Biotech And R&D Jobs

Senior Director – GMP Manufacturing

Our client is a highly innovative biotechnology company specialised in genomic therapies. They are looking for a Senior Director to join their team and play a leading role in the setup of a new manufacturing Production Plant. As Senior Director you will: Direct the build-out and qualification of the new cGMP Production plant Build and develop […]

Senior Frontend Developer

We are looking for a motivated and talented Senior Frontend Developer to join our team in Toulouse, France. The ideal candidate will be an experienced technologist, passionate about software engineering with strong background and experience using top notch technologies. You’ll be responsible for all aspects of presentation layer development and platform-related frontend technologies and collaborating with […]

Research and Development Director

Company Description Phileo Lesaffre Animal Care is part of Lesaffre Group, a global B2B Key Player in yeast and fermentation in general, counting 10.500 employees in about 50 different countries with a turnover of more than 2 billions €, that manufactures and markets innovative solutions for Baking, Food taste & Pleasure, Health care and Biotechnology. Phileo […]

Clinical Project Associate

Clinical Project Associate – France Paris Office-based Who We Are Synteract is a global full-service contract research organization with a successful three-decade track record supporting biotechnology, medical device and pharmaceutical companies. With our mission of ”Bringing Clinical Trials to Life,” we provide customized Phase I through IV services internationally, offering expertise across multiple therapeutic areas including notable […]

Senior Manager Value & Access Alzheimer

Company Description Through cutting-edge science and medicine, Biogen discovers, develops and delivers innovative therapies worldwide for people living with serious neurological and neurodegenerative diseases. Founded in 1978, Biogen is a pioneer in biotechnology and today the Company has the leading portfolio of medicines to treat multiple sclerosis, has introduced the first and only approved treatment […]

Clinical Research Associate Sr

Overview Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach. We leverage local regulatory and deep therapeutic expertise […]

Managing Consultant Quality Compliance

Company Description ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in Australia, Canada, Germany, Japan, the Netherlands, Sweden, United Kingdom, and the United States, ProPharma Group’s fully integrated […]

Communicative Contract Manufacturing Manager for APIs / Pharmaceutical industry

Communicative Contract Manufacturing Manager for APIs / Pharmaceutical industry The main responsibility of this role is to manage the Quality Assurance interface with manufacturing and testing partners for assigned products/projects by ensuring quality of product / process transfers, validations, tracking and resolution in a timely manner of investigations. Other tasks also include the evaluation of […]

CMC Project Lead

You will lead CMC activities in support of our clinical development programs. CMC aspects of the product development, and management of external contributors, will be a priority. These include process development, analytical development, formulation development, manufacturing, analytical testing, fill and finish, packaging and labelling. CMC regulatory filings as well as support of regulatory activities authorities to IND and […]

Clinical Trial Supply Specialist

You will support our activities for drug supply in preclinical and clinical trials. You will be responsible for designing Investigational Medicinal Product (IMP) supply strategies, and overseeing and coordinating execution. Tasks include authoring of trial related CMC documents. The following qualifications are required: Experience with clinical trial supply planning and delivery Solid knowledge in GCP and […]

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