Job Openings at Emzor Pharmaceuticals Limited

Emzor Pharmaceuticals Limited is recruiting suitable candidates to fill the following positions below:

1.) Team Lead, Validation (Quality Assurance)

Job Location: Sagamu, Ogun
Employment Type: Full-time

Job Purpose

• To lead and coordinate all validation activities (equipment, utilities, processes, cleaning, and analytical methods) in compliance with cGMP, regulatory standards, and Emzor’s internal quality systems, ensuring that all systems perform as intended and produce consistent, high-quality products.

Key Responsibilities

• Develop and execute validation protocols (IQ, OQ, PQ) for equipment, facilities, utilities, cleaning, and processes.
• Review and approve validation master plans, protocols, reports, and risk assessments.
• Plan and lead periodic revalidation activities and maintain a validation calendar.
• Ensure compliance with local and international regulatory guidelines (e.g., WHO, NAFDAC, FDA, EU GMP) on validation.
• Coordinate and supervise validation team members, providing guidance and technical support.
• Collaborate with production, QA, QC, engineering, and regulatory departments to ensure validation requirements are integrated into project plans.
• Lead investigations and risk assessments for deviations and non-conformances related to validation.
• Maintain accurate and complete validation documentation and ensure timely archiving.
• Train personnel involved in validation and ensure adherence to validation protocols and SOPs.
• Prepare and support internal and external audits and regulatory inspections related to validation activities.

Qualifications and Experience

• Bachelor's Degree in Pharmacy, Engineering, Industrial Chemistry, or other relevant life science or technical discipline.
• Minimum of 5 years’ experience in pharmaceutical validation with at least 2 years in a lead or supervisory role.
• Hands-on experience with validation of HVAC systems, manufacturing equipment, cleaning procedures, utilities, and analytical methods.
• Strong knowledge of current Good Manufacturing Practices (cGMP), validation life cycle, and applicable regulatory guidelines.
• Experience in preparing for audits by NAFDAC, WHO, and other regulatory bodies.

Key Skills and Attributes:

• Strong project planning and coordination skills
• Excellent technical writing and documentation skills
• Attention to detail and a methodical approach
• Strong leadership and team management abilities
• Effective communication and interpersonal skills
• Analytical thinking and problem-solving mindset
• High integrity and commitment to quality and compliance

Application Closing Date: 10th June, 2025.

Method of Application
Interested and qualified candidates should send their CV and Cover Letter to: recruitment@emzorpharma.com using "Application for Team Lead, Validation" as the subject of the mail.

Note: Only shortlisted candidates will be contacted.

2.) Team Lead, Documentation (Quality Assurance) 

Job Location: Sagamu, Ogun
Employment Type: Full-time

Job Summary

• To lead the documentation team in ensuring accurate, compliant, and timely documentation of all quality-related processes and activities in line with cGMP and regulatory standards, supporting manufacturing, quality control, and quality assurance operations.

Key Responsibilities

• Oversee the preparation, review, issuance, and archiving of all GMP documents including SOPs, batch manufacturing records (BMR), batch packaging records (BPR), protocols, reports, and logbooks.
• Ensure all documents are current, version-controlled, and distributed appropriately in compliance with regulatory and internal requirements.
• Coordinate periodic reviews and updates of controlled documents to reflect operational and regulatory changes.
• Train and guide documentation officers and other relevant personnel on documentation procedures and compliance expectations.
• Liaise with QA, QC, Production, Regulatory Affairs, and other departments to ensure seamless documentation flow.
• Maintain a robust documentation system (manual or electronic) to support traceability and data integrity.
• Support internal and external audits by ensuring availability and retrieval of requested documents.
• Monitor and ensure compliance with documentation-related SOPs across departments.
• Lead and support initiatives on continuous improvement in documentation practices.
• Ensure timely closure of documentation-related deviations, CAPAs, and change controls.

Qualifications and Experience

• Bachelor's Degree in Pharmacy, Chemistry, Microbiology, or a related life science field.
• Minimum of 5 years of experience in pharmaceutical documentation, with at least 2 years in a supervisory or lead role.
• Good understanding of cGMP, GDP (Good Documentation Practices), and regulatory expectations (NAFDAC, WHO, FDA, etc.).
• Proficiency in MS Office and documentation management systems.
• Experience in audits and regulatory inspections is an added advantage.

Key Skills and Attributes:

• Attention to detail and accuracy
• Strong organisational and time management skills
• Excellent written and verbal communication
• Leadership and team coordination abilities
• Analytical thinking and problem-solving skills
• High level of integrity and professionalism.

Application Closing Date: 10th June, 2025.

Method of Application
Interested and qualified candidates should send their CV to: recruitment@emzorpharma.com using "Application for Team Lead, Documentation" as the subject of the mail.

Note: Only shortlisted candidates will be contacted.

3.) Quality Control Supervisor

Job Location: Sagamu, Ogun
Employment Type: Full-time

Responsibilities

• Chemical analysis of all raw materials and document results.
• Chemical analysis of all intermediate/finished products and document results.
• Chemical analysis of stability samples.
• Sampling operations in QC laboratory
• Developing laboratory analytical procedures and validating them.
• Generation of analytical summary report sheets for all raw materials and intermediate/finished products
• Generation of standard operating and testing procedures.
• Adhere to ALL health and safety guidelines.
• Generating reports for equipment qualification, process and methods validation and/or verification
• Clarifying discrepancies in the area of quality control including operating an error prevention system
• Monitoring to ensure that all personnel in the area of quality control take part in the regular trainings
• Participate in internal audits/self-inspections and close out non conformities
• Routine qualification of secondary standards
• Out of specification and out of trend investigation
• Training of IT students, corps members and Interns

Requirements

• B.Sc, HND or equivalent in Chemistry, Industrial Chemistry, Science Laboratory Technology (chemistry option), Biochemistry, Chemistry Education, Pharmaceutical Chemistry or Pharmaceutical Technology with minimum of 1 year of experience (with NYSC inclusive).

Application Closing Date: 23rd June, 2025.

Method of Application
Interested and qualified candidates should send their CV to: recruitment@emzorpharma.com using the Job Position as the subject of the mail.