Gene Therapy Manufacturing Specialist
Vor 2 Tagen
DINAMIQS is a Contract Development and Manufacturing Organization (CDMO) based in Schlieren-Zurich, Switzerland, offering a comprehensive range of services for the manufacturing of viral vector gene therapies.
We are seeking a highly motivated and experienced GMP Upstream Process Supervisor to join our team. This individual will be responsible for the planning, execution, and monitoring of upstream processing operations, ensuring compliance with Good Manufacturing Practices (GMP).
The key responsibilities of this role include:
- Developing and implementing process strategies for efficient and effective upstream processing.
- Leading cross-functional teams to ensure successful technology transfer and scale-up projects.
- Maintaining accurate and detailed records of all upstream processing activities, including batch records and equipment qualifications.
- Coordinating with the quality department to ensure adherence to regulatory requirements and industry standards.
- Identifying and implementing opportunities for process improvements and efficiency gains.
Qualifications:
- Bachelor's degree in biotechnology, bioprocess engineering, or a related field.
- Minimum 3-5 years of experience in upstream processing operations, preferably in a CDMO or pharmaceutical manufacturing environment.
- Excellent communication and leadership skills, with the ability to collaborate effectively with cross-functional teams.
- Strong problem-solving skills, with the ability to analyze complex data and identify opportunities for improvement.
- Knowledge of GMP regulations and industry standards, with the ability to apply this knowledge to ensure compliance.
- Proficient in MS Office and relevant software applications, with the ability to learn new systems quickly.
We offer a competitive salary and benefits package, as well as opportunities for professional growth and development.
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