Senior MSAT Engineer: Sterile Formulation & Tech Transfer

PSC Biotech; South Carolina; On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical premiums

401(k) matching

Paid holidays

Education assistance

Pet insurance

Fitness benefits

Job summary

PSC Biotech in York, United States is seeking a Mid-Level to Senior MSAT Engineer to support sterile injectable formulation development, compounding process design, and tech transfer for clinical and commercial products.

The role involves leading formulation activities, collaborating with Manufacturing, Quality, Validation and Regulatory teams to ensure robust, scalable processes and successful scale-up for GMP manufacturing.

Qualifications

• Bachelor of Science in Chemical Engineering, Pharmaceutical Sciences, Biochemistry, Biotechnology or related discipline.
• 4-7 years of experience in drug product manufacturing and pharmaceutical process development.
• 8+ years of pharmaceutical industry experience and US work authorization.
• No C2C arrangements at this time.

Responsibilities

• Lead formulation assessment and technology transfer activities from clients.
• Review development reports, formulation histories, and manufacturing records.
• Support sterile formulation development and scale-up for clinical to commercial products.
• Identify CPPs/CQAs and ensure robust, scalable processes.
• Author process descriptions and manufacturing instructions.
• Collaborate with clients, quality, validation, and regulatory teams.

Skills

Sterile formulation development

Process transfer

GMP manufacturing

Regulatory knowledge

Education

Bachelor of Science in Chemical Engineering / Pharmaceutical Sciences / Biochemistry / Biotechnology

Job description

PSC Biotech in York, United States is seeking a Mid-Level to Senior MSAT Engineer to support sterile injectable formulation development, compounding process design, and tech transfer for clinical and commercial products.

The role involves leading formulation activities, collaborating with Manufacturing, Quality, Validation and Regulatory teams to ensure robust, scalable processes and successful scale-up for GMP manufacturing.