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• Naples
• US$140000 - US$150000 per year
• Posted about 10 hours 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 10 hours 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...

• Spain
• Negotiable
• Posted about 17 hours ago

🚀 Exciting Opportunity - QARA Consultant - Software Diagnostics 🚀 📅 Contract Length: 12 Months 🌎 Location: Remote 💼 Hours: 20 Hours per week I am partnering with a leading medical device client who is looking for a QARA Consultant focusing on Software Diagnostics Compliance. 🔍 Key Skills & Experi...

• Asheville
• Negotiable
• Posted about 19 hours ago

Title: Associate Director, Microbiology & Sterility Assurance Location: Asheville, NC The Associate Director of Microbiology & Sterility Assurance is a key quality leadership role responsible for overseeing microbiological practices and ensuring compliance with regulatory standards in a manufactu...

• Asheville
• Negotiable
• Posted about 19 hours ago

Title: Associate Director, Microbiology & Sterility Assurance Location: Asheville, NC The Associate Director of Microbiology & Sterility Assurance is a key quality leadership role responsible for overseeing microbiological practices and ensuring compliance with regulatory standards in a manufactu...

• Region Hannover
• Negotiable
• Posted about 21 hours 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 21 hours 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 21 hours 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...

• Japan
• Negotiable
• Posted 1 day ago

Job Title: Quality Assurance Specialist Location: Japan Industry: Biotechnology Company Overview: Join our leading biotechnology company dedicated to advancing healthcare through innovative and high-quality products. We are seeking a dedicated Quality Assurance Specialist to ensure our products m...

• Germany
• Negotiable
• Posted 1 day 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...

• Germany
• Negotiable
• Posted 1 day ago

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

• New York
• Negotiable
• Posted 1 day ago

Job Summary Develop, apply, and maintain quality standards for sample testing processes and comply with regulations. Schedule meetings with management to update them on projects and equipment. Essential Responsibilities Implement management activities within SOPs for the lab and R&D/Validation te...

• Huntersville
• Negotiable
• Posted 1 day 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...

• Negotiable
• Posted 2 days ago

Job Title: Senior Quality Assurance Specialist Location: Japan Industry: Pharmaceutical Company Overview: Join a leading pharmaceutical company dedicated to advancing healthcare through innovative and high-quality products. We are seeking a dedicated Quality Assurance Specialist with a Pharmacist...

• Shizuoka
• Negotiable
• Posted 2 days ago

Job Title: Senior Quality Assurance Specialist Location: Japan Industry: Pharmaceutical Company Overview: Join our leading pharmaceutical company dedicated to advancing healthcare through innovative and high-quality products. We are seeking a dedicated Quality Assurance Specialist with a Pharmaci...

• Japan
• Negotiable
• Posted 2 days ago

Job Title: Senior Quality Assurance Specialist Location: Japan Industry: Pharmaceutical Company Overview: Join a leading pharmaceutical company dedicated to advancing healthcare through innovative and high-quality products. We are seeking a dedicated Quality Assurance Specialist with a Pharmacist...

• Singapore
• Negotiable
• Posted 2 days ago

Job Title: Quality Assurance Director Location: Singapore Company Overview: Our client is a dynamic healthcare organization dedicated to providing top-notch medical services and improving patient outcomes. We are seeking a highly experienced and motivated Quality Assurance Director to lead our qu...

• San Diego
• US$150000 - US$180000 per year
• Posted 2 days ago

We are working with a biotechnology research company in San Diego who is looking for a Associate Director of Supplier Quality. The company has 3 compounds undergoing clinical trials currently, and is looking for someone with an extensive background in supplier quality as well as working with comm...

• Deutschlandsberg
• Negotiable
• Posted 3 days ago

I am currently working with a global leader in medical devices, dedicated to advancing healthcare through innovations in cardiology, orthopedics, surgical robotics, and diagnostics. They are currently looking for a GPO Tender Manager to join their expert team. Key Role Highlights: As a GPO Tender...

• Germany
• Up to €24000 per annum
• Posted 3 days ago

I am working with a global leader in medical devices, dedicated to advancing healthcare through innovations in cardiology, orthopedics, surgical robotics, and diagnostics. They are currently looking for a GPO Tender Manager to join their expert team. Key Role Highlights: As a GPO Tender Manager, ...

• San Diego
• US$120000 - US$140000 per year
• Posted 3 days 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 4 days 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 4 days 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 4 days 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 4 days 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...

• Singapore
• Negotiable
• Posted 4 days ago

Company Overview: Our client is a global leader in life sciences and biopharmaceuticals, offering unparalleled opportunities to impact healthcare. The Regional Quality Director will play a crucial role in leading and inspiring quality teams, ensuring the highest standards of quality, and directly...

• Spain
• Negotiable
• Posted 5 days ago

Estamos buscando un líder en Garantía de Calidad para unirse a nuestro equipo global y desempeñar un papel clave en el desarrollo y lanzamiento de nuevas moléculas, tecnologías y modelos de negocio. Reportando al Chief Quality Officer, esta posición será responsable de garantizar el cumplimiento ...

• Hesseneck
• Negotiable
• Posted 6 days ago

The head of the QM & RA department leads the Quality Management and Regulatory Affairs team, ensuring adherence to regulatory standards and continuous development of the quality management system (QMS). This role encompasses management tasks, strategic oversight, and operational responsibilities,...

• Kaufering
• Negotiable
• Posted 8 days ago

We have a current opportunity for a Quality Manager on a permanent basis. The position will be based in Kaufering. For further information about this position please apply. Your responsibilities include the management and coordination of cross-departmental quality management projects You also sup...

• Sacramento
• US$180000 - US$240000 per year
• Posted 8 days ago

We are currently working with a pharmaceutical company engaged in developing, manufacturing, and marketing pharmaceutical products across generics and specialty drugs The client is seeking an Associate Director (or Higher) Quality officer to head out their Quality department as they are building ...

• Sweden
• Negotiable
• Posted 8 days 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 8 days 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 ...

• Pendleton
• US$90000 - US$105000 per year
• Posted 9 days ago

Quality Systems Senior Auditor A leading global medical device company, renowned for its innovation in product development and medical education within orthopedics, is seeking a Senior Quality Systems Auditor for its manufacturing site in South Carolina. This pivotal role involves conducting inte...

• Brisbane
• US$220000 - US$250000 per year + 401k, Dental, Medical, Vision
• Posted 9 days ago

Position: The Senior Director, Quality Systems will serve as a subject matter expert and will assist in the implementation and maintenance of GxP compliant procedures and operations by managing the GxP systems including electronic document management system and learning management system. This ha...

• Naples
• US$70000 - US$100000 per year
• Posted 10 days ago

A global Medical Device company is seeking a Quality Systems Auditor II to join their manufacturing site in Naples, FL. This role involves conducting internal quality system audits to ensure compliance with industry standards and regulations related to the development, manufacturing, and distribu...

• Walkersville
• Negotiable
• Posted 10 days 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 10 days 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 10 days 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 10 days 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...

• North Dakota
• Negotiable
• Posted 11 days ago

Stability Manager Job Description: Seeking a highly motivated and detail-oriented Stability Manager to join a growing team. As a Stability Manager, you will be responsible for overseeing and managing the stability program as well as a team. This includes designing stability protocols, managing st...

• Stuttgart
• Negotiable
• Posted 11 days 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 11 days 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) ...

• Visp
• Negotiable
• Posted 11 days ago

Unser Kunde sucht einen qualifizierten Biotech Associate, der für einen spannenden 10-Monats-Vertrag dem Team der BIO Biologics Division Services (BDS) beitritt. Dies ist eine hervorragende Gelegenheit für eine detailorientierte Fachkraft, die im Bereich der Qualitätssicherung in einer hochmodern...

• Visp
• Negotiable
• Posted 11 days ago

Unser Kunde sucht einen qualifizierten Biotech Associate, der für einen spannenden 10-Monats-Vertrag dem Team der BIO Biologics Division Services (BDS) beitritt. Dies ist eine hervorragende Gelegenheit für eine detailorientierte Fachkraft, die im Bereich der Qualitätssicherung in einer hochmodern...

• Netherlands
• Negotiable
• Posted 11 days ago

We are currently supporting a Quality Assurance Officer position for a client based in The Netherlands. Quality Assurance Officer Our client is an innovator in Global Health and is currently looking for a Quality Assurance Officer to join the team! Main Responsibilities of a Quality Assurance Off...

• Marlborough
• Negotiable
• Posted 13 days 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 15 days 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...

• Weybridge
• Negotiable
• Posted 15 days ago

We are currently supporting a Qualified Person and Responsible Person position for a client based in the London. Qualified Person and Responsible Person Our client is an innovator in the consumer health space and is currently looking for a Qualified Person and Responsible Person to join the team!...

• Weybridge
• Negotiable
• Posted 15 days ago

We are currently supporting a Qualified Person and Responsible Person position for a client based in the London. Qualified Person and Responsible Person Our client is an innovator in the consumer health space and is currently looking for a Qualified Person and Responsible Person to join the team!...

• Oberhonnefeld-Gierend
• Negotiable
• Posted 15 days ago

We have a current opportunity for a Head of QA/RA on a permanent basis. The position will be based in Oberhonnefeld-Gierend. For further information about this position please apply. Job Summary: The Head of Quality and Regulatory Affairs will oversee and manage all quality and regulatory functio...

• Norway
• Negotiable
• Posted 15 days 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 15 days 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...

• Germany
• Negotiable
• Posted 16 days ago

We are currently working with a reputable Solutions Provider in the pharmaceutical and medical device industry looking for an experienced Quality Management & Compliance professional to join the team in Germany. This is an exciting opportunity to work within a growing team, partnering with leadin...

• Stuttgart
• Negotiable
• Posted 16 days 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 16 days 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 16 days 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 16 days 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...

• Japan
• Negotiable
• Posted 16 days ago

Job Title: Senior Quality Manager (Pharmaceutical) Location: Japan Job Description: Our client is seeking a highly skilled and experienced Senior Quality Manager to join the team in Japan. The successful candidate will be responsible for overseeing and ensuring the highest standards of quality in...

• Grove City
• US$70000 - US$129000 per year
• Posted 16 days ago

We are working with a pharmaceutical manufacturing company who is seeking a Senior Quality Specialist/CQV to support their quality systems and validation activities. This company's core mission is to drive growth and spark innovation within the scientific community, helping a mutitude of pharmace...

• Cincinnati
• Negotiable
• Posted 16 days ago

We are working with a pharmaceutical manufacturing company who is seeking a CQV Validation Engineer 2 to support and collaborate with their current clients. This company's core mission is to drive growth and spark innovation within the scientific community, aiding researchers, organizations, and ...

• Morristown
• US$150000 - US$180000 per year
• Posted 17 days ago

Associate Director, GCP Quality Compliance Summary An industry leader in regenerative health and pain management (non-opioid) is seeking a driven Associate Director, GCP Quality Compliance to join their team. As a Clinical Quality leader working in concert with executive leadership - this person ...

• Naples
• Negotiable
• Posted 17 days ago

Quality Auditor II An Industry-leading medical device company is seeking a Quality Systems Auditing expert for their site in Naples, Florida. They will conduct internal quality system audits to evaluate and ensure conformance to industry standards and regulations related to the development, manuf...

• Devon
• Negotiable
• Posted 17 days ago

We have a current opportunity for a Director of site Quality Management on a permanent basis. The position will be based in Devon. For further information about this position please apply.

• United States of America
• Negotiable
• Posted 17 days ago

ry: We are seeking an experienced GMP Auditor to join our Quality Assurance team. The successful candidate will be responsible for ensuring compliance with Good Manufacturing Practices (GMP) and conducting thorough audits of our processes and systems. Key Responsibilities: Conduct internal and ex...

• Munich
• Swiss Franc80000 - Swiss Franc90000 per annum
• Posted 17 days ago

Senior Quality and Regulatory Affairs Manager - Healthcare Technology (f/m/d) Responsibilities Conduct gap analyses of regulatory documents and QMS documentation, and implement necessary updates. Keep regulatory documentation, including laws, standards, regulations, and guidance documents, curren...

• United States of America
• Negotiable
• Posted 17 days ago

Responsibilities: Minimum 7 years of experience in quality assurance in the biotech or pharmaceutical industry Small Molecules, Solid Oral Dosage experience. Develop, implement, and maintain quality assurance programs, policies, and procedures in compliance with regulatory standards (e.g., FDA, E...

• Albuquerque
• Negotiable
• Posted 18 days ago

Key Responsibilities: Oversee daily operations of the Microbiology laboratory, ensuring smooth and efficient workflow. Lead strategic planning efforts for the laboratory and its staff to meet organizational goals. Serve as the subject matter expert on contamination control and microbiological tes...

• City of London
• Negotiable
• Posted 18 days ago

We are currently supporting a Process Engineer position for a client based in the London. Process Engineer Our client is an innovator in the Medical Device space and is currently looking for a Process Engineer to join the team! Main Responsibilities of a Process Engineer Facilitating the design, ...

• Luxembourg
• Negotiable
• Posted 19 days ago

Role: Leasing Manager Location: Ireland (Homebased) About the Company: A global market leader in the Life Sciences testing space is searching for a Leasing expert to join their team. Responsibilities: Asset management - You will be fully responsible for the inventory, deployment and lifecycle man...

• Stuttgart
• Negotiable
• Posted 19 days 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...

• Secaucus
• US$140000 - US$175000 per year
• Posted 22 days ago

Sr. Manager, Microbiology - Sterility Assurance, EM & Contamination Control An industry leading Global Pharmaceutical company is currently at the forefront of biologics manufacturing. They are seeking a Microbiology/Sterility Assurance leader who is seeking to contribute to life-saving therapies....

• Atlanta
• US$65000 - US$750000 per year
• Posted 22 days ago

Quality Assurance Specialist Position Overview: The Quality Assurance (QA) Specialist is tasked with reviewing a variety of documents, protocols, qualifications, and reports related to Quality Management Systems. This position involves interaction with clients regarding quality issues as needed. ...

• Singapore
• Negotiable
• Posted 22 days ago

Our client is a research organisation that develops vaccines and biologics. They are currently looking for a leader for their Analytical Sciences & Technology team to drive the development and implementation of analytical controls activities. Responsibilities: Develop and manage strategies for th...

• Zurich
• Negotiable
• Posted 23 days 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...

• Hamburg
• Negotiable
• Posted 23 days ago

Your Responsibilities: Ensure compliance with the risk management process according to ISO 14971 for new developments and existing therapy products. Coordinate, create, and maintain risk management files for new developments, the existing portfolio, and change management in therapy products. Anal...

• Morristown
• Negotiable
• Posted 24 days ago

Job Title: Quality Lab Manager Location: Morristown, TN (Can Provide Relocation!) A leading producer of cross-industry FDA-regulated products is expanding their team! They are looking for a Quality Lab Manager to direct all laboratory activities and oversee site quality systems. Job Responsibilit...

• Kaufbeuren
• £60000 - £80000 per annum
• Posted 24 days ago

Senior Test Engineer - Digital Technologies Location: Bavaria, Germany Industry: Medical Devices Shape the Future of Digital Healthcare Join a pioneering team developing cutting-edge digital technologies that enhance surgical precision and patient outcomes. This is an opportunity to work on high-...

• Nyon
• Negotiable
• Posted 24 days ago

Our client is seeking a skilled QC Validation Scientist to join their Product Innovation team for a 2-year contract. This position is ideal for someone with extensive experience in process, cleaning, and analytical validation within the pharmaceutical industry. As a QC Validation Scientist, you w...

• Bethesda
• Negotiable
• Posted 24 days 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 24 days 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 24 days 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...

• Tuttlingen
• Negotiable
• Posted 24 days ago

We have a current opportunity for a QA/RA Manager on a permanent basis. The position will be based in Tuttlingen. For further information about this position please apply. You can look forward to these tasks: * Evaluation, selection and continuous monitoring of suppliers in accordance with intern...

• Albuquerque
• Negotiable
• Posted 25 days ago

Want to join a growing biopharmaceutical manufacturing organization that's rapidly expanding? See the below for more information! Overview: The Manager, Quality Manufacturing oversees daily product manufacturing and lot release, acting as the primary Quality contact for internal teams. This role ...

• Munich
• Negotiable
• Posted 25 days ago

We are looking for a highly skilled individual to assist the quality management and touchpoints with regulatory bodies across various business units or subsidiary companies with a specific focus on Europe and other regions. Responsibilities Establish and maintain Quality System requirements effec...

• Vienna
• Negotiable
• Posted 25 days ago

Job Title: Freelance eQMS Specialist Duration: 6 Months Industry: Pharmaceutical We are looking for a Project Quality Management Specialist to support the modernisation and update of our Electronic Quality Management System (eQMS) on a freelance basis. This is a contract position for six months, ...

• Negotiable
• Posted 25 days ago

CQV - HVAC Specialist Required in Dublin, UK (Contract Position) Are you a seasoned CQV professional with expertise in the pharmaceutical sector? We are seeking an experienced Freelance Commissioning, Qualification and Validation (CQV) specialist to fill a contract role focusing on Heating, Venti...

• North Carolina
• Negotiable
• Posted 25 days ago

. The Contractor Quality Associate, Biologics plays a critical role in data management of commercial biologics executed by contract laboratories. The position requires familiarity with data review, data management in Excel or Minitab, and understanding of LIMS systems. Some understanding or famil...

• Switzerland
• Negotiable
• Posted 25 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...

• Frauenfeld
• Negotiable
• Posted 25 days ago

Job Description: This Exclusive mandate seeks a highly experienced and motivated Global Head of Quality and Regulatory with direct leadership expertise and hands on mentality to join a dynamic client in the medical device field. This leadership role is critical in ensuring our products meet the h...

• Devon
• Negotiable
• Posted 27 days ago

We have a current opportunity for a Director Site Quality Manager - Ilfracombe, Devon on a permanent basis. In this role, you will have the opportunity to: Represent the Ilfracombe site as the Quality Management Representative and lead management reviews Responsible for the leadership & developme...

• England
• Negotiable
• Posted 27 days ago

United Kingdom - Newcastle / Remote Opporunity You will be a part of the Quality Assurance team and report to the Manager, Quality Assurance (Design). You will be responsible for applying in-depth knowledge, experience, expertise in multiple areas of medical device quality assurance, guiding the ...

• Connecticut
• Negotiable
• Posted 29 days ago

Quality Control Supervisor Are you a dedicated Quality Control professional looking for an opportunity to lead and make a significant impact within the biopharma industry? As QC Supervisor, your responsibilities will include: - Overseeing daily operations within the Quality Control department - E...

• Germany
• Negotiable
• Posted 29 days ago

Freelancer Qualification Consultant - Large Pharmaceutical Company Contract Duration: 8 Months (February to November) Location: Germany (Onsite) We're looking for a team of 4x Qualification Consultant to join a global pharmaceutical company! Your main focus will be room, medium, and equipment qua...

• England
• Negotiable
• Posted 29 days ago

United Kingdom - Newcastle / Remote Opporunity You will be a part of the Quality Assurance team and report to the Manager, Quality Assurance (Design). You will be responsible for applying in-depth knowledge, experience, expertise in multiple areas of medical device quality assurance, guiding the ...

• Albuquerque
• Negotiable
• Posted 30 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...

• Atlanta
• Negotiable
• Posted about 1 month ago

Quality Specialist - Regulatory Affairs Overview: Join an industry leading biotech organization leading development of In vitro Diagnostic Medical Devices. This expert role within the Quality Assurance team involves supporting regulatory activities for In vitro Diagnostic Medical Devices. You wil...

• South San Francisco
• Negotiable
• Posted about 1 month ago

Position Summary: We are seeking a talented and driven professional to take a pivotal role in maintaining and enhancing our advanced research ecosystem, comprising diverse datasets, sophisticated processes, and innovative tools. In this dynamic and fast-paced team environment, you will play a cri...

• Santa Barbara
• US$125000 - US$138000 per year
• Posted about 1 month 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...

• United States of America
• Negotiable
• Posted about 1 month ago

Overview: EPM is hiring on behalf of a leading medical device manufacturer recognized for its innovation and excellence in producing active medical devices and software solutions. This hybrid position offers a unique opportunity to play a pivotal role in ensuring the quality and compliance of cut...

• Singapore
• Negotiable
• Posted about 1 month ago

Our client is a research organisation that develops vaccines and biologics. They are currently looking for a leader for their Analytical Sciences & Technology team to drive the development and implementation of analytical controls activities. Responsibilities: Develop and manage strategies for th...

• Singapore
• Negotiable
• Posted about 1 month ago

Join a global biotechnology company as a QC Senior Associate in Singapore! Are you passionate about quality control and quality management system? Do you want to be part of a leading company in the biopharmaceutical industry, known for its cutting-edge manufacturing capability and innovative huma...

• Singapore
• Negotiable
• Posted about 1 month ago

Join a global biotechnology company as a QC Specialist in Singapore! Are you passionate about quality control and quality management system? Do you want to be part of a leading company in the biopharmaceutical industry, known for its cutting-edge manufacturing capability and innovative human ther...

• Singapore
• Negotiable
• Posted about 1 month ago

Our client is a global leader in life sciences and biopharmaceuticals, offering unparalleled opportunities to impact healthcare. The Quality Director will play a crucial role in leading and inspiring quality teams, ensuring the highest standards of quality, directly impacting the safety and effic...

• Swedesboro
• Negotiable
• Posted about 1 month ago

Title: Quality Manager Location: Albany, OH (Can Provide Relocation) A leading pharmaceutical company just launched a brand new 503b facility and is rapidly expanding their site. They are looking for a Quality Manager to lead QA and QC activities for this new site. Responsibilities: Review and ap...

• Marlborough
• Negotiable
• Posted about 1 month ago

Title: Senior Supplier Quality Engineer Location: Marlborough, MA (On-Site) A medical device company is looking to grow their Quality team as they expand their medical device laser product line! The Senior Supplier Quality Engineer will primarily be responsible for overseeing quality of supplier ...

• Portage
• Negotiable
• Posted about 1 month ago

Job Description: Supplier Quality Engineer About the Role: We are seeking a highly skilled and experienced Supplier Quality Engineer to join our client's team. This role involves ensuring the quality and reliability of the company's vendors. The ideal candidate will have a strong background in su...

• Denmark
• Negotiable
• Posted about 1 month ago

Job Title: Freelance CQV Engineer Start Date: March 2025 Contract: 12 Months Location: Denmark - Onsite EPM Scientific is partnering with a leading pharmaceutical company to find an experienced CQV Engineer to be part of their commissioning, qualification, and validation of pharmaceutical manufac...

• Irvine
• US$130000 - US$170000 per year
• Posted about 1 month ago

Responsibilities: Oversee design assurance and development tasks for New Product Development, including risk evaluations, engineering studies, feasibility assessments, drawing analysis, and statistical evaluations. Ensure compliance with relevant regulatory frameworks, such as FDA, EU MDR, and IS...

• Austin
• US$120000 - US$150000 per year
• Posted about 1 month ago

Ideally, we are looking for someone with ablation catheter experience and have done Quality Assurance for new product development. The manufacturing/supplier quality experience is a plus.

• Italy
• Negotiable
• Posted about 2 months ago

ABOUT US We are a European organization recognized as an official Notified Body under Regulation (EU) 2017/745, specializing in verifying the conformity of medical devices with the stringent requirements of the MDR 2017/745 regulation. Our work ensures that medical devices meet the necessary stan...

• Lancaster
• Negotiable
• Posted about 2 months ago

We have a current opportunity for a QC Chemist position within the 2nd shift. This opportunity offers a competitive package including an annual 12% target bonus! The hours are Monday-Thursday from 3:30pm to 11:30pm, and Fridays from 1:30pm - 9:30pm. Roles and Responsibilities: Report to QC Manage...

• United States of America
• Negotiable
• Posted about 2 months ago

Senior Specialist, Quality Systems We are seeking a highly skilled Senior Quality Systems Specialist to join a growing Contract Development and Manufacturing Organization (CDMO). In this role, you will be responsible for managing and enhancing quality management systems (QMS) to ensure compliance...