Pharmaceutical Quality Control Manager Job Vacancy in Tema, Ghana – Pharmaceutical Manufacturing

Job Description

Position: Pharmaceutical Quality Control Manager

Company: Pfizer Ghana Limited

Location: Tema, Ghana

Experience: Minimum 8 years in pharmaceutical quality control, with at least 3 years in a managerial role

Education: Master’s degree in Pharmaceutical Sciences, Chemistry, Biochemistry, or related field

Employment Type: Full-time

Industry: Pharmaceutical Manufacturing

Department: Quality Assurance & Control

Vacancies:1

Company Overview

Pfizer Ghana Limited is a leading global biopharmaceutical company committed to applying science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety, and value in the discovery, development, and manufacture of healthcare products. Our global portfolio includes medicines and vaccines as well as many of the world’s best-known consumer healthcare products. In Ghana, our Tema manufacturing facility is a state-of-the-art production center that serves both the local market and exports to neighboring countries, adhering to the highest international standards including WHO-GMP, FDA, and EMA regulations. We are dedicated to creating a diverse and inclusive workplace and believe in empowering our employees to develop their careers while making a meaningful impact on public health in Ghana and across Africa.

As part of our commitment to Ghana, we invest significantly in local talent development, community health initiatives, and sustainable manufacturing practices. Our Tema facility represents one of the most advanced pharmaceutical manufacturing plants in West Africa, equipped with cutting-edge laboratory instrumentation and production technology. We are currently seeking a highly qualified Pharmaceutical Quality Control Manager to lead our quality control laboratory and ensure the integrity of our life-saving products. This role represents a significant career opportunity in Ghana within a globally respected organization that values scientific excellence and patient safety above all else.

Job Overview

The Pharmaceutical Quality Control Manager will be responsible for overseeing all quality control activities at our Tema manufacturing facility, ensuring that all raw materials, in-process materials, and finished products meet established specifications and regulatory requirements. This leadership role involves managing a team of quality control analysts and technicians, maintaining laboratory equipment and systems, and implementing continuous improvement initiatives to enhance laboratory efficiency and compliance. The successful candidate will play a critical role in maintaining our license to operate and ensuring patient safety through rigorous quality standards.

This position offers an exceptional opportunity for professional growth within a global pharmaceutical leader while contributing directly to healthcare outcomes in Ghana. The manager will interface with regulatory authorities, participate in audits and inspections, and collaborate with production, quality assurance, and supply chain teams to resolve quality issues and implement corrective actions. We are looking for a strategic thinker with strong technical expertise and leadership capabilities who can drive excellence in our quality control operations. For more jobs in Ghana across various sectors, visit our partner site at https://ghanajobsearch.com.

Key Responsibilities

• Lead and manage the quality control laboratory team, including hiring, training, and performance management of analysts and technicians.
• Develop, implement, and maintain quality control procedures, test methods, and specifications in compliance with cGMP, WHO, FDA, and other regulatory requirements.
• Oversee the testing and release of raw materials, packaging materials, in-process samples, and finished pharmaceutical products.
• Manage laboratory investigations, out-of-specification (OOS) results, and deviations, ensuring thorough root cause analysis and effective corrective/preventive actions.
• Maintain laboratory equipment qualification, calibration, and maintenance programs to ensure reliable analytical results.
• Prepare and review quality control documentation, including test records, certificates of analysis, and stability data.
• Participate in regulatory inspections and customer audits, addressing findings and implementing required improvements.
• Develop and manage the laboratory budget, including forecasting resource needs and controlling operational expenses.
• Implement continuous improvement initiatives to enhance laboratory efficiency, data integrity, and compliance.
• Collaborate with quality assurance, production, and supply chain departments to resolve quality issues and support new product introductions.

Required Skills

• Expert knowledge of pharmaceutical analytical techniques including HPLC, GC, UV-Vis spectroscopy, dissolution testing, and microbiological methods.
• Thorough understanding of cGMP, WHO-GMP, ICH guidelines, and pharmaceutical regulatory requirements.
• Strong leadership and team management capabilities with proven ability to develop technical staff.
• Excellent problem-solving and decision-making skills with attention to detail and accuracy.
• Proficient in laboratory information management systems (LIMS) and electronic documentation systems.
• Effective communication and interpersonal skills for collaborating with cross-functional teams and regulatory authorities.
• Project management skills with ability to prioritize multiple tasks and meet deadlines in a fast-paced environment.
• Knowledge of statistical quality control tools and data analysis techniques.
• Commitment to continuous learning and staying current with evolving regulatory expectations and analytical technologies.

Education

A Master’s degree in Pharmaceutical Sciences, Chemistry, Biochemistry, or a related scientific field is required. A PhD in a relevant discipline would be advantageous. Additional certifications in quality management, laboratory management, or regulatory affairs are highly desirable. Candidates must demonstrate comprehensive knowledge of pharmaceutical analysis, quality systems, and regulatory requirements applicable to pharmaceutical manufacturing in Ghana and internationally.

Experience

Minimum of 8 years of progressive experience in pharmaceutical quality control, with at least 3 years in a managerial or supervisory role within a GMP-regulated environment. Experience must include hands-on analytical testing, method validation, laboratory investigations, and regulatory inspections. Previous experience in managing a quality control laboratory in a pharmaceutical manufacturing setting is essential. Familiarity with African regulatory requirements and experience working in multinational pharmaceutical companies will be considered strong advantages.

Benefits

• Competitive salary package with performance-based bonuses
• Comprehensive health insurance for employee and dependents
• Retirement savings plan with company matching contributions
• Professional development opportunities and continuing education support
• Annual leave with travel allowance for international employees
• Relocation assistance for candidates moving to Tema
• Employee assistance program and wellness initiatives
• Opportunities for international assignments and career advancement within Pfizer’s global network

Training

• Comprehensive onboarding program covering Pfizer’s quality systems and procedures
• Regular technical training on new analytical methods and equipment
• Leadership development programs for managerial skills enhancement
• Regulatory compliance training on evolving requirements
• Cross-functional training opportunities in related departments
• Access to Pfizer’s global learning management system with thousands of courses
• Sponsorship for relevant professional certifications and conferences

Working Environment

The Pharmaceutical Quality Control Manager will work in a modern, climate-controlled laboratory environment within our Tema manufacturing facility. The role requires adherence to strict safety protocols and gowning requirements in certain laboratory areas. The position involves regular interaction with manufacturing personnel, quality assurance colleagues, and regulatory professionals. Some flexibility in work hours may be required to support manufacturing schedules and address urgent quality issues. The facility maintains the highest standards of cleanliness and organization, with state-of-the-art equipment and systems to support efficient operations.

Application Process

Interested candidates should submit a detailed CV and cover letter through our online application portal. Applications will be reviewed on a rolling basis until the position is filled. Only shortlisted candidates will be contacted for interviews. The selection process may include technical assessments, panel interviews, and reference checks. Pfizer Ghana Limited is committed to a fair and transparent recruitment process that identifies the most qualified candidates based on merit and fit for the role.

For additional employment in Ghana opportunities in various industries, please explore https://rwandajobsearch.com/job-vacancy-in-rwanda/.

Equal Opportunity Statement

Pfizer Ghana Limited is an equal opportunity employer committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by Ghanaian law. This policy applies to all employment practices within our organization, including hiring, promotion, termination, and compensation. We make hiring decisions based solely on qualifications, merit, and business needs at the time.

Discover more about hiring in Ghana across different sectors by visiting https://somaliajobsearch.com/job-vacancy-in-mogadishu/.