Posted on Mon 19th May, 2025 - hotnigerianjobs.com --- (0 comments)
Nalis Pharmaceuticals Limited is a Nigerian private limited liability company, founded in 2010 and incorporated by the Corporate Affairs Commission (CAC) in 2011. The company was established by Engr. Obinna Magnus Onwunali, a visionary entrepreneur and engineer who followed in the footsteps of his late father, a chemist and business owner who operated in Irete, Imo State. Inspired by this legacy, Engr. Onwunali set out to build a company committed to quality, innovation, and service in Nigeria’s growing pharmaceutical industry.
We are recruiting to fill the position below:
Job Title: Quality Assurance Manager
Location: Nigeria
Employment Type: Full-time
Job Summary
The Quality Assurance Manager holds the critical role of ensuring that all pharmaceutical products meet stringent regulatory and internal quality standards.
This role demands vigilance, scientific rigor, and leadership to maintain compliance with cGMP, WHO, NAFDAC, and international regulatory bodies.
The QA Manager is the company’s final defense against compromise, safeguarding product integrity, patient safety, and company reputation.
Key Responsibilities
Quality Management System (QMS):
Develop, implement, and maintain QMS in alignment with regulatory standards (NAFDAC, WHO-GMP, ISO 9001).
Ensure continuous improvement of QMS through regular audits and management reviews.
Compliance & Documentation:
Oversee compliance with cGMP, GLP, and SOPs across production, QC, and packaging lines.
Ensure accurate and timely documentation, batch record reviews, deviations, and change controls.
Audits & Inspections:
Lead internal audits, host external audits (regulatory bodies, clients), and manage CAPAs.
Prepare the site for regulatory inspections and ensure timely closure of observations.
Process & Product Oversight:
Monitor validation of processes, cleaning, and equipment.
Oversee product release based on conformance to specifications.
Training & Leadership:
Train and mentor QA personnel and cross-functional teams on quality systems and cGMP updates.
Foster a culture of quality and ownership across all departments.
Vendor & Supplier Quality:
Evaluate and audit raw material suppliers and third-party contractors.
Ensure traceability and quality of materials throughout the supply chain.
Educational Qualifications
Bachelor’s Degree in Pharmacy (B.Pharm), Pharmaceutical Sciences, Microbiology, Biochemistry, or related field.
Advanced degrees (M.Sc., MBA) in Quality Management or Regulatory Affairs are an advantage.
Certification in ISO 9001:2015, Six Sigma, or cGMP is highly desirable.
Experience:
Minimum 5 - 7 years of relevant experience in QA/QC in a pharmaceutical manufacturing environment.
At least 2 years in a supervisory or managerial role.
Proven experience managing regulatory inspections and internal audits.
Familiarity with sterile and non-sterile production environments is a plus.
Other Requirements:
Must be registered with relevant professional bodies (e.g., PCN, NAFDAC-recognised body).
Must be conversant with national and international pharmaceutical laws and regulations.
Must exhibit ethical integrity and professional discretion.
Flexibility to work extended hours when required.
Strong leadership presence and ability to make high-stakes decisions under pressure.
Required Skills and Competencies:
Deep knowledge of current Good Manufacturing Practices (cGMP), quality control principles, and pharmaceutical regulations.
Strong analytical and problem-solving skills.
High attention to detail and documentation accuracy.
Excellent communication and interpersonal skills.
Proficiency in Quality Management Software and ERP systems (e.g., Odoo, SAP, TrackWise).
Ability to lead under pressure and drive cross-functional coordination.
Root Cause Analysis (RCA) and risk management expertise.
Salary
Salary: 2,400,000 - 3,600,000 annually.
Competitive and commensurate with experience.
Application Closing Date
31st May, 2025.
How to Apply
Interested and qualified candidates should send their Resume and Cover Letter to:kadiri.abraham@nalispharma.comusing the Job Title as the subject of the mail.
Note: For Inquiries, call 07048154533 for more details.