We are currently looking for a Biopharmaceutical Project Manager (PM) for a leading pharmaceutical company in Valais. This position is a hybrid 6 month contract, with a high likelihood of extension.
Responsibilities:
* Project Leadership & Strategy:Define technical requirements, develop project roadmaps, and ensure alignment with GMP, compliance, and operational goals.
* Technical Oversight:Act as the primary technical contact, coordinate with EPCM teams, and guide production staff on mechanical adaptations and operational improvements.
* Quality & Compliance Management:Ensure adherence to GMP standards, oversee change control processes, and collaborate with QA on validation and documentation.
* Cross-Functional Coordination:Facilitate communication between engineering, operations, maintenance, and quality teams to integrate process changes effectively.
* Execution & Validation:Lead equipment commissioning, qualification (IQ/OQ/PQ), risk assessments, and progress monitoring to ensure timely and budget-compliant project completion.
Requirements:
* Education:Bachelor’s or Master’s degree in Biochemical Engineering, Mechanical Engineering, Life Sciences, or a related field.
* Experience:prior experience in biopharmaceutical manufacturing with a focus on technical project management, GMP compliance, and process improvements.
* Technical Expertise:Strong knowledge and hands-on experience with GMP regulations, change management, commissioning, qualification (CQV), and validation of equipment/processes.
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