What Pharmaceutical Quality Assurance Manager Jobs are in Ibadan?

Our client, a prestigious pharmaceutical company, is actively seeking a highly experienced Senior Pharmaceutical Quality Assurance Manager to oversee quality operations in Lokoja, Kogi, NG . This leadership role is pivotal in ensuring the consistent quality and compliance of all pharmaceutical products manufactured by the company. You will be responsible for developing, implementing, and maintaining the Quality Management System (QMS), leading audit programs, and ensuring adherence to cGMP and other relevant regulatory standards. The ideal candidate possesses a deep understanding of pharmaceutical quality assurance principles, strong leadership capabilities, and a proven track record in managing quality operations. We are looking for a strategic thinker with exceptional problem-solving skills and a commitment to upholding the highest standards of quality in the pharmaceutical industry. This is an excellent opportunity to make a significant impact within a reputable organization.

• Develop, implement, and manage the company's Quality Management System (QMS) to ensure compliance with cGMP and other applicable regulations.
• Lead and conduct internal and external audits of manufacturing sites, suppliers, and partners.
• Oversee the quality review and approval of batch records, validation protocols, and reports.
• Manage deviations, CAPAs (Corrective and Preventive Actions), and change control processes.
• Ensure compliance with all relevant national and international regulatory requirements.
• Provide quality oversight for product lifecycle management, including process validation and stability programs.
• Train and mentor QA staff, fostering a culture of quality and continuous improvement.
• Collaborate with other departments, including Production, R&D, and Regulatory Affairs, to address quality issues and ensure product integrity.
• Manage regulatory inspections and ensure prompt and effective responses to regulatory bodies.
• Stay current with evolving regulatory requirements and industry best practices in pharmaceutical quality assurance.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline.
• Minimum of 8 years of progressive experience in Pharmaceutical Quality Assurance, with at least 3 years in a management or supervisory role.
• Extensive knowledge of cGMP, ICH guidelines, and other relevant regulatory standards.
• Proven experience in developing and implementing Quality Management Systems.
• Strong experience in conducting audits and managing regulatory inspections.
• Excellent leadership, decision-making, and problem-solving skills.
• Proficiency in risk management principles and tools.
• Exceptional communication, interpersonal, and negotiation skills.
• Ability to manage complex projects and prioritize effectively in a demanding environment.
• Familiarity with various pharmaceutical dosage forms and manufacturing processes is advantageous.

Our client offers a competitive salary package and a comprehensive benefits program, including health insurance, retirement savings plans, and generous paid time off. We are committed to employee growth and provide extensive professional development opportunities, including training programs and support for further education. Our facilities in Lokoja, Kogi, NG are modern and well-equipped. We foster a collaborative and supportive work environment with clear opportunities for career advancement. Join our client's dedicated team and play a vital role in ensuring the quality and safety of pharmaceutical products.

• Develop, implement, and maintain the Quality Management System (QMS) in accordance with GMP, GDP, and other relevant regulatory guidelines.
• Lead and mentor the Quality Assurance team, fostering a culture of continuous improvement and compliance.
• Conduct internal audits and host regulatory agency inspections and customer audits.
• Oversee deviation management, CAPA (Corrective and Preventive Actions) implementation, and change control processes.
• Review and approve batch records, validation protocols, and other critical quality documents.
• Ensure all pharmaceutical products meet specified quality standards before release.
• Manage vendor qualification and ongoing supplier quality management.
• Develop and deliver quality training programs to relevant personnel.
• Monitor quality metrics and prepare regular quality reports for senior management.
• Stay abreast of evolving regulatory landscapes and ensure organizational readiness.

• Master's or Ph.D. in Pharmacy, Chemistry, Biology, or a related scientific discipline.
• A minimum of 8 years of progressive experience in Pharmaceutical Quality Assurance/Quality Control.
• Extensive knowledge of pharmaceutical manufacturing operations and regulatory requirements (e.g., NAFDAC, WHO GMP).
• Demonstrated experience in leading QA teams and managing complex quality systems.
• Proven track record in successfully managing audits and inspections.
• Strong understanding of validation principles, risk management, and statistical quality control.
• Excellent analytical, problem-solving, and decision-making skills.
• Exceptional leadership, communication, and interpersonal abilities.
• Proficiency in quality management software and ERP systems.
• Ability to work under pressure and meet strict deadlines in a highly regulated environment, based in **Abuja**.

Our client, a leading pharmaceutical manufacturer, is seeking an experienced and highly capable Pharmaceutical Production Manager to oversee operations in Benin City . This leadership role is critical for ensuring the efficient, safe, and compliant production of high-quality pharmaceutical products. The ideal candidate will have a strong background in GMP environments, a proven ability to manage production teams, and a deep understanding of manufacturing processes. This is a significant opportunity to lead a vital manufacturing function within a respected company, contributing directly to the availability of essential medicines and driving operational excellence.

• Manage and oversee all day-to-day production activities, ensuring adherence to production schedules, quality standards, and safety regulations.
• Lead, mentor, and develop a team of production supervisors and operators, fostering a culture of high performance and continuous improvement.
• Ensure compliance with all current Good Manufacturing Practices (cGMP) and relevant regulatory requirements.
• Develop, implement, and optimize production processes to improve efficiency, reduce costs, and enhance product quality.
• Manage production resources, including personnel, equipment, and materials, to meet production demands.
• Oversee equipment maintenance and calibration programs to ensure operational readiness and compliance.
• Investigate production deviations, implement corrective and preventive actions (CAPAs), and ensure effective root cause analysis.
• Collaborate with Quality Assurance, Quality Control, Engineering, and Supply Chain departments to resolve production issues and support product lifecycle management.
• Prepare and manage the production budget, ensuring cost-effective operations.
• Drive initiatives to enhance workplace safety and promote a strong safety culture within the production department.
• Monitor key performance indicators (KPIs) and implement strategies to achieve production targets.
• Ensure accurate and timely completion of all production batch records and documentation.

• Bachelor's degree in Pharmacy, Chemical Engineering, Industrial Engineering, or a related scientific or technical field. A Master's degree is a plus.
• Minimum of 6 years of progressive experience in pharmaceutical manufacturing, with at least 3 years in a supervisory or managerial role.
• In-depth knowledge of cGMP regulations and guidelines applicable to pharmaceutical manufacturing.
• Proven experience in managing production processes, equipment, and personnel in a fast-paced manufacturing environment.
• Strong leadership, team management, and motivational skills.
• Excellent problem-solving, decision-making, and analytical abilities.
• Proficiency in production planning, scheduling, and resource management.
• Experience with process validation, deviation management, and CAPA systems.
• Strong understanding of EHS (Environment, Health, and Safety) principles.
• Excellent communication, interpersonal, and documentation skills.

Our client offers a competitive salary and benefits package, including comprehensive health insurance, retirement plans, and performance-based bonuses. Employees benefit from extensive training programs, opportunities for professional development, and career advancement within a leading pharmaceutical company. This role offers the chance to significantly impact manufacturing operations and contribute to public health.

Our client, a leading pharmaceutical manufacturer, is seeking an experienced Pharmaceutical Manufacturing Supervisor to oversee operations at their facility in Calabar, Cross River, NG . This role is critical for ensuring the efficient, safe, and compliant production of high-quality pharmaceutical products. The Supervisor will lead a team of production operators, manage daily manufacturing activities, and ensure adherence to all Good Manufacturing Practices (GMP) and regulatory standards. This is an excellent opportunity for a motivated leader with a strong background in pharmaceutical production and a commitment to operational excellence. You will play a key role in optimizing production processes and maintaining the highest standards of quality and safety. We are looking for an individual who can motivate a team and drive continuous improvement in a demanding manufacturing environment.

• Supervise and coordinate the daily activities of the pharmaceutical production team.
• Ensure all manufacturing operations are conducted in compliance with GMP, SOPs, and safety regulations.
• Monitor production schedules and performance metrics, taking corrective actions as needed to meet targets.
• Train, coach, and develop production operators, ensuring they have the necessary skills and knowledge.
• Oversee the operation and maintenance of manufacturing equipment.
• Participate in deviation investigations and implement corrective and preventive actions (CAPAs).
• Ensure accurate and timely completion of batch records and other production documentation.
• Contribute to process improvement initiatives to enhance efficiency, yield, and quality.
• Maintain a safe working environment and promote a strong safety culture within the production team.
• Collaborate with other departments, including Quality Assurance, Quality Control, and Engineering.

• Bachelor's degree in Pharmacy, Chemical Engineering, Biotechnology, or a related field.
• Minimum of 4-6 years of experience in pharmaceutical manufacturing, with at least 2 years in a supervisory or team lead role.
• Thorough understanding of GMP, validation principles, and pharmaceutical manufacturing processes.
• Experience with various dosage forms and manufacturing technologies.
• Strong leadership, team management, and communication skills.
• Proven ability to troubleshoot and resolve production-related issues.
• Excellent organizational and time management skills.
• Proficiency in relevant documentation and record-keeping systems.
• Commitment to quality, safety, and continuous improvement.
• Experience in sterile manufacturing or solid dosage forms is a plus.

Our client offers a competitive salary, a performance-based bonus, and a comprehensive benefits package including health insurance, paid leave, and retirement benefits. We provide excellent opportunities for career advancement and professional development within a growing organization. The role is based at our modern manufacturing facility in Calabar, Cross River, NG . We foster a collaborative and supportive work environment where employee contributions are recognized and valued. Join us in producing high-quality medicines that improve lives.

Our client, a well-established pharmaceutical company, is seeking a dedicated Senior Pharmaceutical Manufacturing Specialist to join their production team in Makurdi, Benue, NG . This role is critical for ensuring the efficient and compliant manufacturing of high-quality pharmaceutical products. You will be responsible for overseeing various aspects of the production process, troubleshooting manufacturing issues, and contributing to process improvements. The ideal candidate will possess a strong understanding of pharmaceutical manufacturing operations, cGMP principles, and a commitment to operational excellence. We are looking for a detail-oriented individual with excellent technical skills and a proactive approach to problem-solving. This position offers an excellent opportunity for career growth within a respected organization known for its commitment to quality and innovation.

• Operate and maintain manufacturing equipment according to Standard Operating Procedures (SOPs) and cGMP guidelines.
• Monitor production processes, ensuring adherence to batch records and quality specifications.
• Troubleshoot and resolve manufacturing issues in a timely and effective manner.
• Participate in process validation and qualification activities.
• Contribute to the continuous improvement of manufacturing processes to enhance efficiency and reduce waste.
• Ensure a safe working environment by adhering to all safety protocols and procedures.
• Accurately document all manufacturing activities in batch records and production logs.
• Collaborate with Quality Assurance, Quality Control, and Engineering departments to address any production-related concerns.
• Train and mentor junior manufacturing staff as needed.
• Maintain inventory of raw materials and consumables required for production.

• Bachelor's degree in Pharmacy, Chemical Engineering, or a related scientific or technical field.
• Minimum of 5 years of experience in pharmaceutical manufacturing operations.
• Solid understanding of current Good Manufacturing Practices (cGMP) and pharmaceutical quality systems.
• Experience with various pharmaceutical manufacturing processes and equipment (e.g., granulation, tablet compression, capsule filling, sterile filling).
• Strong analytical and problem-solving skills.
• Ability to interpret technical documents, SOPs, and batch records.
• Excellent attention to detail and commitment to data accuracy.
• Effective communication and teamwork skills.
• Ability to work flexible shifts, including nights and weekends, if required.
• Willingness to undergo further training and development.

Our client offers a competitive salary and a comprehensive benefits package, including health insurance, retirement savings plans, and paid time off. We provide opportunities for professional development through ongoing training, workshops, and potential for advancement within the company. Our modern manufacturing facilities are located in Makurdi, Benue, NG . We foster a supportive and collaborative work environment. Join our client's dedicated production team and contribute to the manufacturing of essential pharmaceutical products.

• Supervise and provide leadership to pharmaceutical manufacturing teams, ensuring operational efficiency and adherence to production schedules.
• Oversee daily manufacturing activities, including production planning, scheduling, and resource allocation.
• Ensure strict compliance with cGMP, EHS, and other regulatory requirements in all manufacturing processes.
• Monitor production performance metrics, identify areas for improvement, and implement corrective actions.
• Collaborate with Quality Assurance to address deviations, conduct investigations, and implement CAPAs.
• Participate in process validation activities and ensure equipment is maintained and qualified.
• Develop and implement Standard Operating Procedures (SOPs) and manufacturing protocols.
• Foster a culture of continuous improvement, safety, and quality within the manufacturing department.
• Manage and mentor production staff, providing guidance and performance feedback.
• Communicate effectively with site-based teams, senior management, and other departments regarding production status and challenges.

• Bachelor's degree in Pharmacy, Chemical Engineering, or a related scientific/technical field.
• A minimum of 6 years of progressive experience in pharmaceutical manufacturing operations, with at least 2 years in a supervisory or leadership role.
• In-depth knowledge of cGMP regulations and pharmaceutical manufacturing processes (e.g., sterile production, solid dosage forms).
• Proven experience in leading manufacturing teams and driving operational excellence.
• Strong understanding of quality systems, deviation management, and CAPA implementation.
• Excellent leadership, communication, problem-solving, and decision-making skills.
• Ability to effectively manage and motivate teams remotely.
• Proficiency in manufacturing execution systems (MES) and ERP systems is desirable.
• Strong analytical skills and experience with process optimization techniques.

Our client, a reputable pharmaceutical manufacturer, is seeking an experienced and results-driven Pharmaceutical Production Supervisor to oversee and manage daily operations at their facility in Zaria, Kaduna . This hands-on role is essential for ensuring efficient, compliant, and high-quality production of pharmaceutical products. The ideal candidate will have a strong background in pharmaceutical manufacturing processes, a deep understanding of GMP, and exceptional leadership capabilities. This is an on-site position critical for direct supervision and operational excellence within our Zaria, Kaduna plant.

• Supervise and direct the day-to-day activities of the production team, ensuring adherence to production schedules and targets.
• Ensure all manufacturing activities comply with current Good Manufacturing Practices (cGMP), safety regulations, and company policies.
• Monitor production processes, identify potential issues, and implement corrective actions to maintain product quality and efficiency.
• Train and mentor production operators on standard operating procedures (SOPs), equipment operation, and quality standards.
• Oversee the accurate completion of production batch records and related documentation.
• Manage raw material and in-process material flow to ensure uninterrupted production.
• Implement and enforce safety procedures and promote a culture of safety awareness within the production area.
• Participate in process improvement initiatives to enhance productivity, reduce waste, and optimize operational costs.
• Conduct performance reviews for team members and identify training needs.
• Collaborate with Quality Assurance, Quality Control, Maintenance, and Engineering departments to resolve production-related issues.

• Bachelor's degree in Pharmacy, Chemical Engineering, Industrial Engineering, or a related scientific or technical field.
• Minimum of 4 years of progressive experience in pharmaceutical manufacturing, with at least 2 years in a supervisory or team lead capacity.
• In-depth knowledge of pharmaceutical manufacturing processes, equipment, and regulatory requirements (cGMP, FDA, NAFDAC).
• Proven ability to manage and motivate a production team effectively.
• Strong understanding of quality management systems and documentation practices.
• Excellent problem-solving, decision-making, and organizational skills.
• Proficiency in using manufacturing execution systems (MES) and enterprise resource planning (ERP) software is a plus.
• Effective communication and interpersonal skills.
• Ability to work flexible hours, including potential shifts, to meet production demands.
• Commitment to maintaining a safe and compliant manufacturing environment in Zaria, Kaduna .

Our client offers a competitive salary commensurate with experience, along with a comprehensive benefits package including health insurance, life insurance, and paid time off. Opportunities for professional development, continuous training, and career advancement within a growing organization are available. Employees will work in a modern manufacturing facility with opportunities to contribute to the production of vital pharmaceutical products. This role is based in Zaria, Kaduna , offering a stable and rewarding career opportunity.