Bioprocess Associate: GMP Biotech Manufacturing

Bristol Myers Squibb; Harvard (MA); In loco; USD 65.000 - 90.000; Tempo pieno

Descrizione del lavoro

Bristol Myers Squibb in Massachusetts is seeking a Bioprocess Associate/Specialist to assist in executing commercial manufacturing processes for therapeutic proteins according to cGMPs. You will join a team that performs routine manufacturing tasks and maintains compliance with SOPs.

This role requires 1+ years in GMP, a high school diploma with a science-related BS preferred, and comfort with process equipment and automation systems such as DeltaV, SAP, and Maximo.

Competenze

• 1+ years of experience in GMP environment.
• High school diploma required; B.S. in science/engineering/biochemistry or related discipline desirable.

Mansioni

• Works on routine manufacturing assignments per written procedures, where ability to recognize deviation from accepted practice is required.
• Adheres to Good Manufacturing Practices and standard operating procedures.
• Weighs and checks raw materials. Assembles, cleans, and sterilizes process equipment, monitors processes. Completes electronic work instructions and maintains clean room environment to comply with regulatory requirements.
• Trains for proficiency in the operation of primary production equipment within the assigned functional area (i.e. bioreactors, chromatography skids, media or buffer preparation equipment etc.).
• Trains for proficiency in process automation systems (i.e. DeltaV and Syncade Interactions, Pi Vision) and some supporting business systems (i.e. SAP, Infinity, Maximo etc.).
• Assist with the revision and or creation of process documents, such as SOPs and electronic work instructions.
• Assists in maintaining material and components inventory level.
• Supports safe work environment.

Conoscenze

GMP experience

Formazione

High school diploma

B.S. in science/engineering/biochemistry

Descrizione del lavoro

Bristol Myers Squibb in Massachusetts is seeking a Bioprocess Associate/Specialist to assist in executing commercial manufacturing processes for therapeutic proteins according to cGMPs. You will join a team that performs routine manufacturing tasks and maintains compliance with SOPs.

This role requires 1+ years in GMP, a high school diploma with a science-related BS preferred, and comfort with process equipment and automation systems such as DeltaV, SAP, and Maximo.