All jobs near United States of America in the Quality sector

• Naples
• US$140000 - US$150000 per year
• Posted 1 day 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 1 day 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 1 day 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 1 day 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 2 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 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$150000 - US$180000 per year
• Posted 3 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 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....

• Ohio
• Negotiable
• Posted 5 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 8 days ago

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

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

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

• Brisbane
• US$220000 - US$250000 per year + 401k, Dental, Medical, Vision
• Posted 10 days ago

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

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

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

• Walkersville
• Negotiable
• Posted 10 days ago

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

• Walkersville
• Negotiable
• Posted 10 days ago

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

• Walkersville
• Negotiable
• Posted 10 days ago

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

• Warren
• Negotiable
• Posted 10 days ago

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

• North Dakota
• Negotiable
• Posted 11 days ago

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

• 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...

• 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...

• Grove City
• US$70000 - US$129000 per year
• Posted 17 days ago

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

• Cincinnati
• Negotiable
• Posted 17 days ago

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

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

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

• Naples
• Negotiable
• Posted 17 days ago

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

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

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

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

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

• Albuquerque
• Negotiable
• Posted 18 days ago

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

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

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

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

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

• Morristown
• Negotiable
• Posted 24 days ago

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

• 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...

• Albuquerque
• Negotiable
• Posted 25 days ago

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

• North Carolina
• Negotiable
• Posted 25 days ago

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

• Connecticut
• Negotiable
• Posted 29 days ago

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

• 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...

• Atlanta
• Negotiable
• Posted about 1 month ago

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

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

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

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

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

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

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

• Swedesboro
• Negotiable
• Posted about 1 month ago

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

• Marlborough
• Negotiable
• Posted about 1 month ago

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

• Portage
• Negotiable
• Posted about 1 month ago

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

• 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.

• Lancaster
• Negotiable
• Posted about 2 months ago

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

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

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