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.
Sorry, this listing is no longer open.
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