Quality Control Manager at Sagar Vitaceuticals Nigeria Limited

Sagar Vitaceuticals Nigeria Limited formerly known as Strides Vital Nigeria Limited was a strategic partnership comprising Vital Pharmaceuticals Limited and India’s Strides Arcolabs Limited, an 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 Nigeria Limited. The company is a leading household name in the pharmaceuticals and healthcare industry and has many well-known brands such as Vitaclox, Vitacillin, Vitamox, Tropitone, Inbu, Ytacan etc These brands have an established presence in the market and are popular names in Nigeria. An ultra-modern pharmaceutical factory at Ikeja, Lagos, offers consumers quality and affordable products.

We are recruiting to fill the position below:

Job Title: Quality Control Manager

Location: Sagamu, Ogun
Employment Type: Full-time

Job Description

• We are seeking an experienced and detail-oriented Quality Control Manager to join our team.
• The ideal candidate will be responsible for overseeing the quality controlprocesses, ensuring that all products meet the highest standards of quality and compliance with industry regulations.
• The Quality Control Manager will develop and implement quality management systems, lead quality improvement initiatives, and manage a team of quality controlprofessionals.
• Lead the efforts of QC personnel responsible for the testing, investigations, and method transfer activities to ensure compliance with all regulatory requirements, company policies, values, and goals
• Responsible for setting strategy direction for the Quality ControlDept. and team
• Provide leadership for lot release, incoming quality, manufacturing, and labs investigations, change control and corrective and preventative action review/approval, manufacturing support, record review/approval, and ongoing projects support (if any)
• Support team by guidance and coaching and provide direction/approval of activities and decisions
• Cultivate and reinforce appropriate group values, ethics, norms, and behaviors
• Share oversight to individuals and team on personal development, performance, and quality related issues. Write and deliver performance reviews
• Responsible for supporting all planned and unplanned manufacturing and labs deviations, review and approval of product and equipment change controls (including SOPs and master batch records)
• Conduct impact assess to design changes and participate/coordinate CAPA Review Board
• Maintain the structure to ensure that all quality commitments and timelines are tracked and met.
• Work directly with internal and external customers to assure Best-in-Class expectations for quality are met if not exceeded
• Analyze trends, quality metrics and other data to identify quality and compliance gaps.
• Develop, implement, and maintain a comprehensive quality management system (QMS) in line with industry standards and regulations.
• Oversee the inspection and testing of raw materials, in-process products, and finished goods to ensure they meet quality specifications.
• Lead and manage the quality controlteam, providing guidance, training, and performance evaluations.
• Conduct regular audits of the production process to identify areas for improvement and ensure compliance with quality standards.
• Collaborate with production and engineering teams to develop and implement quality control processes and procedures.
• Analyze quality data and trends to identify root causes of quality issues and implement corrective and preventive actions.
• Ensure compliance with environmental, health, and safety regulations related to quality assurance activities.
• Coordinate with suppliers and vendors to ensure the quality of incoming materials meets required standards.
• Prepare and present quality reports to senior management, highlighting key quality metrics and areas for improvement.
• Lead continuous improvement initiatives to enhance product quality, reduce waste, and improve overall process efficiency.
• Develop and maintain documentation related to quality assurance, including standard operating procedures (SOPs), work instructions, and quality records.

Requirements

• Candidates should possess B.Sc Degrees with 10 - 15 years relevant work experience.
• Potential candidates with experience working in Quality Control department of chemical companies are encouraged to apply.
• Candidates with experience working as Quality Control Manager in pharmaceutical companies are also encouraged to apply.
• Candidates must have 10 - 15 years work experience in chemical synthesis Industry.
• Strong knowledge of quality management systems (ISO 9001 or equivalent) and quality control methodologies.
• Proven experience in leading and managing a team of quality controlprofessionals.
• Excellent analytical and problem-solving skills, with the ability to identify and address quality issues effectively.
• Strong communication and interpersonal skills, with the ability to work collaboratively with cross-functional teams.
• Proficiency in using quality management software and tools.

Salary
N150,000 - N250,000 monthly.

Application Closing Date
28th February, 2025.