R&D Associate I

R&D Associate I

Contract Type:

Contractor

Location:

Durham

Industry:

Pharmaceuticals

Contact Name:

Flora Pollack

Contact Phone:

Date Published:

06-Jun-2025

Research and Development Associate I

Research Triangle Park, NC

Schedule: Standard Office Hours

Duration: 6-Month Contract

Pay:$29-34/ph



Job Responsibilities:

In this role, you will support a variety of routine and project-based tasks within the Quality Control (QC) Microbiology department. Key responsibilities include:

  • Supporting microbiological testing, environmental and water sampling activities.
  • Assisting with data review and documentation accuracy to ensure compliance with GMP standards.
  • Initiating and supporting investigations, deviations, and non-conformance documentation.
  • Collaborating with cross-functional teams to maintain laboratory systems and quality standards.
  • Providing assistance in laboratory maintenance and continuous improvement efforts.



    Essential Duties and Job Functions:
  • Perform environmental monitoring and water sampling in accordance with GMP protocols.
  • Support QC testing activities, including sample handling, preparation, and documentation.
  • Conduct timely reviews and corrections of QC documentation; escalate issues as appropriate.
  • Participate in investigations and deviations, ensuring compliance with internal procedures.
  • Maintain cleanliness and readiness of laboratory equipment and spaces.
  • Follow established procedures and documentation practices to ensure data integrity.
  • Assist in maintaining an effective laboratory information system.
  • Collaborate with team members to troubleshoot basic technical issues.
  • Ensure timely completion of assigned tasks under general supervision.
  • Contribute to the continuous improvement of laboratory practices and quality systems.



    Knowledge & Skills:
  • Understanding of basic microbiological and laboratory techniques.
  • Strong attention to detail and commitment to data accuracy.
  • Good written and verbal communication skills.
  • Ability to follow SOPs and regulatory guidelines (GMP/cGMP).
  • Proficiency with documentation systems and lab equipment.
  • Basic knowledge of quality systems and laboratory safety practices.
  • Capability to work in a team-oriented environment with moderate supervision.
  • Ability to manage assigned tasks and meet deadlines in a fast-paced setting.



    Education & Experience:
  • Associate’s or Bachelor’s degree in a scientific or technical discipline.
  • 0–2 years of relevant laboratory experience.
  • Experience working in GMP or cGMP environments preferred.
  • Familiarity with microbiological sampling and QC testing is a plus.

...

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