Technical Project Manager: LZAJP00005293

BioTalent Ltd; Visp; Hybrid; CHF 80’000 - 120’000; Vollzeit

Zusammenfassung

An established industry player is seeking a Biopharmaceutical Project Manager to lead critical projects in a hybrid role. This position promises a dynamic work environment where you will define technical requirements, oversee project execution, and ensure compliance with GMP standards. You will collaborate with cross-functional teams to drive operational improvements and manage quality oversight. If you have a strong background in biopharmaceutical manufacturing and are passionate about project leadership, this role offers an exciting opportunity for professional growth and impact in a vital sector.

Qualifikationen

• 5+ years of experience in biopharmaceutical manufacturing with a focus on project management.
• Strong knowledge of GMP standards and change control processes.

Aufgaben

• Define technical requirements and develop project roadmaps to align with GMP.
• Lead equipment commissioning and ensure timely project completion.

Kenntnisse

Project Leadership

Technical Oversight

Quality Management

Cross-Functional Coordination

Risk Assessment

Ausbildung

Bachelor’s degree in Biochemical Engineering

Master’s degree in Mechanical Engineering

Degree in Life Sciences

Tools

GMP Regulations

Change Management

Commissioning and Qualification

Jobbeschreibung

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.