ASSISTANCE QUALITY CONTROL MANAGER (PHARMACEUTICAL) AT SAGAR VITACEUTICALS NIGERIA LIMITED | QUALITY CONTROL JOBS IN LAGOS & OGUN

About Company:

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. 

Job Description:

We are seeking a highly experienced and technically proficient Assistant Quality Control (QC) Manager to join our pharmaceutical manufacturing team. In this role, you will play a critical part in maintaining the highest standards of product safety and efficacy. You will oversee daily laboratory operations, ensure rigorous adherence to Good Manufacturing Practices (GMP), and mentor a team of analysts to ensure that all raw materials and finished products meet strict regulatory requirements.

Requirements:

• Laboratory Operations: Supervise chemical, microbiological, and physical testing processes. Coordinate workflows to ensure that laboratory results are accurate and released within tight production timelines.

• Quality Compliance: Act as a guardian of compliance. Ensure that all operations align with GMP, GLP, and SOPs. You will lead investigations into Out-of-Specification (OOS) and Out-of-Trend (OOT) results.

• Documentation & Audit Support: Maintain meticulous laboratory records, review Certificates of Analysis (COA), and support the team during internal/external regulatory inspections.

• Equipment & Methodology: Manage the calibration and qualification of analytical instruments. Oversee method validation and ensure the availability of essential reagents and standards.

• Team Leadership: Mentor and train QC analysts, fostering a culture of safety, continuous improvement, and technical excellence.

• Safety & CAPA: Champion laboratory safety procedures and drive the implementation of Corrective and Preventive Actions (CAPA) to mitigate quality risks.

Qualifications and Skills:

• Education: B.Sc./HND, with an MBA/MSc/MA being highly preferred.

• Experience: 6–10 years of progressive experience within the pharmaceutical industry or related scientific field.

• Technical Expertise: Deep understanding of laboratory testing, instrument qualification, and analytical method validation.

• Regulatory Knowledge: Solid foundation in GMP, GLP, and regional pharmaceutical regulatory standards.

• Core Competencies: Strong leadership abilities, exceptional attention to detail, and proven experience in troubleshooting complex analytical deviations.

Salary

Application Closing Date: Not specified

Application Instructions:

Interested and qualified candidates should forward their CV to: recruitment@svnl.in using the position as subject of email.