Job Vacancies at Emzor Pharmaceutical Industries

LOCATION:     Mainland, Lagos State

The hiring company is a leading pharmaceutical company in Nigeria, dedicated to providing premium, affordable medical treatments. We have been manufacturing pharmaceuticals and health products for over 40 years. We aim to promote \'unlimited wellness\' by offering innovative, long-lasting medical solutions.

SUMMARY OF RESPONSIBILITIES·

• Controlling production processes and production facilities to ensure that manufacturing activities are in conformity with the cGMP and safety requirements.
• Participating in planning and organizing the manufacturing activities of the Solids plant.
• Implementing Operations manuals, production plans and programs.
• Ensuring that process delays, which affect production output, are swiftly resolved.
• Allocating work, supervise employees and control production
• Minimizing wastages.
• Ensuring availability of adequate raw and packing materials, utilities and machine size parts.
• Executing the weekly and monthly production plans according to the schedule.
• Ensuring the general cleanliness and hygienic conditions of the manufacturing areas and production personnel.
• Supervising duties of subordinates, operators and rest of workers and ensures discipline and good working culture among the staff.

Qualifications

• Bachelor’s Degree in Pharmacy
• Pharmacist annual license.
• 8 years of relevant pharmaceutical manufacturing experience.
• Knowledgeable in regulatory requirement; WHO, ICH, FDA, GAMP, ISO, USP, BP, EU.

A Few Required Competencies:

• Excellent leadership Skills
• Team work.
• Problem Solving.
• Good communication.
• Good decision making.

What we Offer:

• Competitive salary and performance bonus.
• A dynamic work environment that fosters career development and growth opportunities.
• Medical insurance and retirement benefits, etc.

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SUMMARY OF RESPONSIBILITIES

• Manages and maintains a database for the quality system and prepares/assists in the preparation of monthly and annual reports and quality trending reports
• Reports the status of the quality levels of staff, systems and production activities and participates in improvement program
• Participates in the evaluation of quality events, incidents and possible complaints and the follow-up activities.
• Keep up to date with all related quality legislation and compliance issues
• Coordination of Staff GMP Training
• Handling of obsolete/rejected raw and packaging materials
• Management of deviations and non-conformities in production processes and follow up on CAPA
• Manage internal and external audit programmes which includes preparing CAPA plans and close out of compliance directives
• Writing, reviewing, distributing and filing of completed Quality Management System documents.
• Handling of Product Complaint and reporting on investigations carried out and submission of investigation report

Qualifications

• Bachelor’s Degree in Industrial Chemistry
• A Master’s Degree in Environmental Management.
• 10 years of relevant pharmaceutical manufacturing experience.

A Few Required Competencies:

• Team work.
• Problem Solving.
• Good communication.
• Good decision making.

What we Offer:

• Competitive salary and performance bonus.
• A dynamic work environment that fosters career development and growth opportunities.
• Medical insurance and retirement benefits, etc.