Contract jobs

• Philadelphia
• Negotiable
• Posted 1 day 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...

• Negotiable
• Posted 1 day ago

We have a current opportunity for a Process Development Engineer on a contract basis. if you are interested or know anyone that is then please contact me further. Key Responsibilities: Support R&D activities during the product design phase. Manage process introductions while mitigating product an...

• Negotiable
• Posted 1 day ago

We have a current opportunity for a Process Development Engineer on a contract basis. if you are interested or know anyone that is then please contact me further. Key responsibilities will include: Support R&D activity during the product design phase. Manage a process introduction while mitigatin...

• Northern Ireland
• Negotiable
• Posted 1 day ago

We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis. Please apply if you have the skill set and are interested: 6-12 months project Full time (39 hours per week) Hybrid Start - May/June IVDR Regulatory Knowledge, getting ready for clinical trials. GAP Asse...

• Northern Ireland
• Negotiable
• Posted 1 day ago

We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis in Northern Ireland. Please apply if you have the skill set and are interested: 6-12 months project Full time (39 hours per week) Hybrid Start - May/June IVDR Regulatory Knowledge, getting ready for clini...

• Basel
• Negotiable
• Posted 1 day ago

We are currently searching for a Scientist QC Raw Materials to join our client's team in Basel, Switzerland on a 9-month contract. This is an exciting opportunity to become part of the Primary Packaging and Raw Material QC team, where you will play a critical role in ensuring the quality and comp...

• Basel
• Negotiable
• Posted 1 day ago

We are searching for a Scientist QC Raw Materials to join our team on a 9-month contract. This role plays a key part in the Primary Packaging and Raw Material QC team, ensuring the quality and compliance of raw materials used in drug product manufacturing. The successful candidate will be respons...

• Deutschlandsberg
• Negotiable
• Posted 2 days ago

We are looking to speak with freelance software validation experts in Germany for a fully remote 2-year project - you will play a crucial part in the digitalization efforts of a major pharma company, ensuring that their software systems meet the highest standards of quality and compliance. You wi...

• Boston
• Negotiable
• Posted 2 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...

• Galway
• Negotiable
• Posted 2 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...

• New York
• Negotiable
• Posted 3 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...

• England
• Negotiable
• Posted 5 days ago

EPM Scientific are currently collaborating with a leading Biotechnology Research client who specialise in consulting and clinical development. Our client is seeking a Freelance Global Value Dossier specialist with expertise in the Vaccines space, preferably with a focus on Covid Vaccines. The sco...

• 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...

• Visp
• Negotiable
• Posted 5 days ago

We are currently looking for a Project Engineer - Black Utilities to join the Global Engineering Team based in Valais, Switzerland! Your tasks will include developing and verifying ideas and requests, generating feasibility and conceptual studies, considering regulatory requirements and internal ...

• Visp
• Negotiable
• Posted 5 days ago

We are currently seeking an experienced CQ Manager for a contract position based in Visp, Switzerland. This role is crucial within the pharmaceutical manufacturing sector and involves developing global standard operating procedures across all facilities. Key Responsibilities: Develop Level 2 and ...

• Visp
• Negotiable
• Posted 5 days ago

We are seeking a Quality Assurance Manager to oversee compliance and customer Quality Agreement (QAA) activities for Drug Product manufacturing in Visp. This role involves collaboration with Drug Product Services and Drug Substance teams, acting as the primary QA contact for customer-related qual...

• Deutschlandsberg
• Negotiable
• Posted 6 days ago

We have a current opportunity for a Freelance CRA Germany on a contract basis. The ideal candidate has: 3+ years experience as a CRA Experience in oncology studies Experience working on Phases I-IV Is based in mid to northern Germany For further information about this position please apply with y...

• 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...

• England
• Negotiable
• Posted 9 days ago

Job Title: Medical Writer with Veeva PromoMats Expertise Job Type: Freelance/Contract - 4 days p/w - 6 months Location: Remote Job Description: We are seeking a talented and experienced Medical Writer with expertise in Veeva PromoMats to join our team on a freelance basis. The ideal candidate wil...

• Northern Ireland
• Negotiable
• Posted 9 days ago

We have a current opportunity for a Senior Clinical Project Manager working with IVDs on a contract basis. 6 months contract (possible extension) Clinical protocols, risk management plans, knowledge of IVD regulation within Europe Client-facing position (face-to-face) Remote with occasional site ...

• Morristown
• Negotiable
• Posted 10 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...

• Negotiable
• Posted 11 days ago

We have a current opportunity for a Senior Quality Engineer on a contract basis. - To start ASAP - Fully on-site (hands on role) - Must have injection moulding experience - Previous contract Manufacturing environment would be suitable - CAPA's - Medical Device standard - ISO13485 - Monday - Frida...

• Rome
• Negotiable
• Posted 11 days ago

Cerchiamo un CRA Junior, in Italia, motivato per supportare studi clinici garantendo qualità e conformità. Requisiti: - 1-3 anni di esperienza come CRA (ruolo Junior). - Esperienza in visite pre-site. - Ottima conoscenza delle lingue inglese e italiano. - Capacità di lavorare in modo indipendente...

• 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 ...

• Spain
• Negotiable
• Posted 13 days ago

QARA Consultant - Diagnostics Software Specialist We are excited to announce a contract opportunity for an experienced QARA Consultant specialising in diagnostics software within the medical device sector. This role is fully remote and requires proficiency in Spanish, aligning with our commitment...

• Spain
• Negotiable
• Posted 15 days ago

🚀 Exciting Opportunity - QARA Consultant - Software Diagnostics 🚀 📅 Contract Length: 12 Months 🌎 Location: Remote 💼 Hours: 20 Hours per week I am partnering with a leading medical device client who is looking for a QARA Consultant focusing on Software Diagnostics Compliance. 🔍 Key Skills & Experi...

• Belgium
• Negotiable
• Posted 16 days ago

We have a current opportunity for a Freelance CRA in Belgium on a contract basis. This is a remote role with some site monitoring visits. Candidates located near Leuven are strongly encouraged to apply.

• Germany
• Negotiable
• Posted 16 days ago

Urgent Freelance Quality Assurance Engineering Consultant (Pharmaceutical Industry) Location: Northern Germany Duration: Immediate Start - 12-Month Contract Language: Must be German-speaking We are working exclusively with a large pharmaceutical client to find a highly skilled Quality Assurance E...

• Germany
• Negotiable
• Posted 16 days ago

Urgent Freelance CQV Engineering Consultant (Pharmaceutical Industry) Location: Northern Germany Duration: Immediate Start - 12-Month Contract Language: Must be German-speaking Company Overview: We are working exclusively with a leading pharmaceutical client to find a highly skilled CQV Engineeri...

• Huntersville
• Negotiable
• Posted 16 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...

• Nottingham
• Negotiable
• Posted 17 days ago

We have a current opportunity for a Regulatory / Medical Writer on a contract basis for up to 40 hours per week. The position will be fully remote, dedicated to a renowned CRO. Experience within oncology is desired. Further information about this position please apply.

• 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 ...

• Charlotte
• Negotiable
• Posted 18 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...

• Dublin
• Negotiable
• Posted 19 days ago

I'm currently looking for an experienced DeltaV Automation Lead with expertise in spray drying and a background in API manufacturing for a full-time, on-site role in the South of Ireland. The client is eager for an immediate start but is open to some flexibility for the right candidate. Ideal Can...

• Negotiable
• Posted 19 days ago

𝗗𝗲𝗹𝘁𝗮𝗩 𝗕𝗮𝘁𝗰𝗵 𝗘𝗻𝗴𝗶𝗻𝗲𝗲𝗿 - 12-𝗠𝗼𝗻𝘁𝗵 𝗖𝗼𝗻𝘁𝗿𝗮𝗰𝘁 | 𝗗𝘂𝗯𝗹𝗶𝗻 | 𝗙𝗟𝗦 𝗦𝗵𝗶𝗳𝘁 Currently seeking an experienced 𝗗𝗲𝗹𝘁𝗮𝗩 𝗕𝗮𝘁𝗰𝗵 𝗘𝗻𝗴𝗶𝗻𝗲𝗲𝗿 for a 12-𝗺𝗼𝗻𝘁𝗵 𝗰𝗼𝗻𝘁𝗿𝗮𝗰𝘁 at a leading 𝗽𝗵𝗮𝗿𝗺𝗮 site in Dublin. This role is key to supporting critical manufacturing operations in a fast-paced, high-tech environment. 🔹12-𝗺𝗼𝗻𝘁𝗵 𝗰𝗼𝗻𝘁...

• Negotiable
• Posted 19 days ago

I'm currently looking for an experienced DeltaV Automation Lead with expertise in spray drying and a background in API manufacturing for a full-time, on-site role in the South of Ireland. The client is eager for an immediate start but is open to some flexibility for the right candidate. Ideal Can...

• 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...

• 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...

• Netherlands
• Negotiable
• Posted 19 days ago

EPM Scientific are currently collaborating with a Market Access & Health Economics consultancy who are on the lookout for Senior Health Economist Modellers with a strong acumen in the Oncology space. Our client is seeking a Freelance Senior Health Economics Modeller with expertise in the Oncology...

• United States of America
• Negotiable
• Posted 22 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 22 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 22 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...

• France
• Negotiable
• Posted 22 days ago

EPM Scientific are currently collaborating with a leading Biotechnology Research client who specialise in consulting and clinical development. Our client is seeking a Freelance Health Technology Assessment specialist with expertise in the Medicines space, specifically focusing on the French marke...

• Sweden
• Negotiable
• Posted 22 days ago

About the Role: We are seeking an experienced CQV (Commissioning, Qualification & Validation) Consultant to support Factory Acceptance Testing (FAT) and commissioning for a key project. The successful candidate will play a critical role in ensuring that equipment and systems meet regulatory and o...

• England
• Negotiable
• Posted 23 days ago

Job Title: Freelance Medical Strategist Location: Remote Job Type: Freelance/Contract - 30 hours p/w - 6 months About the Client: Our client is a leading medical communications agency dedicated to delivering high-quality, impactful medical content and strategies. They are passionate about advanci...

• Visp
• Negotiable
• Posted 23 days ago

Our client is seeking a skilled Thermal Validation Subject Matter Expert to join their BIO Biologics Division Services (BDS) team for a 9-month contract in Visp. The successful candidate will be responsible for ensuring the qualification and validation of process and support equipment, including ...

• Switzerland
• Negotiable
• Posted 23 days ago

We are seeking a highly skilled Project Manager to support our pharmaceutical engineering client in Switzerland for 6 months. The ideal candidate will be responsible for: Overseeing development projects with a broad technical perspective. Maintaining a high-level overview of project scope and pro...

• England
• Negotiable
• Posted 23 days ago

EPM Scientific is currently in collaboration with a boutique medical communications agency that is seeking experienced freelance medical writers to join their team and play a pivotal role within their organisations over the course of 2025. The details of the role are as follows: Freelance Medical...

• Ghent
• Negotiable
• Posted 23 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...

• 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...

• Negotiable
• Posted 24 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...

• 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...

• Visp
• Negotiable
• Posted 26 days ago

Unser Kunde sucht einen qualifizierten Biotech Associate, der für einen spannenden 10-Monats-Vertrag dem Team der BIO Biologics Division Services (BDS) beitritt. Dies ist eine hervorragende Gelegenheit für eine detailorientierte Fachkraft, die im Bereich der Qualitätssicherung in einer hochmodern...

• Visp
• Negotiable
• Posted 26 days ago

Unser Kunde sucht einen qualifizierten Biotech Associate, der für einen spannenden 10-Monats-Vertrag dem Team der BIO Biologics Division Services (BDS) beitritt. Dies ist eine hervorragende Gelegenheit für eine detailorientierte Fachkraft, die im Bereich der Qualitätssicherung in einer hochmodern...

• Diegem
• Negotiable
• Posted 26 days ago

Job title: Clinical Contracts & Budget Specialist Location: Diegem, Belgium Role Overview: In this position, you will oversee the development, negotiation, and finalisation of site agreements and budgets for medical device clinical trials in various therapeutic areas. This role requires collabora...

• 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. ...

• City of London
• Negotiable
• Posted 26 days ago

About the Role: We are seeking a highly qualified Medical Director to join a dynamic team at a leading CRO. This is a remote position based on the East Coast, offering a unique opportunity to contribute to groundbreaking clinical trials. Key Responsibilities: Provide medical oversight and leaders...

• Negotiable
• Posted 29 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. ...

• Negotiable
• Posted 29 days ago

We are seeking a DeltaV Automation Engineer with 3+ years of experience in DeltaV Batch systems within pharma manufacturing for a 12-month contract in Dublin. Key Responsibilities: Support automation operations and ensure GMP compliance. FLS Shift Role - supporting 24/7 operations Troubleshoot an...

• 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...

• 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.

• 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...

• Visp
• Negotiable
• Posted about 1 month ago

Our client is seeking a skilled Supplier & Material Qualification Specialist to join their BIO Mammalian team for a 6-Month contract to ensure the efficient and compliant supplier and material qualification process in line with regulatory requirements, corporate standards, and agreements with sta...

• Switzerland
• Negotiable
• Posted about 1 month ago

EPM Scientific are currently working with a small company with an diverse pipeline, who are urgently seeking a Medical Advisor for an exciting project. See a short summary below; Contract Conditions: Start date: ASAP Location: Switzerland, Remote Contract: 0.2-0.3 FTE, Increasing to 1 FTE, 12 mon...

• 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...

• Northern Ireland
• Negotiable
• Posted about 1 month ago

EPM Scientific are partnering with a long-standing Biotechnology client who are seeking a Freelance Global Value Dossier writing specialist on a contract basis to complete an end to end Global Value Dossier. Contract details: 12 month contract 4 to 5 days per week Remote working model Start date:...

• Nyon
• Negotiable
• Posted about 1 month ago

Our client is seeking a skilled QC Validation Scientist to join their Product Innovation team for a 2-year contract. This position is ideal for someone with extensive experience in process, cleaning, and analytical validation within the pharmaceutical industry. As a QC Validation Scientist, you w...

• 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 ...

• 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...

• Denmark
• Negotiable
• Posted about 1 month ago

EPM Scientific is currently supporting a client based in Denmark, who is searching for a CIP Specialist, on a 6 month contract basis. Responsibilities: Lead the validation and verification of Cleaning-in-Place (CIP) processes to ensure compliance with industry standards. Conduct design reviews to...

• Geneva
• Negotiable
• Posted about 1 month ago

Our client is a leader in the pharmaceutical industry. We are currently looking for a Senior Process Engineer to implement pharmaceutical manufacturing processes following Quality by Design (QbD) principles and Continued Process Verification (CPV), on a temporary contract. In this role, you will ...

• 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, ...

• Negotiable
• Posted about 1 month ago

CQV - HVAC Specialist Required in Dublin, UK (Contract Position) Are you a seasoned CQV professional with expertise in the pharmaceutical sector? We are seeking an experienced Freelance Commissioning, Qualification and Validation (CQV) specialist to fill a contract role focusing on Heating, Venti...

• 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...

• 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...

• Negotiable
• Posted about 1 month ago

***Freelance Market Access Contractor - Belgium*** We are seeking a dedicated and experienced freelance Market Access Contractor for an exciting project-based opportunity located in Belgium. Here's what we expect from our ideal candidate: - Availability for 20 hours per week commitment. - In-dept...

• Germany
• Negotiable
• Posted about 1 month ago

Freelancer Qualification Consultant - Large Pharmaceutical Company Contract Duration: 8 Months (February to November) Location: Germany (Onsite) We're looking for a team of 4x Qualification Consultant to join a global pharmaceutical company! Your main focus will be room, medium, and equipment qua...

• 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...

• Switzerland
• Negotiable
• Posted about 2 months ago

We are seeking an ambitious and dynamic OPEX Continuous Improvement Program Head for our contract position in the town of Visp. This pivotal role is not just about streamlining processes-it's about shaping the future of operational performance across our Global Engineering organisation. As a part...

• Switzerland
• Negotiable
• Posted about 2 months ago

We are seeking an experienced EHS (Environmental, Health, and Safety) Design Engineer for our esteemed client based in Visp. This is your chance to join a dynamic project team where safety isn't just policy; it's paramount. As an integral part of this role: Lead the implementation of EHS standard...

• 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...

• Amersham
• Negotiable
• Posted about 2 months ago

One of EPM Scientific's client is seeking a freelancer with a background of experience in the Marketing space (within the Life Sciences industry) to work on-site 5 days per week. We are collaborating with a global Biotechnology client who provides bioprocessing products and services to the biopha...

• 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...

• Groningen
• Negotiable
• Posted about 2 months ago

Senior Health Economist Modeller - Contract Opportunity in Groningen, Netherlands Are you a seasoned professional with expertise in health economics modelling? Our esteemed consultancy is seeking a Senior Health Economist Modeller to join our dynamic team on an initial 3-month contractual basis. ...

• 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...

• Denmark
• Negotiable
• Posted about 2 months ago

Job Title: Freelance CQV Engineer Start Date: March 2025 Contract: 12 Months Location: Denmark - Onsite EPM Scientific is partnering with a leading pharmaceutical company to find an experienced CQV Engineer to be part of their commissioning, qualification, and validation of pharmaceutical manufac...