(CW) Manufacturing Associate DAY SHIFT (Temporary/Contract)
About The Position
BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions. Our Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients. This is a temporary/contract role with multiple openings.
Requirements
- Bachelor’s degree in science related area or engineering
- Associate’s degree in science related area or Biotech certificate with 2+ years of experience in a biotech manufacturing environment or other regulated industry
- Strong communication skills—verbal and written
- Ability to work in a team environment which includes good conflict resolution and collaboration
- Displays good initiative to identify areas for improvement and implement solutions
Nice To Haves
- Understanding of process theory and equipment operation.
- Ability to learn biopharmaceutical manufacturing processes including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, centrifugation, protein purification, and formulation of bulk drug substance.
- Support initiatives for process optimization.
- Identify and elevate processing issues and support solutions.
- Gain experience with automation systems (LIMS, MES, PI, etc.).
- Provide feedback and/or suggested changes to operational procedures.
- Assist in the incorporation of new technologies, practices, and standards into procedures.
- Capable of writing and reviewing process documents.
- Understanding of cGMPs as related to Commercial Operations.
- Ability to utilize Quality systems (Deviations, CAPAs, Change Requests, Action/Alert Reports, etc.).
- Ability to participate on projects and contribute to outcomes.
- Capability to learn and support new business systems (Track wise, ERP, etc.).
- Support trending of defined department metrics.
Responsibilities
- Understanding of process theory and equipment operation.
- Ability to learn biopharmaceutical manufacturing processes including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, centrifugation, protein purification, and formulation of bulk drug substance.
- Support initiatives for process optimization.
- Identify and elevate processing issues and support solutions.
- Gain experience with automation systems (LIMS, MES, PI, etc.).
- Provide feedback and/or suggested changes to operational procedures.
- Assist in the incorporation of new technologies, practices, and standards into procedures.
- Capable of writing and reviewing process documents.
- Understanding of cGMPs as related to Commercial Operations.
- Ability to utilize Quality systems (Deviations, CAPAs, Change Requests, Action/Alert Reports, etc.).
- Ability to participate on projects and contribute to outcomes.
- Capability to learn and support new business systems (Track wise, ERP, etc.).
- Support trending of defined department metrics.
- Support the organisation’s commitment to environmental protection, injury prevention, and continual improvement of EHS management systems.
- Actively contribute to a safe and environmentally responsible workplace by identifying hazards, reporting incidents and participating in EHS initiatives and training.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
