Senior Scientist, Small Molecule Method Development and Validation

Eurofins QTA Inc.; Lancaster (Lancaster County); On-site; USD 60,000 - 100,000; Full time

Job summary

An established industry player in bio/pharmaceutical testing is looking for a Senior Scientist to join their dynamic team. This role involves performing method validations and transfers on APIs and finished products, ensuring compliance with GMP standards. The ideal candidate will have experience in analytical method development and validation, with a strong focus on communication and attention to detail. Join a company that values innovation and offers excellent benefits, including comprehensive medical coverage and a 401(k) plan. If you're passionate about contributing to drug development and thrive in a collaborative environment, this opportunity is perfect for you.

Benefits

Comprehensive Medical Coverage

Dental and Vision Options

Life and Disability Insurance

401(k) with Company Match

Paid Vacation and Holidays

Qualifications

• 3-5 years of experience in LC chromatographic validation in a GMP environment.
• Ability to work independently and as part of a team.

Responsibilities

• Perform method validations, transfers, and verifications on APIs and finished products.
• Conduct analytical investigations and troubleshoot instrumentation.

Skills

Analytical Method Development

Method Validation

Communication Skills

Attention to Detail

Troubleshooting Instrumentation

Education

Higher Education Degree in Analytical Chemistry

Bachelor's Degree

Master's Degree

PhD

Tools

HPLC

GC

UV/Vis Spectroscopy

Dissolution Testing

Job description

Senior Scientist, Small Molecule Method Development and Validation

• Full-time

Eurofins is the world leader in the bio/pharmaceutical testing market. With over €5.3 billion in annual revenues and 55,000 employees across 900 sites in 50 countries, Eurofins is a leading international group of laboratories providing an unparalleled range of testing and support services to the pharmaceutical, biopharmaceutical, food, environmental, and consumer products industries and to governments.

The Eurofins BioPharma Product Testing (BPT) Group is the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide. Eurofins BPT provides comprehensive CMC laboratory services for the world’s largest pharmaceutical and biopharmaceutical companies. The service portfolio supports all stages of the drug development process and all functional areas of bio/pharmaceutical manufacturing, including method development, microbiology, process validation and quality control.

Job Summary: Eurofins Small Molecule Method Establishment is seeking a Senior Scientist to perform method validations, method transfers, and method verification activities on APIs and finished products. The team is seeking candidates with expertise in method development and/or method validation.

• Applies GMP in all areas of responsibility, as appropriate.
• Performing a large variety of analytical tasks for the validation of analytical methods used in the testing of drug products and raw materials by means of various procedures including HPLC, GC, UV/Vis, and dissolution.
• Reading, understanding, and interpreting diverse analytical procedures.
• Conducting analytical investigations.
• Troubleshoot instrumentation and communicate with vendors when required.
• Train and mentor junior staff in laboratory procedures.
• Manage and discuss projects with clients.

The Ideal Candidate would possess:

• 3-5 years of experience with LC chromatographic validation in a GMP environment.
• 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.

Minimum Qualifications:

• Higher education degree in analytical chemistry or other related degree concentration.
• BS and 4+ years of experience, MS and 2+ years of experience, or PhD and 1+ years of experience.
• Authorization to work in the U.S. without restriction or sponsorship.

The position is full-time, Monday-Friday, 8am-4pm, with overtime as needed. Candidates 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.

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.