Aseptic Processing Technician (1st shift) at Planet Pharma in Philadelphia, Pennsylvania

Posted in Other 6 days ago.

Type: full-time





Job Description:

Aseptic Processing Technician (1st shift)

Philadelphia, PA - onsite

$27 per hr

1st shift is 7am - 5:30pm - Tuesday - Friday

6 month CONTRACT TO HIRE

Essential Functions and Responsibilities
  • Complete training sessions and ensure training documentation is maintained.
  • Proficiently carry out procedures to achieve a consistent, error-free execution of daily job assignments
  • Work as part of a team to produce each lot accurately and fully complete batch records, forms, and documentation.
  • At all times, understand and comply with quality standards and safety guidelines.
  • Perform materials stocking, kit preparation, reagent preparation, cleaning activities, and equipment maintenance.
  • Identify errors and report them promptly to lab management. Participate in root cause analysis and implement corrective actions.
  • Adheres to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs), including Good Documentation Practices (GDP).
  • Must adhere to the clients 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.

Required Education, Skills, and Knowledge
  • Research experience with aseptic techniques - MUST HAVE and must be on resume
  • Demonstrated technical knowledge of aseptic processing in cleanroom environments.
  • Cell culture or cell line experience
  • 0-2 years of experience in biopharmaceutical-based GMP manufacturing operations
  • Able to read, write and understand English, and be proficient in Microsoft (Excel, Word, Outlook).
  • Able to accurately perform basic math, including fractions, decimals, and percentages.
  • Able to work effectively with team members and show initiative to assist others on the team.
  • Able to work successfully in a fast-paced, team-oriented environment.
  • Quality mindset, familiar with 21 CFR Part 11 and standard GxP best practices and FDA regulations.

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