Scientist Randstad Pharma – East Syracuse, NY, USA
Position Description
- The Biologics Manufacturing operation produces clinical, commercial and launch biologics drug substance at its 5000L scale manufacturing facility (mammalian cell process).
- Strong communication and technical writing skills are required.
- Must possess good organizational skills and strong attention to details, excellent experimental/troubleshooting aptitude, and be self motivated.
- Possess good verbal and written communication skills, as well as excellent interpersonal skills with the ability to work in a team environment
Position Responsibilities
- Conduct experiments for the purposes of commercial support for downstream biopharmaceutical manufacturing.
- Support ultrafiltration/diafiltration, filtration, bulk fill, freezing, storage and cold chain shipping operations for biologics drug substance.
- Responsibilities include the operation, cleaning and maintenance of laboratory equipment, the preparation of buffers and reagents, documentation of experimental data and results, data verification and the preparation of study protocols and final reports.
- Appropriate GLP/GMP procedures must be followed.
- Involves troubleshooting and problem solving of process related problems observed at manufacturing scale through the effective design of scale-down studies and the evaluation of data from manufacturing lots.
- Will work effectively in cross-functional project teams and also work independently to accomplish project goals.
- Interface with Process Development, Pilot Plant, Manufacturing, Manufacturing Support, Quality Assurance, Analytical, Supply Chain and Global Regulatory Sciences groups.
Position Requirements
- BS or MS degree in Pharmaceutical Sciences, Biological or Chemical Sciences/Engineering or related disciplines.
- Knowledge of common protein analytical tools and demonstrated experimental skills for lab work are required.
- Knowledge of protein freezing/thawing, formulation and stability is desired.
- Ultrafiltration/diafiltration, filtration, process development, characterization, and/or validation experience are desired.
- Experience with cGMP regulations, regulatory requirements, and CMC authoring for biologics processes are a plus.
Benefits
- Medical, Dental, and Vision Insurance
- 401K Plan with Company Match
- Life and AD&D Insurance
