Scientist II: Method Development and Validation

Eurofins USA; Lancaster (Lancaster County); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading company in life sciences is seeking a Scientist II for method development and validation. You will engage in chromatography testing and method transfers while ensuring compliance with GMP standards. The ideal candidate will have a Bachelor's degree in a relevant field and possess solid experience in a pharmaceutical environment. Comprehensive benefits are included for this full-time position.

Benefits

Comprehensive medical coverage

Dental options

Vision options

Qualifications

• 3 years of related pharmaceutical experience in a cGMP environment.
• Authorization to work in the USA without restriction.
• Experience working with protein chromatography is ideal.

Responsibilities

• Perform various type of testing using chromatographic systems and wet chemistry analyses.
• Document work as required for GMP compliance.
• Train technical staff and perform method transfer and feasibility studies.

Skills

Strong computer skills

Scientific skills

Organizational skills

Excellent communication

Attention to detail

Education

Bachelor's degree in chemistry, analytical chemistry, biochemistry

Tools

Chromatographic systems

HPLC

UV/Spec

Karl Fischer

Job description

Scientist II: Method Development and Validation

• 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.

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.

• 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
• 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
• Strong computer, scientific, and organizational skills
• 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 USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.