Job description
Responsibilities:
- Excellent employment opportunity for a Manufacturing Technician in the Fremont, CA area.
- Executes fundamental unit operations in Downstream manufacturing 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.
- Executes independently with adequate training non-complex fundamental operations as parts cleaning, weigh and dispense, equipment prep, kits assembly, and staging.
- Performs internal support duties including stocking consumables/materials, updating controlled SOP binders, appropriately discarding expired reagents, recognizing and reporting process and equipment anomalies.
- Executes with oversight of qualified staff fundamental tasks as CIP and SIP of tanks, manufacturing equipment as well as buffer prep and transfer into tanks and bags
- Daily analytics and maintenance of analytical equipment.
- Cleaning and setup of equipment. Documents work according to cGMP and cGDP.
- Adheres to established regulations and follows cGMP established by site.
- Reports abnormalities and deviations in a timely and accurate manner.
- Adheres to safety standards and identifies unsafe situations / habits and escalates appropriately.
- Maintains production areas according to predefined standards (5s).
- Working in a highly regulated environment following all applicable Company and Company 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.
Experience:
- Completed High School (Diploma or GED)
- Entry level position.
- Associates/Bachelor’s Degree or Biotechnology Vocational training preferred.
- Preferable 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.
- Ability to read and understand SOPs and work instructions and document work in a written format applying cGMP standards.
- Performing highly proceduralized tasks.
- Basic interactions Manufacturing Cell Culture, Manufacturing Purification, Manufacturing Compliance, Engineering & Technology, Supply Chain, Quality Assurance, Quality Control
- Does not require extensive technical knowledge of Manufacturing Operations.
- Low impact, repeatable, highly proceduralized.
- Required Skills: DETAIL ORIENTED, SAFETY STANDARDS, MANUFACTURING TECHNICIAN, SOP, CGMP
- Additional Skills: SOPS, MANUFACTURING OPERATIONS, MAINTENANCE, SIP, OPERATIONS, STOCKING, ENTRY LEVEL, EHS, BIOTECHNOLOGY, BUSINESS INTELLIGENCE, CELL CULTURE, EXCELLENT WRITTEN AND VERBAL COMMUNICATION SKILLS, FERMENTATION, QUALITY ASSURANCE, VOCATIONAL TRAINING, SUPPLY CHAIN, ASSEMBLY, QUALITY CONTROL
Job Type: Contract
Schedule:
- 8 hour shift
Ability to commute/relocate:
- Fremont, CA 94555: Reliably commute or planning to relocate before starting work (Required)
Application Question(s):
- Would you be able to work on the W2 role?
Experience:
- Manufacturing: 1 year (Required)
- BIOTECHNOLOGY: 1 year (Required)
- CGMP: 2 years (Required)
Shift availability:
- Day Shift (Required)
Work Location: One location
Speak with the employer
+91 7602548844
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