Jobs at Centre For Research in Enterprise and Action in Management (CREM) Nigeria

JOB SPECIFICATION.:

• Microbial analysis of raw materials.
• New sampling of materials
• Preparation of media for microbial analysis
• Microbial analysis of finished, bulk and intermediate
• Proper documentation of records.
• Fumigation of the factory.
• Carrying out an environmental check (air sampling)
• Calibrate or maintain Laboratory equipment
• Complete documentation needed to support testing procedures including equipment Log books or inventory forms.
• Maintaining GLP in the Laboratory.
• Instrumental and Microbiological Analysis.

QUALIFICATION AND EXPERIENCE:

• Both Freshers and experienced persons will be considered.
• For experienced persons, work experience of more than 1 year to 2 year is ideal.

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JOB RESPONSIBILITY

• Conduct regular inspections and monitoring of in-process manufacturing activities to ensure compliance with Good Manufacturing Practices (GMP) and other regulatory requirements
• Collaborate with production teams to identify and address any deviations from quality standards
• Review and verify the accuracy and completeness of in-process
• documentation, batch records and related manufacturing records.
• Ensure that all documentation complies with established procedures and regulatory guidelines
• Work closely with the quality control team to implement in-process quality checks
• Collaborate on the resolution of quality-related issues and deviations, providing support for investigations
• Provide training to manufacturing personnel on in-process compliance requirements, quality standards and regulatory expectations
• Promote a culture of awareness and accountability for in-process compliance within the manufacturing teams
• Identify opportunities for process improvements andoptimizationn of in-process compliance procedures
• Implement corrective and preventive actions to enhance overall compliance performance
• Stay updated on relevant regulations and guidelines impacting pharmaceutical manufacturing
• Ensure that manufacturing processes align with current regulatory expectations

Qualification and experience:

• Candidates with a Science background will only be considered.
• HND/OND/B.Sc. in any of the subjects like PURE / INDUSTRIAL/APPLIED CHEMISTRY or MICROBIOLOGY, BIOCHEMISTRY / FOOD SCIENCE/PHYSICAL SCIENCE are candidates we are looking for.
• Freshers with exceptional qualities that can be developed to fit into the post will also be considered.
• 1 to 2 years experience in a similar field of job or experience as
• COMPLIANCE OFFICER in any process/manufacturing company will be
• considered for the experience category.
• Computer operation knowledge is an added advantage

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Job description:

• Individuals shall be able to take care of the incoming raw materials to our stores and inventory management and proper record keeping.
• Responsible for issuing our materials to the user department and keeping and updating the relevant records.

Experience:

• Candidates should have a science background
• Basic knowledge of Computer operation and MS Office operating knowledge.
• Fresher or experienced candidates are required
• Any inventory management software working knowledge is an additional advantage.

Educational Qualification:

• OND/HND/B.Sc from any Science background.
• Any qualification in computer course will be an added advantage

Experience:

• A minimum of 0 to 2 years experience in a raw materials job, especially in a warehouse/depot or in a manufacturing industry.

JOB SPECIFICATION:

• Supervision of raw materials for Pharmaceutical production process and manpower .
• Proper reporting and stock taking
• Coordination of the raw materials department for the required process
• Checks to be carried out from time to time.

TRAITS REQUIRED.:

• INTEGRITY
• HONESTY
• Dynamic
• Adaptability
• Communication.