Eurofins Lancaster Laboratories

Drug Product Formulation Development Scientist - AAV Gene Therapy

Eurofins Lancaster Laboratories • $70K — $95K *
Philadelphia, PA 19120In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
5 days ago
Job Overview by Ladders

Qualifications

  • BS in life sciences (Biology, Molecular Biology, Pharmaceutical Sciences) with 2+ years in drug formulation development.
  • Experience operating HPLC for analytical needs.
  • Proficient in following protocols and collaborating with cross-functional teams.
  • Must be a U.S. citizen or permanent resident without restrictions.

Responsibilities

  • Develop drug product formulation and processes for AAV gene therapy.
  • Conduct stability and release studies and scale-up processes.
  • Operate and troubleshoot HPLC and other analytical instrumentation.
  • Collaborate with various teams throughout the project timeline.
  • Perform data analysis, interpretation, and reporting.

Benefits

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

Eurofins PSS is seeking a Drug Product Formulation Development 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
  • Complete stability and release studies, scale-up and more
  • Utilize analytical characterization techniques via operation and troubleshooting of HPLC, HIAC, HAOL, 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 specifically in drug product formulation development.
  • Must have experience with HPLC
  • 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
  • Experience working with AAV gene therapies


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
Pharmaceuticals & Biotech
* Ladders Estimates

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