Lab Analyst II - Small Molecule Analytical Chemistry

Eurofins QTA Inc.; Lancaster (Lancaster County); On-site; USD 55,000 - 85,000; Full time

Job summary

An established industry player is seeking a skilled Analyst II to join their Small Molecule Method Development team. This exciting role involves performing a variety of analytical tests, troubleshooting instrumentation issues, and ensuring compliance with industry regulations. The ideal candidate will have a strong background in chemistry, with experience in a cGMP compliant lab. You will be part of a dynamic team dedicated to delivering high-quality data and supporting clients in various sectors. This position offers a fantastic opportunity to grow your career in a leading life sciences company committed to making a positive impact on health and safety.

Benefits

Comprehensive medical coverage

Dental and vision options

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Qualifications

• 3+ years in a cGMP compliant lab with a Bachelor's in chemistry.
• Experience with HPLC and data review in compliance with regulations.

Responsibilities

• Perform testing using various analytical methods and instruments.
• Review and ensure quality of laboratory data according to GMP/GLP.

Skills

Chromatographic systems

HPLC

Analytical procedures

Data review

Problem-solving

Education

Bachelor's degree in chemistry or related field

Master's degree in chemistry or related field

Tools

Empower

Karl Fischer

UV/Spec

TLC

Job description

Analyst II - Small Molecule Analytical Chemistry

• 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. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

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. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

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

• 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
• 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

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 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:

• Life and disability 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.