Granulation Officer at Sagar Vitaceuticals Nigeria Limited (SVNL)

Sagar Vitaceuticals Nigeria Limited (SVNL) is a pharmaceutical manufacturing company based in Ikeja, Lagos. Originally established as a joint venture, it is now owned by Sagar Overseas Ltd. SVNL operates a modern facility with high-capacity production lines for tablets, capsules, ointments, and more, adhering to GMP standards.

The company is NAFDAC-approved and partners with Nigeria’s Federal Ministry of Health to support local drug production. Its product portfolio includes vitamins, antibiotics, and over-the-counter supplements.

We are recruiting to fill the position below:

Job Title: Granulation Officer

Location: Makun City, Ogun
Employment Type: Part-time

Job Summary

• A Granulation Officer in a pharmaceutical company is responsible for carrying out the granulation stage of tablet manufacturing in compliance with Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and safety regulations.
• The Granulation Officer is responsible for preparing, operating, monitoring, and documenting granulation processes used in the manufacture of pharmaceutical tablets. The role ensures that products meet quality standards while maintaining compliance with regulatory requirements.

Key Responsibilities

• Operate granulation equipment such as:
  • High-shear granulators
  • Fluid bed dryers (FBD)
  • Rapid mixer granulators (RMG)
  • Multi-mills
  • Vibro sifters
• Weigh and dispense raw materials according to Batch Manufacturing Records (BMRs).
• Perform wet or dry granulation processes as specified in manufacturing procedures.
• Monitor critical process parameters such as mixing time, temperature, moisture content, and drying time.
• Carry out in-process checks and report any deviations.
• Complete and maintain accurate batch documentation and logbooks.
• Clean and sanitize equipment and manufacturing areas according to SOPs.
• Ensure compliance with GMP, cGMP, and company quality policies.
• Coordinate with Quality Assurance (QA), Quality Control (QC), and Production teams.
• Troubleshoot equipment or process issues and escalate when necessary.
• Participate in equipment qualification, validation, and calibration activities.
• Maintain workplace safety and follow health, safety, and environmental (HSE) procedures.

Key Performance Indicators (KPIs)

• Batch completion within schedule
• Compliance with GMP and SOP requirements
• Low batch rejection and deviation rates
• Accurate documentation
• Equipment uptime and cleanliness
• Minimal production downtime
• Zero safety incidents

Required Qualifications

• Bachelor's Degree or HND in Pharmacy, Pharmaceutical Technology, Industrial Chemistry, Biochemistry, Microbiology, Chemical Engineering or a related science discipline
• 1–3 years of experience in pharmaceutical manufacturing (entry-level positions may accept fresh graduates).
• Knowledge of GMP, cGMP, SOPs, and pharmaceutical manufacturing processes.
• Familiarity with tablet manufacturing and granulation techniques.

Required Skills:

• Knowledge of granulation processes (wet and dry granulation)
• Attention to detail and accuracy
• Good documentation practices (GDP)
• Ability to operate pharmaceutical manufacturing equipment
• Problem-solving and troubleshooting skills
• Teamwork and communication
• Time management
• Basic computer proficiency (Microsoft Office and electronic documentation systems)

Working Conditions:

• Production/manufacturing environment.
• Use of personal protective equipment (PPE) is mandatory.
• May involve shift work, weekends, or overtime depending on production schedules.
• Standing for extended periods and handling production equipment.

Career Progression
A typical career path is:

• Granulation Officer
• Senior Granulation Officer
• Production Supervisor
• Production Manager
• Manufacturing Manager
• Plant Manager

Additional Information:

• This role is critical in ensuring that pharmaceutical tablets are manufactured consistently, safely, and in compliance with regulatory standards such as GMP and national regulatory authority requirements.

Salary 
N150,000 - N200,000 per month.

Application Closing Date
Not Specified.

How to Apply
Interested and qualified candidates should send their CVs to: nosa@svnl.in using the job title as the subject of the email.