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Manufacturing Supervisor

2 months ago


Philadelphia, United States Planet Pharma Full time

BIO/PHARMA Manufacturing Supervisor-NIGHT SHIFT


Essential Functions and Responsibilities


  • Develop a Subject Matter Expert (SME)-level understanding of and can execute as skillfully as well as troubleshoot GMP manufacturing process(es).
  • Assists with identifying training needs, establishing a feedback loop to ensure continuous improvement.
  • Deliver training sessions and ensure training documentation is maintained.
  • Understand and comply with quality standards and requirements as documented. Ensure training schedules meet company production and quality targets.
  • Provide operational support functions, including materials stocking and transfer, kit preparation, reagent preparation, room readiness, cleaning activities, and equipment maintenance.
  • Perform document review, including executed Batch Records and Logbooks.
  • Support documentation needs, including drafting and approval of SOPs, Batch Records, Deviations, CAPAs, etc. Perform basic revisions as needed to reflect current procedures accurately.
  • Execute documentation Change Controls of SOPs, Batch records, etc., as needed.
  • Support interdepartmental and departmental projects in a contributor capacity.
  • Supports technical transfer and additional research-level testing activities as needed.
  • May work on moderately complex assignments, requiring judgment to resolve operational issues without negatively impacting manufacturing efforts.
  • Adhere to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs), including Good Documentation Practices (GDP).
  • Completes recording of data to comply with regulatory requirements.
  • Attend or hold the daily huddle meeting and escalates issues/concerns at that forum to Area Management for further investigation.
  • Ability to work in a team environment and independently as required.
  • Works on routine assignments per written procedures, where the ability to recognize deviation from accepted practice is required.
  • Work in a cleanroom with biohazards, human blood components, and chemicals
  • Must adhere to core values, policies, procedures, and business ethics.
  • Comply with Safety SOPs, SDS sheets, and laboratory procedures per company policy and OSHA regulations.
  • Perform miscellaneous duties as assigned.


Travel – 5%


Required Education, Skills, and Knowledge


  • Bachelor's degree or some post-secondary education.
  • Demonstrated technical knowledge of aseptic processing in cleanroom environments is a must.
  • Ability to mentor and provide best practices to other team members.
  • Must be able to work with ambiguity – ready to change gears and plans quickly and manage constant change.
  • Must be able to read, write and understand English for Good Documentation Practices
  • Proficient with computers and Microsoft (Excel, Word, Outlook) programs.
  • Ability to perform arithmetic calculations accurately and reproducibly, including fractions, decimals, percentages, and basic algebraic and geometric calculations.
  • Ability to build relationships quickly and credibly.
  • Ability to work successfully in a fast-paced, team-oriented environment.


Salary Range: $115-130K/yr*** Based on experience