Quality jobs

• United States of America
• Negotiable
• Posted 3 days ago

Position Overview: We are seeking a highly skilled and experienced Drug Product Process Development Consultant to join our team. The ideal candidate will have a strong background in small molecule drug product development, with a focus on early-stage development. This role involves providing tech...

• Albuquerque
• US$135000 - US$175000 per year
• Posted 4 days ago

We have a current opportunity for a Senior Principal Validation Engineer on a permanent basis with a rapidly expanding global organization based in Albuquerque, NM. This position will play a critical role in the expansion including other key projects for this site. If interested, please see the b...

• Copenhagen
• Negotiable
• Posted 7 days ago

We are working with a leading pharmaceutical company based in Copenhagen that are dedicated to the development, manufacturing, and commercialisation of small molecule therapeutics. Their mission is to improve patient outcomes through innovative and high-quality products. We are seeking a detail-o...

• New Jersey
• Negotiable
• Posted 9 days ago

We are seeking a highly skilled Computer System Validation (CSV) Engineer to join our client on a contract basis. This role is crucial for ensuring the validation and compliance of computerized systems in a regulated, GxP-compliant environment, contributing to the production of innovative oncolog...

• Limerick
• Negotiable
• Posted 9 days ago

Acting as a Quality Lead for all phases of production realization including NPD, NPI, Commercialisation, Sustaining, End to Life. Monitor and drive compliance within the development process and/or operations to GMP and the requirements of the QMS within assigned area. Trouble shooting quality iss...

• Zurich
• Negotiable
• Posted 10 days ago

I am on the search for a Quality Engineer for a key client of mine in Switzerland. The ideal candidate must meet the below requirements and expertise. Key Requirements: Proven experience with injection moulding and medical devices. Strong understanding of quality assurance processes and standards...

• Region Hannover
• Negotiable
• Posted 10 days ago

Job Summary: We are seeking a dedicated and detail-oriented Complaint Specialist to join our team. The ideal candidate will have experience as a dialysis technician or nurse and will be responsible for managing and resolving customer complaints related to our medical devices. This role is critica...

• Switzerland
• Negotiable
• Posted 10 days ago

I am on the search for a Quality Engineer for a key client of mine in Switzerland. The ideal candidate must meet the below requirements and expertise. Key Requirements: Proven experience with injection moulding and medical devices. Strong understanding of quality assurance processes and standards...

• Switzerland
• Negotiable
• Posted 11 days ago

I am on the search for a Quality Engineer for a key client of mine in Switzerland. The ideal candidate must meet the below requirements and expertise. Key Requirements: Proven experience with injection moulding and medical devices. Strong understanding of quality assurance processes and standards...

• Doylestown
• Negotiable
• Posted 12 days ago

Title: Quality Engineer Location: Doylestown, PA We are seeking a Quality Engineer to join a local medical device company and play a key role in ensuring the compliance and robustness of their products and processes. This position will focus on quality engineering activities in product developmen...

• Indianapolis
• US$65000 - US$110000 per year
• Posted 12 days ago

We're currently partnered with a top 10 U.S. Biopharma organization that's currently hiring for a Senior CSV Engineer position who have experience and knowledge with benchtop analytical instruments and lab equipment. If you're looking to grow within a renowned organization and hone in on your CSV...

• Netherlands
• Negotiable
• Posted 12 days ago

Quality Engineer - Netherlands About the Role As a Quality Engineer, you will play a key role in ensuring compliance with industry standards, optimising processes, and driving a culture of quality throughout the organisation. You will work closely with cross-functional teams to maintain high-qual...

• California
• Negotiable
• Posted 12 days ago

Field Evaluation Engineer Location: Greater Los Angeles/Southern California (Mandatory) We are looking for a skilled Field Evaluation Engineer to join our team. This role offers an exciting opportunity to work in a dynamic and fast-paced environment, ensuring product safety and compliance through...

• Omaha Township
• US$85000 - US$110000 per year
• Posted 15 days ago

Join a dynamic team as a Manager of Validation! In this pivotal role, you will lead our Validation department, overseeing and driving engineering projects from inception through to completion. You will manage resources, coordinate efforts, and facilitate project progression, ensuring successful o...

• Visp
• Negotiable
• Posted 16 days ago

Head of Process Analytics Engineering and Maintenance We are seeking an experienced and dynamic leader to head the Process Analytics Engineering and Maintenance function at a large-scale manufacturing site in the chemical or pharmaceutical industry. This position offers an exciting opportunity to...

• United States of America
• Negotiable
• Posted 18 days ago

EPM is collaborating with a leading medical device company in the USA to find a skilled Engineer specializing in the evaluation and testing of medical electrical devices. This role is crucial in ensuring products meet regulatory standards and industry requirements. Role Overview The Engineer will...

• Philadelphia
• Negotiable
• Posted 19 days ago

We are working with a leading pharmaceutical company dedicated to the development, manufacturing, and commercialization of small molecule therapeutics. Their mission is to improve patient outcomes through innovative and high-quality products. We are seeking a detail-oriented Quality Assurance Spe...

• Galway
• Negotiable
• Posted 22 days ago

Senior Validations Engineer The requirements of this role within the wider project are to cover the validation activities with respect to the testing and manufacture of the client's device. Role/ Responsibilities: Develop, and/or approve, validation documentation, including protocol, records, and...

• Brooklyn Park
• Negotiable
• Posted 24 days ago

Senior Quality Engineer Opportunity We are excited to offer a promising career opportunity for an experienced Senior Quality Engineer in Brooklyn Park, MN location. This full-time, permanent position is especially suited for a professional who specializes in the medical device industry and posses...

• Philadelphia
• US$80000 - US$151000 per year
• Posted 24 days ago

We have a current opportunity for a Senior Quality Lead/ Manufacturing CSA QA on a permanent basis. The position will be based in Philadelphia, PA with a hybrid model. For further information about this position please apply and see the below: Key Responsibilities: Possesses comprehensive knowled...

• Rahway
• US$120000 - US$140000 per year
• Posted 25 days ago

Lead CQV-CSV Engineer Responsibilities: Manage multiple projects and clients simultaneously. Lead client-facing activities and handle responsibilities. Serve as the escalation point for issues on client projects. Design validation plans and engineering studies. Verify system drawings and electric...

• Naples
• US$135000 - US$145000 per year
• Posted 25 days ago

Job Opportunity: Senior Quality Engineer in Santa Barbara Location: Santa Barbara, CA Company: Privately Owned Company Specializing in Orthopedic and Surgical Devices Position Senior: Quality Engineer (Onsite) About the Company Join a leading company in the orthopedic and surgical device industry...

• Santa Barbara
• US$125000 - US$138000 per year
• Posted 25 days ago

The Senior Quality Engineer to join the team, will work with cutting-edge orthopedic and software surgical devices. This role involves ensuring product quality and compliance from design through manufacturing. Key Responsibilities: - Represent Quality Assurance in product design and development p...

• Negotiable
• Posted about 1 month ago

We have a current opportunity for a Senior Quality Engineer on a contract basis. - To start ASAP - Fully on-site (hands on role) - Must have injection moulding experience - Previous contract Manufacturing environment would be suitable - CAPA's - Medical Device standard - ISO13485 - Monday - Frida...

• Naples
• US$140000 - US$150000 per year
• Posted about 1 month ago

Job Opportunity: Senior Quality Engineer in Santa Barbara Location: Santa Barbara, CA Company: Privately Owned Company Specializing in Orthopedic and Surgical Devices Position Senior: Quality Engineer (Onsite) About the Company Join a leading company in the orthopedic and surgical device industry...

• Naples
• US$140000 - US$145000 per year
• Posted about 1 month ago

Job Opportunity: Senior Quality Engineer in Santa Barbara Location: Santa Barbara, CA Company: Privately Owned Company Specializing in Orthopedic and Surgical Devices Position Senior: Quality Engineer (Onsite) About the Company Join a leading company in the orthopedic and surgical device industry...

• Region Hannover
• Negotiable
• Posted about 1 month ago

Job Summary: We are seeking a dedicated and detail-oriented Complaint Specialist to join our team. The ideal candidate will have experience as a dialysis technician or nurse and will be responsible for managing and resolving customer complaints related to our medical devices. This role is critica...

• Region Hannover
• Negotiable
• Posted about 1 month ago

Job Summary: We are seeking a dedicated and detail-oriented Complaint Specialist to join our team. The ideal candidate will have experience as a dialysis technician or nurse and will be responsible for managing and resolving customer complaints related to our medical devices. This role is critica...

• Region Hannover
• Negotiable
• Posted about 1 month ago

Job Summary: We are seeking a dedicated and detail-oriented Complaint Specialist to join our team. The ideal candidate will have experience as a dialysis technician or nurse and will be responsible for managing and resolving customer complaints related to our medical devices. This role is critica...

• Germany
• Negotiable
• Posted about 1 month ago

Urgent Freelance Quality Assurance Engineering Consultant (Pharmaceutical Industry) Location: Northern Germany Duration: Immediate Start - 12-Month Contract Language: Must be German-speaking We are working exclusively with a large pharmaceutical client to find a highly skilled Quality Assurance E...

• Huntersville
• Negotiable
• Posted about 1 month ago

Job Summary: We are seeking a Quality Engineer with knowledge of Medical Device Manufacturing and a compliance background. This role demands a solid understanding of quality system requirements for medical device companies. The primary responsibility will be to execute Corrective and Preventive A...

• San Diego
• US$120000 - US$140000 per year
• Posted about 1 month ago

About Are you ready to make a real impact in the field of non-opioid pain management? This company is a leading provider of non-opioid pain management and regenerative health solutions. Our commitment to advancing patient care drives us to address unmet medical needs and improve clinical results....

• Dublin
• Negotiable
• Posted about 1 month ago

I'm currently looking for an experienced DeltaV Automation Lead with expertise in spray drying and a background in API manufacturing for a full-time, on-site role in the South of Ireland. The client is eager for an immediate start but is open to some flexibility for the right candidate. Ideal Can...

• Negotiable
• Posted about 1 month ago

𝗗𝗲𝗹𝘁𝗮𝗩 𝗕𝗮𝘁𝗰𝗵 𝗘𝗻𝗴𝗶𝗻𝗲𝗲𝗿 - 12-𝗠𝗼𝗻𝘁𝗵 𝗖𝗼𝗻𝘁𝗿𝗮𝗰𝘁 | 𝗗𝘂𝗯𝗹𝗶𝗻 | 𝗙𝗟𝗦 𝗦𝗵𝗶𝗳𝘁 Currently seeking an experienced 𝗗𝗲𝗹𝘁𝗮𝗩 𝗕𝗮𝘁𝗰𝗵 𝗘𝗻𝗴𝗶𝗻𝗲𝗲𝗿 for a 12-𝗺𝗼𝗻𝘁𝗵 𝗰𝗼𝗻𝘁𝗿𝗮𝗰𝘁 at a leading 𝗽𝗵𝗮𝗿𝗺𝗮 site in Dublin. This role is key to supporting critical manufacturing operations in a fast-paced, high-tech environment. 🔹12-𝗺𝗼𝗻𝘁𝗵 𝗰𝗼𝗻𝘁...

• Negotiable
• Posted about 1 month ago

I'm currently looking for an experienced DeltaV Automation Lead with expertise in spray drying and a background in API manufacturing for a full-time, on-site role in the South of Ireland. The client is eager for an immediate start but is open to some flexibility for the right candidate. Ideal Can...

• Ohio
• Negotiable
• Posted about 1 month ago

Location: Midwest, USA (with Travel Requirements) EPM is working with an exceptional medical device company in the Midwest that is seeking experienced Senior Quality Engineers to join their team. This company specializes in ophthalmology, cardiovascular, and dental medical devices and is dedicate...

• Sweden
• Negotiable
• Posted about 1 month ago

About the Role: We are seeking an experienced CQV (Commissioning, Qualification & Validation) Consultant to support Factory Acceptance Testing (FAT) and commissioning for a key project. The successful candidate will play a critical role in ensuring that equipment and systems meet regulatory and o...

• Visp
• Negotiable
• Posted about 1 month ago

Our client is seeking a skilled Thermal Validation Subject Matter Expert to join their BIO Biologics Division Services (BDS) team for a 9-month contract in Visp. The successful candidate will be responsible for ensuring the qualification and validation of process and support equipment, including ...

• Walkersville
• Negotiable
• Posted about 1 month ago

Lead CQV Engineer Responsibilities: Project Leadership: Guide the team to complete projects on time. Document Review: Ensure validation documents meet standards (e.g., User Requirements, IQ, OQ, PQ, Calibration). Equipment: Handle validation for lab equipment, facility, utility equipment, and pac...

• Walkersville
• Negotiable
• Posted about 1 month ago

Lead CQV Engineer Responsibilities: Project Leadership: Guide the team to complete projects on time. Document Review: Ensure validation documents meet standards (e.g., User Requirements, IQ, OQ, PQ, Calibration). Equipment: Handle validation for lab equipment, facility, utility equipment, and pac...

• Walkersville
• Negotiable
• Posted about 1 month ago

Lead CQV Engineer Responsibilities: Project Leadership: Guide the team to complete projects on time. Document Review: Ensure validation documents meet standards (e.g., User Requirements, IQ, OQ, PQ, Calibration). Equipment: Handle validation for lab equipment, facility, utility equipment, and pac...

• Warren
• Negotiable
• Posted about 1 month ago

Position Title: Senior CSV Engineer Role Overview: We're on the lookout for a seasoned Computer System Validation (CSV) Specialist to enhance our commissioning and qualification (C&Q) activities for a cell therapy manufacturing initiative. This pivotal role ensures our computer systems are compli...

• Stuttgart
• Negotiable
• Posted about 2 months ago

Key Responsibilities: Perform technical assessments of active medical devices, ensuring compliance with MDR 2017/745 and international regulatory standards. Conduct conformity assessments, design dossier reviews, and clinical evaluations for medical devices. Lead and participate in regulatory aud...

• Stuttgart
• Negotiable
• Posted about 2 months ago

Key Responsibilities: Conduct technical file reviews, risk assessments, and clinical evaluations of non-active medical devices. Perform conformity assessments and certification evaluations under MDR 2017/745 and related standards. Lead and participate in regulatory audits (ISO 13485, MDSAP, MDR) ...

• Marlborough
• Negotiable
• Posted about 2 months ago

Title: Senior Design Assurance Engineer Location: Marlborough, MA (On-Site) A MA-based company that develops innovative medical device laser solutions is rapidly growing and seeking additional support on their Quality team. They are looking for a Senior Design Assurance Engineer to lead NPD activ...

• Negotiable
• Posted about 2 months ago

We are seeking a DeltaV Automation Engineer with 3+ years of experience in DeltaV Batch systems within pharma manufacturing for a 12-month contract in Dublin. Key Responsibilities: Support automation operations and ensure GMP compliance. FLS Shift Role - supporting 24/7 operations Troubleshoot an...

• Norway
• Negotiable
• Posted about 2 months ago

Job Description: Medical Device Assessor & Lead Auditor - Non-Active Devices Location: Remote / Hybrid (Flexible) Employment Type: Contract / Permanent Industry: Medical Devices, Regulatory Affairs, Notified Body Key Responsibilities: Conduct technical file reviews, risk assessments, and clinical...

• Germany
• Negotiable
• Posted about 2 months ago

Job Description: Integrated Clinician - Medical Devices (Active & Non-Active) Location: Remote / Hybrid (Flexible) Employment Type: Contract / Permanent Industry: Medical Devices, Regulatory Affairs, Notified Body Key Responsibilities: Conduct clinical evaluations and assessments of active and no...

• Stuttgart
• Negotiable
• Posted about 2 months ago

Do you want to be a driving force in a rapidly expanding environment, making a tangible difference in the process? We have an exciting opportunity for you! Our Client is a market leader in the Biopharmaceutical Industry. They are looking to hire top QA Engineers. Tasks Run tests to make sure the ...

• Visp
• Negotiable
• Posted about 2 months ago

Our client is seeking a skilled Supplier & Material Qualification Specialist to join their BIO Mammalian team for a 6-Month contract to ensure the efficient and compliant supplier and material qualification process in line with regulatory requirements, corporate standards, and agreements with sta...

• Grove City
• Negotiable
• Posted about 2 months ago

CSV/CQV Engineer Responsibilities: Looking for a strong resource with a diverse skillset focused around Data Integrity accompanied by a thorough understanding of both CSV and CQV principles. Authoring, editing, and executing technical commissioning, qualification and validation documentation for ...

• Cincinnati
• Negotiable
• Posted about 2 months ago

Are you an experienced CQV Engineer/Validation Engineer 2 looking for your next opportunity? This is a key role in ensuring the quality and compliance of cutting-edge equipment, systems, and processes in a GMP-regulated environment. Responsibilities and Qualifications would include: -Author, edit...

• Stuttgart
• Negotiable
• Posted about 2 months ago

Head of Non-Active Medical Devices - Leading Notified Body We are representing a leading Notified Body seeking an experienced Head of Non-Active Medical Devices to join their team. This is a pivotal leadership role within a globally recognized organization, providing regulatory expertise, strateg...

• Zurich
• Negotiable
• Posted about 2 months ago

My client are a leader in the medical device industry, dedicated to enhancing patient care with high-quality products and innovative technology. Position Summary: We are seeking a skilled Quality Engineer to maintain quality management systems, and drive continuous improvement in our manufacturin...

• Bethesda
• Negotiable
• Posted about 2 months ago

About the Role A leading Notified Body is seeking an experienced Medical Device Auditor with expertise in IEC 60601-1 (Electrical Safety) and Medical Device Software to join its growing team. This role is crucial in ensuring that medical electrical equipment and software-driven devices comply wit...

• Bethesda
• Negotiable
• Posted about 2 months ago

A leading Notified Body is seeking experienced Medical Device and In Vitro Diagnostic (IVD) Product Reviewers / Auditors to join its growing certification and regulatory compliance team. This role is crucial in ensuring that medical devices and IVD products meet the highest safety, quality, and r...

• London
• Negotiable
• Posted about 2 months ago

A leading provider of certification, audit, and assurance services is seeking a highly skilled professional to join its Assurance Services team as a Lead Auditor. With over 70 years of experience in the UK, the organization ensures that products and systems are safe, reliable, and compliant by of...

• Switzerland
• Negotiable
• Posted about 2 months ago

I am on the search for a Quality Engineer for a key client of mine in Switzerland. The ideal candidate must meet the below requirements and expertise. Key Requirements: Proven experience with injection moulding and medical devices. Strong understanding of quality assurance processes and standards...