Method Transfer 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.

This role is located on-site in Sanford, NC.

 

• Handle the creation, review, and approval of test method transfer protocols, validation documentation, and equipment qualification records.• Support ELISA, plate-based, and other bioanalytical testing and conduct QC Analytical related investigations.

• Maintain compliance with Current Good Manufacturing Practices across Quality Control and Stability laboratory operations.
• Perform testing on various samples, manage Laboratory Information Management System builds, and review laboratory data.
• Serve on cross-functional teams:• Conducting safety inspections
• Participate in investigations, recommend corrective actions
• Training of junior colleagues

Reliable transportation needed to commute to the site, the site is not accessible by public transportation options.

Minimum Qualifications:

• Bachelors degree in a scientific concentration
• Prior experience with method validation and QC testing
• Experience with ELISA and plate-based testing
• Knowledge of pharmaceutical manufacturing, packaging, and quality assurance operations
• Knowledge of quality systems
• Authorization to work in the United States indefinitely without restriction or sponsorship

Preferred Qualifications:

• Proficiency in data analysis and interpretation
• Knowledge of regulatory requirements and guidelines
• Strong problem-solving abilities
• Effective time management and organizational skills
• Experience with Laboratory Information Management Systems (LIMS)
• Ability to mentor and train junior colleagues

Position is full-time, Monday-Friday 8am-5pm with overtime as needed. Candidates currently living within a commutable distance of Sanford, NC are encouraged to apply.

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 PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.