Pharmaceutical Quality Assurance Manager Job Vacancy in Yei, South Sudan – Healthcare Manufacturing
Job Description
Position:Pharmaceutical Quality Assurance Manager
Company:Pfizer
Location:Yei, South Sudan
Experience:5-8 years
Education:Bachelor’s Degree in Pharmacy, Chemistry, or related field
Employment Type:Full-time
Industry:Healthcare Manufacturing
Department:Quality Assurance
Vacancies:1
Company Overview
Pfizer is a global biopharmaceutical company with a mission to deliver breakthroughs that change patients’ lives. With a rich history spanning over 170 years, we have been at the forefront of medical innovation, developing medicines and vaccines that have transformed healthcare worldwide. Our presence in South Sudan represents our commitment to improving health outcomes in emerging markets and ensuring access to high-quality pharmaceutical products. We operate with the highest standards of quality, integrity, and patient safety, making us a trusted partner in healthcare systems globally. Our Yei facility is a state-of-the-art manufacturing plant that produces essential medicines while adhering to international regulatory standards.
Job Overview
We are seeking a dedicated Pharmaceutical Quality Assurance Manager to oversee all quality assurance activities at our Yei manufacturing facility. This critical role ensures that all pharmaceutical products manufactured meet the highest standards of quality, safety, and efficacy. The successful candidate will be responsible for implementing and maintaining quality systems, conducting audits, and ensuring compliance with both local regulations and international standards. This position offers an excellent opportunity for professionals looking to advance their career in pharmaceutical quality assurance while contributing to healthcare improvement in South Sudan. For more South Sudan Jobs and career opportunities, visit https://southsudanjobsearch.com. Discover additional Employment in South Sudan possibilities at https://www.botswanajobsearch.com/.
Key Responsibilities
- Develop, implement, and maintain quality assurance systems and procedures
- Conduct regular internal audits and manage external regulatory inspections
- Review and approve manufacturing batch records and quality control data
- Investigate quality deviations and implement corrective and preventive actions
- Manage quality documentation systems including SOPs, specifications, and validation protocols
- Ensure compliance with Good Manufacturing Practices (GMP) and regulatory requirements
- Train and mentor quality assurance staff on quality systems and procedures
- Collaborate with production and quality control departments to maintain product quality
- Manage product quality reviews and stability studies
- Handle quality-related customer complaints and implement improvements
Required Skills
- Strong knowledge of pharmaceutical GMP regulations and quality systems
- Excellent analytical and problem-solving abilities
- Proven leadership and team management skills
- Effective communication and interpersonal skills
- Attention to detail and commitment to quality excellence
- Ability to work under pressure and meet tight deadlines
- Proficiency in quality management software and documentation systems
- Strong decision-making and risk assessment capabilities
Education
Bachelor’s degree in Pharmacy, Chemistry, Pharmaceutical Sciences, or related field. Advanced degrees or professional certifications in quality assurance are highly desirable. Continuous professional development in pharmaceutical quality management is expected.
Experience
Minimum 5 years of experience in pharmaceutical quality assurance, with at least 2 years in a supervisory or management role. Experience in pharmaceutical manufacturing environment and familiarity with international quality standards is essential. Previous experience in emerging markets is an advantage.
Benefits
- Competitive salary package with performance bonuses
- Comprehensive health insurance for employee and family
- Professional development and training opportunities
- Retirement benefits and savings plan
- Paid time off and holiday benefits
- Relocation assistance for qualified candidates
- Opportunities for international career advancement
Training
- Comprehensive onboarding program
- Regular GMP and quality management training
- Leadership development programs
- Technical skills enhancement workshops
- Regulatory compliance updates
- Cross-functional training opportunities
Working Environment
Our Yei facility offers a modern, safe, and professional working environment with state-of-the-art equipment and technology. We maintain a culture of excellence, innovation, and continuous improvement. The workplace promotes collaboration, professional growth, and work-life balance while adhering to the highest safety and quality standards.
Application Process
Interested candidates should submit their application through our online portal. The selection process includes resume screening, technical assessments, and multiple interview rounds. Only shortlisted candidates will be contacted for further evaluation.
Equal Opportunity Statement
Pfizer 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, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
