Shalina Healthcare is one of the largest pharmaceutical companies in sub-Saharan Africa. For the last 35 years, we have made it our mission to provide quality medicines to those who need it the most. We manufacture and distribute branded prescription and over-the-counter pharmaceutical and consumer products across various therapeutic groups, including anti-malarial, antibiotics, anti-inflammatory, and nutrition. We have a track record few can match and our brands are among the most trusted in Africa.

We are recruiting to fill the position below:

Job Title: Associate Manager – Quality Assurance (External Manufacturing)

Job ID: JOB-686
Location: Ogun

Job Description

• The Associate Manager – Quality Assurance (External Manufacturing) is responsible for overseeing and ensuring compliance of all externally manufactured pharmaceutical products with regulatory requirements, company quality standards, and GMP guidelines.
• This role involves managing contract manufacturing organizations (CMOs), conducting audits, reviewing documentation, and ensuring product quality throughout the supply chain.

Key Responsibilities
External Manufacturing Oversight:

• Ensure all contract manufacturers comply with GMP, regulatory, and company quality standards.
• Act as the primary QA contact for all external manufacturing partners.

Vendor Qualification & Audits:

• Perform qualification, requalification, and periodic audits of CMOs, suppliers, and service providers.
• Prepare audit reports and follow up on corrective and preventive actions (CAPAs).

Batch Documentation & Release:

• Review and approve batch manufacturing records, analytical reports, and related documents from CMOs.
• Support or authorize batch release in compliance with regulatory requirements.

Quality Systems Management:

• Ensure implementation of quality systems at external sites (deviations, change controls, CAPA, OOS/OOT).
• Monitor and track quality metrics for external manufacturing operations.

Regulatory Compliance:

• Ensure products meet NAFDAC, WHO, and other applicable regulatory requirements.
• Support regulatory submissions and inspections related to external manufacturing.

Deviation & Investigation Handling:

• Review and approve deviations, investigations, and CAPAs from external partners.
• Ensure timely closure and effectiveness of corrective actions.

Change Control Management:

• Evaluate and approve changes related to materials, processes, and equipment at CMOs.
• Assess impact on product quality and regulatory compliance.

Qualifications

• Experience: 8–10 years of experience in Quality Assurance within the pharmaceutical industry
• Experience with external manufacturing or contract manufacturing organizations (CMOs) is highly preferred

Skills & Competencies:

• Strong knowledge of GMP, GDP, and regulatory requirements (NAFDAC, WHO,)
• Experience in auditing and vendor management
• Excellent documentation review and attention to detail
• Strong analytical and problem-solving skills
• Effective communication and stakeholder management
• Ability to work independently and manage multiple priorities

Application Closing Date
Nof Specified.