BioMarin Pharmaceutical Inc.
(CW) Manufacturing Associate
BioMarin Pharmaceutical Inc., Novato, California, United States, 94949
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(CW) Manufacturing Associate
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BioMarin Pharmaceutical Inc.
Who We Are BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.
Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.
Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need and empower our teams to pursue bold, innovative science.
Manufacturing Associate Process Knowledge : 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 processing issues and support solutions. Gain experience with automation systems (LIMS, MES, PI, etc.).
Technical Documentation : 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.
Quality and Compliance : Understanding of cGMPs as related to Commercial Operations. Ability to utilize Quality systems (Deviations, CAPAs, Change Requests, Action/Alert Reports, etc.).
Business : 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.
Work Environment / Physical Demands
Consists of strenuous, repetitive work; daily movements include bending, reaching, climbing stairs and ladders, kneeling, and making numerous equipment connections using hands.
Independently able to regularly lift, dispense, push, and/or pull items with an average weight of 25 pounds.
May require work around loud equipment.
Requires use of personal protective equipment.
Requires various shift-based work and off hours.
Skills
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.
Education
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.
Hours: 6:00 PM to 7:00 AM. Alternating Sat/Sun - Tues.
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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(CW) Manufacturing Associate
role at
BioMarin Pharmaceutical Inc.
Who We Are BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.
Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.
Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need and empower our teams to pursue bold, innovative science.
Manufacturing Associate Process Knowledge : 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 processing issues and support solutions. Gain experience with automation systems (LIMS, MES, PI, etc.).
Technical Documentation : 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.
Quality and Compliance : Understanding of cGMPs as related to Commercial Operations. Ability to utilize Quality systems (Deviations, CAPAs, Change Requests, Action/Alert Reports, etc.).
Business : 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.
Work Environment / Physical Demands
Consists of strenuous, repetitive work; daily movements include bending, reaching, climbing stairs and ladders, kneeling, and making numerous equipment connections using hands.
Independently able to regularly lift, dispense, push, and/or pull items with an average weight of 25 pounds.
May require work around loud equipment.
Requires use of personal protective equipment.
Requires various shift-based work and off hours.
Skills
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.
Education
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.
Hours: 6:00 PM to 7:00 AM. Alternating Sat/Sun - Tues.
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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