Senior MSAT Engineer: Formulation & Transfer Lead

PSC Biotech® Corporation; York (York County); On-site; USD 120,000 - 180,000; Full time

Benefits offered by this job

Medical premiums covered for employee

401(k) and matching

Paid Holidays

Education Assistance

Pet Insurance

Fitness Benefits

Job summary

PSC Biotech Corporation is seeking a Senior MSAT Engineer to support formulation development, process design, technology transfer, scale‑up and commercial manufacturing readiness for sterile injectable products.

The successful candidate will lead formulation and compounding activities, collaborate with Manufacturing, Quality, Validation and Regulatory teams to ensure robust, scalable processes suitable for aseptic manufacturing and regulatory compliance.

Qualifications

• BS in a related field with 7+ years in sterile formulation development
• Experience in drug product manufacturing and pharmaceutical process development
• Authorized to work in the U.S. and no C2C at this time

Responsibilities

• Lead formulation assessment and process transfer activities from client organizations.
• Review development reports, formulation histories, and manufacturing records.
• Support development and optimization of sterile injectable formulations.
• Identify CPPs and CQAs and ensure process robustness during scale‑up.
• Author process descriptions and manufacturing instructions.
• Collaborate with clients to establish manufacturing strategies for clinical and commercial production.
• Provide technical guidance during development and manufacturing campaigns.
• Troubleshoot processing deviations and formulation‑related challenges.
• Investigate batch failures, yield losses, or process excursions.

Skills

Sterile formulation development

Drug product manufacturing

Process development

MSAT engineering

GMP knowledge

Client collaboration

Education

Bachelor of Science in Chemical Engineering or related field

Job description

PSC Biotech Corporation is seeking a Senior MSAT Engineer to support formulation development, process design, technology transfer, scale‑up and commercial manufacturing readiness for sterile injectable products.

The successful candidate will lead formulation and compounding activities, collaborate with Manufacturing, Quality, Validation and Regulatory teams to ensure robust, scalable processes suitable for aseptic manufacturing and regulatory compliance.