Process Development Engineer

BioTalent; Wallis; Vor Ort; CHF 80’000 - 120’000; Vollzeit

Zusammenfassung

A leading company in pharmaceutical innovation is seeking a Process Development Engineer in Basel, Switzerland. This role involves developing and optimizing biopharmaceutical manufacturing processes, ensuring compliance with regulatory standards, and collaborating with cross-functional teams. Ideal candidates will possess a relevant degree and substantial experience in process development within the biopharmaceutical industry.

Leistungen

Competitive salary and comprehensive benefits package

Opportunities for career growth and professional development

Support with relocation and integration for international candidates

Qualifikationen

• Minimum 3 years’ experience in biopharmaceutical process development.
• Strong knowledge of biopharmaceutical techniques and GMP compliance.
• Fluent in English; German or French is a plus.

Aufgaben

• Design, develop, and optimize bioprocesses.
• Conduct process characterization studies and support technology transfer.
• Collaborate with teams to ensure compliance with GMP standards.

Kenntnisse

Cell culture

Purification techniques

Analytical techniques

Data analysis

Problem-solving

Communication

Ausbildung

Bachelor’s or Master’s degree in Chemical Engineering, Biochemical Engineering, Biotechnology

Tools

JMP

Minitab

Excel

Jobbeschreibung

Job Title: Process Development Engineer

Location: Basel, Switzerland

Company: Global Pharmaceutical Leader

About Us:

Join a world-renowned pharmaceutical company dedicated to innovation and excellence in drug development and manufacturing. Located in Basel, our cutting-edge R&D facilities focus on advancing new therapies for patients worldwide.

Role Overview:

As a Process Development Engineer, you will play a critical role in developing, optimizing, and scaling up biopharmaceutical manufacturing processes. You will collaborate closely with cross-functional teams in R&D, manufacturing, and quality to deliver robust, scalable processes that meet regulatory and commercial requirements.

Key Responsibilities:

• Design, develop, and optimize upstream and downstream bioprocesses for clinical and commercial manufacturing.
• Conduct small and large-scale process characterization studies to understand process parameters and their impact on product quality.
• Support technology transfer of processes from development to manufacturing sites.
• Develop process models and execute process scale-up activities to ensure smooth transition to commercial manufacturing.
• Analyze process data using statistical tools to identify trends, troubleshoot issues, and recommend improvements.
• Prepare and review technical documentation including batch records, process descriptions, and validation protocols.
• Work collaboratively with quality, manufacturing, analytical, and regulatory teams to ensure compliance with GMP and internal standards.
• Participate in risk assessments and continuous improvement initiatives to enhance process efficiency and robustness.

Qualifications:

• Bachelor’s or Master’s degree in Chemical Engineering, Biochemical Engineering, Biotechnology, or related field.
• Minimum 3 years’ experience in biopharmaceutical process development or related roles.
• Strong knowledge of cell culture, purification, and analytical techniques used in biologics manufacturing.
• Experience with process scale-up, technology transfer, and GMP compliance.
• Proficiency in data analysis software and statistical methods (e.g., JMP, Minitab, Excel).
• Excellent problem-solving and communication skills with the ability to work effectively in multidisciplinary teams.
• Fluent in English; knowledge of German or French is advantageous.

What We Offer:

• Competitive salary and comprehensive benefits package.
• Work in a dynamic, innovative environment at the forefront of pharmaceutical science.
• Opportunities for career growth and professional development.
• Support with relocation and integration for international candidates.