Supervisor, Formulation and Fill - 2nd shift

Sun Pharmaceutical Industries Ltd

  • Billerica, MA
  • 7 days ago

    Highlights

    Supervise and perform the activities of technicians on the second shift in equipment and component preparation operations; dispensing API and excipients; formulation and filling and capping of parenteral drug products. Physical Requirements: Stand, walk, sit, use hands and fingers to handle or feel, reach or push with hands and arms, stoop, kneel, crouch or crawl, climb, talk and hear.

    Numbers & Facts

    LocationBillerica, MA

    Description

    Job Summary

    This position is a 2nd shift role, 1:30PM - 10:00PM. Supervise and perform regularly the preparation, formulation and dispensing of pharmaceutical products according to our current Good Manufacturing (cGMPs) and utilize Standard Operating Procedures (SOPs) in a clean room environment. Write and complete investigations, CAPAs, deviations and change controls utilizing root cause analysis tools and reporting software.

    Area Of Responsibility

    • Supervise and perform the activities of technicians on the second shift in equipment and component preparation operations; dispensing API and excipients; formulation and filling and capping of parenteral drug products. Also responsible for overseeing the formulation and filling of dermatological drug products.
    • Schedule weekly plan of floor activities for technicians on second shift
    • Author and track to close investigations, CAPAS, deviations and change controls as required
    • Troubleshoot and solve moderate to complex problems related to the equipment, processes; existing or new products
    • Oversee inventory control in the production area and order supplies as needed for production to assure no delay in the manufacturing plan
    • Use systems like SAP, Track Wise, EDMS etc.
    • Evaluate team performance by conducting midyear and yearly reviews
    • Review completed batch records to ensure product is made in accordance with specifications
    • Review SOPs and Batch Records, and update through DCRs as needed
    • Work under limited supervision and follows clearly described procedures
    • Other duties as assigned
    • Education in Life sciences or technical discipline

    Work Conditions:

    • Lab
    • Clean room/controlled classified areas
    • Manufacturing/production areas
    • Office
    • Exposure to noise
    • Exposure to Chemical/Biological hazards
    • Exposure to non-hazardous chemicals
    • Exposure to radiation within NRC limits
    • Exposure to/use of syringes and needles
    • Must wear scrubs/coveralls, safety glasses, safety shoes, gloves as required

    Physical Requirements:

    • Stand, walk, sit, use hands and fingers to handle or feel, reach or push with hands and arms, stoop, kneel, crouch or crawl, climb, talk and hear
    • Able to operate lab equipment, production equipment and computer/office machines
    • Ability to wear Personal Protection Equipment
    • Lift up to 50 lbs.

    Travel Estimate

    Up to 0%

    Education and Job Qualification

    • Bachelors degree in related field or equivalent experience
    • 6 to 8 years of experience in pharmaceutical manufacturing
    • Excellent verbal, written and interpersonal communication skills
    • High level of initiative and self-motivation
    • Strong computer skills
    • Attention to detail
    • Ability to plan, prioritize and organize diversified workload
    • Team management skills
    • Record keeping skills
    • Safe chemical handling techniques
    • Knowledge of SAP, GMP, GDP, FDA, and OSHA regulations and standards

    Experience

    • Minimum 2 - 5 years of supervisory or team lead experience
    • 5 to 7 years of aseptic processing and aseptic area techniques experience
    • Experience with technical writing, root cause analysis and completing investigations, CAPAs, deviations and change controls

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