Quality Assurance Manager Job at Sagar Vitaceuticals Nigeria Limited
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 Nigeria Limited.
The company is a leading household name in 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 Position: Quality Assurance Manager
Job Location: Sagamu, Ogun
Employment Type: Full-time
Job Description
- We are seeking an experienced and detail-oriented Quality Assurance Manager to join our team.
- The ideal candidate will be responsible for overseeing the quality assurance processes, ensuring that all products meet the highest standards of quality and compliance with industry regulations.
- The Quality Assurance Manager will develop and implement quality management systems, lead quality improvement initiatives, and manage a team of quality assurance professionals.
- Lead the efforts of QA personnel responsible for the testing, investigations, and method transfer activities to ensure compliance with all regulatory requirements, company policies, values, and goals
- 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)
- Responsible for setting strategy direction for the Quality Assurance Dept. 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)
- 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 assurance team, 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 of relevant work experience.
- Potential candidates with experience working in Quality Assurance department of chemical companies are encouraged to apply.
- Candidates with experience working as Quality Assurance Manager in pharmaceutical companies are also encouraged to apply.
- Candidates must have 10 - 15years 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 assurance professionals.
- 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
N200,000 - N250,000 Monthly.
Method of Application
Interested and qualified candidates should send their Applications and CV to: hr@svnl.in using the Job Position as the subject of the mail.
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