Pharmacist at Sagar Vitaceuticals Nigeria Limited


Posted on: Wed 09-09-2026

Sagar Vitaceuticals Nigeria Limited formerly known as Strides Vital Nigeria Limited was a strategic partnership comprising Vital Pharmaceuticals Ltd and India’s Strides Arcolabs Ltd,a NSE listed company. In 2017, Management of Sagar Overseas Limited, acquired 100% shares in Strides Vital Nigeria Limited and the company was re-named to Sagar Vitaceuticals N...

We are  recruiting to fill the position below:

Job Title: Pharmacist

Locations: Ikeja, Lagos and Makun, Sagamu - Ogun

Employment Type: Full-time

Reports To: Pharmacy Manager / Managing Director

 

Job Summary

  • The Pharmacist is responsible for supporting the development, manufacturing, quality assurance, regulatory compliance, and distribution of pharmaceutical products.
  • The role ensures that all products meet regulatory requirements, Good Manufacturing Practice (GMP) standards, and company quality policies while promoting patient safety and product effectiveness.
  • A pharmacist in a pharmaceutical company is responsible for ensuring that medicines are developed, manufactured, tested, stored, and distributed in compliance with regulatory standards while maintaining product quality, safety, and efficacy.

Key Responsibilities

  • Ensure compliance with Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and applicable pharmaceutical regulations.
  • Supervise and monitor the manufacturing process to ensure products meet quality standards.
  • Review and approve batch manufacturing and packaging records.
  • Conduct quality assurance and quality control activities, including reviewing test results and investigating deviations.
  • Monitor product stability and ensure proper storage and handling of pharmaceutical products.
  • Prepare and maintain accurate documentation in accordance with regulatory requirements.
  • Participate in internal and external audits and implement corrective and preventive actions (CAPA).
  • Support product registration, licensing, and regulatory submissions.
  • Investigate customer complaints, product defects, and recalls when necessary.
  • Provide technical guidance and training to production and quality personnel.
  • Collaborate with research and development, production, engineering, and regulatory teams during product development and commercialization.
  • Ensure compliance with health, safety, and environmental policies.
  • Keep up to date with changes in pharmaceutical regulations and industry best practices.

Key Performance Indicators (KPIs)

  • Compliance with GMP and regulatory standards.
  • Reduction in manufacturing deviations and quality incidents.
  • Successful completion of audits with minimal observations.
  • Timely completion of documentation and batch record reviews.
  • Product quality and customer satisfaction.
  • Effective implementation of corrective and preventive actions (CAPA).

Requirements

  • Bachelor of Pharmacy (B.Pharm) or Doctor of Pharmacy (Pharm.D.).degree from a recognized institution.
  • Valid pharmacist license / registration with the appropriate regulatory authority.
  • 2- 8 years of experience in pharmaceutical manufacturing, quality assurance, quality control, or regulatory affairs is preferred.
  • Knowledge of GMP, GDP, GLP, and pharmaceutical quality systems.
  • Strong analytical and problem - solving skills.
  • Excellent communication and teamwork abilities.
  • Proficiency in Microsoft Office and pharmaceutical documentation systems.

Key Skills:

  • Pharmaceutical manufacturing.
  • Quality assurance and quality control.
  • Regulatory compliance.
  • Documentation and record management.
  • Risk assessment and problem-solving.
  • Attention to detail.
  • Time management.
  • Leadership and teamwork.
  • Communication and presentation skills.

Working Conditions:

  • Work is primarily performed in manufacturing plants, laboratories, offices, or warehouse environments.
  • May require the use of personal protective equipment (PPE).
  • May involve shift work depending on production schedules.

Application Closing Date

9th October, 2026.

 

Method of Application

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