Downstream Process Development Scientist
2 weeks ago
Pharmaron is seeking a Downstream Process Development Scientist to contribute to the design, development, and scale-up of cGMP clinical manufacturing processes for bulk drug substances.
In this role, you will play a key part in ensuring the successful production of high-quality pharmaceutical products. You will work closely with a team of scientists and engineers to develop and optimize downstream processes, including purification, formulation, and characterization.
Key Responsibilities:
- Lead the development and validation of cGMP manufacturing processes for bulk drug substances.
- Plan, execute, and analyze experiments to optimize process parameters and improve product quality.
- Prepare comprehensive documentation, including protocols, reports, and regulatory submissions.
- Collaborate with cross-functional teams, including research scientists, engineers, and quality assurance personnel.
- Stay abreast of industry best practices and emerging technologies in downstream processing.
Qualifications:
- Bachelor's or Master's degree in a relevant life sciences or process engineering field.
- PhD or equivalent industrial experience in bioprocess development, cGMP manufacturing, or process validation.
- Proven experience in mammalian, microbial, or viral-based processes.
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal skills.
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