Viral Vector Production Supervisor
Vor 2 Tagen
Viral vector gene therapy manufacturing is a rapidly evolving field, requiring continuous innovation and improvement to ensure high-quality products.
As a GMP Upstream Process Supervisor at DINAMIQS, you will be at the forefront of this evolution, contributing to the development and implementation of cutting-edge process technologies and innovative solutions for our clients.
The role involves a wide range of responsibilities:
- Managing upstream processing operations, including mammalian cell culture, bioreactor management, and aseptic techniques for cell line handling.
- Ensuring compliance with GMP standards through rigorous quality control and assurance measures.
- Collaborating with cross-functional teams to achieve project objectives and deadlines.
- Staying up-to-date with industry developments and trends, identifying opportunities for process improvements and efficiency gains.
- Communicating effectively with colleagues and stakeholders to ensure seamless integration of upstream processing operations.
To succeed in this role, you will require:
- A degree in biotechnology, bioprocess engineering, or a related field.
- 3-5 years of experience in upstream processing operations, preferably in a CDMO or pharmaceutical manufacturing environment.
- Excellent communication and collaboration skills, with the ability to work effectively in a fast-paced environment.
- Strong analytical and problem-solving skills, with the ability to identify and troubleshoot process issues.
- 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 in a dynamic and innovative environment.
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