All Contract jobs near North America

• Philadelphia
• Negotiable
• Posted 2 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...

• Boston
• Negotiable
• Posted 3 days ago

We have a current opportunity for a Quality Assurance Engineer on a contract basis. Our client is a leading innovator in the medical device industry, dedicated to improving patient outcomes through cutting-edge technology and rigorous quality standards. They are seeking a talented Quality Assuran...

• New York
• Negotiable
• Posted 4 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...

• Morristown
• Negotiable
• Posted 11 days ago

Job Title: Senior Associate, Regulatory Affairs Location: Morristown, New Jersey About the Role: We are seeking a highly motivated and detail-oriented Senior Associate, Regulatory Affairs to join our team. In this role, you will help author, compile, review, and submit high-quality regulatory sub...

• Huntersville
• Negotiable
• Posted 17 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...

• United States of America
• Negotiable
• Posted 17 days ago

* Authoring high-quality CMC documentation for US/ EU / UK countries, with support and guidance, applying agreed CMC global regulatory strategies, assuring technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements throughout project lifecycle. * P...

• Charlotte
• Negotiable
• Posted 19 days ago

We have a current opportunity for a Quality CAPA Consultant on a contract basis. The position will be based in Huntersville, NC. We are seeking a Quality Engineer who has knowledge of Medical Device Manufacturing with a compliance background. Duties will include CAPA execution (currently have app...

• United States of America
• Negotiable
• Posted 19 days ago

A leading organization in the pharmaceutical and regulatory affairs industry, dedicated to increasing project efficiency and establishing project management standards; are looking for a talented and experienced Project Manager to join the Project Management Office (PMO) team. Key Responsibilities...

• Redwood City
• Negotiable
• Posted 19 days ago

We have a current opportunity for a Associate Director Of Clinical Development on a contract basis. The position will be based in Redwood City. For further information about this position please apply. Position Summary The Associate Director of Clinical Development will play a key role in plannin...

• United States of America
• Negotiable
• Posted 23 days ago

We have a current opportunity for a Indirect Buyer on a contract basis. The position will be based in Westminster. For further information about this position please apply. To be successful in this role, you will need negotiation skills; a moderate understanding of Contract Management (e.g., comm...

• United States of America
• Negotiable
• Posted 23 days ago

We have a current opportunity for a Supply Planner on a contract basis. The position will be based in either Westminster, Co or Olive Branch, Ms For further information about this position please apply. The Associate Supply Planner is responsible for forecasting, supply planning, new products lau...

• United States of America
• Negotiable
• Posted 23 days ago

We have a current opportunity for a 1 Assoc Supply Planner on a contract basis. The position will be based in either Westminster, Co or Olive Branch, Ms For further information about this position please apply. The Associate Supply Planner is responsible for forecasting, supply planning, new prod...

• San Francisco
• Negotiable
• Posted 24 days ago

Associate Director, Clinical Development (Consultant/Contract - Hybrid) Redwood City, CA Hybrid/Remote (Bay Area) Position Summary The Associate Director of Clinical Development will play a key role in planning and executing clinical trials while providing strategic input into clinical developmen...

• Westminster
• Negotiable
• Posted 24 days ago

EPM Scientific are on the lookout for 2 top level candidates to come onboard as a Indirect Buyer and Direct Buyer for a Medical Device Client of ours based in Westminster, Co. Job description and duties will be listed below. Indirect Buyer: Principal Duties and Responsibilities: Ensure that all a...

• Town of Westminster
• Negotiable
• Posted 24 days ago

EPM Scientific are on the lookout for 2 top level candidates to come onboard as a Indirect Buyer and Direct Buyer for a Medical Device Client of ours based in Westminster, Co. Job description and duties will be listed below. Indirect Buyer: Principal Duties and Responsibilities: Ensure that all a...

• Denver
• Negotiable
• Posted 25 days ago

We have a current opportunity for a Indirect Buyer on a contract basis. The position will be based in Westminster. For further information about this position please apply.

• Denver
• Negotiable
• Posted 25 days ago

The Indirect Buyer will be responsible for commercializing low complexity supplier agreements, driving total cost reduction, and creating and capturing value for Operations by partnering with internal stakeholder and suppliers. You will be a trusted advisor that delivers value and fosters innovat...

• United States of America
• Negotiable
• Posted 26 days ago

EPM Scientific are on the lookout for a top tier candidate to fill a vacancy with a client of ours on a 2 year contract as a Medical Director, Duties and responsibilities will be listed below. We are seeking a highly experienced Senior / Medical Director, Neuroscience with a focus on Psychiatry. ...

• Town of Westminster
• Negotiable
• Posted about 1 month ago

We have a current opportunity for a Technical Project Operations Manager on a contract basis. The position will be based in Westminster. For further information about this position please apply.

• Town of Westminster
• Negotiable
• Posted about 1 month ago

We have a current opportunity for a Indirect Buyer on a contract basis. The position will be based in Westminster. For further information about this position please apply.

• Town of Westminster
• Negotiable
• Posted about 1 month ago

We have a current opportunity for a Buyer on a contract basis. The position will be based in Westminster. For further information about this position please apply.

• 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...

• San Francisco
• Negotiable
• Posted about 1 month ago

Position Summary The Associate Director of Clinical Development will play a key role in planning and executing clinical trials while providing strategic input into clinical development programs. This position requires a combination of scientific expertise, project management skills, and leadershi...

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

Job Description: We are seeking an experienced Clinical Data Manager. The successful candidate will ensure that CDM deliverables are completed on time, within budget, and in accordance with quality standards and study requirements. Key Responsibilities: Leadership & Oversight: Provide leadership ...

• 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...

• Minnetonka
• Negotiable
• Posted about 1 month ago

Position Summary: As a Design Assurance Engineer II, you will lead quality engineering activities for development projects from conception to commercialization. This includes developing risk management files, completing DHF deliverables, and being significantly involved in design verification/val...

• 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...

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

Job Description: We are seeking a talented and experienced Medical Writer with a strong background in Acute Myeloid Leukemia (AML) to join our dynamic team. The ideal candidate will have a deep understanding of AML, excellent writing skills, and the ability to translate complex scientific informa...

• South San Francisco
• Negotiable
• Posted about 2 months ago

Position Summary: We are seeking a highly motivated Biosample Operations Manager with a passion for new cancer therapy development. This role will be responsible for providing leadership to Clinical Development Execution and/or Study Management Team and oversight of laboratory vendors for our cli...

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

Regulatory Affairs Contractor (Remote, USA) As a Regulatory Affairs Contractor, you will support the development and implementation of global regulatory CMC strategies for our partners' marketed and development products. You will assist with regulatory activities for both internal and external pr...

• Portage
• Negotiable
• Posted about 2 months 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...

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

Job Overview The Clinical Evaluation Reporting Specialist is tasked with creating Clinical Evaluation Reports (CERs) for Terumo Blood and Cell Technologies (TBCT) products. This involves utilizing product labeling, preclinical and clinical data, published literature, risk management documents, co...