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Biopharm Manufacturing Associate - Level 3 US_AGS

LanceSoft Inc
  • 🇺🇸 United States
  • On-site
  • 1 day ago
  • GMP
  • 5S
  • SAP
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Title: GMP Cleaning Associate/Biopharm Manufacturing Associate
Duration: 11/16/2026 to 11/15/2027
Location: King of Prussia, PA 19406

Hiring for overnight shifts (C and D shift).
12 hours 3-4 times a week. Including every other weekend and overnight. Rotating 2-2-3 overnight schedules from 5:00 PM to 5:00 AM. The schedule consists of two days on, two days off, and alternating three-day weekends on or off.

Job Description:
Job Purpose:
  • To clean the production, lab, and warehouse areas according to site procedures and complying to safety[br role="presentation"]and quality requirements.
  • Conduct GMP Cleaning operations in accordance with Biopharm Safety[br role="presentation"]Procedures and cGMPs.
  • Off-shift hours (including night work) may be required. Must be able to work every[br role="presentation"]other weekend (Saturdays and Sundays)

Key Responsibilities:
Safety
  • Follow all EHS procedures, standards and PPE requirements
  • Notify appropriate personnel of any incident and accident in respective area.
  • Raise ZAPs for any EHS concerns.
  • Attended Stop for Safety Sessions in respective shift / area

Quality
  • Follow GMP procedures
  • Report any abnormalities /adverse event to FLL (OLN, Rapid Response, deviation) in a timely manner.
  • Perform area cleaning and record per procedure.[br role="presentation"]

Performance
  • Adhere to site cleaning procedure and schedule
  • Ontime attendance
  • Maintain 5S, area cleanness and tidiness.
  • Interact professionally with other staff

Knowledge / Experience Required
  • Reading and comprehension skills required to execute GMP Cleaning activities and ensure operations occur in safe, compliant and efficient manner.
  • Minimum of 1 year experience in Sterile or GMP Cleaning operations within Pharmaeutical or Biotechnology industry or 5 or more years of equivanlent experience
  • Prior experience with pharmaceutical manufacturing
  • Familiar with cGMP’s, regulatory guidelines, governmental codes, and standard operating procedures.
  • Strong communications skills, both verbal and written.
  • Basic knowledge and understanding of safety and GMP requirements
  • Demonstrates proficiency on the following systems: SAP/MERPS, VQD, Syncade, Microsoft software packages
  • Ensure the proper procurement of appropriate materials for tasks.
  • Ensure proper documentation is completed appropriately to sufficiently document cleaning tasks.
  • Strong quality/compliance orientation and track record.

Minimum Education:
  • GED or high school diploma

Biopharm Manufacturing Associate - Level 3 US_AGS · LanceSoft Inc

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