Eurofins - Lancaster, PA

posted 5 months ago

Full-time - Entry Level
Onsite - Lancaster, PA
10,001+ employees
Professional, Scientific, and Technical Services

About the position

Eurofins Biopharmaceutical is seeking an Associate Scientist to join our Biochemistry team, focusing on Data Review. This entry-level position offers a unique opportunity for hands-on development and growth within a laboratory environment, adhering to prescribed processes such as protocols, standard operating procedures, and methods. The role emphasizes the importance of data review, allowing the Associate Scientist to take on responsibilities that include reviewing scientific reports under CGMP guidelines, assisting with internal audits, and ensuring that all regulatory requirements are met. The position also involves data tracking and reporting, providing a balanced schedule that supports both laboratory and data tracking operations. We are looking for a candidate who is eager to learn and grow in both aspects of laboratory work. In this role, the Associate Scientist will ensure that clients receive high-quality data by meticulously reviewing laboratory data for accuracy, clarity, and compliance with GMP and/or GLP regulations. The responsibilities include reviewing both simple and complex routine and non-routine data across multiple areas, following departmental, corporate, and client SOPs. The Associate Scientist will be expected to read and understand analytical procedures, ensuring that all work is performed according to GLP/GMP requirements. Strong organizational skills, effective communication, and attention to detail are essential for success in this position. The ability to work independently and collaboratively within a team, along with self-motivation and adaptability, will be key attributes for the ideal candidate.

Responsibilities

  • Review laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations.
  • Review simple and complex routine and non-routine data according to departmental, corporate, and client SOPs.
  • Read and understand analytical procedures to ensure compliance with GLP/GMP requirements.
  • Assist with internal audits and ensure regulatory requirements are met.
  • Track and report data accurately and efficiently.
  • Maintain good organizational skills and follow directions effectively.

Requirements

  • Bachelor's Degree in a Life Science (Chemistry, Biochemistry, or Biology preferred).
  • Experience in a laboratory setting or GMP pharmaceutical setting is preferred.
  • Strong computer, scientific, and organizational skills.
  • Excellent oral and written communication skills with attention to detail.
  • Ability to work independently and as part of a team.

Nice-to-haves

  • Experience with data tracking and reporting in a laboratory setting.
  • Familiarity with CGMP guidelines and regulatory compliance.

Benefits

  • Comprehensive medical coverage
  • Life and disability insurance
  • 401(k) with company match
  • Paid holidays and vacation
  • Personal days
  • Dental and vision options
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