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Found 47 jobs
    • Switzerland
    • Negotiable
    • Posted 1 day ago

    We are looking for an experienced Quality Assurance Consultant (GMP/GDP) to work on a 12 months contract with possibility for extension. Our client is a leading pharmaceutical company based in Switzerland. The successful candidate will be responsible for developing and implementing a standardized...

    • Amsterdam
    • Negotiable
    • Posted 6 days ago

    Experience: Over 5 years of quality management experience within the medical device, consumer healthcare, or pharmaceutical industries. Expertise in ISO 13485 or GMP Pharma and ISO 14971, with a preference for ISO 22000 experience. Extensive track record in ensuring compliance with the Medical De...

    • Slovakia
    • Negotiable
    • Posted 9 days ago

    I am currently working with a long standing reputable pharmaceutical company seeking a Key Account Manager for Slovakia/Croatia. They have been serving as the regional affiliate for world's most important pharmaceutical and biotechnology companies. They are looking for someone with experience as ...

    • Czech Republic
    • Negotiable
    • Posted 9 days ago

    I am currently working with a long standing reputable pharmaceutical company seeking a Key Account Manager for Czech Republic. They have been serving as the regional affiliate for world's most important pharmaceutical and biotechnology companies. They are looking for someone with experience as a ...

    • Poland
    • £250 - £251 per day
    • Posted 9 days ago

    I am currently working with a long standing reputable pharmaceutical company seeking a Key Account Manager for Poland. They have been serving as the regional affiliate for world's most important pharmaceutical and biotechnology companies. They are looking for someone with experience as a Key Acco...

    • Germany
    • Negotiable
    • Posted 9 days ago

    Account Manager/ Inside Sales Role Introduction We are looking for an Account Manager/ Inside Sales Representative for a leading company in the Life Sciences sector. The company provides innovative products and services for the EPM and Diagnostics industry. The role will be based in Bavaria, Germ...

    • Sachsen
    • Negotiable
    • Posted 10 days ago

    Account Manager - Dresden, Jena, Leipzig Our client is searching for an Account Manager, responsible for the active sale of their capital equipment products in the region with the aim of increasing market share and sales Responsibilities: Personal and digital customer visits in life science resea...

    • Germany
    • Negotiable
    • Posted 10 days ago

    Company Overview: I am partnered with a global leader in genomics who have been at the forefront of developing technologies for NGS, DNA sequencing and genome editing for over 20 years. The organisation are enlarging its portfolio to deliver life-changing technology to Life Science researchers & ...

    • France
    • Negotiable
    • Posted 10 days ago

    Quality Director - Medical Devices A global medical device manufacturer is looking for a Quality Director to join their expanding French site, overseeing a team of 50 quality professionals, providing them with guidance, coaching, and support. As a Quality Director, you will: Develop and implement...

    • Norway
    • Negotiable
    • Posted 10 days ago

    Regional Manager Nordics Introduction Our client is a leading B company that provides innovative solutions in Next Generation Sequencing (NGS) with a focus on EPM. They are looking for a Regional Manager for the Nordics region. As Regional Manager, you will be responsible for driving sales of our...

    • Deutschlandsberg
    • Negotiable
    • Posted 10 days ago

    We are looking for a Head of Regulatory Affairs to manage a team of regulatory affairs professionals for a leading medical device company in Germany. The ideal candidate will have a minimum of 5 years experience in regulatory affairs in the medical device industry. Responsibilities - Develop, imp...

    • Düsseldorf
    • Negotiable
    • Posted 12 days ago

    As a member of the QA Release team, the QA Release Specialist (f/m/d) conducts the quality audit of all pertinent manufacturing and testing records to ensure compliance before the qualified person certifies the batch. The QA release team is also in charge of ensuring that the underlying processes...

    • Germany
    • Negotiable
    • Posted 12 days ago

    Senior Regulatory Affairs Specialist We are currently seeking a Senior Regulatory Affairs Specialist to join our client's team in Jena, Germany. Our client is a leading medical device company dedicated to improving health-care through innovative products. The successful candidate will work closel...

    • Netherlands
    • Negotiable
    • Posted 15 days ago

    Job Title: Quality Assurance Manager Location: Amsterdam, Netherlands Salary: Negotiable Position Overview: This company is seeking a highly qualified and experienced Quality Manager to join their team. Reporting directly to the CEO and one of the owners, the Quality Manager will play a pivotal r...

    • Switzerland
    • Negotiable
    • Posted 15 days ago

    This is an opportunity to join a leading Medical Device manufacturer that is looking to expand their talent within Switzerland with a real focus on Regulatory activities. You would be joining a dynamic team of both Regulatory and Quality talent located in Switzerland Responsibilities: Help us to ...

    • Nürnberger Land
    • Negotiable
    • Posted 15 days ago

    Global leader in medical technology (radiation therapy and X-ray diagnostics. Innovation, quality and customer focus make us a trendsetter in the industry. Our approximately 200 highly qualified employees work at our HQ in Germany and in our subsidiaries globally Tasks Preparation, implementation...

    • England
    • Negotiable
    • Posted 19 days ago

    We have a current opportunity for a Assoc. Director, DMPK Discovery on a permanent basis. The position will be based in Durham. For further information about this position please apply. Responsibilities Designs, plans, and conducts DMPK studies to support lead identification, lead optimization, a...

    • Munich
    • Negotiable
    • Posted 19 days ago

    Project Manager Qualitätskontrolle (f/m/d) Aufgaben: * Vertretung der QK in internen oder firmenübergreifenden Projekten * Selbständige Koordination aller QK-internen Projektaktivitäten * Sicherstellung der GMP- und termingerechten Durchführung von Stabilitätsunter-suchungen in der QK einschließl...

    • Switzerland
    • Negotiable
    • Posted 21 days ago

    We currently have an open position as Supplier Quality Professional for a 6-month contract for our client in Basel, starting asap or latest 1st of December. Responsibilities Supplier Life cycle management for project global QAA remediation to manage end to end QAA establishment process from autho...

    • Düsseldorf
    • Negotiable
    • Posted 21 days ago

    We are currently looking for a QA Validation Specialist to join our client´s team in Düsseldorf. The Specialist Quality Validation is part of the QA Validation team and supports all qualification and validation activities, including equipment and utility qualification, validation of computerized ...

    • Belgium
    • £1 - £2 per annum
    • Posted 22 days ago

    Sales Representative Responsibilities In this role, you will be responsible for: Selling medical devices across Belgium Building relationships with key clients Providing technical support to clients Keeping up to date with market developments Representing the company at trade shows and conference...

    • Germany
    • Negotiable
    • Posted 26 days ago

    Our client, a Global CDMO, is growing their Quality Control team. As a Stability Testing QC Expert, you will support the Quality Control team onsite. Your responsibilities include both the creation and adherence to stability testing plans and the evaluation of data, along with communication with ...

    • Germany
    • Negotiable
    • Posted 26 days ago

    Our client, a global CDMO, is growing their Quality control team. In this role, you will closely collaborate with other laboratory departments on-site, as well as with the Production, Quality, and Supply Chain teams. You will report directly to the Head of Quality Control. Job Duties: -Managing a...

    • England
    • Negotiable
    • Posted 27 days ago

    We are currently partnered with a global CRO, who are seeking a Senior Regulatory Writer to handle their complex regulatory documents for regulatory submissions. Key responsibilities: Prepare, develop and finalise clinical documents for submission to regulatory authorities including briefing docu...

    • Norway
    • Negotiable
    • Posted 29 days ago

    A global leader in diagnostics who are expanding across the Nordics is looking for a Market Development & Solution Manager to join their team. In this pivotal role, you will represent the company with senior stakeholders to accelerate access and integrate end to end solutions for customer needs. ...

    • Germany
    • Negotiable
    • Posted about 1 month ago

    Business Development Manager - CRO Bavaria, Company Overview: Company Overview: We are proud to partner with a global leading CRO that has been providing all Phases of clinical development services to medical device, biotechnology and pharmaceutical industries for over 20 years. The organization ...

    • Belgium
    • Negotiable
    • Posted about 1 month ago

    Account Manager Introduction Our client is a leading medical device manufacturer looking for a Sales Representative to join their team in Belgium. The successful candidate will be responsible for selling medical devices across Belgium and will require fluency in the French and Dutch languages. Re...

    • England
    • Negotiable
    • Posted about 1 month ago

    We are currently partnered with a global biotechnology company, who are seeking an experienced regulatory writer to contribute to the development of complex clinical, nonclinical, and safety documents for regulatory submissions. Key responsibilities: Prepare, develop and finalise clinical documen...

    • England
    • Negotiable
    • Posted about 1 month ago

    We are currently partnered with a global biotechnology company, who are seeking an experienced regulatory writer to contribute to the development of complex clinical, nonclinical, and safety documents for regulatory submissions. Key responsibilities: Prepare, develop and finalise clinical documen...

    • England
    • US$110000 - US$130000 per year
    • Posted about 1 month ago

    The Global Product Manager develops global and holistic product portfolio, product category, supplier, and sales strategies. The candidate will translate those strategies into global business go to market plans and tactical programs to drive revenue and profit for the business unit and corporatio...

    • Germany
    • Negotiable
    • Posted about 1 month ago

    The Project Engineer takes care of effort estimation, execution and review of test & certification projects within the field of functional safety of industrial machinery. The Engineer assures accurate project execution and authority to review correctness of other project executions & documentatio...

    • Baden-Württemberg
    • Negotiable
    • Posted about 1 month ago

    The position holder is supporting EU Head of Regulatory in administrative tasks in regards of Regulatory projects, Quality Management System and Corrective and Preventive actions. JOB DUTIES & RESPONSIBILITIES: The position holder is responsible for: Managing projects and activities to further im...

    • England
    • Negotiable
    • Posted about 1 month ago

    Position Summary: In charge of designing and executing the PMX strategy at the program level; building, validating, and implementing models for disease, placebo, exposure-response, and mechanistic PKPD to assess risk/benefit and aid in drug development decisions, in close partnership with TS coll...

    • England
    • US$85000 - US$105000 per year
    • Posted about 1 month ago

    Salary: $85,000-105,000 A global Food Services company is seeking a Business Development Manager to support their operations in the USA. In this role, you will be responsible for driving profitable revenue growth in The United States and Canada within key service sectors of the company. Key respo...

    • Switzerland
    • Negotiable
    • Posted about 1 month ago

    I've partnered up with a trailblazing medical device manufacturer looking to expand their Regulatory team. This roles requires a specialised technical skillset of working within the Otology space. Requirements Bachelors degree, or equivalent experience, ideally in a scientific or healthcare disci...

    • Switzerland
    • Negotiable
    • Posted about 1 month ago

    We have a current opportunity to join a global medical device manufacturer that are based in Switzerland and looking to expand their regulatory team. Regulatory Affairs Manager TASKS International registration and approval of our medical devices (risk classes I, lla, IIb) Assembling the relevant ...

    • Berlin
    • Negotiable
    • Posted about 1 month ago

    We are currently looking for an Associate Quality Assurance Manager to join our client's team in Berlin. Our client is a pharmaceutical company that has been expanding its operations in Germany and is now looking for a talented individual to join their team. Responsibilities: - Work closely with ...

    • England
    • US$240000 - US$300000 per annum
    • Posted about 2 months ago

    Senior Director Strategy, Surgical Franchise Introduction We are looking for a Senior Director of Strategy for our Surgical Franchise. The successful candidate will be responsible for leading the annual strategic planning exercise, including long-range sales forecasts, portfolio management, and e...

    • Switzerland
    • Negotiable
    • Posted about 2 months ago

    QA Manager (GDP/GMP) We are looking for a QA Manager (GDP/GMP) for a 12-month contract in Switzerland. Our client is a leading pharmaceutical and biotech company and has a reputation for quality and innovation. They are seeking an experienced Quality Assurance Manager who can work independently. ...

    • England
    • Negotiable
    • Posted about 2 months ago

    Contract Product Access Lead - Europe A global Pharmaceutical client is seeking an experienced Product Access Lead to join their team, to work on a fully remote capacity. This role is a 12-18 month contract, with initial training taking place in the office. You will be responsible for developing ...

    • Belgium
    • Negotiable
    • Posted about 2 months ago

    A large and well-established medical manufacturer with global offices is looking to introduce a Director of Quality and Regulatory Affairs to their site in Belgium. This role is advertised as on site but a hybrid working structure is up for negotiation. Responsibilities: Lead and expand a large q...

    • England
    • Negotiable
    • Posted about 2 months ago

    Our client is a large and well-established medical manufacturer with global offices looking to introduce a QA Manager to their site in Belgium. This role is advertised as on site but a hybrid working structure is up for negotiation. Responsibilities as QA Manager: Lead and expand a large quality ...

    • England
    • Negotiable
    • Posted about 2 months ago

    We have a current opportunity for a Product Access Lead on a contract/ interim basis. The position is fully remote. Key Responsibilities: - Maintain existing pricing, contracts and access across EUR/INT markets including managing the regional pricing corridor - Evaluate, develop and implement opt...

    • England
    • Negotiable
    • Posted about 2 months ago

    EPM Scientific are currently partnered with a reputable company seeking a Marketing Manager with experince in Rare Diseases. See a short summary below: Contract Conditions: Start Date: ASAP Location: London (Office travel) Language: English Therapy Area: Rare Diseases Fix Term Contract or Temp to...

    • Basel
    • Negotiable
    • Posted about 2 months ago

    The Regulatory Affairs Manager, CMC will support the initial registration of products and will be the lead for life cycle management of other products, including determining regulatory reporting, and global filing requirements for post-approval variations related to synthetics (small molecule) pr...

    • Switzerland
    • Negotiable
    • Posted about 2 months ago

    We are currently searching for a QA Ops for one of our clients, a global bio-pharmaceutical company located in Switzerland. Responsibilities: Execute, Write and Review of deviation Change and Deviation management. Document review and approval. Expectations: Experience in Biotech industry At least...

    • Netherlands
    • Negotiable
    • Posted about 2 months ago

    Job Type: Permanent , Full time Location: South Netherlands Our client is looking for a Medical Device Quality Specialist, within this role you are responsible for managing quality technical support within EMEA. Your manager will also be your mentor to guide you as you take your next steps in qua...

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