Nalis Pharmaceuticals Limited | Full-time

QUALITY ASSURANCE MANAGER

Nigeria | Posted on 19/05/2025

About Company:

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 Description:

  • 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.

Requirements:

  • 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.

Qualifications and Skills:

  • 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

Application Instructions:

Interested and qualified candidates should send their Resume and Cover Letter to: kadiri.abraham@nalispharma.com using the Job Title as the subject of the mail.

Note: For Inquiries, call 07048154533 for more details.



Click here to Apply

Job Information

Deadline

31/05/2025

Job Type

Full-time

Industry

Pharmaceutical

Work Level

Experienced

State

Nigeria

Country

Nigeria

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