Description
Media/Buffer Validation EngineerA global biotech company is looking for an experienced Project Engineer to support a site transformation from chemicals to biotech manufacturing.
Location: Paris Region France.
Duration: 3-6 months
Start: ASAP
Seeking a highly motivated individual to be responsible for the validation of new media and buffer equipment.
Role and Responsibilities:
• Oversee and coordinate the validation of media and buffer equipment to support the biotech transformation programme.
• Provide technical input and knowhow based upon knowledge and experience of the biopharmaceutical industry, specifically media and buffer equipment.
• The successful candidate will be responsible for the full project lifecycle including protocol writing, sampling, planning and data review and conclusion.
• Work closely with the QA team to drive GMP and FDA compliance.
Requirements:
• Experience working in a biopharmaceutical environment is essential.
• Biopharmaceutical QA or Engineering background required.
• Previous experience of the validation of media and buffer equipment.
• Able to communicate and build relationships with stakeholders from various different backgrounds.
• Fluent French language skills essential.
• Knowledge of English language desirable.