All jobs near North America in the Quality sector

• Indianapolis
• US$65000 - US$110000 per year
• Posted about 17 hours 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...

• Omaha Township
• US$85000 - US$110000 per year
• Posted about 17 hours 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...

• Massachusetts
• Negotiable
• Posted 1 day 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...

• United States of America
• Negotiable
• Posted 3 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 4 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...

• United States of America
• US$120000 - US$140000 per year
• Posted 6 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 7 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 7 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...

• New York
• Negotiable
• Posted 9 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...

• Albuquerque
• US$103000 - US$130000 per year
• Posted 9 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 9 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...

• Massachusetts
• US$120000 - US$150000 per year
• Posted 9 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 10 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 10 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 10 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 10 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...

• Doylestown
• US$90000 - US$120000 per year
• Posted 16 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...

• Trenton
• US$95000 - US$106000 per year
• Posted 18 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...

• Naples
• US$140000 - US$150000 per year
• Posted 20 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...

• Naples
• US$140000 - US$145000 per year
• Posted 20 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...

• Asheville
• Negotiable
• Posted 21 days 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 21 days 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...

• New York
• Negotiable
• Posted 22 days 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 22 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$150000 - US$180000 per year
• Posted 22 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...

• San Diego
• US$120000 - US$140000 per year
• Posted 23 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....

• Ohio
• Negotiable
• Posted 24 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...

• Sacramento
• US$180000 - US$240000 per year
• Posted 28 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 ...

• Pendleton
• US$90000 - US$105000 per year
• Posted 29 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 29 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 30 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 30 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 30 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 30 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 30 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 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...

• 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...

• Grove City
• Negotiable
• Posted about 1 month 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 1 month 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...

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

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

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

• Secaucus
• US$140000 - US$175000 per year
• Posted about 1 month 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 1 month 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. ...

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

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

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

• Connecticut
• Negotiable
• Posted about 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...

• Albuquerque
• Negotiable
• Posted about 2 months 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 2 months 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 2 months 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 2 months 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 2 months 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...

• Swedesboro
• Negotiable
• Posted about 2 months 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...