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• Albuquerque
• US$135000 - US$175000 per year
• Posted about 11 hours 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...

• Harleysville
• Negotiable
• Posted about 11 hours ago

Quality Manager Role Overview: A growing company in the pharmaceutical testing accessories sector who is seeking a Quality Manager to lead their quality department. This role involves both management and hands-on inspection tasks, making it ideal for someone who enjoys a dynamic work environment....

• United States of America
• Up to US$150000 per year
• Posted about 24 hours ago

We are seeking a Quality Management System (QMS) Manager to lead and enhance our audit program, ensuring compliance with regulatory standards in the medical device industry. If you have expertise in audit program management and hosting external audits, we want to hear from you! Key Responsibiliti...

• Frankfurt am Main
• Negotiable
• Posted 1 day 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 a global leading German bank is looking for a Product Manager Tasks You use AI and LLMs to improve our chatbot and make customer i...

• Philadelphia
• US$135000 - US$160000 per year
• Posted 4 days ago

A renowned biopharmaceutical organization is looking to hire a strong microbiology leader that'll be responsible for leading key activities within the microbiology team and provide oversight of the QC Microbiology team including managing the training of junior microbiology staff and the qualifica...

• Denmark
• Negotiable
• Posted 4 days ago

Project Coordinator / Junior Project Manager (Operational Readiness - Downstream) Duration: 12 months, possible extension Location: Denmark - on-site Start Date: ASAP -12month contract We are looking for an experienced Project Coordinator or Junior Project Manager with pharmaceutical industry exp...

• Copenhagen
• Negotiable
• Posted 4 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...

• Visp
• Negotiable
• Posted 4 days ago

We are currently seeking a highly skilled and dedicated Lab Scientist to join our client's Analytical Department. If you have a strong background in analytical chemistry and a passion for process optimization, we would love to hear from you! Responsibilities Provide analytical support for chemica...

• Visp
• Negotiable
• Posted 4 days ago

We are currently seeking a highly skilled and dedicated Lab scientist to join our client's Analytical department. Main tasks and responsibilities: Analytical support of chemical process development and process optimisation. Preparation, execution and documentation of analyses, method developments...

• Cork
• Up to €50 per hour
• Posted 5 days ago

Responsibilities Researches, develops, designs, and evaluates mechanical and electro-mechanical materials, components, assemblies, processes and/or equipment. Conducts feasibility studies to verify capability and functionality. Develops new concepts from initial design to market release. Write an...

• Cork
• Up to €50 per hour
• Posted 5 days ago

Responsibilities Researches, develops, designs, and evaluates mechanical and electro-mechanical materials, components, assemblies, processes and/or equipment. Conducts feasibility studies to verify capability and functionality. Develops new concepts from initial design to market release. Write an...

• New Jersey
• Negotiable
• Posted 5 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 6 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...

• Princeton
• US$240000 - US$280000 per year
• Posted 6 days ago

Senior Director of Quality Assurance (GCP) - Drive Excellence in Cutting-Edge Oncology Innovation! Backed by $500 MILLION in Funding | Transforming Oncology Treatments | A Culture of Innovation & Impact Are you a Quality Assurance leader passionate about revolutionizing oncology therapies? This i...

• Zurich
• Negotiable
• Posted 7 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...

• Singapore
• Negotiable
• Posted 7 days ago

Job Title: QA Validation Manager Location: Singapore Job Type: Full-time Job Description: Position Overview: Our client is a global pharmaceutical company, seeking a highly motivated and experienced QA Validation Manager to join their dynamic team. The successful candidate will be responsible for...

• Region Hannover
• Negotiable
• Posted 7 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 7 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 7 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 8 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...

• New Hampshire
• Negotiable
• Posted 8 days ago

QA Manager, USA Location: Hybrid in NH or PA Are you an experienced Quality Assurance professional with a passion for compliance, continuous improvement, and leadership? We are seeking a Quality Assurance Manager to join a new Quality team and lead QA operations in the USA for a local medical dev...

• Indianapolis
• US$65000 - US$110000 per year
• Posted 8 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 8 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 9 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...

• Deutschlandsberg
• Negotiable
• Posted 11 days ago

Exciting Career Opportunity: Freelance CQV Consultant We are currently seeking an experienced Freelance CQV Consultant to join our client in Germany for a 12-month contract role. This is a full-time, on-site position with an immediate start. Key Details: Location: On-site, Germany Contract Durati...

• Valais
• Negotiable
• Posted 12 days ago

We are currently looking for a Project Engineer - Black Utilities to join the Global Engineering Team based in Valais, Switzerland! Summary: Your tasks will include developing and verifying ideas and requests, generating feasibility and conceptual studies, considering regulatory requirements and ...

• Stein
• Negotiable
• Posted 12 days ago

We are currently seeking a highly skilled and motivated GMP High Bay Warehouse Specialist to join our client's team in Stein. The Specialist will be driving the execution and coordination of the defined CQV activities in the warehouse for both cold and ambient temperatures and support building. R...

• Stein
• Negotiable
• Posted 12 days ago

We are seeking a skilled and motivated Instrumentation & Controls Engineer to join our client's team in Stein. Summary: The Instrumentation and Control (I&C) Engineer will report directly to the Automation Technical Lead and is responsible for providing hands on support to the commissioning and q...

• Omaha Township
• US$85000 - US$110000 per year
• Posted 12 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...

• Bern
• Negotiable
• Posted 13 days ago

We are currently working with a leading pharmaceutical company looking for an MES Engineer to join their team in Switzerland. This is an exciting opportunity to build a long-term career in one of the fastest-growing CDMOs globally. You will be responsible for: Developing, testing, and optimizing ...

• Switzerland
• Negotiable
• Posted 13 days ago

We are currently working with a leading pharmaceutical company looking for an MES Engineer to join their team in Switzerland. This is an exciting opportunity to build a long-term career in one of the fastest-growing CDMOs globally. You will be responsible for: Developing, testing, and optimizing ...

• Massachusetts
• Negotiable
• Posted 13 days ago

Sr. GCP Quality Specialist Location: Hybrid in MA We are seeking a Senior GCP Quality Specialist to play a critical role in maintaining the integrity and compliance of clinical research operations. In this global role, you will lead audits of clinical processes and vendors, ensuring they meet reg...

• Zurich
• Negotiable
• Posted 13 days ago

We are seeking two skilled and motivated QC Analysts to join our client's team in Zurich. As a QC Analyst, you will play a crucial role in performing laboratory testing, ensuring the highest standards of quality control, and supporting the development of pharmaceutical products. Your expertise in...

• Visp
• Negotiable
• Posted 13 days ago

We are seeking a Process Analytics Technician to join a global leader in the specialty chemicals industry. This is a fantastic opportunity to contribute to cutting-edge projects and work in an innovative, sustainable environment. Key Responsibilities: Ensure the optimum availability of process an...

• Visp
• Negotiable
• Posted 13 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...

• Singapore
• Negotiable
• Posted 15 days ago

Job Opportunity: Senior Quality Operations Manager Location: Singapore About Us: We are a leading pharmaceutical company committed to delivering exceptional quality and innovative solutions. We are seeking a highly experienced and motivated Senior Quality Operations Manager to join our dynamic te...

• United States of America
• Negotiable
• Posted 15 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 16 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...

• Japan
• Negotiable
• Posted 16 days ago

Job Title: Quality Manager - Pharmaceutical Industry Location: Japan Company Overview: Join our innovative and forward-thinking pharmaceutical company, committed to improving health and well-being worldwide. We are dedicated to producing high-quality, safe, and effective pharmaceutical products, ...

• United States of America
• US$120000 - US$140000 per year
• Posted 18 days ago

We are seeking a Quality Management System (QMS) Manager to lead and enhance our audit program, ensuring compliance with regulatory standards in the medical device industry. If you have expertise in audit program management and hosting external audits, we want to hear from you! Key Responsibiliti...

• Albuquerque
• US$116000 - US$130000 per year
• Posted 18 days ago

Our client is urgently hiring for a critical position within the Microbiology vertical. This is a rapidly expanding organization that offers growth opportunities and stability. If interested in learning more, apply below and let's set up a time to chat! Key Responsibilities: Oversee daily operati...

• Saint Albans
• US$80000 - US$120000 per year
• Posted 18 days ago

Lead QA Specialist - Operations A global industry pharmaceutical leader with commercial products available across multiple therapeutic areas is seeking an experience Lead QA Specialist to take a key position in their Quality Assurance organization. You will be supporting the development of truste...

• Germany
• Negotiable
• Posted 18 days ago

Seeking Freelance Automation Specialist - Large Pharma Project Location: Southern Germany Duration: Immediate Start - 12-Month Contract Language: Must be German-speaking We are currently seeking an Automation Specialist to work exclusively with a large pharmaceutical company based in Southern Ger...

• Basel
• Negotiable
• Posted 19 days ago

We are currently searching for a Scientist QC Raw Materials to join our client's team in Basel, Switzerland on a 9-month contract. This is an exciting opportunity to become part of the Primary Packaging and Raw Material QC team, where you will play a critical role in ensuring the quality and comp...

• Basel
• Negotiable
• Posted 19 days ago

We are searching for a Scientist QC Raw Materials to join our team on a 9-month contract. This role plays a key part in the Primary Packaging and Raw Material QC team, ensuring the quality and compliance of raw materials used in drug product manufacturing. The successful candidate will be respons...

• Singapore
• Negotiable
• Posted 19 days ago

Position: Quality Director Location: Singapore Company Overview: Our client is a leading pharmaceutical manufacturing organization, committed to delivering high-quality medications and healthcare solutions. Job Summary: The Quality Director will oversee and manage all aspects of quality assurance...

• Galway
• Negotiable
• Posted 19 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...

• Belgium
• Negotiable
• Posted 20 days ago

We are currently working with a leading CDMO looking for a MSAT Packaging Engineer to join their team in Belgium. This is an exciting opportunity to build a long-term career in one of the fastest-growing CDMOs globally. You will be responsible for: Leading closure and shipping validation projects...

• New York
• Negotiable
• Posted 20 days ago

We are seeking a highly skilled QA Supervisor to join a leading Medical Device company. In this role, you will be responsible for: Maintaining a Quality Management System compliant with FDA regulations and driving continuous improvement. Managing complaint handling and adverse event reporting, en...

• Belgium
• Negotiable
• Posted 20 days ago

We are currently working with a leading CDMO looking for a MSAT Packaging Engineer to join their team in Belgium. This is an exciting opportunity to build a long-term career in one of the fastest-growing CDMOs globally. You will be responsible for: Leading closure and shipping validation projects...

• Albuquerque
• US$103000 - US$130000 per year
• Posted 20 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 ...

• Brooklyn Park
• Negotiable
• Posted 20 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...

• Belgium
• Negotiable
• Posted 21 days ago

We are currently working with a leading CDMO looking for a MSAT Packaging Engineer to join their team in Belgium. This is an exciting opportunity to build a long-term career in one of the fastest-growing CDMOs globally. You will be responsible for: Leading closure and shipping validation projects...

• Massachusetts
• US$120000 - US$150000 per year
• Posted 21 days ago

I'm currently working with a start-up biotech company that accelerates drug development for a specific rare disease by leveraging innovative research models and collective expertise. Their partient advocacy group has funded over 90 translational research grants, leading to 13 therapeutic programs...

• Philadelphia
• US$80000 - US$151000 per year
• Posted 21 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 21 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 22 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 22 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...

• Visp
• Negotiable
• Posted 22 days ago

We are seeking a Quality Assurance Manager to oversee compliance and customer Quality Agreement (QAA) activities for Drug Product manufacturing in Visp. This role involves collaboration with Drug Product Services and Drug Substance teams, acting as the primary QA contact for customer-related qual...

• Germany
• Negotiable
• Posted 22 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, ...

• Tokyo
• Negotiable
• Posted 23 days ago

Job Title: Head of Quality Location: Japan Company Overview: Our client is a global leading pharmaceutical company committed to delivering high-quality, innovative therapies to improve patient health and well-being. Our dedication to excellence and compliance ensures that our products meet the hi...

• Shizuoka
• Negotiable
• Posted 23 days ago

Job Title: Senior QA Specialist Location: Shizuoka About Us: Our client is a global leader in the development, supply, and support of specialty excipients and fully formulated products for the pharmaceutical and nutritional industries. They have established a strong reputation for providing high-...

• Deutschlandsberg
• Negotiable
• Posted 26 days ago

Job Title: Quality Control Team Lead Location: Germany Company Overview: Join an innovative Medical Device company dedicated to developing products that prevent fatalities from heart attacks. Position Overview: We are seeking a highly experienced QC Team Lead to join our dynamic team. The ideal c...

• Netherlands
• Negotiable
• Posted 28 days ago

Job Title: Quality Management System (QMS) Specialist Location: The Netherlands About our client: Innovative medical device company focused on improving the lives of people with diabetes through our advanced insulin pump. Job Description: We are looking for a QMS Specialist to ensure top-quality ...

• Singapore
• Negotiable
• Posted 28 days ago

Our client is a life science service provider based in Singapore with presence across the region. They are currently looking for a Laboratory Director to join and oversee the operations in the Singapore lab. Responsibilities: Hire, train, and manage lab staff; promote teamwork and manage the lab'...

• Germany
• €100000 - €120000 per annum
• Posted 28 days ago

Job Title: Associate Director - Qualified Person (QP) with Vaccine Expertise Location: Germany Job Description: We are seeking a highly qualified and experienced Associate Director to join our team. The ideal candidate will be a Qualified Person (QP) with a strong background in vaccines and holdi...

• Japan
• Negotiable
• Posted 28 days ago

Job Title: Quality Director Location: Japan Our client is a leading pharmaceutical company dedicated to improving health and well-being through innovative medicines and therapies. They are committed to maintaining the highest standards of quality and compliance in all our operations. Seeking an e...

• Doylestown
• US$90000 - US$120000 per year
• Posted 28 days ago

Quality Assurance Supervisor A growing ophthalmic medical device company is seeking a quality assurance leader to join their organization in a crucial position. This role is vital for ensuring the highest standards of quality and regulatory compliance within the company. Role and Responsibilities...

• Negotiable
• Posted 28 days 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...

• Trenton
• US$95000 - US$106000 per year
• Posted 29 days ago

Supervisor, Quality Systems As a key member of the Quality Systems team, you will lead the daily operations of our Quality Specialists, ensuring their productivity and compliance with both internal and external regulatory standards. This role involves active participation in audits, meticulous pr...

• Spain
• Negotiable
• Posted about 1 month ago

QARA Consultant - Diagnostics Software Specialist We are excited to announce a contract opportunity for an experienced QARA Consultant specialising in diagnostics software within the medical device sector. This role is fully remote and requires proficiency in Spanish, aligning with our commitment...

• 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...

• Spain
• Negotiable
• Posted about 1 month 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 1 month 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 1 month 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 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...

• Japan
• Negotiable
• Posted about 1 month 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 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...

• Germany
• Negotiable
• Posted about 1 month 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 about 1 month 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 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...

• Negotiable
• Posted about 1 month 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 about 1 month 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 about 1 month 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 about 1 month 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 about 1 month 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 about 1 month 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 about 1 month 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 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...

• Singapore
• Negotiable
• Posted about 1 month 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 about 1 month 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 about 1 month 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 about 1 month 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 about 1 month 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 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 ...

• Pendleton
• US$90000 - US$105000 per year
• Posted about 1 month 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 about 1 month 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 about 1 month 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 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...

• North Dakota
• Negotiable
• Posted about 1 month 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 about 1 month 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 1 month 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 about 1 month 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 about 1 month 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 about 1 month 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 about 1 month 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...

• Weybridge
• Negotiable
• Posted about 2 months 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 about 2 months 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 about 2 months 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 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...

• Germany
• Negotiable
• Posted about 2 months 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 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...

• Japan
• Negotiable
• Posted about 2 months 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...

• Cincinnati
• Negotiable
• Posted about 2 months 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 about 2 months 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 about 2 months 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 about 2 months 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 about 2 months 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 about 2 months 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 about 2 months 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...

• City of London
• Negotiable
• Posted about 2 months 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 about 2 months 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 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...

• Secaucus
• US$140000 - US$175000 per year
• Posted about 2 months 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 about 2 months 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 about 2 months 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 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...

• Hamburg
• Negotiable
• Posted about 2 months 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 about 2 months 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 about 2 months 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 about 2 months 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 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...

• Tuttlingen
• Negotiable
• Posted about 2 months 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...

• Munich
• Negotiable
• Posted about 2 months 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 about 2 months 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 about 2 months 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 about 2 months 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 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...

• Frauenfeld
• Negotiable
• Posted about 2 months 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 about 2 months 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 about 2 months 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 2 months 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 2 months 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 2 months 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 ...