Scientist - Small Molecule Analytical Chemistry

ZipRecruiter; Lancaster; On-site; USD 50,000 - 80,000; Full time

Job summary

An established industry player is looking for a dedicated Scientist to join their dynamic team in Lancaster. This full-time role involves performing a variety of analytical tests, troubleshooting methods, and ensuring data quality in compliance with industry regulations. The ideal candidate will have a strong background in chemistry and experience in a cGMP compliant lab. With a focus on method validation and data review, this position offers a chance to contribute to important projects while enjoying excellent benefits, including comprehensive medical coverage and a 401(k) plan. If you are passionate about science and eager to make an impact, this opportunity is perfect for you.

Benefits

Comprehensive medical coverage

Dental insurance

Vision insurance

401(k) with company match

Paid vacation

Paid holidays

Qualifications

• 3+ years in a cGMP compliant lab with a Bachelor's in chemistry or related field.
• 1+ year in a cGMP compliant lab with a Master's in chemistry or related field.

Responsibilities

• Perform testing using various analytical methods and equipment.
• Review laboratory data for accuracy and compliance with regulations.
• Train technical staff and carry out method transfers.

Skills

Chromatographic systems

HPLC

Data analysis

Troubleshooting

Method validation

Education

Bachelor's degree in chemistry

Master's degree in chemistry

Tools

Empower

Karl Fischer

UV/Spec

IC

IR

ICP

AA

TLC

Job description

Job Summary: Eurofins' BPT Small Molecule Method Development and Validation team is seeking a Scientist to join their team full time in Lancaster, PA. This individual will work in a dual analyst and data reviewer role. The Scientist will be able to:

• 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.
• Execute specialized analyses and method transfer and feasibility testing.
• 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.
• Determine if data is compliant and defendable based on industry regulations and methodology.
• Verify scientific data is of sound quality following all method, industry, and client requirements where applicable.
• Ensure that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations.
• Review simple and complex routine and non-routine data (for three or more areas) according to departmental, corporate, and client SOPs; read and understand analytical procedures; ensure all work is performed according to GLP/GMP requirements and apply GLP/GMP in all areas of responsibility as appropriate.
• Diagnose problems, solve simple problems, and suggest solutions to complex problems in professional area.
• Review methods to ensure procedures are followed.
• Authorize written reports (e.g., SOP, OMC, client reports).

Minimum Qualifications:

• Bachelor's degree in chemistry, pharmaceutical science, or other related degree concentration and a minimum of 3 years of experience in a cGMP compliant industry lab.
• Master's degree in chemistry, pharmaceutical science, or other related degree concentration and a minimum of 1 year of experience in a cGMP compliant industry lab.
• Experience with HPLC and Empower.
• Authorization to work in the U.S. without restriction or sponsorship.

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 insurance.
• 401(k) with company match.
• Paid vacation and holidays.

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