QM Associate Scientist

About the role

The QM Associate Scientist will perform various laboratory testing, data analysis, and documentation activities to ensure product quality and compliance with regulatory standards. This role requires a strong understanding of GMP/GDP/GLP regulations and quality management systems.

Responsibilities

• Execute routine and non-routine quality control (QC) testing on raw materials, in-process samples, and finished products according to established Standard Operating Procedures (SOPs) and specifications.
• Handle hazardous materials, including chemicals and infectious agents, in the accurate manner as established by safety and company policy.
• May be required to perform testing of Mycobacterium tuberculosis (TB) and other similar organisms requiring Biosafety Level 3 Laboratory containment with strict adherence to safety policies associated with this manner of testing.
• Operate and maintain laboratory equipment, including calibration and troubleshooting, and ensure all equipment is in good working order.
• Document all results and observations accurately and thoroughly on test sheets and electronic systems (SAP).
• Absorb and participate in the investigation of out-of-specification (OOS) results, identifying root causes and recommending corrective actions.
• Contribute to continuous improvement initiatives within the quality management system.
• Ensure compliance with all applicable Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), Good Laboratory Practices (GLP), and company policies.
• Collaborate effectively with cross-functional teams, including manufacturing and scientific ops.
• Work in any of the laboratories within the QC department without a permanent assignment.

Qualifications

• Bachelor's degree in Biology, Microbiology or other related Life Science preferred.
• Minimum of laboratory related certificate from accredited institution required.
• Minimum of one year practical experience in Microbiological or medical technology laboratory preferred.
• Strong understanding of GMP/GDP/GLP regulations and quality management systems.
• Excellent written and verbal communication skills.
• Strong attention to detail and ability to maintain accurate records.
• Ability to work independently and as part of a team in a fast-paced environment.
• Good problem solving and trouble-shooting skills.

Skills

• Strong understanding of GMP/GDP/GLP regulations and quality management systems.
• Excellent written and verbal communication skills.
• Strong attention to detail and ability to maintain accurate records.
• Ability to work independently and as part of a team in a fast-paced environment.
• Good problem solving and trouble-shooting skills.

Benefits

At BD, we offer a comprehensive Total Rewards program that includes competitive compensation, benefits, and a supportive culture. We value our associates and provide opportunities for growth and development.

Pay

$27.10 - $43.40 USD per hour

Schedule

PR 700am-330pm M-F (United States of America)