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Principal Scientist, Biologics Analytical Research & Development

USA - New Jersey - Rahway

Job Description

The Biologics Analytical Research & Development department of our company's Research Laboratories Division is seeking applicants for a Principal Scientist position available at our company's research facility. The Principal Scientist is a senior scientific role tasked with working closely with the group Director to define group strategy and to lead a team of scientists in solving complex analytical problems at the interface of biology, chemistry, and lab informatics disciplines to enable development of biologics active pharmaceutical ingredients (APIs). 

We are looking for a team player with strong leadership skills and the passion for mentoring and working along others in a laboratory setting. Applicants must have effective organizational and multi-tasking skills, have demonstrated excellent scientific leadership, and have superior communications skills, both written and oral. A track record of delivering impactful solutions to complex problems, and evidence of strong cross-functional collaboration is expected. Experience in leading small groups of technical personnel, leading projects, and defining group or departmental strategy will aid in distinguishing candidates. An established reputation for scientific excellence supported by publications and external presentations is expected. 

Qualifications
 

Education Minimum Requirements:

  • Ph.D. in analytical chemistry/biochemistry or related field with a minimum of 8 years of experience in the pharmaceutical industry, M.S. in analytical chemistry/biochemistry or related field with a minimum of 12 years of experience in the pharmaceutical industry, or B.S. in analytical chemistry/biochemistry or related field with a minimum of 16 years of experience in the pharmaceutical industry. 

Required Experience and Skills:

  • Extensive experience in analysis of biologics (separation methods such as Size Exclusion Chromatography (SEC), Ion Exchange Chromatography (IEX) and Capillary Electrophoresis (CE) techniques, and immunoassays such as residual and PCR-based assays).

  • Strong background in analytical control strategy development and execution.

  • Demonstrated ability to develop talent through good mentoring skills.

  • Demonstrated ability for taking initiative, creativity, and innovation in problem solving.

  • Background in Analytical Methodologies and sound scientific understanding of Critical Quality Attributes/QbD/DOE principles as well as data analysis and statistics for setting specifications.

  • Ability to design, execute and/or direct the development and qualification of release, characterization, and stability assays for testing of clinical trial material and in support of product and process development.

  • A strong team player with excellent oral and written communication skills; ability to work both independently for development of assays and cross-functionally for successful transfer of assays. Plan assay optimization and documentation to meet program deadlines.

  • Authoring and reviewing internal technical …

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Job Profile

Regions

North America

Countries

United States

Restrictions

Hybrid Hybrid work Hybrid work model

Benefits/Perks

Bonus eligibility Diverse workplace Equal opportunity employer Flexible work arrangements Hybrid work Hybrid work model Inclusion Inclusive environment Insurance Meetings Mentoring Paid holidays Retirement benefits Sick Days Vacation

Tasks
  • Coaching
  • Collaboration
  • Communication
  • Communications
  • Cross-Functional Collaboration
  • Data Analysis
  • Innovation
  • Leadership
  • Mentoring
  • Mentor team members
  • Problem solving
  • Strategy development
  • Validation
Skills

Analysis Analytical Analytical Chemistry Analytical Research APIs Biochemistry Biologic Biologics Biology Business Operations CE Characterization Chemistry Chromatography Clinical Coaching Collaboration Commercial Communication Communications Cross-functional Collaboration Data Data analysis Design Documentation DOE Execution GLP ICH Immunoassays Inclusion Innovation Laboratory Leadership Management Manufacturing Matrix management Mentoring Method development Methodologies Multi-tasking Optimization Organizational PCR Pharmaceutical Pharmaceutical Industry Process Development QbD Qualification Quality Regulatory Regulatory filings Research Scientific Excellence Scientific Leadership Scientific publications SEC Statistics Strategy Strategy Development Technical Validation Written communication

Experience

12 years 8 years

Education

Biochemistry Biology B.S. Business Chemistry Communications Management MS Ph.D. Related Field Statistics

Timezones

America/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9