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Work as Pharmaceutical Manufacturing Team Lead at Gilead Sciences | San Dimas, US

 

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Gilead Sciences, Inc. is a research-based biopharmaceutical company that discovers, develops and commercialises innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. Gilead’s therapeutic areas of focus include HIV/AIDS, liver diseases, cancer and inflammation, and serious respiratory and cardiovascular conditions.

Post : Pharmaceutical Manufacturing Team Lead - Formulation/Hydration

Job Description
• Provides hands-on guidance to Manufacturing Technicians.
• Conducts Technicians’ performance evaluations and one-to one meetings
• Assigns daily job responsibilities.
• Expedites production scheduling through communication with QA/QC and Inventory Control personnel.
• Participates in production processes, including cleaning and set-up.
• Complies with all established SOPs in performance of job. Adheres consistently to GMPs.
• Investigates and reports on variance or deviations from standard procedures..
• Has daily contact with Compliance, Inventory Control and Maintenance to ensure equipment and materials are ready and available for use.

Physical Requirements for the role:
• Must be able to work on a rotational shift schedule alternating between day shift and grave shift
• Must be able to work weekends
• Must be able to work holidays
• Must be able to operate and qualify for respirator usage
• Must be able to see and distinguish all colors and shades
• Must be able to stand for a continuous 4 hours
• Must be able to change into Gilead gowns and work attire as required for the task
• Occasionally lift 50 lbs
• Routinely lift 25 lbs

Candidate Profile
• 6+ years of relevant experience and a BS or BA.
• 4+ years of relevant experience and a MS.
• Prior experience in a cGMP related industry is required, within Biopharmaceutical or Pharmaceutical industry preferred.
• Proficient knowledge of Good Manufacturing Practices (GMPs)
• Audit and Investigation Skills, Report Writing Skills.
• Strong verbal, technical writing and interpersonal skills are required.
• Proficiency in Microsoft Office applications.
• Must possess a strong knowledge of the FDA/IMB and cGMP standards as well as regulatory guidance documents.

Additional Information:
Requisition ID:  R0001732
Job Location : San Dimas
Industry Type: Pharma
Functional Area: Formulation/Hydration
End Date: 18th April, 2018

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