Enable job alerts via email!

Scientist II: Method Development and Validation

Eurofins QTA Inc.

Lancaster (Lancaster County)

On-site

USD 80,000 - 100,000

Full time

30+ days ago

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

Job summary

An established industry player in life sciences is seeking a dedicated Scientist II for method development and validation. This exciting role involves performing a variety of tests using advanced chromatographic systems and ensuring compliance with GMP standards. The ideal candidate will possess a strong background in analytical chemistry, excellent communication skills, and the ability to work both independently and collaboratively. Join a dynamic team committed to making life safer and healthier through innovative testing services. This full-time position offers a supportive work environment with comprehensive benefits, making it an excellent opportunity for career growth.

Benefits

Comprehensive medical coverage
Dental options
Vision options

Qualifications

  • 3 years of pharmaceutical experience in a cGMP environment required.
  • Strong computer skills and experience with protein chromatography preferred.

Responsibilities

  • Perform various testing using chromatographic systems and wet chemistry analyses.
  • Document work for GMP compliance and troubleshoot method problems.

Skills

Chromatography
Analytical Chemistry
Attention to Detail
Communication Skills
Organizational Skills
Troubleshooting
Teamwork
Self-Motivation

Education

Bachelor's degree in Chemistry
Bachelor's degree in Analytical Chemistry
Bachelor's degree in Biochemistry

Tools

HPLC
UV/Spec
Karl Fischer
IC
IR
ICP
AA
TLC
Dissolution Apparatus
Auto-titrators

Job description

Scientist II: Method Development and Validation
  • Full-time

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries.

  • Perform various type of testing using chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus
  • Execute specialized analyses and method transfer and feasibility testing
  • Document work as required for GMP compliance
  • Perform tests accurately
  • Troubleshoot method and instrumentation problems
  • Use office and instrumentation specific computer software
  • Develop and execute validation plans
  • Carry out method transfers and feasibility studies
  • Train technical staff
  • Some travel to client sites for technical meetings could be required

Minimum Qualifications:

  • Bachelor's degree in chemistry, analytical chemistry, biochemistry, or other related degree concentration
  • 3 years of related pharmaceutical experience in a cGMP environment
  • Authorization to work in the United States indefinitely without restriction or sponsorship

The Ideal Candidate Would Possess:

  • Strong computer, scientific, and organizational skills
  • Experience working with protein chromatography
  • Excellent communication (oral and written) and attention to detail
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies

Position is full-time position, Monday - Friday 8:00am - 4:00pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply.

  • Excellent full time benefits including comprehensive medical coverage, dental, and vision options

Eurofins is an M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.

Similar jobs

Scientist II: Method Development and Validation

Eurofins BioPharma Product Testing North America

Lancaster

On-site

USD 70,000 - 90,000

7 days ago
Be an early applicant

HPLC Scientist - Med Device Production Testing

Eurofins BioPharma Product Testing North America

Lancaster

On-site

USD 70,000 - 90,000

4 days ago
Be an early applicant

Scientist II: Method Development and Validation

Eurofins Viracor, Inc.

Lancaster

On-site

USD 60,000 - 90,000

30+ days ago

Scientist II Method Development and Validation

Eurofins USA BioPharma Services

Lancaster

On-site

USD 50,000 - 90,000

30+ days ago