Parenteral Formulation Scientist I

Socket.dev; Cambridge (MA); On-site; USD 103,000 - 134,000; Full time

Benefits offered by this job

Medical, Dental, Vision insurance

401(k) with company match

Stock purchase plan

Tuition reimbursement

Paid time off

Job summary

Biogen is seeking a Scientist I/II in Parenteral Formulation and Drug Product Development to drive formulation and process development for parenteral programs. The role requires collaboration within a matrix team and strong analytical, communication, and problem-solving skills.

Responsibilities include design of studies, technology transfer, support during GMP campaigns, and preparation of CMC documentation for regulatory submissions. PhD/MS/BS with relevant pharmaceutical experience is required.

Qualifications

• Ph.D./MS/BS in a pharmaceutical or biotech field with relevant experience.
• Experience in sterile parenteral drug product development preferred.
• Strong analytical and communication skills; ability to work in a matrix environment.
• Exposure to IND/IMPD/NDA regulatory submissions is a plus.

Responsibilities

• Design and execute formulation and process development studies for parenteral programs.
• Develop sterile parenteral products, including formulation optimization and transfer.
• Provide technical support during GMP campaigns and PPQ activities.
• Collaborate with cross-functional teams to support program objectives.
• Prepare CMC documentation and technical reports for regulatory submissions.

Skills

Parenteral development

Sterile formulations

Process development

Analytical methods

Regulatory submissions

Independent work

Education

PhD in Chemical Eng

MS in related field

BS in related field

Tools

Statistical software

Job description

Biogen is seeking a Scientist I/II in Parenteral Formulation and Drug Product Development to drive formulation and process development for parenteral programs. The role requires collaboration within a matrix team and strong analytical, communication, and problem-solving skills.

Responsibilities include design of studies, technology transfer, support during GMP campaigns, and preparation of CMC documentation for regulatory submissions. PhD/MS/BS with relevant pharmaceutical experience is required.