Jobs at Sagar Vitaceuticals Nigeria Limited

Job Summary

• The role financial operational, compliance, and technology audits, ensuring adherence to CBN, NDIC, AML/CFT, and IFRS requirements while identifying control weaknesses, strengthening governance, and supporting continuous improvement across Manufacturing ,Sagar Vitaceuticals both Lagos and Ogun state.

Responsibilities

• Develop and execute risk-based audit plans, conducting financial, operational, compliance, and Manufacturingaudits across the operations.
• Evaluate the effectiveness of internal controls, governance processes, and risk management frameworks, recommending practical improvements to mitigate operational and financial risks.
• Audit banking payment, payment systems, lending activities, customer onboarding, and other technology-enabled business functions.
• Ensure compliance with CBN, NDIC, AML/CFT regulations, IFRS, and internal policies while supporting regulatory examinations and statutory audits.
• Prepare comprehensive audit reports, communicate findings, track remediation plans, and validate the implementation of corrective actions.
• Provide advisory support on emerging risks, internal control enhancements, governance best practices, and evolving regulatory requirements within payment financial system
• Collaborate with Risk Management, Compliance, external auditors, regulators, and the Board Audit Committee to strengthen the bank's overall control environment.
• Promoting professionalism, continuous improvement, and adherence to audit standards and ethical practices.

Requirements

• Bachelor's degree in Accounting, Finance, Economics, or a related field. Professional certifications such as ACA, ACCA, CIA, or CISA are required, while CIBN certification is an added advantage.
• 3–5 years of experience in internal or external audit within the Manufacturingcompany, pharmacyticals company,financial services, or other regulated industries.
• Proven experience conducting financial, operational, compliance,
• Strong understanding of internal audit methodologies, enterprise risk management frameworks, internal controls, and governance principles.
• Sound knowledge of CBN regulations, NDIC guidelines, AML/CFT requirements, IFRS, and applicable regulatory standards.
• Proficiency in Microsoft Office, audit software, and data analytics tools, with strong analytical, investigative, and report-writing skills.

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Job Summary

• The Mechanical Engineer is responsible for maintaining the mechanical integrity, operational efficiency, and safety of all manufacturing equipment, packaging lines, and plant utilities across the pharmaceutical facility
• This role ensures that all mechanical systems operate in full compliance with Current Good Manufacturing Practices (cGMP), NAFDAC regulatory guidelines, and internal Standard Operating Procedures (SOP)

Key Responsibilities
Machinery Maintenance & Operations:

• Execute scheduled Preventive Maintenance (PM) and rapid troubleshooting/repair for processing machinery, including:
• High-shear granulators, Fluid Bed Dryers (FBD), Rapid Mixer Granulators (RMG), tablet compression machines, and coating pans.
• Blister packing machines, liquid filling/capping machines, sachet machines, and strip packagers.
• Lead mechanical setups, tool/die changes, and mechanical adjustments during production batch changeovers to ensure zero damage and minimal downtime.

Engineering & Projects:

• Support the execution of engineering projects, equipment installations, and facility upgrades.
• Participate in qualification and validation activities for new equipment and systems.
• Assist in monitoring engineering budgets, spare parts inventory, and maintenance costs.
• Ensure proper documentation of maintenance activities, equipment history, and engineering records.

Compliance & Safety:

• Ensure compliance with GMP, SOPs, safety regulations, and pharmaceutical industry standards.
• Support audits, inspections, and regulatory compliance activities.
• Promote workplace safety and ensure adherence to HSE policies and procedures.
• Ensure calibration and maintenance activities are carried out according to approved schedules.

Utilities & Facilities Management:

• Oversee the maintenance of utility systems including HVAC, boilers, generators, compressors, purified water systems, and electrical installations.
• Ensure uninterrupted utility supply to support production operations.
• Monitor facility conditions and coordinate repairs when necessary.

Utility & HVAC Management:

• Maintain Air Handling Units (AHUs), HEPA filtration systems, and ducting to preserve pressure cascades and environmental controls required for cleanrooms.
• Oversee the operation, servicing, and pressure-testing of plant utilities:
  • Industrial boilers and steam distribution systems.
  • Oil-free air compressors and pneumatic supply networks.
  • Chillers, cooling towers, and water generation/distribution plants (Purified Water / Water for Injection).
  • Effluent Treatment Plants (ETP) and water recycling systems.

Compliance, Safety & Documentation:

• Ensure all mechanical repairs, modifications, and lubrications use food/pharma-grade materials (e.g., NSF/H1 lubricants) and comply with sanitary standards.
• Maintain audit-ready engineering logbooks, equipment maintenance history cards, Equipment Qualification (IQ/OQ/PQ) records, and change control documentation.
• Enforce safety protocols, including Lockout/Tagout (LOTO), pressure vessel safety, hot  work permits, and factory floor health and safety regulations.

Job Specifications & Qualifications
Required Education & Experience:

• B.Sc. or HND in Mechanical Engineering from a recognized institution.
• COREN registration or NSE membership is an added advantage.

Experience:

• 3 to 8 years of hands-on mechanical maintenance experience in a pharmaceutical manufacturing, FMCG, or food processing environment.
• Proven experience working with high-speed automated packaging and tableting machinery.

Key Technical & Functional Skills:

• Strong command of pneumatic circuits, valves, cylinders, and hydraulic actuators.
• In-depth knowledge of industrial steam systems, air compressors, and HVAC/AHU setups.
• Ability to read and interpret mechanical fabrication drawings, piping and instrumentation diagrams (P&ID), and assembly schematics.
• Practical experience with pharmaceutical equipment will added more advantage.

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Job Summary

• The Liquid Filling Operator is responsible for setting up, running, and monitoring high-speed liquid filling and capping machinery.
• The core objective of this role is to ensure that liquid pharmaceutical products are filled with extreme volume accuracy, safely sealed, and processed efficiently in compliance with standard operating procedures (SOPs) and Good Manufacturing Practices (GMP).

Qualifications

• Candidates should possess a Bachelor's Degree / HND / OND /Trade Test/ City & Guilds, SSCE qualification.
• Conduct regular checks to ensure filled containers meet strict volume and weight specifications (preventing underfill or overfill)
• Relevant qualification as applicable to role applied for.
• Clean, sanitize, and sterilize (CIP/SIP) filling machines, product lines, and tanks before and after production according to strict hygiene guideline
• Ccurately document production data, batch numbers, run quantities, waste counts, and equipment usage in the Batch Manufacturing Record (BMR) or logbook
• Must be very detailed and self-driven
• In-depth knowledge of the MS-Office

Experience:

• 1 - 4 years in liquid filling operation roles in Pharma, Foods and chemical Production Industry
• Ability to operate a filling Machine.
• High drive and interest in taking on new tasks.
• Strong analytical skills and interpersonal skill

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Job Summary

• The Assistant Quality Control Manager is responsible for supporting the QC Manager in overseeing daily laboratory operations, ensuring strict compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
• This role involves supervising laboratory personnel, reviewing analytical data for raw materials, in-process, and finished products, leading Out-of-Specification (OOS) investigations, and maintaining inspection readiness for global regulatory bodies

Key Responsibilities
Laboratory Operations:

• Assist in managing daily Quality Control laboratory activities.
• Supervise chemical, microbiological, and physical testing of raw materials, packaging materials, in-process samples, and finished products.
• Ensure timely analysis and reporting of laboratory results.
• Coordinate laboratory workflow to meet production and release timelines.

Quality Compliance:

• Ensure compliance with GMP, GLP, SOPs, and regulatory requirements.
• Support internal and external audits, including regulatory inspections.
• Monitor adherence to quality systems and laboratory best practices.
• Participate in investigations related to deviations, out-of-specification (OOS), and out-of-trend (OOT) results.

• Develop and execute Corrective and Preventive Actions (CAPA) to address root causes and prevent recurrence of quality issues.

• Write, review, and update Quality Control Standard Operating Procedures (SOPs) to reflect changing regulations and process improvements.

Documentation & Reporting:

• Review analytical reports, laboratory records, certificates of analysis, and test documentation.
• Ensure proper documentation, filing, and record retention in compliance with regulatory standards.
• Assist in preparing quality metrics and management reports.

Equipment & Method Management:

• Oversee calibration, qualification, and maintenance of laboratory instruments and equipment.
• Support analytical method validation, verification, and transfer activities.
• Ensure availability of laboratory reagents, standards, and consumables.

Team Leadership:

• Supervise and mentor QC analysts and laboratory staff.
• Assist in staff training and competency development programs.
• Promote a culture of quality, safety, and continuous improvement.

Safety & Continuous Improvement:

• Ensure compliance with laboratory safety procedures and environmental standards.
• Identify process improvement opportunities within QC operations.
• Support implementation of CAPA (Corrective and Preventive Actions).
• Required Education & Experience

Requirements

• Bachelor’s or Master’s degree in Chemistry, Pharmacy, Pharmaceutical Sciences, Biochemistry, or a closely related scientific discipline.
• Minimum of 5 to 8 years of hands-on experience in a pharmaceutical QC laboratory.
• At least 2+ years in a supervisory, team-lead, or senior analyst role.