Analytical Chemist I

Eurofins; Lancaster (Lancaster County); Vor Ort; USD 65.000 - 85.000; Vollzeit

Benefits dieser Stelle

Medical coverage

Dental coverage

Vision coverage

Life insurance

Disability insurance

401(k) with company match

Paid vacation and holidays

Zusammenfassung

Eurofins USA BioPharma Services is seeking a chemistry-focused analyst to perform chromatographic testing and method transfer in a GMP environment. The role requires a Bachelor's degree in chemistry or related field and 1–2 years of pharmaceutical experience, with HPLC and validation experience.

The position is full-time, on-site in Lancaster, PA, with potential travel to client sites. Excellent benefits are offered, including medical and retirement plans.

Qualifikationen

• 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.
• Experience in cGMP environments is preferred.
• HPLC and validation experience is required.

Aufgaben

• Perform various types of testing using chromatographic systems including HPLC and related instruments.
• Execute specialized analyses and method transfer and feasibility testing.
• Document work as required for GMP compliance.
• Perform tests accurately and troubleshoot method and instrumentation problems.
• Use office and instrumentation-specific computer software.
• Produce written reports (e.g., SOP, OMC, client reports).
• 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.

Kenntnisse

Excellent communication

Attention to detail

Independent work

Self-motivation

Ausbildung

Bachelor's degree in chemistry/analytical chemistry/biochemistry

Tools

HPLC

Jobbeschreibung

Company Description

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 Organization 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 Organizations. It also has a rapidly developing presence in highly specialized 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 decentralized 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.

In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

• Applicants MUST have authorization to work in the United States indefinitely without restriction or sponsorship**
• 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
• Produce written reports (e.g., SOP, OMC, client reports)
• 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
• 1-2 years of related pharmaceutical experience in a cGMP environment
• HPLC and validation experience
• 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
• Strong computer, scientific, and organizational skills
• Excellent communication (oral and written) and attention to detail
• Ability to work independent 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

Working schedule will be Full-Time, First Shift, Mon-Fri, 8am-4pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. 25% travel may be required. This position is NOT remote.

What We Offer

• 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.