Eurofins Lancaster Laboratories

Gene Therapy Drug Product Development Scientist

Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BS in life sciences (Biology, Molecular Biology, Pharmaceutical Sciences) and 2+ years in drug formulation development.
  • Experience with biophysical characterization (XRD, DLS, DSC) and analytical techniques (HPLC, ELISA).
  • Ability to follow protocols and coordinate across teams.
  • Eligibility to work in the US without restrictions or sponsorship.
  • Preferred: Experience with HIAC and HALO instruments.

Responsibilities

  • Conduct drug product formulation and process development for AAV gene therapy.
  • Apply biophysical characterization techniques and instrumentation.
  • Perform analytical characterization using HPLC and other tools.
  • Collaborate with cross-functional teams throughout the project.
  • Analyze data, prepare reports, and present findings.

Benefits

  • Comprehensive medical, dental, and vision coverage.
  • Life and disability insurance.
  • 401(k) plan with company match.
  • Paid vacation and holidays.
Full Job Description
Job Description

Eurofins PSS is seeking a Drug Product Formulation Scientist to permanently work at a client site to support drug product formulation, biophysical characterization, and process development for gene therapy research. The successful employee will thrive in a high throughput environment, working with small-scale drug product manufacturing process development and scale-up activities.

Position Responsibilities:
  • Drug product formulation, delivery, and process development activities in support of AAV gene therapy research in a small-scale manufacturing facility
  • Utilize biophysical characterization techniques, administration, and instrumentation
  • Analytical characterization via operation and troubleshooting of HPLC, HIAC, HALO, and other instrumentation on raw materials and drug products
  • Collaborate with multiple teams throughout study timeline
  • Data analysis, interpretation, reporting, and presentation


Qualifications

Basic Minimum Qualifications:
  • BS in a life sciences discipline (Biology, Molecular Biology, Pharmaceutical Sciences, etc.) with at least 2 yearsof pharmaceutical industry experience working in drug product formulation development.
  • Must have experience with a mixture of biophysical characterization techniques (XRD, DLS, DSC, etc.) and analytical techniques (HPLC, ELISA, etc.)
  • Ability to understand and follow report protocols and coordinate with multiple cross-functional teams
  • Must be eligible to work in the United States indefinitely without restriction or sponsorship

Preferred Qualifications:
  • Experience with HIAC and HAOL is highly preferred


Additional Information

The position is full-time, first shift, Monday-Friday with overtime as needed. Candidates living within a commutable distance of Philadelphia, PA are encouraged to apply.

Excellent full-time benefits include:
  • Comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

About Eurofins Lancaster Laboratories

Eurofins Lancaster Laboratories is a leading contract research organization (CRO) providing analytical, research and testing services to clients in the pharmaceutical, biopharmaceutical, biotechnology, crop protection, chemical, food, environmental and consumer products industries. The company was founded in 1961 and has grown to become one of the largest CROs in the world, with over 50 locations in 20 countries. Eurofins Lancaster Laboratories is part of the Eurofins Scientific Group, a global leader in bioanalytical testing and laboratory services. The company's services include method development and validation, stability testing, quality control testing, and regulatory compliance support.
Learn more about Eurofins Lancaster Laboratories
Size
12,000 employees
Industry

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