Quality Control Officer

Shalina Healthcare

Supply Chain & Procurement

About Shalina Healthcare:

We are one of the largest, privately owned pharmaceutical businesses across Africa (Global Head Quarters- Dubai, UAE) with recent forays across multiple, new lines of businesses, viz., Digital Healthcare, Diagnostics, Consumer Healthcare, etc.

Over the last 40 years, operating across multiple geographies, 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 a broad range of therapeutic groups, including anti-malarial, antibiotics, anti-inflammatory, respiratory, gastrointestinal, nutrition, oral care, dermatology, sexual well-being, and antiseptic liquids & soaps. Leading brands, great teams and a focus on influencing the well-being of people have made Shalina a household name in Africa.

We have a track record few can match, and our brands are among the most trusted in Africa. We are proud of our history and have big ambitions for the future. Our vision for 2030 is to be the health champion of Sub-Saharan Africa. To achieve this, we are looking for the right people to join us and create a lasting impact not just within our company but on the communities that we serve; people who identify with our Core Values and are as passionate about our Mission as we are.

Website http://www.shalina.com/

Role : Quality Control Officer

Department: Quality

Reporting to : Head Quality

Location : Nigeria

Job Purpose:

To ensure that all raw materials, in-process materials, and finished products are tested according to approved specifications and meet quality standards, ensuring compliance with GMP, regulatory requirements, and company policies.

Key Responsibilities:

• Perform physical, chemical, and instrumental analysis of raw materials, packaging materials, in-process, and finished products.
• Ensure sampling, testing, and release are conducted in accordance with SOPs and cGMP requirements.
• Prepare and review test reports, COAs, and maintain accurate documentation.
• Calibrate and operate laboratory instruments such as HPLC, UV-Vis Spectrophotometer, FTIR, pH meter, etc.
• Participate in method validation, method transfer, and stability studies.
• Conduct environmental and water testing as required.
• Report and investigate OOS (Out of Specification) and OOT (Out of Trend) results.
• Maintain laboratory cleanliness and ensure safety practices are followed.
• Support internal and external audits and implement corrective/preventive actions (CAPAs).
Collaborate with Production, QA, and other departments to resolve quality-related issues.

Qualifications and Experience:

• B.Sc. or HND in Chemistry, Biochemistry, Microbiology, or related sciences.
• 2–5 years of relevant QC experience in a pharmaceutical manufacturing environment.
• Good knowledge of cGMP, GLP, and regulatory guidelines (e.g., NAFDAC, WHO, FDA).
Experience with analytical instruments like HPLC, UV, FTIR, etc.

Key Skills and Competencies:

• Attention to detail and accuracy.
• Strong analytical and problem-solving skills.
• Good documentation and communication skills.
• Proficiency in Microsoft Office tools.
• Ability to work independently and as part of a team.
Time management and ability to handle multiple tasks.

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