Preclinical Qc Associate
3 weeks ago
**Company Description**
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
**Job Description****:
The Preclinical QC Associate performs a variety of quality control reviews of nonclinical studies, or aspects thereof, within Research, Pharmaceutical, and Preclinical Sciences (RPPS). Working in concert with the client Preclinical Operations team, this position will perform program management activities, with client oversight, in support of the client’s research and development goals.
**POSITION RESPONSIBILITIES**:
- Performs quality control of routine nonclinical documents.
- May be responsible for limited independent initiatives, working with client in setting the objectives of these initiatives.
- Coordinates and maintains QC calendar.
- Provides management of aspects of outsourced, or insourced, projects.
**Qualifications**
**BASIC MINIMUM QUALIFICATIONS**:
- Bachelor’s degree or Master’s Degree in relevant discipline, with science background preferred.
- More than one year of experience.
**PREFERRED QUALIFICATIONS**:
- QC experience for nonclinical protocols, reports, IND and NDA data/reports.
- Assist Study Monitors with ad hoc reviews of reports and special projects.
- Provides support in formatting documents.
- Ability to multitask effectively to manage efforts on multiple projects.
- Demonstrates ability to understand processes and explain the intended use.
- Possesses computer skills to support and maintain department software programs.
**Additional Information**
- 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
- Eligibility for potential yearly Bonus & Merit-Based Pay Increases
**Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
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