Responsibilities:
1. Provide support and troubleshooting in Drug Substance Manufacturing areas like USP, DSP, and Solution Preparation.
2. Oversee equipment installation, maintenance, and calibration as the process owner, ensuring top performance and adherence to industry standards.
3. Ensure quality, safety, and compliance by reviewing exceptions, supporting batch record reviews, and leading deviation investigations and CAPAs.
4. Represent operations in facility design, tech transfer, commissioning, and validation of new production lines.
5. Drive continuous quality and process improvements using Practical Process Improvement (PPI) methodologies.
6. Collaborate with various departments and represent DS Manufacturing in external interactions.
Qualifications:
1. Bachelor/Master/PhD in Chemistry, Biochemistry, Biotechnology, Biology, or related field.
2. Proficiency in English; German advantageous.
3. In-depth experience in pharmaceutical companies in a GMP environment.
4. Experience in biotech processes, sterile processes, and production equipment handling.
5. Ability to thrive in a matrix environment and collaborate with multi-functional teams.
Additional Information:
Exciting tasks in a renowned company with challenging and varied tasks in a forward-looking and innovative industry.
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