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Process Improvement Engineer in Pharmaceutical Manufacturing

vor 2 Wochen


Neuenburg, Neuenburg, Schweiz Randstad Vollzeit
Job Description
We are searching for a skilled Process Improvement Engineer in Pharmaceutical Manufacturing for our client, an international pharma company based in Neuchâtel.

Key Tasks:
Develop and optimize process parameters, ensure process performances through Quality by Design (QbD) and Continuous Process Verification (CPV) approaches. Lead and/or support investigations related to deviation/CAPA process, perform product impact assessments, and lead projects or activities related to FF process or equipment. Support validation activities, present topics during regulatory inspections, and support technology transfer.

Responsibilities and Requirements:
45% - Manufacturing support activities (deviation, process follow-up), 45% - Projects, 10% - Audit and Regulatory questions related activities. Minimum 3-5 years of experience in FF area for recombinant protein, previous MSAT exposure, engineering or university degree in biotechnology. Fluent in English and French, knowledge of cGMP and quality requirements, ability to deal with statistics, strong energetic team player with good communication skills.