Quality Control Research Associate
- Permanent
- Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP)
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is currently recruiting for a Quality Control Research Associate with a pharmaceutical company located in Gaithersburg, MD.
Job Responsibilities:
- Conducts routine analyses based on written procedures
- Reviews data and results of testing to ensure compliance to appropriate specifications and protocols.
- Performs maintenance and calibration of analytical instrumentation.
- Begins to learn and apply knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Practices (GLPs) on a daily basis.
- Writes simple protocols and reports.
- Must have working knowledge of Microsoft Office software.
- Participates in group meetings.
- May present data or prepare information for others to present.
Skills and Requirements:
- Bachelor's or master's degree with 1-2 years of relevant experience
- Knowledge of cGMP manufacturing or GLP.
- Experience calibrating/ maintaining laboratory equipment
- Must have understanding of laboratory instrumentation.
- Self-motivated, collaborative with excellent time management and organizational skills.
- Must have basic computer skills. General use of word processing, spreadsheets, databases, etc. for the purposes of work execution, training, performance management, and self-service.
- Good interpersonal skills and able to work effectively and efficiently in a team environment.
If you are having difficulty in applying or if you have any questions, please contact Nikki Ranieri at 215-531-5288.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
#LI-NR1
Related jobs
Highly Competitive
Visp, Switzerland
Join a leading Swiss team as a QC Associate driving excellence in biopharmaceutical quality control.
Highly Competitive
Rockville, USA
Step into a role where precision meets purpose-become a Materials Technician supporting essential pharma and respiratory operations
Highly Competitive
Liverpool, England
Are you passionate about quality and precision? Join our client in this Quality Assurance Representative and help ensure top-tier standards every day.
Highly Competitive
Bristol, USA
Drive cGMP excellence by powering large‑scale downstream manufacturing that brings life‑changing therapies to reality.