Quality jobs

• Naples
• US$140000 - US$150000 per year
• Posted about 19 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 19 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...

• Region Hannover
• Negotiable
• Posted 1 day 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 1 day 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 1 day ago

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

• Germany
• Negotiable
• Posted 2 days ago

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

• Huntersville
• Negotiable
• Posted 2 days ago

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

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

• 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 ...

• 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...

• 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) ...

• 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...

• 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...

• 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 17 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 17 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...

• 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...

• 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...

• 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...

• 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...

• 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 ...

• 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 about 1 month 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...

• 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...

• 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...

• 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...