Scientist II: Method Development and Validation

Eurofins Viracor, Inc.; Lancaster (Lancaster County); On-site; USD 60,000 - 90,000; Full time

Job summary

An established industry player is seeking a dedicated Scientist II for Method Development and Validation. This full-time role offers the chance to engage in cutting-edge analytical testing across various platforms, ensuring the safety and authenticity of critical products. You will be responsible for executing specialized analyses, troubleshooting instrumentation, and documenting work to meet compliance standards. With a focus on collaboration and innovation, this position promises a dynamic work environment where your contributions will directly impact the quality of essential services. If you're ready to advance your career in a supportive and growth-oriented company, this opportunity is for you.

Benefits

Comprehensive medical coverage

Dental options

Vision options

Training and development opportunities

Qualifications

• 3 years of experience in a cGMP environment with a chemistry-related degree.
• Strong computer skills and ability to work independently or in a team.

Responsibilities

• Perform various types of testing using advanced analytical methods.
• Document work for GMP compliance and troubleshoot method issues.
• Train technical staff and develop validation plans.

Skills

Chromatographic systems

HPLC

Analytical chemistry

Protein chromatography

GMP compliance

Documentation

Troubleshooting

Education

Bachelor's degree in chemistry

Degree in biochemistry

Tools

Karl Fischer

UV/Spec

IC

IR

ICP

AA

TLC

Job description

Scientist II: Method Development and Validation

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.

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Responsibilities:

• 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.
• Document work as required for GMP compliance.
• Perform tests accurately.
• 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.

Minimum Qualifications:

• Bachelor's degree in chemistry, analytical chemistry, biochemistry, or other related degree concentration.
• 3 years of related pharmaceutical experience in a cGMP environment.
• 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.
• 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.

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.

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