Sagar Vitaceuticals Nigeria Limited formerly known as Strides Vital Nigeria Limited was a strategic partnership comprising Vital Pharmaceuticals Ltd and India’s Strides Arcolabs Ltd,a NSE listed company. In 2017, Management of Sagar Overseas Limited, acquired 100% shares in Strides Vital Nigeria Limited and the company was re-named to Sagar Vitaceuticals N...
We are recruiting to fill the position below:
Job Title: Assistance Quality Control Manager (Pharmaceutical)
Locations: Ikeja - Lagos & Sagamu - Ogun
Employment Type: Full-time
Job Summary
- The Assistant Quality Control Manager is responsible for supporting the QC Manager in overseeing daily laboratory operations, ensuring strict compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
- This role involves supervising laboratory personnel, reviewing analytical data for raw materials, in-process, and finished products, leading Out-of-Specification (OOS) investigations, and maintaining inspection readiness for global regulatory bodies
Key Responsibilities
Laboratory Operations:
- Assist in managing daily Quality Control laboratory activities.
- Supervise chemical, microbiological, and physical testing of raw materials, packaging materials, in-process samples, and finished products.
- Ensure timely analysis and reporting of laboratory results.
- Coordinate laboratory workflow to meet production and release timelines.
Quality Compliance:
- Ensure compliance with GMP, GLP, SOPs, and regulatory requirements.
- Support internal and external audits, including regulatory inspections.
- Monitor adherence to quality systems and laboratory best practices.
- Participate in investigations related to deviations, out-of-specification (OOS), and out-of-trend (OOT) results.
-
Develop and execute Corrective and Preventive Actions (CAPA) to address root causes and prevent recurrence of quality issues.
-
Write, review, and update Quality Control Standard Operating Procedures (SOPs) to reflect changing regulations and process improvements.
Documentation & Reporting:
- Review analytical reports, laboratory records, certificates of analysis, and test documentation.
- Ensure proper documentation, filing, and record retention in compliance with regulatory standards.
- Assist in preparing quality metrics and management reports.
Equipment & Method Management:
- Oversee calibration, qualification, and maintenance of laboratory instruments and equipment.
- Support analytical method validation, verification, and transfer activities.
- Ensure availability of laboratory reagents, standards, and consumables.
Team Leadership:
- Supervise and mentor QC analysts and laboratory staff.
- Assist in staff training and competency development programs.
- Promote a culture of quality, safety, and continuous improvement.
Safety & Continuous Improvement:
- Ensure compliance with laboratory safety procedures and environmental standards.
- Identify process improvement opportunities within QC operations.
- Support implementation of CAPA (Corrective and Preventive Actions).
- Required Education & Experience
Requirements
- Bachelor’s or Master’s degree in Chemistry, Pharmacy, Pharmaceutical Sciences, Biochemistry, or a closely related scientific discipline.
- Minimum of 5 to 8 years of hands-on experience in a pharmaceutical QC laboratory.
- At least 2+ years in a supervisory, team-lead, or senior analyst role.
Application Closing Date
13th August, 2026.
How to Apply
Interested and qualified candidates should forward their CV to: recruitment@svnl.in using the position as subject of email.
https://www.hotnigerianjobs.com/hotjobs/922804/assistance-quality-control-manager-pharmaceutical.html