Downstream Process Development Scientist (Viral Vector)

Minaris; Philadelphia (Philadelphia County); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Medical insurance

Vision insurance

Dental insurance

401(k) plan

Tuition assistance

Job summary

Minaris is seeking an experienced Downstream Process Development Associate Scientist to advance viral vector processes—from design to manufacturing transfer—ensuring robust, scalable production. The role emphasizes collaboration, rigorous documentation, and GMP-compliant practices to deliver high‑quality therapies.

Ideal candidates will have hands-on experience in chromatography, filtration, and fill/finish steps, plus strong analytical and problem‑solving skills.

Qualifications

• Master or Bachelor's in Biological/Chemical Engineering or Biological Sciences.
• Experience in GLP/GMP environments desirable.
• Strong written and verbal communication skills in a GMP setting.

Responsibilities

• Contribute to design and independently execute experiments to improve recovery, consistency, and robustness.
• Support development and troubleshooting of analytical methods.
• Coordinate and interpret analytical testing to generate reports and present in client meetings.
• Support technology transfer to manufacturing and provide floor support during GMP runs.
• Maintain accurate and organized experimental records.
• Regular and reliable attendance on a full-time basis.
• Maintain professional behavior reflecting company policies and practices.
• Align actions with Minaris Advanced Therapies values.

Skills

Downstream processing

Chromatography

TFF

Viral filtration

Fill/finish

GMP documentation

Analytical methods

Cross-functional collaboration

Technical problem-solving

Report generation

Communication skills

Education

Master or Bachelor's in Biological/Chemical Engineering or Biological Sciences

Job description

Minaris is seeking an experienced Downstream Process Development Associate Scientist to advance viral vector processes—from design to manufacturing transfer—ensuring robust, scalable production. The role emphasizes collaboration, rigorous documentation, and GMP-compliant practices to deliver high‑quality therapies.

Ideal candidates will have hands-on experience in chromatography, filtration, and fill/finish steps, plus strong analytical and problem‑solving skills.