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• Groningen, Netherlands
• €55000 - €60000 per annum + 25 days holiday
• Posted about 6 hours ago

Senior Product Quality Lead The Company A global Contract Manufacturing Organisation (CMO), who specialise in producing clinical trial batches for Pharmaceutical and Biotechnology companies all over the world, is recruiting a Senior Product Leader at their site in the Netherlands. Not only do...

• Cambridge, Massachusetts
• Negotiable
• Posted about 6 hours ago

Title: CMC Project Manager (Contract) Company Summary An advancing pharma company focused on gastrointestinal diseases, in Cambridge, is looking to bring on a CMC Project Manager to join their Development and Manufacturing team, on a 1-year contract-to-extension basis. You will play a key r...

• Zürich, Switzerland
• Negotiable
• Posted about 7 hours ago

Description: This is an exciting opportunity to lead an exciting new department and develop your international medical device standards experience with an international manufacturer, based in the Zurich area. This company specialises in unique spinal implant and is a rapidly growing, innovative ...

• Frankfurt am Main, Hessen
• Negotiable
• Posted about 15 hours ago

Marketing Manager: A Leading medical device company is seeking a product marketing manager to be based in Berlin or South-West Germany. The Manager will join an experienced marketing team and will be responsible for product research and development within the company's Medical device department...

• Hamburg, Germany
• Negotiable
• Posted about 18 hours ago

Responsibilities: Lead a team in QM/RA Creating technical documentations Involvement in product development and project management Improving QMS Responsible in planning international approvals for the medical devices What awaits you An competitive salary Learning and training Ca...

• Hamburg, Germany
• Negotiable
• Posted 1 day ago

Responsibilities: Lead a team in QM/RA Creating technical documentations Involvement in product development and project management Improving QMS Responsible in planning international approvals for the medical devices What awaits you An competitive salary Learning and training Ca...

• Tuttlingen, Baden-Württemberg
• Negotiable
• Posted 1 day ago

Senior Regulatory Affairs Manager Job type: Permanent Location: Tuttlingen A reputable Medical Device Manufacturer is currently looking to hire a Senior Regulatory/Quality Manager to join their growing team on their site in Tuttlingen. Employees will have the chance to work on ground b...

• New York, USA
• Negotiable
• Posted 4 days ago

You are the liaison between the client and internal departments and will provide a clear direction on plans of execution to ensure they are aligned with committed timelines and budgets You have the opportunity to work directly with clients on deliverables such as Advisory Boards, Slide Decks...

• New York, USA
• PTO, Healthcare, Dental and 401K
• Posted 4 days ago

You will lead the account and have a thorough understanding of the market, brand, and strategy in order to support Execution plans. Assist in organic business growth and actively manage budgets and forecasting You will engage in strategic, tactical and execution oversight of all deliverables ...

• Los Angeles, California
• Negotiable
• Posted 4 days ago

You will develop professional relationships with thought leaders, translate those relationships into business and research opportunities, as well as provide timely, accurate, unbiased, fair-and-balanced product information to internal and external customers. You will disseminate technical and sc...

• New York, USA
• Negotiable
• Posted 4 days ago

Title: Senior Medical Writer (REMOTE) Salary: $85,000 - 95,000 A cutting edge Medical Communications agency is searching for a Senior Medical Writer with a passion for oncology to work remotely. You will play a pivotal role in the content creation of the organization and will be mentored to gr...

• California, USA
• Negotiable
• Posted 4 days ago

As the Senior Director - Medical Science Liaisons - West, you will be responsible for managing a growing, high-performing team of field-based Medical Science Liaisons (MSLs). This is a high visibility position accountable for defining and executing the Medical Affairs field strategy for the comp...

• Philadelphia, Pennsylvania
• US$90000 - US$110000 per year + Healthcare, Vacation, 401k, etc.
• Posted 4 days ago

Job Summary: An excellent agency within a growing network of agencies is looking for an outgoing Senior Medical Writer to join the team. This position has been opened as a growth position and it is a great time to join the organization as the continued growth will open doors to whichever career...

• Denver, Colorado
• US$165000 - US$200000 per year
• Posted 4 days ago

Medical Science Liaison A leading pharmaceutical company focused on bringing innovative products to patients with unmet medical needs. Due to consistent growth, they are actively building their MSL team. Medical Science Liaison Responsibilities Systematically identify and develop new as well...

• San Diego, California
• US$165000 - US$200000 per year
• Posted 4 days ago

Medical Science Liaison A leading pharmaceutical company focused on bringing innovative products to patients with unmet medical needs. Due to consistent growth, they are actively building their MSL team. Medical Science Liaison Responsibilities Systematically identify and develop new as well...

• Zürich, Switzerland
• Negotiable
• Posted 4 days ago

Key Account Manager EMEA ** Based in the Zurich ** An international business specialised in life sciences and diagnostics and laboratory automation is seeking an senior level experienced Key Account Manager to join the business for the EMEA region. This fantastic opportunity is a highly str...

• Frankfurt am Main, Hessen
• Negotiable
• Posted 4 days ago

Working with a Medical Technology company to assist the teams improve their Regulatory system for a 6 month contract working flexibly from client site just outside of Frankfurt. Senior Regulatory Associate consultant's Responsibilities: Maintenance of Regulatory Files- Globally including F...

• Frankfurt am Main, Hessen
• Negotiable
• Posted 4 days ago

A growing Medical Technology company specialised in the manufacture of Class IIb and Class II products is looking for an Independent CSV Expert consultant to work on upgrading and working on current systems. Job Overview Looking at a risk based validation strategy for all QMS Procedures and...

• Berlin, Germany
• Negotiable
• Posted 5 days ago

MAIN TASKS Performing and monitoring of medical device registration with prime focus in the EU Market; lifecycle management activities for devices of risk Class I-III from regulatory perspective. Additionally, creating and maintaining Technical Documentation for class I - III devices. MAIN...

• Switzerland
• Negotiable
• Posted 5 days ago

The Consultant will be responsible for planning, coordinating and driving validation activities from initiation to successful completion. Furthermore, the consultant will act as the primary decision maker for assigned validation responsibilities, including deviation investigations, risk / impac...