Quality Assurance Associate
Eurofins EAG Agroscience, LLC

Easton, Maryland

This job has expired.


*#main-wrapper { background: rgb(204,204,204); width: 100.0%; }

Eurofins is the world leader in the food, bio/pharmaceutical product testing. It is also number one in the field of environmental laboratory services and one of the global market leaders in agroscience, genomics, discovery pharmacology, and central laboratory services. With over $2 billion in annual revenues and 25,000 employees across 250 sites in 39 countries, Eurofins is a leading international group of laboratories providing an unparalleled range of testing and support services to the pharmaceutical, biopharmaceutical, food, environmental, and consumer products industries and to governments.

With over 25 years of experience in the crop protection industry, Eurofins Agroscience Services offers outstanding technical knowledge and project management skills. By acquiring a carefully selected range of CRO's, Eurofins Agroscience Services has created a unique portfolio of expertise that provides analytical, regulatory, and field support to plant breeders, agrochemical, biopesticide, biocide, and fine chemical manufacturers.

Eurofins Agroscience Services is searching for a Quality Assurance Associate to work in Easton, MD.

Quality Assurance Associate responsibilities include, but are not limited to, the following :

  • Review protocols, procedures, data, reports, and other documents for internal accuracy, consistency and to ensure compliance with specified regulatory requirements, protocol, project plan, methods and SOPs.
  • Prepares, issues, and tracks reports of observations noted during audits and inspections. Reviews and evaluates addressed deficiencies for clarity, completeness, correctness, and potential impact on compliance status. Works with staff to correct any noted deficiencies/inconsistencies.
  • Works with staff, study directors, principal investigators, and management to detect and resolve any quality issues.
  • Performs phase inspections of ongoing study activities.
  • Ability to assess noncompliance situations and create an audit report.
  • Files protocols, amendments, deviations, inspections, and other quality documents appropriately.
  • Maintains computerized files to support audit activities.
  • Maintains Master Schedule in accordance with specified regulations and standard operating procedures.
  • Reviews equipment calibrations, qualifications, and validations for adherence to company procedures (e.g., SOPs) and federal regulations.
  • Keeps supervisor informed of significant issues or developments identified during quality assurance activities.
  • Assists with implementation and monitoring of quality systems and procedures (e.g., CAPA, Metrics, Change Control, Training, etc.).
  • Perform facility audits to ensure departmental compliance with the regulations.
  • Effectively works independently or in a team and demonstrates a commitment to achieving company goals.
  • Efficiently prioritizes assigned daily workload and uses time productively.
  • Adheres to schedule according to company's or contracting organization's timetable and establishes daily or weekly routines necessary to ensure on-time delivery.
  • Ability to work effectively under minimal supervision for the specific tasks, once signed off to perform independently.Performs other related duties as required and directed.
The ideal candidate would possess :
  • 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
Basic Minimum Qualifications :
  • Bachelor's degree is required. A degree in a relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field or degree with comparable coursework is preferred.
  • Authorization to work in the United States indefinitely without restriction or sponsorship
Position is full-time, Monday-Friday, 8 a.m.-5 p.m., with overtime as needed. Candidates currently living within a commutable distance of Easton, MD are encouraged to apply.

As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options.

To learn more about Eurofins, please explore our website www.eurofinsus.com .

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


This job has expired.

Get Hired Faster

Subscribe to job alerts and upload your resume!

*By registering with our site, you agree to our
Terms and Privacy Policy.

More Science and Research jobs


Eurofins Lancaster Laboratories Professional Scientific Services, LLC
Lancaster, Pennsylvania
Posted about 1 hour ago
TestAmerica Laboratories
Pittsburgh, Pennsylvania
Posted about 1 hour ago
TestAmerica Laboratories
Sacramento, California
Posted about 1 hour ago
View Science and Research jobs ยป