IPQC Officer at Shalina Healthcare


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Shalina Healthcare is a market leader in making quality healthcare products affordable and available across Africa. We achieve this by sourcing from WHO-approved production facilities in India and China and by focusing on our first-class distribution expertise. Shalina Healthcare is privately owned and part of the Shalina Group.

Experience1 – 3 years
Location Ogun

Job Summary:

  • To ensure that in-process materials and production processes comply with GMP standards and defined specifications by carrying out routine inspections and sampling during production activities.

Key Responsibilities

  • Conduct in-process quality checks on manufacturing activities including granulation, compression, coating, filling, and packaging processes.
  • Monitor critical process parameters and ensure adherence to approved batch manufacturing records (BMR) and standard operating procedures (SOPs).
  • Perform sampling and testing of in-process materials (e.g., weight variation, hardness, friability, disintegration time, leak test, etc.).
  • Ensure line clearance before the start of any batch or product changeover.
  • Report any deviations or non-conformities observed during the process to the QA/QC Supervisor or Manager.
  • Ensure proper segregation, labeling, and handling of in-process and intermediate materials.
  • Maintain accurate and timely documentation of observations and test results.
  • Assist in the investigation of process deviations and support CAPA implementation.
  • Ensure compliance with cGMP, safety, and hygiene standards during operations.
  • Participate in routine training on GMP and SOPs.
  • Support continuous improvement initiatives in quality and production operations.

Qualifications and Experience

  • B.Sc / HND in Chemistry, Biochemistry, Microbiology, Industrial Chemistry, or related science discipline.
  • 1–3 years of experience in IPQC or a related quality role in a pharmaceutical manufacturing environment.
  • Good knowledge of cGMP, in-process testing procedures, and pharmaceutical manufacturing operations.
  • Familiarity with regulatory requirements (e.g., NAFDAC, PCN is an advantage.

Key Skills & Competencies

  • Strong attention to detail and observation skills.
  • Ability to work independently and as part of a team.
  • Excellent written and verbal communication.
  • Good documentation and record-keeping skills.
  • Ability to work under pressure and in a fast-paced environment.
  • Proficient in MS Office applications (Word, Excel, etc.).

Method of Application

Interested and qualified candidates should send a recent copy of their CV to: [email protected] using the Job Title as the subject of the email.

Closing date: Not specified

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