Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

Job Description

Join the Thermo Fisher team for impactful work and chances to contribute to the world.

Job Description

Review and release drug substances, purchased and in-house material. Support various departments during facility establishment and operation activities.

Responsibilities:Timely exceptions review and event assessmentActive on-the-floor supportReview and approval of operational elements such as procedures and related documents including specificationsAssist with continuous improvement initiatives related to quality documents and processesSupervision of the preparation of the Annual Product Review (APQR) and guarantees its execution within the due dateBe on the floor during critical manufacturing stepsRespect and share data integrity rules (ALCOA+)Make proposals to improve flows, manufacturing activities, and organization

Qualifications:Pharmacist or scientist with a master’s degree or equivalent experience. At least 3-5 years in the pharmaceutical industry (biotech company) and not less than 1 year in commercial batch release.Knowledge of pharmaceutical manufacturing processes with a focus on biologic drug substances.Proficient communication (oral and written) in German and English.Experience in SAP and electronic MES (manufacturing execution system) is an asset.

Join us to help customers globally for a healthier, cleaner, and safer world.

Apply today! http://jobs.thermofisher.com

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.

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