Contract jobs
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- 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...
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- 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...
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- Galway
- Negotiable
- Posted 3 days ago
Senior Validations Engineer The requirements of this role within the wider project are to cover the validation activities with respect to the testing and manufacture of the client's device. Role/ Responsibilities: Develop, and/or approve, validation documentation, including protocol, records, and...
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- 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...
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- Ghent
- Negotiable
- Posted 5 days ago
Job Title: Supply Chain Manager Location: Ghent, Belgium Company: EPM Scientific Job Description: We are seeking an experienced and dynamic Supply Chain Manager to join our team. The successful candidate will be responsible for overseeing distribution, project management, sales and operations pla...
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- Cambridge
- Negotiable
- Posted 6 days ago
We are seeking a highly organised and detail-oriented Manager to lead our Clinical Procurement Team. In this role, you will be responsible for managing the procurement process for clinical supplies and equipment, ensuring that all purchases meet the organisation's quality standards and budget req...
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- 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...
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- Switzerland
- Negotiable
- Posted 12 days ago
We are seeking a skilled CSV Engineer to join our team on a 6-month initial contract in Basel. The ideal candidate will have a robust background in Computer System Validation (CSV) and Automated systems within the pharmaceutical and biotechnology industries. This role involves leading validation ...
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- Switzerland
- Negotiable
- Posted 17 days ago
We are seeking a skilled CSV Engineer to join our team on a 6-month initial contract in Basel. The ideal candidate will have a robust background in Computer System Validation (CSV) and Automated systems within the pharmaceutical and biotechnology industries. This role involves leading validation ...
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- 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...
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- Negotiable
- Posted 19 days ago
๐๐ฒ๐น๐๐ฎ๐ฉ ๐๐ฎ๐๐ฐ๐ต ๐๐ป๐ด๐ถ๐ป๐ฒ๐ฒ๐ฟ - 12-๐ ๐ผ๐ป๐๐ต ๐๐ผ๐ป๐๐ฟ๐ฎ๐ฐ๐ | ๐๐๐ฏ๐น๐ถ๐ป | ๐๐๐ฆ ๐ฆ๐ต๐ถ๐ณ๐ Currently seeking an experienced ๐๐ฒ๐น๐๐ฎ๐ฉ ๐๐ฎ๐๐ฐ๐ต ๐๐ป๐ด๐ถ๐ป๐ฒ๐ฒ๐ฟ for a 12-๐บ๐ผ๐ป๐๐ต ๐ฐ๐ผ๐ป๐๐ฟ๐ฎ๐ฐ๐ at a leading ๐ฝ๐ต๐ฎ๐ฟ๐บ๐ฎ site in Dublin. This role is key to supporting critical manufacturing operations in a fast-paced, high-tech environment. ๐น12-๐บ๐ผ๐ป๐๐ต ๐ฐ๐ผ๐ป๐...
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- Basel
- Negotiable
- Posted 19 days ago
Senior Engineer - Small Molecules We are currently seeking an experienced Senior Engineer specializing in small molecules for a contract position based in Visp, Switzerland. This role is crucial within the pharmaceutical manufacturing sector and involves developing global standard operating proce...
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- 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...
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- 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...
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- Ghent
- Negotiable
- Posted 24 days ago
Job title: Clinical Supplies Manager Location, Belgium, Germany, Netherlands Key Responsibilities: Represents product supply in the Clinical Study Team, driving the development of tailored clinical trial supply strategies aligned with the relevant clinical trial protocol. Creates and maintains co...
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- 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...
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- 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...
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- 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...
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- Negotiable
- Posted 25 days ago
I am currently looking to fill the below vacancy. If you are interested then please send your CV and contact me for further information: Must-Haves: 6-8 years of experience as an engineer within R&D in medical devices Experience with product management activities, including design, validation, an...
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- 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...
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- Negotiable
- Posted 30 days ago
Job Description Ensure compliance with Design Control and Risk Management activities and processes, managing and completing Quality deliverable for R&D projects. Provide Quality support and guidance to R&D project leads and team members, and direct Design Quality Engineers and Quality Engineers. ...
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- Negotiable
- Posted about 1 month ago
We have a current opportunity for a Freelance Clinical Trial Lead on a contract basis. The position will be based in Ireland. The ideal candidate: Is immediately available at 1.0 FTE Has at least 5 years experience in Clinical Research, with at least 2 as a CTM or equivalent Has oncology experien...
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- 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.
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- 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.
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- Barcelona
- Negotiable
- Posted about 1 month ago
I am working with a highly innovative biotech company based in Barcelona, specializing in the development of groundbreaking medical devices. We are looking for a Regulatory Affairs & Quality Assurance Specialist to join their team. Ideal Profile: Experience in regulatory strategies and documentat...
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- Zurich
- Negotiable
- Posted about 1 month ago
We currently have an opportunity for a Operational Buyer (Indirect Purchasing) on a contract basis within the Industrial Engineering sector in canton Zurich. Duration: Max. 6 months (potential for permanent employment) Your Responsibilities: Procurement Operations: Ensure timely procurement of go...
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- Vienna
- Negotiable
- Posted about 1 month ago
Job Title: Freelance eQMS Specialist Duration: 6 Months Industry: Pharmaceutical We are looking for a Project Quality Management Specialist to support the modernisation and update of our Electronic Quality Management System (eQMS) on a freelance basis. This is a contract position for six months, ...
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- Italy
- Negotiable
- Posted about 1 month ago
Freelance CRA Opportunity in Italy Are you a Clinical Research Associate (CRA) looking for an exciting freelance opportunity? We are on the hunt for a dedicated and experienced professional to oversee clinical trial activities throughout Italy. This role is tailored for someone who has mastered s...
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- 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...
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- 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...