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/Bachelors 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) years work experience in GMP regulated industry Associates/Bachelors 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.
