Jobs at Sagar Vitaceuticals Nigeria Limited

Reports To: Packaging Supervisor / Production Manager

Job Summary

• The Blistering Machine Operator is responsible for operating, setting up, monitoring, and maintaining blister packaging machines to ensure pharmaceutical products are packaged accurately, efficiently, and in compliance with Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and company quality standards.
• The operator ensures product integrity, minimizes downtime, and maintains accurate production documentation.

Key Responsibilities

• Set up, operate, and adjust blister packaging machines according to production schedules and batch manufacturing records.
• Verify packaging materials, including PVC, aluminum foil, cartons, leaflets, and labels, before production.
• Perform line clearance before and after production to prevent product mix-ups and cross-contamination.
• Conduct machine start-up, in-process checks, and shutdown procedures in accordance with SOPs.
• Monitor machine performance and make necessary adjustments to maintain optimal operating efficiency.
• Inspect blister packs for defects such as missing tablets, damaged blisters, incorrect sealing, printing errors, and coding issues.
• Record production data, equipment parameters, downtime, rejects, and material usage accurately.
• Ensure products are packaged according to approved specifications and regulatory requirements.
• Perform routine cleaning, lubrication, and minor preventive maintenance of blistering equipment.
• Report equipment malfunctions, deviations, or quality issues promptly to supervisors and maintenance personnel.
• Minimize material waste while maximizing production efficiency.
• Follow GMP, safety regulations, hygiene requirements, and company policies at all times.
• Participate in validation activities, equipment qualification, and process improvement initiatives when required.
• Assist during internal, customer, and regulatory audits.
• Maintain a clean and organized work environment following 5S principles.

Key Performance Indicators (KPIs)

• Production output achieved versus target
• Packaging quality and defect rate
• Machine uptime and operating efficiency
• Downtime reduction
• Material waste percentage
• Compliance with GMP and SOP requirements
• Accuracy and completeness of production documentation
• Safety and housekeeping compliance.

Qualifications

• High school diploma, technical certificate, or equivalent qualification; diploma in Engineering, Industrial Technology, or related field is an advantage.
• Previous experience operating blister packaging machines in a pharmaceutical, food, or FMCG manufacturing environment is preferred.
• Knowledge of pharmaceutical packaging processes and GMP requirements.
• Ability to read and understand batch records, SOPs, and packaging specifications.
• Basic mechanical troubleshooting skills.
• Good numerical and documentation skills.
• Ability to work rotating shifts, weekends, and overtime when required.

Required Skills:

• Blister machine setup and operation
• Equipment troubleshooting
• Attention to detail
• GMP and GDP compliance
• Documentation accuracy
• Quality inspection
• Teamwork and communication
• Time management
• Problem-solving
• Safety awareness

Physical Requirements:

• Ability to stand and walk for long periods.
• Good manual dexterity and hand-eye coordination.
• Ability to lift materials in accordance with company safety guidelines.
• Normal or corrected vision sufficient to detect packaging defects.
• Ability to work in a cleanroom environment while wearing appropriate PPE.

Working Conditions:

• Manufacturing and pharmaceutical packaging environment.
• Requires standing for extended periods.
• May involve lifting packaging materials within approved safety limits.
• Use of personal protective equipment (PPE) is mandatory.
• Work is performed in controlled cleanroom or packaging areas with strict hygiene requirements.

go to method of application »

Reports To: Pharmaceutical Manager / Quality Manager / Production Manager

Job Summary

• The Pharmacist is responsible for supporting the development, manufacturing, quality assurance, regulatory compliance, and distribution of pharmaceutical products.
• The role ensures that all products meet regulatory requirements, Good Manufacturing Practice (GMP) standards, and company quality policies while promoting patient safety and product effectiveness.
• A pharmacist in a pharmaceutical company is responsible for ensuring that medicines are developed, manufactured, tested, stored, and distributed in compliance with regulatory standards while maintaining product quality, safety, and efficacy.

Key Responsibilities

• Ensure compliance with Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and applicable pharmaceutical regulations.
• Supervise and monitor the manufacturing process to ensure products meet quality standards.
• Review and approve batch manufacturing and packaging records.
• Conduct quality assurance and quality control activities, including reviewing test results and investigating deviations.
• Monitor product stability and ensure proper storage and handling of pharmaceutical products.
• Prepare and maintain accurate documentation in accordance with regulatory requirements.
• Participate in internal and external audits and implement corrective and preventive actions (CAPA).
• Support product registration, licensing, and regulatory submissions.
• Investigate customer complaints, product defects, and recalls when necessary.
• Provide technical guidance and training to production and quality personnel.
• Collaborate with research and development, production, engineering, and regulatory teams during product development and commercialization.
• Ensure compliance with health, safety, and environmental policies.
• Keep up to date with changes in pharmaceutical regulations and industry best practices.

Key Performance Indicators (KPIs)

• Compliance with GMP and regulatory standards.
• Reduction in manufacturing deviations and quality incidents.
• Successful completion of audits with minimal observations.
• Timely completion of documentation and batch record reviews.
• Product quality and customer satisfaction.
• Effective implementation of corrective and preventive actions (CAPA).

Required Qualifications

• Bachelor of Pharmacy (B.Pharm) or Doctor of Pharmacy (Pharm.D.).
• Valid pharmacist license / registration with the appropriate regulatory authority.
• Experience in pharmaceutical manufacturing, quality assurance, quality control, or regulatory affairs is preferred.
• Knowledge of GMP, GDP, GLP, and pharmaceutical quality systems.
• Strong analytical and problem - solving skills.
• Excellent communication and teamwork abilities.
• Proficiency in Microsoft Office and pharmaceutical documentation systems.

Key Skills:

• Pharmaceutical manufacturing.
• Quality assurance and quality control.
• Regulatory compliance.
• Documentation and record management.
• Risk assessment and problem-solving.
• Attention to detail.
• Time management.
• Leadership and teamwork.
• Communication and presentation skills.

Working Conditions

• Work is primarily performed in manufacturing plants, laboratories, offices, or warehouse environments.
• May require the use of personal protective equipment (PPE).
• May involve shift work depending on production schedules.

go to method of application »

Reports To: Pharmaceutical Manager / Quality Manager / Production Manager

Job Summary

• The Pharmacist is responsible for supporting the development, manufacturing, quality assurance, regulatory compliance, and distribution of pharmaceutical products.
• The role ensures that all products meet regulatory requirements, Good Manufacturing Practice (GMP) standards, and company quality policies while promoting patient safety and product effectiveness.
• A pharmacist in a pharmaceutical company is responsible for ensuring that medicines are developed, manufactured, tested, stored, and distributed in compliance with regulatory standards while maintaining product quality, safety, and efficacy.

Key Responsibilities

• Ensure compliance with Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and applicable pharmaceutical regulations.
• Supervise and monitor the manufacturing process to ensure products meet quality standards.
• Review and approve batch manufacturing and packaging records.
• Conduct quality assurance and quality control activities, including reviewing test results and investigating deviations.
• Monitor product stability and ensure proper storage and handling of pharmaceutical products.
• Prepare and maintain accurate documentation in accordance with regulatory requirements.
• Participate in internal and external audits and implement corrective and preventive actions (CAPA).
• Support product registration, licensing, and regulatory submissions.
• Investigate customer complaints, product defects, and recalls when necessary.
• Provide technical guidance and training to production and quality personnel.
• Collaborate with research and development, production, engineering, and regulatory teams during product development and commercialization.
• Ensure compliance with health, safety, and environmental policies.
• Keep up to date with changes in pharmaceutical regulations and industry best practices.

Key Performance Indicators (KPIs)

• Compliance with GMP and regulatory standards.
• Reduction in manufacturing deviations and quality incidents.
• Successful completion of audits with minimal observations.
• Timely completion of documentation and batch record reviews.
• Product quality and customer satisfaction.
• Effective implementation of corrective and preventive actions (CAPA).

Required Qualifications

• Bachelor of Pharmacy (B.Pharm) or Doctor of Pharmacy (Pharm.D.).
• Valid pharmacist license / registration with the appropriate regulatory authority.
• Experience in pharmaceutical manufacturing, quality assurance, quality control, or regulatory affairs is preferred.
• Knowledge of GMP, GDP, GLP, and pharmaceutical quality systems.
• Strong analytical and problem - solving skills.
• Excellent communication and teamwork abilities.
• Proficiency in Microsoft Office and pharmaceutical documentation systems.

Key Skills:

• Pharmaceutical manufacturing.
• Quality assurance and quality control.
• Regulatory compliance.
• Documentation and record management.
• Risk assessment and problem-solving.
• Attention to detail.
• Time management.
• Leadership and teamwork.
• Communication and presentation skills.

Working Conditions

• Work is primarily performed in manufacturing plants, laboratories, offices, or warehouse environments.
• May require the use of personal protective equipment (PPE).
• May involve shift work depending on production schedules.

go to method of application »

Reports To: Pharmaceutical Manager / Quality Manager / Production Manager

Job Summary

• The Pharmacist is responsible for supporting the development, manufacturing, quality assurance, regulatory compliance, and distribution of pharmaceutical products.
• The role ensures that all products meet regulatory requirements, Good Manufacturing Practice (GMP) standards, and company quality policies while promoting patient safety and product effectiveness.
• A pharmacist in a pharmaceutical company is responsible for ensuring that medicines are developed, manufactured, tested, stored, and distributed in compliance with regulatory standards while maintaining product quality, safety, and efficacy.

Key Responsibilities

• Ensure compliance with Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and applicable pharmaceutical regulations.
• Supervise and monitor the manufacturing process to ensure products meet quality standards.
• Review and approve batch manufacturing and packaging records.
• Conduct quality assurance and quality control activities, including reviewing test results and investigating deviations.
• Monitor product stability and ensure proper storage and handling of pharmaceutical products.
• Prepare and maintain accurate documentation in accordance with regulatory requirements.
• Participate in internal and external audits and implement corrective and preventive actions (CAPA).
• Support product registration, licensing, and regulatory submissions.
• Investigate customer complaints, product defects, and recalls when necessary.
• Provide technical guidance and training to production and quality personnel.
• Collaborate with research and development, production, engineering, and regulatory teams during product development and commercialization.
• Ensure compliance with health, safety, and environmental policies.
• Keep up to date with changes in pharmaceutical regulations and industry best practices.

Key Performance Indicators (KPIs)

• Compliance with GMP and regulatory standards.
• Reduction in manufacturing deviations and quality incidents.
• Successful completion of audits with minimal observations.
• Timely completion of documentation and batch record reviews.
• Product quality and customer satisfaction.
• Effective implementation of corrective and preventive actions (CAPA).

Required Qualifications

• Bachelor of Pharmacy (B.Pharm) or Doctor of Pharmacy (Pharm.D.).
• Valid pharmacist license / registration with the appropriate regulatory authority.
• Experience in pharmaceutical manufacturing, quality assurance, quality control, or regulatory affairs is preferred.
• Knowledge of GMP, GDP, GLP, and pharmaceutical quality systems.
• Strong analytical and problem - solving skills.
• Excellent communication and teamwork abilities.
• Proficiency in Microsoft Office and pharmaceutical documentation systems.

Key Skills:

• Pharmaceutical manufacturing.
• Quality assurance and quality control.
• Regulatory compliance.
• Documentation and record management.
• Risk assessment and problem-solving.
• Attention to detail.
• Time management.
• Leadership and teamwork.
• Communication and presentation skills.

Working Conditions

• Work is primarily performed in manufacturing plants, laboratories, offices, or warehouse environments.
• May require the use of personal protective equipment (PPE).
• May involve shift work depending on production schedules.

go to method of application »

Reports To: Pharmaceutical Manager / Quality Manager / Production Manager

Job Summary

• The Pharmacist is responsible for supporting the development, manufacturing, quality assurance, regulatory compliance, and distribution of pharmaceutical products.
• The role ensures that all products meet regulatory requirements, Good Manufacturing Practice (GMP) standards, and company quality policies while promoting patient safety and product effectiveness.
• A pharmacist in a pharmaceutical company is responsible for ensuring that medicines are developed, manufactured, tested, stored, and distributed in compliance with regulatory standards while maintaining product quality, safety, and efficacy.

Key Responsibilities

• Ensure compliance with Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and applicable pharmaceutical regulations.
• Supervise and monitor the manufacturing process to ensure products meet quality standards.
• Review and approve batch manufacturing and packaging records.
• Conduct quality assurance and quality control activities, including reviewing test results and investigating deviations.
• Monitor product stability and ensure proper storage and handling of pharmaceutical products.
• Prepare and maintain accurate documentation in accordance with regulatory requirements.
• Participate in internal and external audits and implement corrective and preventive actions (CAPA).
• Support product registration, licensing, and regulatory submissions.
• Investigate customer complaints, product defects, and recalls when necessary.
• Provide technical guidance and training to production and quality personnel.
• Collaborate with research and development, production, engineering, and regulatory teams during product development and commercialization.
• Ensure compliance with health, safety, and environmental policies.
• Keep up to date with changes in pharmaceutical regulations and industry best practices.

Key Performance Indicators (KPIs)

• Compliance with GMP and regulatory standards.
• Reduction in manufacturing deviations and quality incidents.
• Successful completion of audits with minimal observations.
• Timely completion of documentation and batch record reviews.
• Product quality and customer satisfaction.
• Effective implementation of corrective and preventive actions (CAPA).

Required Qualifications

• Bachelor of Pharmacy (B.Pharm) or Doctor of Pharmacy (Pharm.D.).
• Valid pharmacist license / registration with the appropriate regulatory authority.
• Experience in pharmaceutical manufacturing, quality assurance, quality control, or regulatory affairs is preferred.
• Knowledge of GMP, GDP, GLP, and pharmaceutical quality systems.
• Strong analytical and problem - solving skills.
• Excellent communication and teamwork abilities.
• Proficiency in Microsoft Office and pharmaceutical documentation systems.

Key Skills:

• Pharmaceutical manufacturing.
• Quality assurance and quality control.
• Regulatory compliance.
• Documentation and record management.
• Risk assessment and problem-solving.
• Attention to detail.
• Time management.
• Leadership and teamwork.
• Communication and presentation skills.

Working Conditions

• Work is primarily performed in manufacturing plants, laboratories, offices, or warehouse environments.
• May require the use of personal protective equipment (PPE).
• May involve shift work depending on production schedules.