Exciting Career Opportunity: Granulation Machine Operator at Sagar Vitaceuticals Nigeria Limited
Are you looking to advance your career in the pharmaceutical manufacturing sector? Sagar Vitaceuticals Nigeria Limited, a leading household name in the healthcare industry, is seeking a dedicated and detail-oriented Granulation Machine Operator to join its state-of-the-art production team in Ikeja, Lagos.
Sagar Vitaceuticals Nigeria Limited (formerly known as Strides Vital Nigeria Limited) has a rich history of strategic partnerships and growth. Following a 100% acquisition by Sagar Overseas Limited in 2017, the company has solidified its position as an industry leader, producing highly trusted brands such as Vitaclox, Vitacillin, Vitamox, Tropitone, Inbu, and Ytacan. Operating from an ultra-modern pharmaceutical facility, the company is dedicated to offering consumers affordable, top-tier quality healthcare products.
Role Overview
As a Granulation Machine Operator, you will play a critical role in the manufacturing process. You will be responsible for operating, monitoring, and maintaining specialized granulation equipment to ensure the highest standards of product quality. Operating in strict compliance with Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and approved Batch Manufacturing Records (BMRs), you will ensure that all operations are safe, efficient, and consistent with regulatory requirements.
Key Responsibilities
In this role, your daily tasks will include but are not limited to:
- Operating specialized granulation equipment such as high-shear granulators, fluid bed granulators, and rapid mixer granulators (RMG) in accordance with approved SOPs.
- Reviewing Batch Manufacturing Records (BMRs) to ensure all necessary raw materials and equipment are prepared and available before commencing production.
- Weighing, loading, and processing raw materials according to the designated formulation specifications.
- Monitoring critical process parameters, including mixing times, impeller/chopper speeds, temperature, and moisture content, to ensure batch consistency.
- Performing wet or dry granulation processes as defined by manufacturing instructions.
- Conducting routine in-process checks and immediately reporting any deviations or technical abnormalities.
- Accurately recording all relevant production data in batch records and equipment logbooks.
- Cleaning, sanitizing, and maintaining granulation equipment and workstations to meet strict cleaning SOPs.
- Conducting proper line clearance procedures before and after every production run.
- Assisting in machine setups, changeovers, and basic preventive maintenance to minimize downtime.
- Ensuring absolute compliance with Good Documentation Practices (GDP), GMP, and health, safety, and environmental (HSE) standards.
Key Performance Indicators (KPIs)
Success in this position will be measured by:
- Strict adherence to GMP guidelines and SOP requirements.
- Meeting or exceeding planned production targets.
- Achieving exceptional Batch Right-First-Time (RFT) performance.
- Maintaining precise, error-free production documentation.
- Optimizing equipment uptime and operational efficiency while minimizing material waste.
- Zero critical process deviations caused by operator error.
Qualifications & Experience
To be considered for this role, candidates should possess:
- A High School Diploma, National Diploma (ND), Higher National Diploma (HND), or a Bachelor's degree in Pharmacy, Chemistry, Microbiology, Biochemistry, Industrial Chemistry, Chemical Engineering, or a related scientific discipline.
- Prior experience within a pharmaceutical manufacturing facility is highly preferred.
- A solid understanding of pharmaceutical production processes and GMP regulations.
- The ability to interpret and execute Batch Manufacturing Records (BMRs) and SOPs accurately.
Required Skills & Competencies
- Technical Expertise: Proven experience operating and troubleshooting pharmaceutical granulation equipment.
- Attention to Detail: Strong commitment to accuracy, precision, and quality control.
- Documentation Skills: Excellent record-keeping skills with a strong command of Good Documentation Practices.
- Problem-Solving & Adaptability: Basic mechanical aptitude with the ability to work under pressure to meet tight manufacturing targets.
- Core Values: Demonstration of integrity, accountability, safety awareness, and teamwork.
Working Conditions & Operational Authority
This role operates within a controlled, sterile pharmaceutical manufacturing environment where the use of Personal Protective Equipment (PPE) is strictly mandatory. Candidates should be comfortable standing for extended periods and handling production materials. Due to the nature of manufacturing schedules, shift work, overtime, or weekend work may be required.
Authority: The operator is fully empowered to halt equipment if quality concerns or unsafe working conditions are detected, report deviations immediately, and recommend process modifications to boost efficiency and safety.
Method of Application
Interested and qualified candidates should send their CVs to: nosa@svnl.in using the job title as the subject of the email.
