Overview
We are seeking a QC Analyst Team Lead to join a leading pharmaceutical company’s Quality Control (QC) laboratory. In this role, you will provide leadership and support to the QC team, oversee laboratory operations, and ensure compliance with Good Manufacturing Practice (GMP) standards. You will be responsible for managing daily QC activities, optimizing resources, and ensuring efficient testing processes to support pharmaceutical production.
Key Responsibilities
1. Lead and support the QC team in daily operations, ensuring tasks are completed efficiently and in compliance with regulatory standards.
2. Monitor and report on Key Performance Indicators (KPIs) to track team and laboratory performance.
3. Oversee the preparation of media, buffers, and analytical reagents for QC testing.
4. Assign and delegate tasks within the team to maintain workflow efficiency.
5. Ensure the proper operation, calibration, and maintenance of laboratory equipment, including autoclaves, balances, pH meters, and incubators.
6. Maintain a clean, organized, and compliant laboratory environment.
7. Manage inventory levels by ordering consumables and raw materials to ensure continuous lab operation.
8. Oversee sample receipt, handling, and shipping, including vendor Preventative Maintenance (PM) coordination.
9. Support and oversee analytical testing across various methodologies in alignment with GMP requirements.
10. Participate in bioreactor builds and equipment calibration processes.
11. Conduct stock checks and ensure timely replenishment of laboratory supplies.
12. Review and verify process data integrity to maintain compliance with quality and regulatory standards.
Qualifications
1. Bachelor’s degree in Biotechnology, Microbiology, Biochemistry, or a related scientific discipline.
2. Minimum of 2 years of relevant experience in a QC, Microbiology, or Biochemistry laboratory.
3. At least 1 year of supervisory or team lead experience in a GMP-regulated environment.
4. Strong knowledge and practical application of GMP principles.
5. Preference for candidates with an analytical background.
6. Excellent organizational, problem-solving, and time management skills.
7. Experience documenting and recording scientific studies, with a strong understanding of data integrity and electronic lab notebook systems.
8. Demonstrated experience in maintaining laboratory safety and compliance standards.
9. Strong leadership and communication skills, with the ability to mentor and develop team members.
Who You Are
1. A proactive leader with the ability to manage multiple tasks and priorities effectively.
2. Detail-oriented with a strong commitment to upholding laboratory safety, quality, and regulatory compliance.
3. A collaborative team player who can engage with cross-functional teams to ensure seamless lab operations.
What We Offer
1. Competitive salary and comprehensive benefits package.
2. Professional development and career growth opportunities within a dynamic pharmaceutical environment.
3. A collaborative, innovative, and supportive workplace that values continuous improvement.
4. The opportunity to contribute to high-quality pharmaceutical production and scientific excellence.
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