit regulatory documents and applications to health authorities Global Registration Support: Assist the team in obtaining and retaining country-specific regulatory registrations worldwide MDSAP Implementation: Manage the implementation of the Medical Device Single Audit Program within the organization Regulatory Compliance Monitoring: Ensure compliance with national and international regulatory requirements and quality standards Risk Assessment: Identify and assess potential regulatory risks and propose effective mitigation strategies Cross-Functional Collaboration: Work closely with QA, R&D, Operations, Clinical Affairs, and other departments to integrate regulatory requirements into QMS and product development processes Regulatory Updates: Stay current with changing regulations, guidelines, and industry trends Maintain high-quality standards within the organization by assessing risk profiles and creating mitigation programs/tools. Post Market Surveillance: Manage activities including logging customer complaints and adverse events, coordinating investigations, and conducting regulatory trending and reporting CE Mark Submissions: Handle submissions, significant change notifications, and interactions with Notified Bodies International Filings: Support the team with the preparation of international regulatory filings, including 510(k) submissions and FDA correspondence Material Review: Ensure public-facing materials comply with regulatory standards Skills and Qualifications Bachelor's degree in Engineering or Science or practical expertise Regulatory experience in the medical device industry Understanding of ISO 13485, ISO 14971, EU MDR, UK, MDSAP, 21 CFR 820, and supporting standards Please visit our website to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement. 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
03/04/2025
Project-based
We're looking for a Senior Regulatory Affairs Specialist for a fast growing med tech company based Cork (Ireland). The successful candidate will collaborate with cross-functional teams to facilitate regulatory approvals, manage submissions, and maintain compliance with evolving regulatory requirements. This position offers an excellent compensation package and potentially hybrid working. Responsibilities Regulatory Strategy Development: Formulate and execute strategies for product registration, approval, and compliance Daily Regulatory Management: Oversee day-to-day regulatory activities and manage multiple projects related to regulatory compliance Submission Management: Prepare, maintain, review, and submit regulatory documents and applications to health authorities Global Registration Support: Assist the team in obtaining and retaining country-specific regulatory registrations worldwide MDSAP Implementation: Manage the implementation of the Medical Device Single Audit Program within the organization Regulatory Compliance Monitoring: Ensure compliance with national and international regulatory requirements and quality standards Risk Assessment: Identify and assess potential regulatory risks and propose effective mitigation strategies Cross-Functional Collaboration: Work closely with QA, R&D, Operations, Clinical Affairs, and other departments to integrate regulatory requirements into QMS and product development processes Regulatory Updates: Stay current with changing regulations, guidelines, and industry trends Maintain high-quality standards within the organization by assessing risk profiles and creating mitigation programs/tools. Post Market Surveillance: Manage activities including logging customer complaints and adverse events, coordinating investigations, and conducting regulatory trending and reporting CE Mark Submissions: Handle submissions, significant change notifications, and interactions with Notified Bodies International Filings: Support the team with the preparation of international regulatory filings, including 510(k) submissions and FDA correspondence Material Review: Ensure public-facing materials comply with regulatory standards Skills and Qualifications Bachelor's degree in Engineering or Science or practical expertise Regulatory experience in the medical device industry Understanding of ISO 13485, ISO 14971, EU MDR, UK, MDSAP, 21 CFR 820, and supporting standards Please visit our website to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement. 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
We are recruiting for a Stores Assistant for a leading IT Service provider based on site in Colnbrook. You must have a valid UK driving licence for this role. Job Summary: Responsible for efficiently managing the storage, organization, and distribution of stock within the stores. This role involves receiving, inspecting, and storing incoming materials and products, as well as maintaining stock level by ordering materials for existing and new projects. Maintaining accurate inventory records and ensuring a clean and organized workspace. In addition, management of vehicle fleet and test & plant equipment. To assist the existing PM/PE onsite team with administrative tasks as required. Key Responsibilities: Stock Control Receiving and Inspection : Receive incoming shipments of materials and products. Inspect and verify the accuracy of received items. Report and document any discrepancies or damages. Storage and Organization : Safely store items in designated locations within the warehouse. Maintain an organized and clean storage area. Ensure proper labelling and identification of products. Inventory Management : Keep accurate inventory records using appropriate software or tools. Conduct regular stock counts to reconcile inventory levels. Assist in the ordering of materials to replenish stock as needed. Documentation : Maintain detailed records of received and dispatched items. Generate reports on inventory levels and movement. Assist with paperwork related to shipping and receiving. Equipment Maintenance/Office Maintenance : Maintaining PAT testing records and Yearly Fire Inspections. Ensure proper care and maintenance of stores equipment. COSHH Management. Report any equipment malfunctions or issues. Ensuring Network Test Equipment is maintained and annually calibrated. Fleet Management: Weekly Vehicle Checks Booking and managing Yearly Service, MOT & Safety Inspections Booking and managing repairs Qualifications: Previous experience in store management or a similar role is desirable. Familiarity with inventory management software is desirable. Excellent communication and teamwork skills. MS Excel experience and knowledge required. Must have a full drivers licence This is an umbrella contract, the role is Inside IR35
03/04/2025
Project-based
We are recruiting for a Stores Assistant for a leading IT Service provider based on site in Colnbrook. You must have a valid UK driving licence for this role. Job Summary: Responsible for efficiently managing the storage, organization, and distribution of stock within the stores. This role involves receiving, inspecting, and storing incoming materials and products, as well as maintaining stock level by ordering materials for existing and new projects. Maintaining accurate inventory records and ensuring a clean and organized workspace. In addition, management of vehicle fleet and test & plant equipment. To assist the existing PM/PE onsite team with administrative tasks as required. Key Responsibilities: Stock Control Receiving and Inspection : Receive incoming shipments of materials and products. Inspect and verify the accuracy of received items. Report and document any discrepancies or damages. Storage and Organization : Safely store items in designated locations within the warehouse. Maintain an organized and clean storage area. Ensure proper labelling and identification of products. Inventory Management : Keep accurate inventory records using appropriate software or tools. Conduct regular stock counts to reconcile inventory levels. Assist in the ordering of materials to replenish stock as needed. Documentation : Maintain detailed records of received and dispatched items. Generate reports on inventory levels and movement. Assist with paperwork related to shipping and receiving. Equipment Maintenance/Office Maintenance : Maintaining PAT testing records and Yearly Fire Inspections. Ensure proper care and maintenance of stores equipment. COSHH Management. Report any equipment malfunctions or issues. Ensuring Network Test Equipment is maintained and annually calibrated. Fleet Management: Weekly Vehicle Checks Booking and managing Yearly Service, MOT & Safety Inspections Booking and managing repairs Qualifications: Previous experience in store management or a similar role is desirable. Familiarity with inventory management software is desirable. Excellent communication and teamwork skills. MS Excel experience and knowledge required. Must have a full drivers licence This is an umbrella contract, the role is Inside IR35
Title: Technical & Quality Assistant Junior Salary: Negotiable Hours: 42 per week Location: London Education level: Diploma or equivalent experience My client is one of the nations biggest food manufactures to some of the largest restaurant and prestigious hotel groups in the UK. With over 50 years in the industry, they have proven they have the strength and determination to withstand any obstacles encountered and exceed their customers' expectations every time. In order to keep up with the demands this industry has, they are seeking a proactive and detail-oriented Technical and Quality Assistant to join our dynamic team at our UK-based food manufacturing facility. This role supports the delivery of high-quality products by ensuring compliance with UK and international food safety standards, quality systems, and regulatory requirements. The ideal candidate will be passionate about food quality and safety and have excellent organisational and communication skills. Key Responsibilities Quality Control & Assurance: Perform quality checks on raw materials, in-process products, and finished goods to ensure compliance with specifications Maintaining and monitoring of HACCP systems and CCP records Implementation and verification of quality standards and procedures across the production process Compliance and Audits: Preparing for third-party audits (eg, BRCGS, SALSA) and customer inspections Ensure all documentation complies with UK food safety regulations (eg, Food Standards Agency requirements) Managing non-conformances and implementing corrective actions Technical Support: Work closely with the production team to address quality-related issues and identify process improvements Assist in developing and maintaining product specifications, technical documentation, and labelling compliance under UK/EU regulations. Provide technical support during new product development trials Record Keeping & Reporting: Maintain accurate records of quality checks, test results, and incidents in line with BRCGS standards. Prepare quality performance reports and KPIs for internal review. Training & Development: Help train production staff on food safety, HACCP principles, and quality standards. Contribute to fostering a culture of quality and continuous improvement across the company. Requirements Degree or diploma in Food Science, Food Technology, Microbiology, or a related discipline. Experience in a food manufacturing or quality assurance environment (preferred) Familiarity with HACCP, GMP, and UK/EU food safety regulations Strong attention to detail and organisational skills Excellent communication skills and the ability to work effectively with cross-functional teams Experience in Google environment (Doc, Sheet, Slides ) Analytical mindset with a problem-solving approach Familiarity with UK and EU food safety regulations and labelling requirements Understanding of BRCGS standards, SALSA accreditation, or similar food safety certification schemes is advantageous. Please note: As per my clients request, your CV will not be considered if any of the following apply: You require sponsorship now or within the next 5+ years You are on a dependant/graduate visa. Not living in the UK currently or have residency in the UK currently. In addition to this, as part of our compliance, you will be asked to provide the proof you have to confirm you have the right to work in the UK before your CV is submitted.
02/04/2025
Full time
Title: Technical & Quality Assistant Junior Salary: Negotiable Hours: 42 per week Location: London Education level: Diploma or equivalent experience My client is one of the nations biggest food manufactures to some of the largest restaurant and prestigious hotel groups in the UK. With over 50 years in the industry, they have proven they have the strength and determination to withstand any obstacles encountered and exceed their customers' expectations every time. In order to keep up with the demands this industry has, they are seeking a proactive and detail-oriented Technical and Quality Assistant to join our dynamic team at our UK-based food manufacturing facility. This role supports the delivery of high-quality products by ensuring compliance with UK and international food safety standards, quality systems, and regulatory requirements. The ideal candidate will be passionate about food quality and safety and have excellent organisational and communication skills. Key Responsibilities Quality Control & Assurance: Perform quality checks on raw materials, in-process products, and finished goods to ensure compliance with specifications Maintaining and monitoring of HACCP systems and CCP records Implementation and verification of quality standards and procedures across the production process Compliance and Audits: Preparing for third-party audits (eg, BRCGS, SALSA) and customer inspections Ensure all documentation complies with UK food safety regulations (eg, Food Standards Agency requirements) Managing non-conformances and implementing corrective actions Technical Support: Work closely with the production team to address quality-related issues and identify process improvements Assist in developing and maintaining product specifications, technical documentation, and labelling compliance under UK/EU regulations. Provide technical support during new product development trials Record Keeping & Reporting: Maintain accurate records of quality checks, test results, and incidents in line with BRCGS standards. Prepare quality performance reports and KPIs for internal review. Training & Development: Help train production staff on food safety, HACCP principles, and quality standards. Contribute to fostering a culture of quality and continuous improvement across the company. Requirements Degree or diploma in Food Science, Food Technology, Microbiology, or a related discipline. Experience in a food manufacturing or quality assurance environment (preferred) Familiarity with HACCP, GMP, and UK/EU food safety regulations Strong attention to detail and organisational skills Excellent communication skills and the ability to work effectively with cross-functional teams Experience in Google environment (Doc, Sheet, Slides ) Analytical mindset with a problem-solving approach Familiarity with UK and EU food safety regulations and labelling requirements Understanding of BRCGS standards, SALSA accreditation, or similar food safety certification schemes is advantageous. Please note: As per my clients request, your CV will not be considered if any of the following apply: You require sponsorship now or within the next 5+ years You are on a dependant/graduate visa. Not living in the UK currently or have residency in the UK currently. In addition to this, as part of our compliance, you will be asked to provide the proof you have to confirm you have the right to work in the UK before your CV is submitted.
We have an opportunity for a hands-on, career minded Facility and Equipment Repair Manager to join our growing team and help lead our maintenance department! This is an opportunity for a motivated individual to work in a fast paced, rapidly growing organization. If working with high-technology, semiconductor type equipment is interesting to you then this is the right opportunity. The ideal candidate is pursuing a career with a growing company where they can demonstrate our core values: driven, positive energy, and embodies a Here to Help attitude. This person has a strong problem-solving mindset with a focus on attention to detail. North American Coating Laboratories (NACL) is an industry leading optical coating provider servicing customers across the United States as well as around the globe. At NACL, we provide hi-technology coatings for endless industries including: Lasers and Photonics Aviation and Aerospace Medical Consumer Electronics LIDAR Virtual/Augmented and Mixed Reality Military Entertainment/Film Responsibilities for this hands-on opportunity, including but not limited to: Establish maintenance policies and procedures Preventive maintenance - schedule regular inspections and preventive maintenance to avoid equipment breakdowns Troubleshooting - Diagnose and repair machinery and equipment; primary equipment is vacuum coating machines Electrical/electronic troubleshooting Identify and resolve HVAC issues, specifically refrigeration Prepare maintenance reports, document and communicate actions, irregularities and continuing needs through the use of preventive maintenance software CNC machine operation Fabrication and welding Supervise maintenance staff Preferred knowledge/skills: Previous maintenance leadership/supervisory experience Computer savvy - proficient in MS Office Suite (Word, Excel and Outlook) Knowledge and familiarity with vacuum pumps and technology Experience with a preventive maintenance program, such as Maintain X Strong mechanical aptitude for accurately assessing, diagnosing and resolving equipment issues with a sense of urgency Motivated self-starter who works well independently and as part of a team Deadline and detail oriented Strong communication skills, verbal and written Education: HVAC Certification a plus High school diploma/GED required Previous experience: 5+ years prior experience in an equipment maintenance role with proven growth 3-years CNC machining experience Welding experience a plus We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.
02/04/2025
Full time
We have an opportunity for a hands-on, career minded Facility and Equipment Repair Manager to join our growing team and help lead our maintenance department! This is an opportunity for a motivated individual to work in a fast paced, rapidly growing organization. If working with high-technology, semiconductor type equipment is interesting to you then this is the right opportunity. The ideal candidate is pursuing a career with a growing company where they can demonstrate our core values: driven, positive energy, and embodies a Here to Help attitude. This person has a strong problem-solving mindset with a focus on attention to detail. North American Coating Laboratories (NACL) is an industry leading optical coating provider servicing customers across the United States as well as around the globe. At NACL, we provide hi-technology coatings for endless industries including: Lasers and Photonics Aviation and Aerospace Medical Consumer Electronics LIDAR Virtual/Augmented and Mixed Reality Military Entertainment/Film Responsibilities for this hands-on opportunity, including but not limited to: Establish maintenance policies and procedures Preventive maintenance - schedule regular inspections and preventive maintenance to avoid equipment breakdowns Troubleshooting - Diagnose and repair machinery and equipment; primary equipment is vacuum coating machines Electrical/electronic troubleshooting Identify and resolve HVAC issues, specifically refrigeration Prepare maintenance reports, document and communicate actions, irregularities and continuing needs through the use of preventive maintenance software CNC machine operation Fabrication and welding Supervise maintenance staff Preferred knowledge/skills: Previous maintenance leadership/supervisory experience Computer savvy - proficient in MS Office Suite (Word, Excel and Outlook) Knowledge and familiarity with vacuum pumps and technology Experience with a preventive maintenance program, such as Maintain X Strong mechanical aptitude for accurately assessing, diagnosing and resolving equipment issues with a sense of urgency Motivated self-starter who works well independently and as part of a team Deadline and detail oriented Strong communication skills, verbal and written Education: HVAC Certification a plus High school diploma/GED required Previous experience: 5+ years prior experience in an equipment maintenance role with proven growth 3-years CNC machining experience Welding experience a plus We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.
Fleet Specialist (Warehouse) Are you ready to embark on an exciting journey in the micro-mobility industry? Our client is seeking enthusiastic individuals to join their team as Fleet Specialists in the warehouse! This is a fantastic opportunity to be part of a dynamic environment where your contributions will make a real difference. Position: Fleet Specialist (Warehouse) Contract Duration: 1 month - potential extension Working Pattern: 8:30am - 4pm Mon - Fri What You'll Do: As a Fleet Specialist, your main focus will be on replacing steering columns and performing various warehouse tasks. You'll be pivotal in ensuring our fleet of scooters is in top-notch condition! Here's a sneak peek of your responsibilities: Steering Column Replacement: Dive into training and learn how to efficiently replace steering columns. Your dedication will keep our scooters safe and functional! Scooter Movement: Help keep our warehouse organised by moving scooters around to designated areas. Quick Fixes: Utilise your skills to tackle minor repairs and maintenance tasks, ensuring our fleet is always ready for action. What We're Looking For: We want motivated team players who are eager to support our warehouse operations. Here's what you need to qualify: Warehouse Experience: Previous experience in a warehouse setting is a plus. Familiarity with tools (hand tools and power tools) will help you shine in this position. Team Spirit: A positive attitude and a willingness to learn are essential. We want individuals who are excited to contribute to our vibrant team! Why Join Us? Training Provided: Don't worry if you're new to steering column replacement; we'll provide comprehensive training to set you up for success. Dynamic Environment: Join a lively team dedicated to revolutionising urban mobility. Your work will directly impact the community! Opportunity for Growth: This contract may lead to further opportunities within our organisation, so show us what you've got! Ready to roll with us? If you're excited about joining a fast-paced, innovative industry and want to make a difference, we want to hear from you! Join us in shaping the future of micro-mobility- apply today and let's get started on this thrilling adventure together! Note: This is a temporary position with a duration of 1 month, so be sure to apply soon! We can't wait to welcome you aboard! Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.
01/04/2025
Project-based
Fleet Specialist (Warehouse) Are you ready to embark on an exciting journey in the micro-mobility industry? Our client is seeking enthusiastic individuals to join their team as Fleet Specialists in the warehouse! This is a fantastic opportunity to be part of a dynamic environment where your contributions will make a real difference. Position: Fleet Specialist (Warehouse) Contract Duration: 1 month - potential extension Working Pattern: 8:30am - 4pm Mon - Fri What You'll Do: As a Fleet Specialist, your main focus will be on replacing steering columns and performing various warehouse tasks. You'll be pivotal in ensuring our fleet of scooters is in top-notch condition! Here's a sneak peek of your responsibilities: Steering Column Replacement: Dive into training and learn how to efficiently replace steering columns. Your dedication will keep our scooters safe and functional! Scooter Movement: Help keep our warehouse organised by moving scooters around to designated areas. Quick Fixes: Utilise your skills to tackle minor repairs and maintenance tasks, ensuring our fleet is always ready for action. What We're Looking For: We want motivated team players who are eager to support our warehouse operations. Here's what you need to qualify: Warehouse Experience: Previous experience in a warehouse setting is a plus. Familiarity with tools (hand tools and power tools) will help you shine in this position. Team Spirit: A positive attitude and a willingness to learn are essential. We want individuals who are excited to contribute to our vibrant team! Why Join Us? Training Provided: Don't worry if you're new to steering column replacement; we'll provide comprehensive training to set you up for success. Dynamic Environment: Join a lively team dedicated to revolutionising urban mobility. Your work will directly impact the community! Opportunity for Growth: This contract may lead to further opportunities within our organisation, so show us what you've got! Ready to roll with us? If you're excited about joining a fast-paced, innovative industry and want to make a difference, we want to hear from you! Join us in shaping the future of micro-mobility- apply today and let's get started on this thrilling adventure together! Note: This is a temporary position with a duration of 1 month, so be sure to apply soon! We can't wait to welcome you aboard! Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.
We are currently looking on behalf of one of our important clients for a German Speaking Supply Chain Manager (Medical Device Sector). The role is a permanent position based across locations in Bern & Solothurn Cantons & comes with good home office allowance. Your Role: Participate in Process Optimization via the independent analysis & further development of existing supply chain processes in order to continuously increase efficiency, quality, transparency & resilience of the supply chain (Global Process Owner). Manage & implement overall & partial projects in the area of supply chain development, including budget planning, cost planning, resource management, time frame control & change management. Closely cooperate with internal departments such as IT, Production, Purchasing, SCM, QA/RA & Sales & also with external partners to ensure the efficient implementation of project requirements. Analyze current IT systems & develop requirements to optimize supply chain software solutions. Observe market trends, new technologies & best practices to integrate innovative solutions in the supply chain. Your Skills: At least 5 years of relevant operational Supply Chain experience, including experience in Supply Chain Development Management. Experienced in Project Management & Leading Interdisciplinary Teams (Stakeholder Management). An in-depth knowledge of Process Optimization & Implementation. A strong affinity for IT & an in-depth knowledge of SAP modules MM, PP & SD. Experience in S/4 HANA & other Supply Chain Management tools are considered advantageous. Ideally experienced in International Global Production Environments in the MedTech or Pharmaceutical Sectors. Your Profile: Completed Higher Education/University Degree in Industrial Engineering, Supply Chain Management or similar. Fluent English & German language skills (to at least C1 level) are mandatory requirements.
31/03/2025
Full time
We are currently looking on behalf of one of our important clients for a German Speaking Supply Chain Manager (Medical Device Sector). The role is a permanent position based across locations in Bern & Solothurn Cantons & comes with good home office allowance. Your Role: Participate in Process Optimization via the independent analysis & further development of existing supply chain processes in order to continuously increase efficiency, quality, transparency & resilience of the supply chain (Global Process Owner). Manage & implement overall & partial projects in the area of supply chain development, including budget planning, cost planning, resource management, time frame control & change management. Closely cooperate with internal departments such as IT, Production, Purchasing, SCM, QA/RA & Sales & also with external partners to ensure the efficient implementation of project requirements. Analyze current IT systems & develop requirements to optimize supply chain software solutions. Observe market trends, new technologies & best practices to integrate innovative solutions in the supply chain. Your Skills: At least 5 years of relevant operational Supply Chain experience, including experience in Supply Chain Development Management. Experienced in Project Management & Leading Interdisciplinary Teams (Stakeholder Management). An in-depth knowledge of Process Optimization & Implementation. A strong affinity for IT & an in-depth knowledge of SAP modules MM, PP & SD. Experience in S/4 HANA & other Supply Chain Management tools are considered advantageous. Ideally experienced in International Global Production Environments in the MedTech or Pharmaceutical Sectors. Your Profile: Completed Higher Education/University Degree in Industrial Engineering, Supply Chain Management or similar. Fluent English & German language skills (to at least C1 level) are mandatory requirements.
QA Validation Expert (EN/FR) vacancy for our Neuchatel based client in the pharmaceutical sector . The QA Validation Expert plays a key role in regulatory compliance and quality assurance for processes and equipment within a pharmaceutical industry operating under GMP (Good Manufacturing Practices). Working closely with technical teams, they ensure the review and approval of validation protocols to guarantee the safety, efficiency, and reliability of pharmaceutical products. Your tasks: Assess validation protocols related to equipment, processes, CIP, SIP, computerized systems, and HVAC/Utilities. Ensure compliance with GMP requirements, internal company standards, and international regulatory guidelines (FDA, EMA, etc.). Evaluate validation results to confirm that all requirements defined in the protocols are fully met. Identify discrepancies and propose corrective actions when necessary. Collaborate closely with technical departments (Production, Engineering, Validation, etc.) to foster an integrated quality approach. Participate in project meetings and provide expertise on quality aspects related to validations. Your experience/knowledge: Degree in a scientific field (pharmacy, biotechnology, chemistry, or equivalent). Significant experience (2 years or more) in a similar role within the pharmaceutical industry, in a GMP environment. Expertise in process, equipment, CIP, SIP, computerized systems validation. Experience in filling line, freeze-dryer validation is a plus Strong knowledge of GMP standards and international regulations (FDA, EMA, ICH). Familiarity with risk management methodologies (Risk Assessment) and validation protocols (IQ, OQ, PQ). Language skills: Oral and written skills in English and French, fluency is an asset Your soft skills: Analytical mindset and attention to detail in document reviews. Excellent communication skills to effectively collaborate with multidisciplinary teams. Solution-oriented approach and ability to manage multiple projects under tight deadlines. Location: Neuchatel, Switzerland Sector: Pharmaceutical Start: 04/2025 Duration: 12 MM+ Ref .Nr.: BH22761 Take the next step and send us your CV and contact phone number on which we can reach you during working hours. 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 welcome, we will support you all the way. By applying, you agree to the storage and processing of your data for the application process. We strictly comply with the applicable data protection laws.
31/03/2025
Project-based
QA Validation Expert (EN/FR) vacancy for our Neuchatel based client in the pharmaceutical sector . The QA Validation Expert plays a key role in regulatory compliance and quality assurance for processes and equipment within a pharmaceutical industry operating under GMP (Good Manufacturing Practices). Working closely with technical teams, they ensure the review and approval of validation protocols to guarantee the safety, efficiency, and reliability of pharmaceutical products. Your tasks: Assess validation protocols related to equipment, processes, CIP, SIP, computerized systems, and HVAC/Utilities. Ensure compliance with GMP requirements, internal company standards, and international regulatory guidelines (FDA, EMA, etc.). Evaluate validation results to confirm that all requirements defined in the protocols are fully met. Identify discrepancies and propose corrective actions when necessary. Collaborate closely with technical departments (Production, Engineering, Validation, etc.) to foster an integrated quality approach. Participate in project meetings and provide expertise on quality aspects related to validations. Your experience/knowledge: Degree in a scientific field (pharmacy, biotechnology, chemistry, or equivalent). Significant experience (2 years or more) in a similar role within the pharmaceutical industry, in a GMP environment. Expertise in process, equipment, CIP, SIP, computerized systems validation. Experience in filling line, freeze-dryer validation is a plus Strong knowledge of GMP standards and international regulations (FDA, EMA, ICH). Familiarity with risk management methodologies (Risk Assessment) and validation protocols (IQ, OQ, PQ). Language skills: Oral and written skills in English and French, fluency is an asset Your soft skills: Analytical mindset and attention to detail in document reviews. Excellent communication skills to effectively collaborate with multidisciplinary teams. Solution-oriented approach and ability to manage multiple projects under tight deadlines. Location: Neuchatel, Switzerland Sector: Pharmaceutical Start: 04/2025 Duration: 12 MM+ Ref .Nr.: BH22761 Take the next step and send us your CV and contact phone number on which we can reach you during working hours. 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 welcome, we will support you all the way. By applying, you agree to the storage and processing of your data for the application process. We strictly comply with the applicable data protection laws.
Outsystems CoE Lead My client has a requirement for a CoE lead who can drive their Centre of excellence in Outsystems. S/He will have to work with the Outsystems Development team and Client senior management to ensure they deliver the best Outsystems quality projects keeping clients organization goals/roadmap in place. 1)Architecture and Quality of all ongoing development projects . Ensure designing designing applications that are scalable, secure, and maintainable. By establishing architectural best practices and governance frameworks, the CoE ensures that all solutions adhere to high-quality standards. Key responsibilities include: Defining application architecture patterns and standards. Enforcing compliance with security, scalability, and performance guidelines. Conducting code reviews to maintain technical excellence. Utilizing tools like OutSystems Lifetime for monitoring and auditing. 2)Ensure Code Reusability Reusability is at the heart of efficient low-code development. This pillar emphasizes creating shared components, libraries, and templates that developers can leverage across projects, reducing redundancy and accelerating delivery. Key responsibilities include: Building a repository of reusable modules, widgets, and connectors. Promoting standardization in UI/UX and Back End processes. Enabling teams to adopt reusable components through documentation and training. Fostering collaboration between teams to share best practices and innovations. 3)Release Management: Establish a process of release management, planning releases, talking to multiple development teams and Product owners and come up with release plan to ensure all stages of environment are not impacted, none of the development team is getting impacted by the release. To ensure no last minute glitches, hindrances, better planning would be required. This foundation ensures smooth, efficient, and reliable application releases while managing the underlying platform's performance and scalability. It emphasizes operational excellence and continuous delivery. Key responsibilities include: Managing CI/CD pipelines for automated deployments. Overseeing environment management (development, staging, production). Monitoring platform health, performance, and usage metrics. Defining processes for version control, rollback, and disaster recovery. By establishing a robust Center of Excellence, organizations can: Enhance Quality: Through architecture governance and reusable components. Accelerate Development: By leveraging reusable code and streamlining release processes. Ensure Scalability: With platform operations optimized for performance. Promote Innovation: By enabling teams to focus on solving business challenges rather than reinventing the wheel. Align Business and IT: Through standardized processes and strategic oversight. 4)Platform Operations - To manage, govern, and enable the efficient use of the OutSystems platform across the organization. By defining processes, enforcing standards, and driving technical excellence, the CoE ensures that teams deliver scalable, secure, and high-quality applications in alignment with business needs. This CoE Lead should provide expertise, tools, and methodologies to accelerate delivery while mitigating risks, enabling organizations to achieve both short-term results and long-term digital transformation goals. 5)To Strengthen the CoE Maintaining the technical quality of OutSystems applications-especially across multiple suppliers and distributed teams-can be challenging. Ensuring scalability, reusability, and adherence to best practices
31/03/2025
Project-based
Outsystems CoE Lead My client has a requirement for a CoE lead who can drive their Centre of excellence in Outsystems. S/He will have to work with the Outsystems Development team and Client senior management to ensure they deliver the best Outsystems quality projects keeping clients organization goals/roadmap in place. 1)Architecture and Quality of all ongoing development projects . Ensure designing designing applications that are scalable, secure, and maintainable. By establishing architectural best practices and governance frameworks, the CoE ensures that all solutions adhere to high-quality standards. Key responsibilities include: Defining application architecture patterns and standards. Enforcing compliance with security, scalability, and performance guidelines. Conducting code reviews to maintain technical excellence. Utilizing tools like OutSystems Lifetime for monitoring and auditing. 2)Ensure Code Reusability Reusability is at the heart of efficient low-code development. This pillar emphasizes creating shared components, libraries, and templates that developers can leverage across projects, reducing redundancy and accelerating delivery. Key responsibilities include: Building a repository of reusable modules, widgets, and connectors. Promoting standardization in UI/UX and Back End processes. Enabling teams to adopt reusable components through documentation and training. Fostering collaboration between teams to share best practices and innovations. 3)Release Management: Establish a process of release management, planning releases, talking to multiple development teams and Product owners and come up with release plan to ensure all stages of environment are not impacted, none of the development team is getting impacted by the release. To ensure no last minute glitches, hindrances, better planning would be required. This foundation ensures smooth, efficient, and reliable application releases while managing the underlying platform's performance and scalability. It emphasizes operational excellence and continuous delivery. Key responsibilities include: Managing CI/CD pipelines for automated deployments. Overseeing environment management (development, staging, production). Monitoring platform health, performance, and usage metrics. Defining processes for version control, rollback, and disaster recovery. By establishing a robust Center of Excellence, organizations can: Enhance Quality: Through architecture governance and reusable components. Accelerate Development: By leveraging reusable code and streamlining release processes. Ensure Scalability: With platform operations optimized for performance. Promote Innovation: By enabling teams to focus on solving business challenges rather than reinventing the wheel. Align Business and IT: Through standardized processes and strategic oversight. 4)Platform Operations - To manage, govern, and enable the efficient use of the OutSystems platform across the organization. By defining processes, enforcing standards, and driving technical excellence, the CoE ensures that teams deliver scalable, secure, and high-quality applications in alignment with business needs. This CoE Lead should provide expertise, tools, and methodologies to accelerate delivery while mitigating risks, enabling organizations to achieve both short-term results and long-term digital transformation goals. 5)To Strengthen the CoE Maintaining the technical quality of OutSystems applications-especially across multiple suppliers and distributed teams-can be challenging. Ensuring scalability, reusability, and adherence to best practices
