Coordination Scientist
Eurofins

Worcester, Pennsylvania

This job has expired.



Company 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

Employee Responsibilities:

  • Act as a single point of contact for resolving laboratory and facility related issues in a fast-paced environment with tight timelines.
  • Communicate effectively with leadership and client staff members
  • Entering and reviewing data following GMP guidelines
  • Filing documents consistent with cGMP record keeping, including electronic document systems
  • Liaises closely with cross-functional teams to support compliance activities.
  • Carries out all assignments to the standards of efficiency, innovation, accuracy and safety in accordance with applicable requirements.

Qualifications

The Ideal Candidate would possess:
  • Strong computer, scientific, and organizational skills
  • Familiarity with LIMs systems
  • 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
  • Ability to develop and maintain effective, trusting work and customer relationships
  • Self-starter, able to prioritize work and work efficiently with minimal supervision

Minimum Qualifications:
  • No degree with at least two years of directly related industry/Pharmaceutical GMP experience
  • Minimum of 0-2 years' experience in the Pharmaceutical or equivalent industry with an Associate's degree
  • Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

Position is full-time, Monday - Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of West Point, PAare 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
All your information will be kept confidential according to EEO guidelines.

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


This job has expired.

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