Parenteral Drug Product Development Scientist I

Biogen; Cambridge (MA); On-site; USD 103,000 - 134,000; Full time

Benefits offered by this job

Medical Insurance

401(k) match

Tuition reimbursement

Stock purchase plan

Paid vacation

Job summary

Biogen is seeking a Scientist I/II to advance parenteral drug product development within a collaborative, matrixed team. You will design and execute formulation and process development studies for preclinical and clinical programs, support sterile product development, and contribute to tech transfer and manufacturing readiness.

The role requires strong analytical skills, ability to work cross-functionally with regulatory, device engineering, and quality teams, and to manage timelines effectively

Qualifications

• Ph.D. holders with 0–4 years experience in pharma/biotech settings or MS with 2–4+ years, or BS with 4–6+ years.
• Experience with sterile drug product development and parenteral formulations preferred.
• Hands-on experience with oligonucleotide, peptide, antibody, or conjugated therapeutics is a plus.

Responsibilities

• Design and execute formulation and process development studies for preclinical and clinical drug product programs.
• Contribute to sterile parenteral product development including formulation optimization, process development, and technology transfer.
• Provide technical support during GMP manufacturing campaigns, engineering runs, process validation, and PPQ activities.
• Execute studies supporting formulation/process optimization and product/process characterization.

Skills

Parenteral formulation

Sterile formulation

Analytical techniques

Tech transfer

Regulatory submissions

Cross-functional collaboration

Independent work

Education

Ph.D. in Chemical Engineering, Pharmaceutical Sciences, Pharmaceutics, Analytical Chemistry or related fields

MS with 2–4+ years of relevant experience

BS with 4–6+ years of relevant experience

Job description

Biogen is seeking a Scientist I/II to advance parenteral drug product development within a collaborative, matrixed team. You will design and execute formulation and process development studies for preclinical and clinical programs, support sterile product development, and contribute to tech transfer and manufacturing readiness.

The role requires strong analytical skills, ability to work cross-functionally with regulatory, device engineering, and quality teams, and to manage timelines effectively