Scientist II Method Development and Validation

Eurofins USA BioPharma Services; Lancaster (Lancaster County); On-site; USD 50,000 - 90,000; Full time

Job summary

An established industry player is seeking a dedicated professional to join their team as a full-time analyst. In this role, you will perform a range of testing and analyses using advanced chromatographic systems and other scientific methods. Your expertise will contribute to ensuring compliance with GMP standards while producing high-quality reports. This position offers a collaborative environment where you can thrive, develop your skills, and make a significant impact in the pharmaceutical industry. With excellent benefits and a supportive team, this opportunity is perfect for those looking to advance their careers in a dynamic field.

Benefits

Comprehensive medical coverage

Dental and vision options

Life and disability insurance

401(k) with company match

Paid vacation

Paid holidays

Qualifications

• 3 years of pharmaceutical experience in a cGMP environment.
• Strong computer, scientific, and organizational skills.

Responsibilities

• Perform various testing using chromatographic systems and HPLC.
• Document work for GMP compliance and produce written reports.

Skills

Chromatographic systems

HPLC

Analytical chemistry

GMP compliance

Protein chromatography

Scientific writing

Troubleshooting

Technical training

Education

Bachelor's degree in chemistry or related field

Tools

UV/Spec

Karl Fischer

Office software

Job description

Job Description

1. Perform various types 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.
2. Execute specialized analyses and method transfer and feasibility testing.
3. Document work as required for GMP compliance.
4. Perform tests accurately.
5. Troubleshoot method and instrumentation problems.
6. Use office and instrumentation specific computer software.
7. Produce written reports (e.g., SOP, OMC, client reports).
8. Develop and execute validation plans.
9. Carry out method transfers and feasibility studies.
10. Train technical staff.
11. Some travel to client sites for technical meetings could be required.

Qualifications:

Minimum Qualifications:

1. Bachelor's degree in chemistry, analytical chemistry, biochemistry, or other related degree concentration.
2. 3 years of related pharmaceutical experience in a cGMP environment.
3. Authorization to work in the United States indefinitely without restriction or sponsorship.

The Ideal Candidate Would Possess:

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

Additional Information:

Position is full-time, 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, life and disability insurance, 401(k) with company match, paid vacation and holidays.

To learn more about Eurofins, please explore our website www.eurofinsus.com.

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