What are the responsibilities and job description for the Product Protection Specialist position at Eurofins?
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
BS in the field of Chemistry, Biology, or a related field
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
- Perform routine operational support and Investigative tasks involved in the investigation of suspect samples (e.g., sample log-in, photographs, packaging variable data verification, packaging evaluations, physical appearance, etc.).
- Perform non-routine sample analyses of suspect samples utilizing screening technologies.
- Produce quality documentation for internal and external use and ensure data documentation meets ALCOA plus expectations.
- Learn and utilize basic development, manufacturing, and regulatory processes, and develop an awareness of analytical and pharmaceutical industry trends related to product authentication.
- Work collaboratively with people in AQCO and with cross-functional business partners.
- Work safely and in compliance with applicable quality, environmental, and safety expectations. Ensure compliance with applicable Lilly global standards and regulatory guidelines.
- As needed within the AQCO organization, this position will help with shipping and purchasing needs
BS in the field of Chemistry, Biology, or a related field
- Fundamental knowledge of cGMP/GLP compliance requirements.
- 1-3 years of pharmaceutical experience.
- Capable of evaluating safety/quality compliance and supporting efforts to perform needed activities.
- Effective oral and written communication skills, self-management, task planning, and organization.
- Must be able to work productively in an interdisciplinary team environment.
- Ability to execute well-defined protocols/procedures with minimal oversight.
- Experience with basic analytical techniques (e.g., balances, pH meter, etc.).
- Theoretical experience with more sophisticated analytical techniques (e.g., microscopy, IR, NIR, Raman, HPLC, GC-MS, LC-MS, SEM-EDS), as required.
- Experience using IT tools such as: Veeva (QDocs), SmartLab, BLUE, NuGenesis, Empower, Tableau, CIMS, Trackwise, SAP, Fiori, etc.
- Experience with handling confidential/privileged information.
- The position is full-time, M- F 8 am to 5 pm
- May be requested to work on weekends, overtime, and holidays based on business needs.
- 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