Animal care Services Konsult Nig. Ltd is a foremost operator in the livestock industry, we are into the business of Commercial Poultry production, procurement and Marketing of Livestock Products such as feed, Premix, Poultry products, vaccines & Biotechnology products, technical laboratory and intallation of new cages and repair/maintenance of cages of all kinds. We are a dynamic and fast growing company that that combines a resourceful management team with young, result-oriented and highly motivated staff with a vision to emerge as a leader in the nation's agro-allied industry.
We are recruiting to fill the position below:
Job Title: Production Laboratory Manager
Location: Ogere Remo, Ogun
Employment Type: Full-time
Job Summary
We are seeking an experienced and highly motivated Technical Laboratory Production Manager to oversee the manufacturing operations of our animal health vaccines and drugs production facility.
The ideal candidate will ensure that production processes are efficient, compliant with regulatory standards, and aligned with company goals.
The Production Manager will be responsible for managing production schedules, optimizing workflows, leading a team of production staff, and ensuring the highest standards of quality and safety.
Key Responsibilities
Production Management:
Plan, organize, and oversee daily production activities to meet production targets and deadlines.
Ensure efficient utilization of resources, including personnel, equipment, and materials.
Monitor production processes to ensure compliance with Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and regulatory requirements.
Implement and maintain production schedules to meet customer demand and inventory requirements.
Quality Assurance and Compliance:
Ensure all products are manufactured in compliance with regulatory standards (e.g., FDA, EMA, USDA) and company quality policies.
Collaborate with the Quality Assurance (QA) team to resolve any production-related quality issues.
Conduct regular audits and inspections to ensure adherence to GMP and other regulatory guidelines.
Maintain accurate production records and documentation for regulatory submissions and audits.
Team Leadership and Development:
Lead, mentor, and motivate a team of production supervisors, technicians, and operators.
Conduct performance evaluations, provide feedback, and identify training needs to enhance team skills.
Foster a culture of safety, quality, and continuous improvement within the production team.
Process Optimization and Continuous Improvement:
Identify opportunities to improve production efficiency, reduce waste, and optimize workflows.
Implement lean manufacturing principles and other process improvement methodologies.
Collaborate with the R&D and Engineering teams to scale up new products and processes.
Health, Safety, and Environmental Compliance:
Ensure a safe working environment by enforcing safety protocols and conducting regular safety training.
Monitor and comply with environmental regulations related to waste disposal and emissions.
Investigate and report any safety incidents or near-misses, and implement corrective actions.
Budget and Resource Management:
Develop and manage the production budget, including labor, materials, and equipment costs.
Monitor production expenses and identify cost-saving opportunities without compromising quality.
Coordinate with the procurement team to ensure timely availability of raw materials and supplies.
Stakeholder Collaboration:
Work closely with cross-functional teams, including R&D, QA/QC, Supply Chain, and Maintenance, to ensure seamless operations.
Communicate production updates, challenges, and achievements to senior management.
Liaise with regulatory bodies and external auditors during inspections and audits.
Liaising with regulatory affair Manager on NAFDAC issues.
Qualifications and Skills
Education:
Bachelor’s Degree in Biotechnology, Pharmaceutical Sciences, Chemical Engineering, or a related field. A Master’s degree is a plus.
Experience:
Minimum of 3 years of experience in a production or manufacturing role within the pharmaceutical, biotech, technical Production Laboratory in animal health and production industry.
Proven experience in managing GMP-compliant production facilities.
Experience with vaccines and/or sterile drug production is highly desirable.
Technical Skills:
Strong knowledge of GMP, FDA, EMA, and other regulatory requirements.
Proficiency in production planning and inventory management software
Familiarity with lean manufacturing, Six Sigma, or other process improvement methodologies.
Soft Skills:
Excellent leadership and team management abilities.
Strong problem-solving and decision-making skills.
Effective communication and interpersonal skills.
Ability to work under pressure and meet tight deadlines.
Working Conditions:
This role requires working in a manufacturing environment, which may involve exposure to chemicals, biologics, and controlled environments.
Occasional overtime or weekend work may be required to meet production deadlines.
Compensation and Benefits
Competitive salary based on experience.
Comprehensive benefits package, including health insurance, retirement plans, and paid time off.
Opportunities for professional development and career advancement.
Application Closing Date
10th February, 2025.
How to Apply
Interested and qualified candidates should send their resume and a cover letter detailing their relevant experience and qualifications to: [email protected] using the Job Title as the subject of the mail.