Associate Scientist III - Parenteral Formulation & DP

Biogen

Cambridge (MA)

On-site

USD 77,000 - 100,000

Full time

2 days ago
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Benefits offered by this job

Medical Insurance
Dental Insurance
Vision Insurance
Life Insurance
Fitness Reimbursement
Disability Insurance
Vacation time
Paid holidays
Sick time

Job summary

Biogen is seeking an Associate Scientist III in Parenteral Formulation and Drug Product Development. You will contribute to developing parenteral formulations and DP manufacturing processes to support Biogen’s pipeline, working in a matrix environment with the technical development team.

You will plan and execute experiments, prepare formulations, analyze data, draft development protocols and technical reports for CMC submissions, and maintain GDP-compliant records while collaborating with

Qualifications

  • Bachelor’s Degree in a related field with 0-2 years of experience, or a Master’s with 0+ years of experience.
  • Experience in a pharmaceutical/biotechnology laboratory environment.
  • Experience in formulation development for sterile parenteral drug products.
  • Experience performing laboratory experiments, analyzing data, and documenting results using GDP.
  • Working knowledge of laboratory instrumentation and analytical techniques used for characterization of drug products.
  • Familiarity with sterile laboratory practices and aseptic techniques is preferred.
  • Strong organizational skills with the ability to manage multiple assignments.

Responsibilities

  • Plan and execute laboratory experiments supporting formulation development, product characterization, process development and evaluation of new technologies.
  • Independently manage assigned development activities while working under guidance of senior scientists on more complex initiatives.
  • Prepare formulations, perform laboratory studies, collect and analyze data, and communicate findings to project teams.
  • Author development protocols, perform data analysis, prepare technical reports, and documentation for support of CMC submissions.
  • Maintain accurate laboratory records in accordance with GDP and support activities in compliance with GLP as applicable.
  • Collaborate with cross-functional partners including Analytical Development, Drug Substance Development, Manufacturing Sciences, Quality, Device Engineering, and Regulatory to support project objectives.
  • Contribute to continuous improvement initiatives, laboratory organization, and implementation of new technologies.

Skills

Pharma lab experience
Formulation development
GDP documentation
Analytical techniques
Aseptic techniques
Cross-functional teamwork
Communication skills

Education

Bachelor's degree in Chemistry, Chemical Engineering, Biochemistry, Pharmaceutical Sciences
Master's degree

Job description

Biogen is seeking an Associate Scientist III in Parenteral Formulation and Drug Product Development. You will contribute to developing parenteral formulations and DP manufacturing processes to support Biogen’s pipeline, working in a matrix environment with the technical development team.

You will plan and execute experiments, prepare formulations, analyze data, draft development protocols and technical reports for CMC submissions, and maintain GDP-compliant records while collaborating with

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