Description
Direct Employment with a Pharmaceutical Company, Quick apply to learn more. We are hiring multiple levels of experience for new product lines.
Description:Executes routine unit operations in Downstream manufacturing as assigned related to the manufacturing of bulk drug substance in a multi-product facility. Performs duties under limited supervision and according to standard operating and manufacturing procedures.
Pharma Manufacturing Associate - Downstream
Requirements:- High school degree plus minimum one (1) year work experience in GMP regulated industry
- Associates/Bachelor's degree from an accredited institution or biotechnology vocational training preferred.
- One (1) or more years of experience in cGMP regulated industry.
- Ability to concentrate on detail oriented work in a complex technical setup with a Quality and Right the first time mindset.
- Strong written and verbal communication skills.
- Ability to work with computer-based systems and ideally experience with process control systems (e.g. Delta V) and manufacturing execution systems (MES).
- Ability to read and understand SOPs and work instructions and document work in a written format applying cGMP standards.
- Ability to work as part of a high performing team and collaborate effectively with staff.
- Basic knowledge of fundamental manufacturing concepts is preferred. Does not require extensive technical knowledge of manufacturing operations.
- Working in a highly regulated environment following all applicable BI and BI Fremont SOPs, OCPs and BGSs for cGMP, EHS and Compliance policies.
- Required to work according to given schedules in a 24/7 shift structure and flexibility to adapt working schedule upon prior given notice.
Pharma Master Manufacturing Associate - Downstream
Requirements:- High school degree plus minimum four (4) year's work experience in GMP regulated industry
- Associates/Bachelor's degree from an accredited institution or biotechnology vocational training preferred.
- Four (4) or more years of experience in cGMP regulated industry.
- Ability to concentrate on detail oriented work in a complex technical setup with a Quality and Right the first time mindset.
- Strong written and verbal communication skills.
- Ability to work with computer-based systems and ideally experience with process control systems (e.g. Delta V) and manufacturing execution systems (MES).
- Ability to read and understand SOPs and work instructions and document work in a written format applying cGMP standards.
- Ability to work as part of a high performing team and collaborate effectively with staff.
- Subject Matter Expert of biopharmaceutical manufacturing practices, as well as a high technical knowledge of biologics principles required.
- Working in a highly regulated environment following all applicable BI and BI Fremont SOPs, OCPs and BGSs for cGMP, EHS and Compliance policies.
- Required to work according to given schedules in a 24/7 shift structure and flexibility to adapt working schedule upon prior given notice.
