Senior MSAT Engineer - Sterile Formulation & Transfer

PSC Biotech; York (York County); On-site; USD 120,000 - 160,000; Full time

Benefits offered by this job

Medical, Dental, and Vision benefits

PTO and Holidays

Education Assistance

401(k) retirement plan

Job summary

PSC Biotech is seeking a Senior MSAT Engineer to support formulation development, compounding process design, technology transfer, scale-up, and commercial manufacturing readiness for sterile injectable products. The role requires leading drug product formulation activities and collaborating with clients and internal teams to ensure robust, scalable processes for clinical and commercial production.

The candidate should have strong expertise in sterile formulation development, compliance with GMP

Qualifications

• Bachelor of Science in Chemical Engineering, Pharmaceutical Sciences, Biochemistry, Biotechnology, or related discipline.
• 7+ years of experience in drug product manufacturing.
• 8+ years pharmaceutical industry experience.

Responsibilities

• Lead formulation assessment and transfer from clients.
• Support development and optimization of sterile injectable formulations.
• Assist with process characterization and scale-up activities.
• Ensure compliance with cGMP, FDA and EU guidelines during development and manufacturing.
• Collaborate with Manufacturing, Quality, Validation and Regulatory teams.

Skills

GMP manufacturing

Process development

Technology transfer

Scale-up

Cross-functional collaboration

Education

B.S. in Chemical Engineering

B.S. in Pharmaceutical Sciences

B.S. in Biochemistry

B.S. in Biotechnology

Job description

PSC Biotech is seeking a Senior MSAT Engineer to support formulation development, compounding process design, technology transfer, scale-up, and commercial manufacturing readiness for sterile injectable products. The role requires leading drug product formulation activities and collaborating with clients and internal teams to ensure robust, scalable processes for clinical and commercial production.

The candidate should have strong expertise in sterile formulation development, compliance with GMP