Stability / Reference Standard Specialist

Job Description

Job Description

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 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.

Job Description

• Build and maintain stability studies in Lab Information Management System (LIMS)
• Manage label request program
• Manage inventory system
• Receive, store, forecast, submit, and deliver stability and analytical samples
• Understands and follows all relevant policies relating to this job including business, compliance, quality, environmental and safety expectations
• Supports the development, registration and launch of new pharmaceutical products
• Support the client's work requests as needed 
• Support domestic and international shipping of material
• Additional duties as needed

Qualifications

The Ideal Candidate would possess:

• Fundamental knowledge of cGMP compliance requirements
• Excellent communication (oral and written) and attention to detail
• Strong computer and organizational skills and experience with Microsoft Office
• Ability to work independently and as part of a team, have self-motivation, adaptability, and a positive attitude
• Ability to learn new techniques, prioritize multiple tasks, keep accurate records, follow instructions, and comply with company policies
• Must be able/authorized to handle Controlled Drugs or Controlled Substances under the guidance of DEA requirements 

Minimum Qualifications:

• Bachelor's degree
• 2 years professional experience

Additional Information

• Position is full-time, working Monday-Friday 8:00 a.m.-5:00p.m overtime as needed
• Candidates currently living within a commutable distance of Indianapolis, IN  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
• #LI-EB1
• Authorization to work in the United States indefinitely without restriction or sponsorship

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