Lead Aseptic Fill-Finish Manufacturing Associate

PSC Biotech® Corporation; York (York County); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Medical, Dental, Vision benefits

401(k) and matching

Paid time off and holidays

Relocation assistance

Education assistance

Wellness programs

Job summary

PSC Biotech is seeking a Level III Manufacturing Associate to perform complex aseptic filling and related activities in a GMP environment. You will work under general guidance, coordinating with engineering, QA, and facilities to ensure compliant operations and timely production.

You will lead manufacturing tasks, review documentation, and participate in investigations while supporting continuous improvements and cross-functional training.

Qualifications

• Bachelor’s Degree in Life Sciences or Liberal Arts or equivalent experience.
• 5–7 years of professional manufacturing experience in an aseptic, FDA-regulated pharmaceutical facility.

Responsibilities

• Maintain aseptic gowning certification and use proper aseptic technique.
• Perform equipment prep including CIP and SIP operations.
• Execute manufacturing instructions for compounding, filtration, formulation, and fill activities.
• Complete production documentation and batch records with GDP compliance.
• Sanitize rooms and maintain controlled environment conditions.
• Identify deviations and participate in investigations; support GMP facility improvements.
• Lead routine and critical operations, commissioning and validation activities.
• Assist cross-functional departments to build cross-functional skills.

Skills

Excellent communication

Attention to detail

Analytical skills

Self-motivated

Team collaboration

Education

Bachelor’s Degree in Life Sciences or Liberal Arts

Tools

MS Office/Excel

Job description

PSC Biotech is seeking a Level III Manufacturing Associate to perform complex aseptic filling and related activities in a GMP environment. You will work under general guidance, coordinating with engineering, QA, and facilities to ensure compliant operations and timely production.

You will lead manufacturing tasks, review documentation, and participate in investigations while supporting continuous improvements and cross-functional training.