Garonit Pharmaceutical
The QC Supervisor is primarily responsible for the daily operation of pharmaceutical Quality Control Laboratory. This position will manage the staff to schedule and perform all necessary testing to support manufacturing and release requirements. Responsible for training and personnel development. This is a hands‑on position. In addition to managerial responsibilities, this position will be performing wet chemistry testing, HPLC and GC testing, etc. as needed.
What You’ll Do
Lead, coach and manage a team of chemists to ensure data integrity and performance to meet business objectives
Train and develop chemists
Formulate, document, and maintain quality control standards and on‑going quality control objectives
Schedule workload to meet release objectives and deadlines
Review, interpret, analyze and report HPLC data according to USP/NF/BP/EP/IP/JP/CEP/cGMP, and internal guidelines
Author analytical methods and SOPs
Clean, maintain, and troubleshoot HPLC instruments
Develop analytical methods and specifications
Develop analytical method validation protocols and reports
Perform Laboratory Investigations, root cause analysis, CAPA, Change Controls, Validations, Stability Programs
Manage the outsourcing process of testing to contract laboratories
Ensure lab safety and manage chemical inventory
Improve the compliance of the laboratory operations as well improve the efficiency and reduce the cost of the operations
Perform duties of QC Chemist as needed including HPLC sample preparation and testing and any other testing requirements
Audit the work of QC Chemists
Other duties assigned by Management
What You’ll Bring
Bachelor’s degree in Chemistry or a related scientific field.
2+ years in a supervisory or management role in a pharmaceutical QC lab.
Strong experience with Empower 3, HPLC, GC, and wet chemistry.
Deep understanding of cGMP, ICH, CFR, and USP testing requirements.
Experience in method development, validation, and stability testing.
Proven leadership, training, and coaching skills.
Excellent problem‑solving, documentation, and communication abilities.
High attention to detail, strong work ethic, and commitment to quality.
Why Garonit Pharma
Work with cutting‑edge equipment in a collaborative, growth‑oriented environment.
Play a key role in ensuring product quality and regulatory success.
Competitive compensation and career growth opportunities.
Seniority level
Mid‑Senior level
Employment type
Full‑time
Job function
Quality Assurance
Industries
Pharmaceutical Manufacturing
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What You’ll Do
Lead, coach and manage a team of chemists to ensure data integrity and performance to meet business objectives
Train and develop chemists
Formulate, document, and maintain quality control standards and on‑going quality control objectives
Schedule workload to meet release objectives and deadlines
Review, interpret, analyze and report HPLC data according to USP/NF/BP/EP/IP/JP/CEP/cGMP, and internal guidelines
Author analytical methods and SOPs
Clean, maintain, and troubleshoot HPLC instruments
Develop analytical methods and specifications
Develop analytical method validation protocols and reports
Perform Laboratory Investigations, root cause analysis, CAPA, Change Controls, Validations, Stability Programs
Manage the outsourcing process of testing to contract laboratories
Ensure lab safety and manage chemical inventory
Improve the compliance of the laboratory operations as well improve the efficiency and reduce the cost of the operations
Perform duties of QC Chemist as needed including HPLC sample preparation and testing and any other testing requirements
Audit the work of QC Chemists
Other duties assigned by Management
What You’ll Bring
Bachelor’s degree in Chemistry or a related scientific field.
2+ years in a supervisory or management role in a pharmaceutical QC lab.
Strong experience with Empower 3, HPLC, GC, and wet chemistry.
Deep understanding of cGMP, ICH, CFR, and USP testing requirements.
Experience in method development, validation, and stability testing.
Proven leadership, training, and coaching skills.
Excellent problem‑solving, documentation, and communication abilities.
High attention to detail, strong work ethic, and commitment to quality.
Why Garonit Pharma
Work with cutting‑edge equipment in a collaborative, growth‑oriented environment.
Play a key role in ensuring product quality and regulatory success.
Competitive compensation and career growth opportunities.
Seniority level
Mid‑Senior level
Employment type
Full‑time
Job function
Quality Assurance
Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr