Jobs at HRLeverage Africa

Description 

• We are seeking a skilled and experienced Microbiologist to join our Quality Control team at our pharmaceutical factory. The Microbiologist will be responsible for performing microbiological testing and analysis of raw materials, in-process samples, and finished products to ensure compliance with regulatory requirements and quality standards.

Key Responsibilities

• Microbiological Testing:

  • Perform routine and non-routine microbiological testing of raw materials, in-process samples, and finished products using standard microbiological techniques and procedures.
  • Conduct microbial enumeration, identification, and antimicrobial effectiveness testing to assess the microbial quality of pharmaceutical products.

• Environmental Monitoring:

  • Conduct environmental monitoring of cleanrooms, manufacturing areas, and utilities to assess microbial contamination levels and ensure compliance with Good Manufacturing Practices (GMP).

• Method Development and Validation:

  • Develop and validate microbiological test methods in accordance with regulatory requirements and industry standards.
  • Optimize test methods to improve sensitivity, accuracy, and efficiency while ensuring reproducibility and reliability of results.

• Documentation and Record Keeping:

  • Maintain accurate and detailed records of all microbiological testing activities, including test results, observations, and data analysis.
  • Prepare and review technical reports, protocols, and standard operating procedures (SOPs) related to microbiological testing and analysis.

• Quality Control and Compliance:

  • Ensure compliance with regulatory requirements from agencies such as the FDA, EMA, and USP.
  • Participate in internal and external audits, inspections, and regulatory submissions as needed.
  • Investigate and resolve deviations, out-of-specification results, and quality-related issues through effective root cause analysis and corrective actions.

• Continuous Improvement:

  • Identify opportunities for process improvements and efficiency gains in microbiological testing and analysis.
  • Implement best practices and innovative techniques to enhance the quality and efficiency of microbiological operations.

Requirements

• Interested candidates should possess a Bachelor's Degree in relevant fields.

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Job Summary

• As a Production Supervisor in our pharmaceutical factory, you will oversee and coordinate the manufacturing operations to ensure efficient production of high-quality pharmaceutical products.
• You will lead a team of production workers, monitor production processes, and enforce safety and quality standards to meet production targets while adhering to regulatory requirements.

Key Responsibilities
Supervise Production Operations:

• Direct and supervise production staff to ensure adherence to production schedules and quality standards.
• Coordinate and prioritize production activities to meet production targets and customer demands.
• Monitor production processes, troubleshoot issues, and implement corrective actions as needed to optimize efficiency and minimize downtime.

Quality Control and Compliance:

• Ensure compliance with Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and regulatory requirements.
• Conduct regular inspections of production areas to ensure cleanliness, organization, and compliance with safety protocols.
• Implement and enforce quality control measures to maintain product quality and consistency.

Training and Development:

• Train and mentor production staff on proper operating procedures, safety protocols, and quality standards.
• Provide ongoing coaching and feedback to ensure continuous improvement and skill development among team members.
• Identify training needs and coordinate training programs to enhance the skills and capabilities of production personnel.

Inventory Management:

• Monitor inventory levels of raw materials, packaging materials, and finished products to ensure adequate supplies for production.
• Coordinate with procurement and warehouse teams to optimize inventory levels and minimize stockouts or overages.

Performance Monitoring and Reporting:

• Track production metrics, such as yield, efficiency, and downtime, and prepare regular reports for management review.
• Analyze production data to identify trends, inefficiencies, and areas for improvement, and implement corrective actions as necessary.

Safety and Environmental Compliance:

• Promote a culture of safety and environmental stewardship among production staff through training, awareness, and enforcement of safety regulations.
• Conduct safety audits and inspections to identify hazards and ensure compliance with occupational health and safety standards.

Qualifications and Skills

• Candidates should possess a Bachelor's Degree or HND with 2-7 years experience.
• Proven experience in a production supervisory role within the pharmaceutical or manufacturing industry.
• Strong knowledge of pharmaceutical manufacturing processes, equipment, and regulations
• Excellent leadership and communication skills, with the ability to motivate and inspire a diverse team.
• Solid problem-solving abilities and decision-making skills, with a focus on continuous improvement.
• Detail-oriented with strong organizational and time-management skills.
• Ability to work effectively in a fast-paced, dynamic environment and adapt to changing priorities.

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Job Description

• We are seeking a highly motivated and experienced R&D Assistant Manager to join our Research and Development team at our pharmaceutical factory.
• The R&D Assistant Manager will play a key role in supporting the development and optimization of pharmaceutical formulations, processes, and analytical methods.

Key Responsibilities

• Collaborate with R&D team members to design and execute experiments for the development and optimization of pharmaceutical formulations, processes, and analytical methods.
• Perform laboratory experiments, analyze data, and interpret results to support product development and process optimization efforts.
• Assist in the preparation and review of technical documents, including study protocols, reports, and regulatory submissions.
• Maintain accurate records of experimental procedures, results, and observations in accordance with Good Laboratory Practices (GLP) and regulatory guidelines.
• Coordinate with cross-functional teams, including Quality Assurance, Regulatory Affairs, and Manufacturing, to ensure alignment and compliance with project timelines and regulatory requirements.
• Stay informed about industry trends, scientific advancements, and regulatory updates relevant to pharmaceutical research and development.
• Contribute to a culture of innovation, collaboration, and continuous improvement within the R&D team and across the organization.

Qualifications

• Bachelor's Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related field. Advanced degrees (e.g., Master's or PhD) are preferred.
• Minimum of [3] years of experience in pharmaceutical research and development, with a focus on formulation development and process optimization.
• Strong knowledge of pharmaceutical dosage forms, drug delivery systems, and analytical techniques commonly used in pharmaceutical R&D.
• Experience with laboratory equipment, instrumentation, and software for formulation development, characterization, and analysis.
• Familiarity with regulatory requirements from agencies such as the FDA, EMA, and ICH guidelines.
• Excellent communication skills, both verbal and written, with the ability to effectively communicate technical information to cross-functional teams.
• Strong organizational skills, attention to detail, and ability to manage multiple projects simultaneously.
• Ability to work independently as well as part of a team in a fast-paced, collaborative environment.