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• United States of America
• US$140000 - US$190000 per year
• Posted about 16 hours ago

Manager/Sr. Manager Clinical Quality Assurance - Remote Our team is collaborating with a leading global pharmaceutical company to fill an exciting Clinical Quality Assurance role. This position is pivotal in managing GCP quality activities across several key therapeutic programs. As the Clinical ...

• San Diego
• US$150000 - US$180000 per year
• Posted 1 day 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...

• Los Angeles
• US$150000 - US$180000 per year
• Posted 1 day ago

We're working with a client who aims to develop and provide high quality formulations and exceptional service to healthcare practitioners and their patients as they are dedicated to helping unlock the full potential of sterile injectables through a specialized approach. The client is seeking a hi...

• Pleasanton
• Negotiable
• Posted 2 days ago

Position Summary Reporting directly to the CSO, the Director of Quality Assurance (QA) is responsible for developing and overseeing quality systems to ensure compliance with Good Laboratory Practice (GLP) for nonclinical studies and Good Clinical Laboratory Practice (GCLP) for clinical studies. T...

• Denver
• US$120000 - US$130000 per year
• Posted 2 days ago

My client, a leading medical device company specializing in class 2 devices is looking for an experienced Full Time Supplier Quality Engineer to join their growing team paying 130K+ a bonus. You would work shoulder to shoulder with R&D and sustaining engineering as you qualify component suppliers...

• Denver
• US$125000 - US$130000 per year
• Posted 2 days ago

We have a current opportunity for a Supplier Quality Engineer 3 on a permanent basis. The position will be based in Lakewood. For further information about this position please apply and feel free to reach out to Adam.tizabi@epmscientific.org Collaborate with Suppliers and R&D on new product deve...

• Germany
• Negotiable
• Posted 8 days ago

EPM Scientific are looking for 3 Project Engineers to join a global Medical Device client of ours as they look to set up a new site. You would be part of the team working on vendor management, and the development, purchasing and installation of new machinery through to validation stage. Contract ...

• Visp
• Negotiable
• Posted 8 days ago

We are seeking a QA Validation Specialist with expertise in Product Quality Review (PQR) to join our Client team in Visp on a one-year contract. In this role, you will: Ensure the trainings required to the Process Validation Specialist with focus on Product Quality Review are completed Active par...

• Los Angeles
• Negotiable
• Posted 8 days ago

EPM Scientific are currently on the search for 4 candidates to fill roles as a Cleaning and Process Validation Engineer. Planned Start date of ASAP as a W2 Contractor on a 6 - 12 month contract located in Los Angeles, CA Details below: Process Validation Engineer · Ensure that all qualifications ...

• Japan
• Negotiable
• Posted 9 days ago

Join a global medical device company as a QA Specialist in Yokohama! Are you passionate about quality assurance and regulatory affairs? Do you want to be part of a leading company in the medical device industry, known for its cutting-edge clinical diagnostics and innovative medical devices? If so...

• Singapore
• Negotiable
• Posted 9 days ago

Join a global medical device company as a QARA Manager in Tokyo! Are you passionate about quality assurance and regulatory affairs? Do you want to be part of a leading company in the medical device industry, known for its cutting-edge clinical diagnostics and innovative medical devices? If so, we...

• Singapore
• Negotiable
• Posted 9 days ago

Join a global medical device company as a QARA Manager in Tokyo! Are you passionate about quality assurance and regulatory affairs? Do you want to be part of a leading company in the medical device industry, known for its cutting-edge clinical diagnostics and innovative medical devices? If so, we...

• Deutschlandsberg
• Negotiable
• Posted 9 days ago

Job Title: Qualified Person (QP) - Cell & Gene Therapy and Vaccines Location: Southern Germany Industry: Pharmaceutical Contract: 12-month About Us: We are a leading pharmaceutical company based in southern Germany, specialising in the development and production of Cell & Gene Therapy and vaccine...

• Neuchâtel
• Negotiable
• Posted 9 days ago

We are currently looking for an experienced Senior QC Analyst to join our dynamic client team a leading CDMO. In this role, you will perform a wide variety of chemical and biological analyses, ensuring the highest quality standards in support of quality assurance and control programs. Key Respons...

• Omaha
• Negotiable
• Posted 11 days ago

Title: Quality Assurance Manager Location: Omaha, NE (can provide relocation) A leading pharmaceutical and health product manufacturer is seeking a Quality Manager to join their team. The Quality Manager will be responsible for managing the site's quality systems and QA department. Responsibiliti...

• Denmark
• Negotiable
• Posted 12 days ago

EPM Scientific are looking for a team of experienced consultants, to join our Medical Device client based near Copenhagen, Denmark. The initial project is focussed around a 510k submission, once completed focus will shift towards improving and maintaing compliance to ISO 13485. We are looking for...

• Lancaster
• US$60000 - US$75000 per year + 12% Bonus
• Posted 15 days ago

We have a current opportunity for a QC Chemist - 2nd shift position with a competitive package! The hours are M-Th 3:30pm to 11:30pm, and Fridays 1:30pm - 9:30pm. Roles and Responsibilities: Report to QC Management. Perform testing of finished products and raw materials per SOPs and methods. Oper...

• King of Prussia
• Negotiable
• Posted 15 days ago

A global biopharmaceutical organization is hiring for a global leadership role that works cross functionally with R&D, Quality Control, and Regulatory. If you're an innovative leader that's looking for a strategic focused position that impacts an organization globally, then please apply in! Job T...

• Seattle
• US$150000 - US$170000 per year
• Posted 15 days ago

Sr. Manager, Microbiology - Environmental Monitoring An industry leading biologics CDMO is currently at the forefront of a revolution in biologics manufacturing, where your leadership in environmental monitoring can directly contribute to life-saving therapies. Their team is offering an extraordi...

• Fargo
• Negotiable
• Posted 15 days ago

Title: Sr. QA Specialist - Labeling Location: Fargo, ND (Can offer FULL relocation) Position Summary: A leading CDMO for the cell and gene therapy space is seeking a Quality Labeling SME to join their growing team! You will oversee all labeling activities throughout the product lifecycle. This in...

• Singapore
• Negotiable
• Posted 15 days ago

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

• Houston
• Up to US$110000 per year
• Posted 16 days ago

Sr. Quality Training Specialist Our team is working with one of the fastest growing pharmaceutical companies in the industry on a pivotal Sr. Quality Training Specialist role. As a Sr. Quality Training Specialist, you will partner closely with site leadership and technical subject-matter experts ...

• New Jersey
• US$200000 - US$260000 per year
• Posted 16 days ago

Director/Sr. Director IT QA Auditing - Q1/2 2025 Join an internationally renowned organization at the forefront of pharmaceutical innovation and quality assurance. This team has identified a leadership need in their IT Quality Auditing organization to execute a global position that will reverbera...

• New Jersey
• Up to US$130000 per year
• Posted 16 days ago

Quality Engineering Manager Our team is working with one of the fastest growing pharmaceutical companies in the industry on a dynamic Manager of Quality Engineering to lead their quality engineering buildout in New Jersey. This permanent role focuses on establishing robust engineering functions a...

• Singapore
• Negotiable
• Posted 16 days ago

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

• Princeton
• US$260000 - US$280000 per year
• Posted 16 days ago

We are working with a biopharmaceutical firm dedicated to creating innovative bi-specific and multi-specific antibodies, along with antibody-drug conjugates (ADCs), aimed at cancer treatment. The company's ultimate mission is to develop biologics that systematically target tumor microenvironments...

• Austin
• US$120000 - US$150000 per year
• Posted 16 days 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.

• Denver
• US$125000 - US$130000 per year
• Posted 16 days ago

We have a current opportunity for a Supplier Quality Engineer 3 on a permanent basis. The position will be based in Lakewood. For further information about this position please apply and feel free to reach out to Adam.tizabi@epmscientific.org Collaborate with Suppliers and R&D on new product deve...

• Germany
• Negotiable
• Posted 18 days ago

QA Specialist - Supply Qualification & Auditing Location: West Germany Job Type: 3-Month Contract (Start Date: January) We are urgently seeking an experienced QA Specialist for a 3-month contract starting in January in West Germany. This role focuses on supply qualification and auditing within th...

• Watertown
• Negotiable
• Posted 19 days ago

We have a current opportunity for a Contract QA Operation Consultant on a contract basis with Small molecules experiace. The position will be based in fully remote. Please see the responsibilities below: Support the compliance oversight of manufacture and analysis of Drug Substance and Drug Produ...

• Muniz Freire
• Negotiable
• Posted 22 days ago

We have a current opportunity for a CQV Consultant on a contract basis. The position will be based in Sligo. For further information about this position please apply. Reaching out as we are searching for a Senior CQV Consultant to join one of EPM's clients on the West Coast of Ireland. Would you ...

• Germany
• Negotiable
• Posted 22 days ago

Exciting Opportunity: Senior CQV Consultant Join one of our clients in Germany this January! 🔑 Key Experience 🔹 Proven expertise in authoring, reviewing, and executing CQV activities for Facility, Utility, and Process Equipment 🔹 Strong knowledge of clean utilities and aseptic processing faciliti...

• Geneva
• Negotiable
• Posted 22 days ago

We are seeking a CSV Engineer for one of our client on a 6 to 12 months contract, in Geneva. The ideal candidate will have a strong background in Computer System Validation (CSV) and Quality Assurance within the pharmaceutical and biotechnology industries. This role involves leading validation pr...

• Missouri River Township
• Negotiable
• Posted 25 days ago

Title: Quality Engineer II Location: St. Louis, MO A leading pharmaceutical company is seeking to expand their Quality Engineering team! This is a really exciting opportunity to join a large company that can fast track your career. The Quality Engineer II will perform a variety of investigations ...

• New Albany
• Negotiable
• Posted 25 days ago

Title: Quality Assurance Supervisor 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 currently looking for a Quality Supervisor oversee QA activities for the team and provide any on...

• Denver
• US$125000 - US$130000 per year
• Posted 25 days ago

We have a current opportunity for a Supplier Quality Engineer 3 on a permanent basis. The position will be based in Lakewood. For further information about this position please apply and feel free to reach out to Adam.tizabi@epmscientific.org Collaborate with Suppliers and R&D on new product deve...

• Brisbane
• US$220000 - US$250000 per year + 401k, Dental, Medical, Vision
• Posted 26 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...

• Visp
• Negotiable
• Posted 29 days ago

We are seeking a QC Analyst for a 6-Month Contract in Visp, starting January 2025. As a QC Analyst, you'll play a key role in ensuring product quality and compliance at our client's Visp site. Your responsibilities will include: Conducting and releasing in-process controls (HPLC, CE, icIEF, etc.)...

• Switzerland
• Negotiable
• Posted about 1 month ago

Join our client's Audit & Inspections Team as a Supplier Quality Management. You will be responsible for conducting supplier audits, enhancing Supplier Qualification Management processes, and maintaining accurate supplier data in Veeva. This is a 12 Months contract. Responsibilities: Conduct onsi...

• Irvine
• US$130000 - US$170000 per year
• Posted about 2 months 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...

• Switzerland
• Negotiable
• Posted about 2 months ago

We are seeking a highly independent and experienced Global Specialist with a strong background in compliance within cell therapy and biopharmaceuticals. This role will focus on ensuring compliance across enterprise-level QMS, with particular emphasis on supporting system updates and enabling func...

• Middlesex
• Negotiable
• Posted about 2 months ago

We're currently partnered with a global pharmaceutical organization hiring for a full-time metrology position to join their bigger QC Team! This is an urgent hire and offers a very competitive relocation package if needed. Should you be interested, please feel free to apply in! Key Responsibiliti...

• New Albany
• 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...

• Hunt Valley
• Negotiable
• Posted about 2 months ago

We have a current opportunity for a Director Quality Control (Maryland) on a permanent basis. The position will be based in the Baltimore County area with a rapidly growing Pharmaceutical Organization! If interested, please apply directly and we'd reach out with further information. Responsibilit...

• Baltimore
• Negotiable
• Posted about 2 months ago

We have a current opportunity for a Director Quality Control (Maryland) on a permanent basis. The position will be based in Baltimore County with a growing pharmaceutical manufacturing organization! Responsibilities: Oversee daily operations and personnel in the Quality Control (QC) Laboratory. D...

• Stein
• Negotiable
• Posted about 2 months ago

We are seeking a QA Specialist, CSV & Automation. The ideal candidate will be responsible for overseeing the qualification and validation compliance of equipment and computerized systems related to aseptic facilities, utilities, and GMP manufacturing as part of Lonza's CAPEX project portfolio in ...

• New Albany
• Negotiable
• Posted about 2 months ago

Title: Validation Engineer 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 Validation Engineer to lead site validation activities across equipment, cleaning, process,...

• Swedesboro
• Negotiable
• Posted about 2 months ago

Title: Validation Engineer 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 Validation Engineer to lead site validation activities across equipment, cleaning, process,...

• New Albany
• 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...

• Singapore
• Negotiable
• Posted about 2 months ago

Join a global medical device company as a QARA Manager in Tokyo! Are you passionate about quality assurance and regulatory affairs? Do you want to be part of a leading company in the medical device industry, known for its cutting-edge clinical diagnostics and innovative medical devices? If so, we...

• Singapore
• Negotiable
• Posted about 2 months ago

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

• New Jersey
• Up to US$120000 per year
• Posted about 2 months ago

POSITION SUMMARY This role involves overseeing internal and supplier audits while driving quality initiatives like change control and risk management. The individual will work cross-functionally, acting as a technical point of contact for quality-related matters, and will represent the Quality De...