Sagar Vitaceuticals Nigeria Limited Recruitment 2026: Production Pharmacist, Etc. Jobs

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Sagar Vitaceuticals Nigeria Limited Recruitment 2026: Production Pharmacist, Etc. Jobs

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: Production Pharmacist

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

Job Summary

  • The Production Pharmacist is responsible for supervising and coordinating pharmaceutical manufacturing activities to ensure that products are manufactured according to approved procedures, Good Manufacturing Practices (GMP), quality standards, and Regulatory requirements.
  • The role involves Overseeing Production processes, ensuring accurate documentation, Monitoring Personnel and equipment, and maintaining Compliance with company Policies and applicable Regulatory standards.
  • The ideal candidate must have relevant pharmaceutical manufacturing experience, sound Knowledge of GMP, and the Ability to manage Production Activities efficiently while ensuring product quality, safety, and timely delivery.

Key Duties and Responsibilities
Pharmaceutical Production Operations:

  • Supervise daily pharmaceutical manufacturing activities, including dispensing, mixing, granulation, compression, capsule filling, coating, liquid preparation, and filling, as applicable to the company’s products.
  • Ensure that production activities are carried out according to approved Batch Manufacturing Records (BMRs), Standard Operating Procedures (SOPs), and work instructions.
  • Monitor production processes to ensure compliance with approved manufacturing specifications and established quality standards.
  • Ensure Proper Line clearance before the commencement of Production and between product batches.
  • Coordinate with production supervisors and operators to achieve daily and monthly production targets.
  • Monitor production yields, material usage, and process losses, and investigate significant discrepancies.
  • Ensure that equipment and production areas are properly cleaned, maintained, and ready for use.

Good Manufacturing Practice (GMP) and Quality Assurance:

  • Ensure strict adherence to current Good Manufacturing Practices (cGMP) and applicable regulatory requirements.
  • Ensure compliance with approved manufacturing procedures, hygiene standards, gowning requirements, and contamination-control measures.
  • Identify and report deviations, non-conformances, and out-of-specification process results.
  • Participate in investigations, root-cause analysis, corrective and preventive actions (CAPA), and other quality improvement activities.
  • Work closely with Quality Assurance (QA) and Quality Control (QC) to Resolve production-related quality issues.
  • Ensure that products are manufactured under appropriate conditions to prevent cross-contamination, mix-ups, and other quality risks.
  • Support internal and external audits and regulatory inspections.

Production Documentation and Reporting:

  • Ensure accurate, complete, and timely documentation of all manufacturing activities.
  • Review Batch Manufacturing Records and associated production documents for completeness and compliance.
  • Ensure proper recording of batch numbers, raw materials, equipment details, process parameters, yields, and Personnel involved.
  • Ensure that all entries comply with Good Documentation Practices (GDP), including correction of errors in accordance with approved procedures.
  • Prepare daily, weekly, and monthly production reports.
  • Report production deviations, equipment breakdowns, material shortages, and other operational challenges to the Production Manager.
  • Maintain proper records of production activities, cleaning, equipment usage, and in-process controls.

Personnel Supervision and Training:

  • Supervise production operators, line leaders, and other assigned production personnel.
  • Allocate duties and monitor staff performance to ensure operational efficiency.
  • Train production personnel on GMP, SOPs, hygiene, safety, and correct equipment operation.
  • Ensure that personnel follow approved gowning procedures and maintain good housekeeping practices.
  • Promote discipline, teamwork, accountability, and continuous improvement within the production department.
  • Identify staff Training needs and recommend appropriate Training programmes.

Equipment and Material Management:

  • Ensure the proper handling, storage, dispensing, and use of raw materials and packaging materials.
  • Verify material identity, status labels, and required documentation before use.
  • Ensure that production equipment is used only when appropriately cleaned, qualified where required, and released for use.
  • Coordinate with Engineering and Maintenance to address equipment breakdowns and preventive maintenance requirements.
  • Monitor material reconciliation and investigate discrepancies in quantities issued, used, rejected, or returned.
  • Minimise wastage and promote efficient utilisation of materials, manpower, and equipment.

Health, Safety, and Environmental Compliance:

  • Ensure compliance with workplace health, safety, and environmental procedures.
  • Enforce the proper use of personal protective equipment (PPE).
  • Ensure safe handling of Pharmaceutical ingredients, chemicals, and cleaning agents.
  • Report accidents, incidents, unsafe practices, and potential hazards promptly.
  • Maintain clean, organised, and Safe Production Areas in accordance with company requirements.

Key Performance Indicators (KPIs)
The Production Pharmacist’s performance will be assessed using the following indicators:

  • Production target achievement: Percentage of planned production targets achieved.
  • Batch documentation accuracy: Completeness and accuracy of batch records.
  • GMP compliance: Number and severity of production-related GMP deviations.
  • Product quality: Rate of batch rejection, rework, and production-related defects.
  • Production yield: Achievement of approved yield targets and reduction of
  • Production efficiency: Reduction in downtime and avoidable process delays.
  • Safety compliance: Adherence to safety procedures
  • Staff development: Completion of required training and improvement in staff competence.
  • Audit readiness: Timely closure of assigned audit findings and CAP
  • Housekeeping and hygiene: Compliance with production-area cleanliness and hygiene standards.

Qualifications and Experience

  • Bachelor of Pharmacy (B.Pharm) or Doctor of Pharmacy (Pharm.D.) from a recognised institution.
  • Current registration and practising licence with the  Pharmacists Council of Nigeria (PCN), as applicable to the position and duties.
  • Minimum of 2–5 years of relevant experience in pharmaceutical manufacturing or production.
  • Demonstrated experience in pharmaceutical production processes and batch documentation.
  • Good knowledge of cGMP, SOPs, GDP, and pharmaceutical quality systems.
  • Experience with production equipment, process controls, and manufacturing documentation.
  • Familiarity with applicable NAFDAC Requirements and pharmaceutical Regulatory standards.
  • Experience in oral solid dosage forms, liquids, capsules, tablets, or other relevant dosage forms is an advantage.

Required Skills and Competencies:

  • Strong leadership and personnel management skills.
  • Good analytical, problem-solving, and decision-making abilities.
  • Excellent documentation and report-writing skills.
  • Strong attention to detail and commitment to product quality.
  • Good communication and Interpersonal skills.
  • Ability to work under pressure and meet production deadlines.
  • Good understanding of GMP compliance and quality risk management.
  • Proficiency in Microsoft Office and production reporting systems.

Reporting Relationship:

  • Reports to: Production Manager or Head of Production.
  • Supervises: Production Supervisors, Line Leaders, Machine Operators, and other assigned production staff.
  • Works closely with: Quality Assurance, Quality Control, Engineering and Maintenance, Warehouse, Regulatory Affairs, and Supply Chain departments.

Working Conditions:

  • Work is primarily within pharmaceutical manufacturing facilities.
  • May require the use of protective clothing and entry into controlled production areas.
  • May involve shift work or extended hours depending on production schedules.
  • Must comply with all company safety, hygiene, and quality requirements.

General Responsibilities:

  • The Production Pharmacist shall perform other reasonable duties assigned by management that are consistent with the position, professional competence, and applicable regulatory requirements.

Salary
N300,000 – N400,000 monthly.

Application Closing Date
30th November, 2026.

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

 

Job Title: Capsule Filling Machine Operator

Location: Makun City, Ogun
Employment Type: Full-time
Department: Production
Section: Solid Dosage Manufacturing
Reports To: Production Supervisor / Production Manager

Job Purpose

  • To operate and monitor capsule filling machines for the accurate, efficient, and hygienic filling of pharmaceutical powders, granules, or pellets into empty capsules in accordance with approved batch manufacturing records, Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMP), and established safety and quality requirements.
  • The operator is responsible for ensuring consistent capsule quality, compliance with production specifications, proper documentation, and achievement of assigned production targets without compromising product quality or patient safety.

Key Responsibilities and Duties
Machine Operation:

  • Operate automatic, semi-automatic, or other assigned capsule filling machines in accordance with approved SOPs.
  • Ensure that the correct machine settings, tooling, and capsule sizes are selected as specified in the batch manufacturing record.
  • Set up the machine and perform routine operational checks before production.
  • Feed approved empty capsules and the designated product into the machine according to approved procedures.
  • Monitor machine performance, filling speed, capsule separation, powder dosing, capsule closing, and ejection throughout production.
  • Make only authorized adjustments to machine settings to maintain consistent filling performance.
  • Report abnormal machine noise, vibration, malfunction, or process irregularities to the Production Supervisor or Engineering team.

Pre-Operational Checks and Line Clearance:

  • Verify that the machine, surrounding area, tools, and product-contact parts are clean and suitable for use.
  • Confirm completion and approval of line clearance before starting a new batch.
  • Ensure that previous product remnants, labels, documents, and materials have been removed from the area.
  • Verify the identity and status of the approved product, raw materials, and empty capsules before use.
  • Check equipment identification, cleanliness status labels, calibration status where applicable, and maintenance status.
  • Confirm that the correct batch number, product name, capsule size, and manufacturing instructions are available.

In-Process Quality Control:

  • Monitor capsule fill weight in accordance with the approved sampling plan and specified frequency.
  • Check capsule appearance, locking, closure, integrity, and overall uniformity.
  • Inspect for empty capsules, underfilled or overfilled capsules, loose caps, split capsules, damaged capsules, and other visible defects.
  • Conduct or assist with in-process checks as authorized by approved procedures.
  • Record all required results accurately and report results outside established limits immediately.
  • Segregate and identify rejected capsules to prevent accidental mixing with acceptable products.
  • Stop the machine and inform the supervisor when a critical quality defect or process deviation is detected.

Documentation and GMP Compliance:

  • Complete batch manufacturing records, equipment logbooks, machine usage records, and other required production documents accurately and contemporaneously.
  • Record start and stop times, quantities processed, material usage, yield, rejects, and downtime as required.
  • Follow Good Documentation Practices and applicable data integrity requirements.
  • Report deviations, discrepancies, equipment malfunctions, and unexpected events promptly.
  • Never falsify records, backdate entries, or make unauthorized alterations to production documents.
  • Ensure that all entries are traceable to the person performing the activity.

Material Handling and Reconciliation:

  • Verify material identity and status before charging materials into the machine.
  • Handle powders, granules, pellets, and empty capsules carefully to prevent contamination, mix-ups, and material loss.
  • Ensure that materials are transferred and used in accordance with approved instructions.
  • Reconcile issued, used, rejected, and returned materials as required by the batch record.
  • Maintain proper segregation and identification of approved, rejected, and unprocessed materials.
  • Report material shortages, discrepancies, or suspected contamination to the supervisor.

Cleaning and Housekeeping:

  • Perform routine cleaning of the machine and surrounding work area according to approved cleaning SOPs.
  • Assist with equipment changeover and product-contact part cleaning as trained and authorized.
  • Ensure that cleaned equipment is properly identified and protected against contamination.
  • Maintain good housekeeping and comply with applicable hygiene and sanitation requirements.
  • Dispose of waste and rejected capsules according to approved procedures.
  • Complete equipment cleaning records and obtain verification where required.

Safety and Environmental Compliance:

  • Wear the prescribed personal protective equipment (PPE), including appropriate protective clothing and respiratory protection where required by the product risk assessment.
  • Follow occupational health, safety, and environmental procedures.
  • Never bypass machine guards or safety interlocks.
  • Stop the equipment and report unsafe conditions or mechanical hazards.
  • Follow approved procedures for handling pharmaceutical powders and controlling dust exposure.
  • Report accidents, near misses, spills, and injuries immediately.

Preventive Maintenance and Teamwork:

  • Perform routine operator-level checks as specified in the equipment SOP.
  • Assist Engineering and Maintenance personnel during equipment servicing when required.
  • Report worn parts, unusual machine performance, and maintenance needs promptly.
  • Participate in production meetings, GMP training, and continuous improvement activities.
  • Work collaboratively with Production, Quality Assurance, Quality Control, Engineering, and Warehouse personnel.

Requirements
Educational Qualifications:

  • Minimum of Senior Secondary School Certificate (SSCE/WAEC/NECO) or equivalent.
  • OND, NCE, HND, or relevant technical qualification in Mechanical Engineering, Electrical / Electronic Engineering, Pharmaceutical Technology, Science Laboratory Technology, or a related discipline is an advantage.
  • Relevant pharmaceutical manufacturing or machine operation training is desirable.

Work Experience:

  • 2 – 4 years of experience operating capsule filling machines or similar pharmaceutical production equipment is preferred.
  • Candidates with relevant technical aptitude and demonstrated machine operation skills may be considered for entry-level training.
  • Experience in pharmaceutical solid dosage manufacturing and GMP-regulated environments is an advantage.

Required Skills and Competencies:

  • Ability to operate and monitor capsule filling equipment safely.
  • Basic understanding of capsule filling processes and in-process quality checks.
  • Good numerical and record-keeping skills.
  • Strong attention to detail and ability to identify defects.
  • Knowledge of GMP, personal hygiene, line clearance, and contamination prevention.
  • Ability to follow written procedures and instructions.
  • Good communication, teamwork, and problem-solving skills.
  • Ability to work shifts and meet production schedules where required.
  • High level of discipline, honesty, and commitment to product quality.

Salary
N180,000 – N250,000 monthly.

Application Closing Date
17th November, 2026.

How to Apply
Interested and qualified candidates should send their updated CV to: nosa@svnl.in using the Job Title as the subject of the email.

 

 

 

Job Title: Compression Machine Operator

Location: Makun City, Ogun
Employment Type: Full-time
Industry: Pharmaceutical Manufacturing

Job Summary

  • We are seeking an experienced Compression Machine Operator to operate and monitor tablet compression machines in a pharmaceutical manufacturing environment.
  • The successful candidate will ensure that tablets are produced safely, efficiently, and in accordance with Good Manufacturing Practice (GMP), approved batch manufacturing procedures, and quality standards.

Key Responsibilities

  • Set up, operate, and monitor tablet compression machines according to approved procedures.
  • Perform machine changeover, tooling installation, and basic adjustments.
  • Monitor compression parameters such as tablet weight, hardness, thickness, and appearance.
  • Conduct in-process checks and document results accurately.
  • Identify and report machine abnormalities, product defects, and process deviations.
  • Maintain proper documentation, including batch manufacturing records and equipment logbooks.
  • Clean and sanitize compression equipment and the production area according to SOPs.
  • Follow GMP, safety, hygiene, and contamination-control requirements.
  • Minimize machine downtime and material wastage while maintaining product quality.
  • Work closely with Production, Quality Assurance, Quality Control, and Maintenance teams.
  • Assist with troubleshooting and routine preventive maintenance activities.
  • Ensure proper handling and reconciliation of raw materials and packaging / production materials.

Requirements

  • 2–3 years of experience operating tablet compression machines in a pharmaceutical manufacturing environment.
  • Knowledge of GMP and pharmaceutical production procedures.
  • Experience with tablet compression equipment and tooling.
  • Ability to perform in-process quality checks.
  • Good understanding of batch documentation and SOP compliance.
  • Ability to troubleshoot basic machine and process problems.
  • Good attention to detail and ability to work shifts.

Education:

  • OND / HND / B.Sc. in Pharmaceutical Technology, Mechanical Engineering, Chemical Engineering, Industrial Chemistry, or a related field is preferred, depending on the employer’s requirements.

Key Skills:

  • Tablet compression machine operation
  • Machine setup and changeover
  • GMP compliance
  • In-process quality control
  • Troubleshooting
  • Documentation and record keeping
  • Equipment cleaning and maintenance
  • Attention to detail
  • Teamwork and communication.

Salary
N200,000 – N250,000 monthly.

Application Closing Date
30th October, 2026.

Method of Application
Interested and qualified candidates should send their detailed CV to: nosa@svnl.in using the Job Title as the subject of the email.

 

 

 

Job Title: Capsule Filling Operator (Pharmaceutical)

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

Responsibilities

  • Operate and monitor capsule filling machines in accordance with approved Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP).
  • Perform capsule filling, weight checks, in-process testing, and machine adjustments to ensure products meet established specifications.
  • Accurately dispense and load pharmaceutical powders or granules into capsule-filling equipment while maintaining product integrity.
  • Conduct equipment setup, cleaning, assembly, disassembly, and line clearance before and after production activities.
  • Monitor production processes and identify abnormalities, machine faults, or deviations, reporting them promptly to supervisors.
  • Perform routine in-process quality checks, including capsule weight, appearance, fill consistency, and defects.
  • Complete batch manufacturing records, equipment logbooks, cleaning records, and other required production documentation accurately.
  • Maintain a clean, safe, and controlled manufacturing environment in compliance with GMP, health, safety, and hygiene requirements.
  • Minimize product loss and downtime by following correct operating procedures and performing basic troubleshooting where authorized.
  • Work closely with Quality Control, Quality Assurance, Maintenance, and Production teams to ensure smooth and compliant manufacturing operations.
  • Follow proper procedures for handling pharmaceutical materials, including identification, segregation, labeling, and storage.
  • Adhere strictly to safety procedures, personal protective equipment (PPE) requirements, and pharmaceutical manufacturing regulations.

Application Closing Date
31st October, 2026.

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

 

 

 

Job Title: Electrical Maintenance Engineer

Location: Makun City, Ogun
Employment Type: Full-time
Industry: Pharmaceutical Manufacturing

Job Summary

  • We are seeking an experienced Electrical Maintenance Engineer to maintain, troubleshoot, and improve electrical systems and equipment within a pharmaceutical manufacturing facility.
  • The successful candidate will ensure reliable plant operations while maintaining compliance with Good Manufacturing Practice (GMP), safety standards, and company procedures.

Key Responsibilities

  • Perform preventive, corrective, and breakdown maintenance on electrical equipment and systems.
  • Troubleshoot and repair electrical faults affecting production machinery and utility systems.
  • Maintain electrical panels, motors, control circuits, sensors, switches, contactors, relays, and other electrical components.
  • Support the maintenance of pharmaceutical production equipment, including tablet compression, granulation, coating, filling, packaging, and other process equipment.
  • Maintain and troubleshoot PLC, VFD, motor control, and automation systems where applicable.
  • Conduct routine inspection and testing of electrical installations and equipment.
  • Respond promptly to equipment breakdowns to minimize production downtime.
  • Develop and implement preventive maintenance schedules.
  • Maintain accurate maintenance records, equipment history, and work orders.
  • Participate in equipment installation, commissioning, qualification, and modification activities.
  • Ensure electrical maintenance activities comply with GMP, electrical safety requirements, SOPs, and company policies.
  • Support maintenance activities involving HVAC, compressors, generators, pumps, water systems, and other pharmaceutical utilities.
  • Assist with root-cause analysis of recurring equipment failures and recommend corrective actions.
  • Coordinate with Production, Engineering, Quality Assurance, and other departments to resolve equipment-related issues.
  • Maintain appropriate spare parts and recommend replacement of obsolete or defective components.
  • Participate in emergency response, safety inspections, and maintenance improvement projects.

Pharmaceutical / GMP Responsibilities:

  • Follow GMP requirements when working in production and controlled areas.
  • Ensure maintenance activities do not compromise product quality or cause contamination.
  • Complete maintenance documentation accurately and in accordance with Good Documentation Practices.
  • Support equipment qualification and validation activities where required.
  • Follow approved procedures for maintenance work in cleanrooms and other controlled environments.

Requirements

  • B.Eng. / B.Sc. / HND in Electrical Engineering, Electrical/Electronics Engineering, or a related field.
  • 2–5 years of electrical maintenance experience, preferably in pharmaceutical manufacturing or a regulated production environment.
  • Practical experience with industrial electrical systems, motors, control panels, PLCs, VFDs, and automation systems.
  • Knowledge of preventive and corrective maintenance practices.
  • Understanding of GMP, electrical safety, and pharmaceutical manufacturing requirements.
  • Ability to read and interpret electrical drawings and schematics.
  • Strong troubleshooting and problem-solving skills.
  • Ability to work shifts and respond to equipment breakdowns when required.

Key Skills:

  • Industrial electrical maintenance
  • Preventive and corrective maintenance
  • PLC and automation troubleshooting
  • Motor and control systems
  • VFDs and electrical panels
  • Equipment installation and commissioning
  • Pharmaceutical utilities
  • GMP compliance
  • Electrical safety
  • Root-cause analysis
  • Maintenance documentation
  • Teamwork and communication.

Salary
N250,000 – N380,000 monthly.

Application Closing Date
30th October, 2026.

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

 

 

Job Title: Blistering Machine Operator

Location: Makun City, Ogun
Employment Type: Full-time
Department: Production / Manufacturing
Reports To: Production Supervisor / Production Manager

Job Summary

  • We are seeking an experienced Blistering Machine Operator with pharmaceutical manufacturing experience to operate, monitor, and maintain blister packing equipment in accordance with approved Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMP), and company quality standards.

Key Responsibilities

  • Operate and monitor blister packing machines efficiently and safely.
  • Set up the machine according to approved batch manufacturing and packaging instructions.
  • Perform machine changeovers, adjustments, and basic troubleshooting.
  • Ensure correct feeding, forming, filling, sealing, coding, and cutting of blister packs.
  • Conduct in-process quality checks, including pack appearance, seal integrity, print quality, batch number, expiry date, and tablet/capsule placement.
  • Complete batch documentation, machine logs, and production records accurately.
  • Follow GMP, SOPs, safety procedures, and hygiene requirements at all times.
  • Identify and report machine faults, product defects, deviations, and abnormal operating conditions.
  • Carry out routine cleaning and basic preventive maintenance of the blister machine.
  • Minimize product wastage, downtime, and packaging-material losses.
  • Maintain a clean and organized production area.
  • Work closely with Quality Assurance, Quality Control, Engineering, and Production teams.
  • Participate in line clearance and ensure correct packaging materials are used for each batch.
  • Support investigations into production deviations and equipment-related issues when required.

Requirements

  • 2 – 3 years of experience operating blister packing machines in a pharmaceutical manufacturing environment.
  • Knowledge of pharmaceutical packaging processes and GMP requirements.
  • Practical experience with machine setup, changeover, operation, and troubleshooting.
  • Ability to read and follow SOPs, batch packaging records, and work instructions.
  • Good understanding of pharmaceutical packaging quality requirements.
  • Ability to identify common machine and packaging defects.
  • Strong attention to detail and commitment to product quality and safety.
  • Good communication and teamwork skills.
  • Technical, mechanical, pharmaceutical, or related qualification is an advantage.

Preferred Experience:

  • Experience operating or working with pharmaceutical blister machines such as PVC / PVDC-Alu, Alu-Alu, or similar blister packaging systems is highly desirable.

Key Competencies:

  • GMP compliance
  • Machine operation and setup
  • Troubleshooting
  • Quality awareness
  • Documentation and record keeping
  • Attention to detail
  • Preventive maintenance awareness
  • Teamwork and communication
  • Production efficiency and waste reduction

Salary
N200,000 – N250,000 monthly.

Application Closing Date
31st October, 2026.

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

 

 

Job Title: Production Pharmacist

Location: Makun City, Sagamu, Ogun
Employment Type: Full-time

Requirements

  • Interested candidates must have strong pharma background to be considered.

Salary
N250,000 – N350,000 monthly.

Application Closing Date
30th October, 2026.

Method of Application
Interested and qualified candidates should send their detailed CV to: hr@svnl.in using the Job Title as the subject of the email.

 

 

 

Job Title: Pharmacovigilance Officer

Location: Makun City, Sagamu – Ogun
Employment Type: Full-time

Requirements

  • Must be science background with experience in pharmacovigilance.

Salary
N120,000 – N200,000 monthly.

Application Closing Date
31st October, 2026.

Method of Application
Interested and qualified candidates should send their detailed CV to: hr@svnl.in using the Job Title as the subject of the email.

 

 

 

Job Title: Quality Control Officer 

Location: Makun City, Ogun
Employment Type: Full-time
Department: Quality Control
Reports to: QC Manager / Head of Quality Control

Job Summary

  • The Quality Control (QC) Officer is responsible for conducting laboratory tests, inspections, sampling, and analysis of raw materials, packaging materials, in-process materials, finished pharmaceutical products, and other relevant samples to ensure compliance with approved specifications, pharmacopoeial standards, Good Manufacturing Practices (GMP), and applicable regulatory requirements.
  • The role involves maintaining accurate laboratory records, operating and maintaining laboratory equipment, reporting out-of-specification results, and supporting the production of safe, effective, and high-quality pharmaceutical products.

Responsibilities

  • Conduct physical, chemical, microbiological, and other relevant tests on raw materials, in-process materials, finished products, and packaging materials, according to assigned responsibilities.
  • Collect and sample materials and products in accordance with approved sampling procedures.
  • Perform quality tests on pharmaceutical products, including tablets, capsules, syrups, suspensions, creams, and other dosage forms, as applicable.
  • Verify that raw materials and packaging materials meet approved specifications before use.
  • Conduct in-process quality control checks during manufacturing and packaging operations.
  • Analyse finished products to confirm compliance with approved specifications before batch disposition.
  • Operate laboratory equipment such as analytical balances, pH meters, dissolution testers, disintegration testers, friability testers, hardness testers, UV-visible spectrophotometers, and HPLC systems, where applicable and within the officer’s competence.
  • Prepare reagents, standard solutions, and laboratory materials in accordance with approved procedures.
  • Ensure that laboratory equipment is properly calibrated, qualified where required, cleaned, and maintained.
  • Record all test results accurately, contemporaneously, and in accordance with Good Documentation Practices (GDP) and data integrity requirements.
  • Immediately report out-of-specification (OOS), out-of-trend (OOT), atypical results, and other laboratory discrepancies to the QC Manager.
  • Participate in laboratory investigations, root cause analysis, and the implementation of corrective and preventive actions (CAPA).
  • Maintain laboratory records, analytical worksheets, equipment logbooks, reference standards, reagents, and sample registers.
  • Ensure proper labelling, storage, retention, and disposal of samples in accordance with approved procedures.
  • Monitor laboratory environmental conditions and maintain good housekeeping and laboratory safety practices.
  • Support stability studies and conduct stability sample testing according to approved protocols.
  • Assist in method verification, method validation, and transfer activities as assigned.
  • Ensure compliance with GMP, GLP where applicable, SOPs, pharmacopoeial standards, and relevant regulatory requirements, including applicable NAFDAC requirements.
  • Participate in internal audits, regulatory inspections, and laboratory compliance assessments.
  • Collaborate with Production, Quality Assurance, Engineering, and other relevant departments to resolve quality-related issues.
  • Ensure that rejected or non-conforming materials and products are appropriately documented and communicated to authorised personnel.
  • Perform any other duties related to quality control as assigned by Management.

General Responsibilities:

  • The QC Officer shall maintain confidentiality, uphold professional ethics, comply with company policies, and ensure that all laboratory activities are performed according to approved procedures.
  • The officer must promptly report any test failure, suspected data integrity issue, equipment malfunction, or other condition that may affect product quality.

Key Performance Indicators

The QC Officer’s performance will be measured by:

  • Accuracy and reliability of laboratory test results.
  • Timeliness of raw material, in-process, and finished-product testing.
  • Compliance with approved testing methods and specifications.
  • Completeness and accuracy of laboratory documentation.
  • Timely reporting and investigation of OOS and OOT results.
  • Compliance with laboratory SOPs, GMP, and safety requirements.
  • Proper maintenance and availability of laboratory equipment.
  • Timely completion of assigned stability studies and laboratory activities.
  • Reduction of documentation errors and repeat testing attributable to procedural errors.
  • Readiness for internal and regulatory inspections.

Requirements

  • B.Sc. or HND in Chemistry, Industrial Chemistry, Biochemistry, Microbiology, Pharmaceutical Chemistry, or another relevant scientific discipline.
  • Previous experience working in the Quality Control Department of a pharmaceutical manufacturing company.
  • Practical knowledge of pharmaceutical laboratory testing, sampling, and analytical procedures.
  • Familiarity with GMP, laboratory documentation, data integrity, and applicable quality standards.
  • Experience with laboratory instruments and analytical techniques relevant to the company’s products.
  • Knowledge of OOS investigations, stability testing, calibration, and laboratory safety is an advantage.
  • Ability to interpret analytical results and compare them with approved specifications.

Required Skills:

  • Strong analytical and numerical skills.
  • Attention to detail and accuracy.
  • Good laboratory practices and safe handling of chemicals.
  • Knowledge of pharmaceutical testing procedures and specifications.
  • Accurate documentation and report-writing skills.
  • Problem-solving and investigation skills.
  • Ability to work independently and as part of a team.
  • Good communication and organisational skills.
  • High level of integrity and commitment to product quality.

Working Relationships:

  • QC Manager / Head of Quality Control
  • Quality Assurance Department
  • Production Department
  • Warehouse and Inventory Department
  • Engineering and Maintenance Department
  • Regulatory Affairs Department

Authority And Accountability:

  • The QC Officer is responsible for the accuracy and integrity of assigned laboratory activities and for reporting results to authorised personnel.
  • Final decisions on material approval, rejection, and finished-product release must follow the company’s approved quality system and delegated authority.

Recommended Qualifications:

  • For a pharmaceutical manufacturing company in Nigeria, tailor the educational requirement to the actual testing responsibilities. For example, microbiological testing requires appropriate microbiology competence, while chemical and instrumental analysis requires relevant analytical chemistry skills.
  • The job description should also reflect applicable NAFDAC requirements and the company’s approved procedures.

Application Closing Date
30th November, 2026.

How to Apply
Interested and qualified candidates should send their updated CV to: nosa@svnl.in using the Job Title as the subject of the email.

 

 

Job Title: Automatic Capsule Filling Machine Operator

Location: Makun City, Ogun
Employment Type: Full-time
Department: Production
Industry: Pharmaceutical Manufacturing
Reports To: Production Supervisor / Production Pharmacist

Job Summary

  • The Automatic Capsule Filling Machine Operator is responsible for setting up, operating, monitoring, and cleaning automatic capsule-filling machines used in pharmaceutical manufacturing.
  • The role ensures that capsules are filled accurately, efficiently, and consistently in accordance with approved batch manufacturing records, Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMP), and established quality standards.
  • The successful candidate must have practical experience operating automatic capsule-filling machines in a pharmaceutical manufacturing environment, with a strong understanding of in-process quality checks, production documentation, machine troubleshooting, and contamination prevention.

Key Duties and Responsiblites 
Machine Operation:

  • Operate automatic capsule-filling machines for the production of pharmaceutical hard-shell capsules.
  • Set up and adjust machine parameters according to approved batch instructions and product specifications.
  • Ensure correct installation of machine parts, change parts, dosing systems, and capsule-handling components.
  • Verify that the correct capsule size, formulation, and batch details are used before commencing production.
  • Monitor capsule feeding, capsule separation, powder or granule filling, capsule closing, and ejection throughout the production process.
  • Adjust machine settings within authorised limits to maintain consistent capsule weight, filling accuracy, and production output.
  • Monitor machine speed and performance to achieve approved production targets.
  • Identify and report machine malfunctions, unusual noise, blockages, and operational abnormalities promptly.
  • Ensure proper line clearance before starting production and during product or batch changeovers.

In-Process Quality Control:

  • Perform routine in-process checks according to approved procedures and sampling frequencies.
  • Monitor capsule fill weight and weight variation to ensure compliance with approved specifications.
  • Inspect capsules for defects, including improper locking, denting, cracking, leakage, deformation, and incomplete filling.
  • Check capsule separation, closing, and ejection to minimise defective products.
  • Monitor powder or granule flow and report issues that may affect filling consistency.
  • Segregate rejected capsules and ensure they are identified and handled according to approved procedures.
  • Immediately report out-of-specification results, process deviations, and other quality concerns to the Production Supervisor and Quality Assurance (QA) Department.
  • Ensure that production continues only when required quality and process conditions are met.

GMP and Production Documentation:

  • Comply strictly with current Good Manufacturing Practices (cGMP), approved SOPs, and applicable regulatory requirements.
  • Complete Batch Manufacturing Records (BMRs), machine logbooks, equipment usage records, and other required production documents accurately and promptly.
  • Record machine settings, batch numbers, production quantities, rejected units, capsule weight checks, and downtime as required.
  • Ensure that all entries comply with Good Documentation Practices (GDP).
  • Verify that equipment cleaning and status labels are completed and current before use.
  • Report deviations, discrepancies, and documentation errors in accordance with company procedures.
  • Maintain complete traceability of production activities and materials used.

Cleaning and Preventive Maintenance:

  • Clean the capsule-filling machine, hoppers, dosing components, tooling, and associated parts according to approved cleaning SOPs.
  • Ensure that equipment is properly cleaned between batches and product changeovers to prevent cross-contamination.
  • Carry out pre-start checks and routine operator-level maintenance as authorised.
  • Inspect machine components for wear, damage, or abnormal operation.
  • Ensure equipment is properly assembled after cleaning and maintenance.
  • Coordinate with the Engineering and Maintenance Department for repairs and scheduled preventive maintenance.
  • Never perform unauthorised machine adjustments, repairs, or maintenance activities.

Materials and Production Control:

  • Confirm the identity and status of capsule shells and approved powder or granule formulations before use.
  • Ensure that only materials released for production are used.
  • Handle materials in accordance with approved dispensing, storage, and handling procedures.
  • Monitor material consumption, production yield, and rejected quantities.
  • Report material shortages, spillage, wastage, and reconciliation discrepancies.
  • Ensure proper segregation and identification of materials and products throughout production.

Safety and Housekeeping:

  • Wear approved protective clothing and personal protective equipment (PPE).
  • Follow Pharmaceutical hygiene, gowning, and safety procedures.
  • Ensure machine guards and safety devices remain functional and in place.
  • Follow approved procedures for equipment shutdown and isolation before cleaning or maintenance.
  • Maintain cleanliness and orderliness in the production area.
  • Report accidents, unsafe conditions, and potential hazards immediately.

Key Performance Indicators (KPIs)
The operator’s performance will be evaluated based on:

  • Achievement of daily capsule production targets.
  • Compliance with approved capsule fill-weight specifications.
  • Reduction in capsule defects and rejection rates.
  • Machine uptime and reduction of avoidable downtime.
  • Compliance with GMP, SOPs, and safety procedures.
  • Accuracy and completeness of batch production records.
  • Timely completion of machine cleaning and changeover activities.
  • Reduction in material wastage and improvement in production yield.
  • Prompt reporting of machine faults and process deviations.
  • Maintenance of a clean and organised production area.

General Responsibilities:

  • Perform other reasonable duties assigned by management that are consistent with the position, the employee’s competence, approved procedures, and applicable pharmaceutical manufacturing requirements.

Requirements and Experiences

  • Minimum of SSCE,OND or HND in Mechanical Engineering, Electrical/Electronic Engineering, Pharmaceutical Technology, Science Laboratory Technology, or a related discipline.
  • Minimum of 2–3 years of hands-on experience operating automatic capsule-filling machines in a pharmaceutical manufacturing company.
  • Demonstrable knowledge of hard-shell capsule-filling operations and machine setup.
  • Practical experience in capsule weight monitoring, in-process checks, cleaning, and batch documentation.
  • Good knowledge of GMP, SOPs, GDP, and pharmaceutical hygiene requirements.
  • Experience with capsule-filling machine changeovers and basic troubleshooting is an advantage.

Required Skills and Competencies:

  • Strong technical knowledge of automatic capsule-filling machines.
  • Good understanding of capsule filling, dosing, locking, and ejection processes.
  • Attention to detail and commitment to product quality.
  • Ability to identify machine faults and report problems promptly.
  • Accurate documentation and record-keeping skills.
  • Good communication and teamwork skills.
  • Ability to work under production pressure and meet deadlines.
  • Strong commitment to GMP compliance, safety, and discipline.

Reporting Relationship:

  • Reports to: Production Supervisor / Production Pharmacist.
  • Works closely with: Quality Assurance, Quality Control, Engineering and Maintenance, Warehouse, and other Production Personnel.

Salary
N250,000 – N280,000 monthly.

Application Closing Date
30th November, 2026

Method of Application
Interested and qualified candidates should send their detailed CV to: hr@svnl.in using the Job Title as the subject of the email.

 

 

 

Job Title: Mechanical Maintenance Engineer

Location: Makun City, Ogun
Employment Type: Full-time
Industry: Pharmaceutical Manufacturing

Job Summary

  • We are seeking an experienced Mechanical Maintenance Engineer to maintain, troubleshoot, and improve mechanical equipment and utility systems within a pharmaceutical manufacturing facility.
  • The successful candidate will ensure equipment reliability, minimize production downtime, and maintain compliance with GMP, safety standards, and company procedures.

Key Responsibilities

  • Perform preventive, predictive, and corrective maintenance on pharmaceutical production and utility equipment.
  • Diagnose and repair mechanical faults to minimize equipment downtime.
  • Maintain and troubleshoot equipment such as tablet compression machines, granulators, mixers, coating machines, filling machines, packaging machines, conveyors, and pumps.
  • Maintain mechanical components including bearings, gears, shafts, couplings, valves, seals, belts, chains, and pneumatic systems.
  • Carry out equipment installation, assembly, alignment, commissioning, and modification.
  • Perform routine inspection and condition monitoring of production and utility equipment.
  • Develop and implement preventive maintenance schedules for mechanical equipment.
  • Respond promptly to equipment breakdowns and carry out effective repairs.
  • Support maintenance of pharmaceutical utilities such as HVAC systems, air compressors, boilers, chillers, water treatment systems, and pumps.
  • Investigate recurring equipment failures and perform root-cause analysis.
  • Maintain accurate maintenance records, equipment history, work orders, and spare-parts records.
  • Ensure availability and proper management of critical mechanical spare parts.
  • Work closely with Production, Electrical, Quality Assurance, Quality Control, and other departments to resolve equipment-related issues.
  • Participate in equipment installation, qualification, validation, and commissioning activities where required.
  • Ensure all maintenance activities are performed according to approved SOPs, safety procedures, and GMP requirements.

Pharmaceutical/GMP Responsibilities:

  • Follow Good Manufacturing Practice (GMP) requirements during maintenance activities.
  • Ensure maintenance work does not compromise product quality or cause contamination.
  • Follow approved procedures when working in cleanrooms and controlled production areas.
  • Complete maintenance documentation accurately and according to Good Documentation Practices.
  • Support equipment qualification and validation activities.
  • Maintain proper housekeeping and safety standards within maintenance and production areas.

Requirements

  • B.Eng./B.Sc./HND in Mechanical Engineering, Mechatronics Engineering, or a related discipline.
  • 2–5 years of mechanical maintenance experience, preferably within pharmaceutical manufacturing or another regulated manufacturing environment.
  • Practical experience with industrial machinery, pumps, compressors, HVAC, pneumatic systems, and production equipment.
  • Good knowledge of preventive and corrective maintenance techniques.
  • Understanding of GMP, equipment maintenance, safety requirements, and pharmaceutical manufacturing practices.
  • Ability to read and interpret mechanical drawings, equipment manuals, and technical specifications.
  • Strong troubleshooting, analytical, and problem-solving skills.
  • Ability to work independently and as part of a multidisciplinary engineering team.
  • Willingness to work shifts and respond to equipment breakdowns when required.

Key Skills:

  • Mechanical maintenance
  • Preventive and corrective maintenance
  • Equipment troubleshooting
  • Pumps and compressors
  • HVAC and utilities
  • Pneumatic and hydraulic systems
  • Bearings, gears, shafts, and couplings
  • Equipment installation and commissioning
  • Root-cause analysis
  • GMP compliance
  • Maintenance documentation
  • Spare-parts management
  • Health, safety, and environmental compliance.

Salary
N250,000 – N380,000 monthly.

Application Closing Date
30th October, 2026.

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

 

 

Sagar Vitaceuticals Nigeria Limited Recruitment 2026: Production Pharmacist, Etc. Jobs

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Important Notes

  • The above statements are intended to describe the general nature and level of work to be performed by those assigned to this function.
  • It should not be construed as an exhaustive list of all responsibilities, tasks and skills required of persons so classified.
  • All employees may be required to undertake other responsibilities in addition to those specified from time to time, as required.
  • We do not charge any application, processing, training, interview, testing or any other fees in connection with the application or recruitment process. If you receive a fee request, please ignore it.
  • Also, please note that logos, slogans, names and titles are easily copied and reproduced. Therefore, particular care should be taken when submitting personal information on the web.
  • We are an equal opportunity employer that values ​​inclusiveness and diversity. We do not discriminate on the basis of color, race, nationality, religion, age, ethnic origin, disability, gender, marital status or orientation gender in our employment practices
  • Our employees are all equally talented in unique ways: we come from diverse traditions, personal experiences and perspectives. And we want to include your ideas, are you ready to inspire us with your ideas?
  • We encourage all applicants to apply and do not discriminate in any recruitment process.
  • Applications submitted after the deadline will not be considered.
  • Due to the necessity of the position, we are entitled to appoint a candidate who matches the required profile before the above deadline
  • Only qualified candidates will be invited for an interview

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