Jobs at Chemo-Pharma Laboratories

Responsibilities

• Microbial analysis of raw materials, packaging materials, intermediates, and finished goods, raw, portable, and purified water
• Sample and analyze packaging materials supplied by vendors to ensure they meet required specifications and standards before approval for payment
• Preparation of media for microbial analysis, and microbial bioassay of specific products; while maintaining Good Laboratory Practice (GLP)
• ensure thorough supervision of raw materials dispensing, so as to achieve accurate weight of materials for production purposes
• Regular monitoring of microbial load of machine surfaces and personnel in the production environment
• Planning and coordinating microbial environmental survey/monitoring of the premises with particular emphasis on the production areas and production personnel with the aim of identifying possible critical points or sources of contamination.

Requirements

• Candidates must possess a B.Sc. Microbiology from a reputable institution or its equivalent.
• In addition, candidates must have at least one (1) post-NYSC working experience as a microbiologist in a pharmaceutical company or other manufacturing organisation.

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Responsibilities

• Perform routine and non-routine chemical analysis of products using standard operating procedures.
• Write and execute chemical testing procedures.
• Maintain up-to-date documents for chemical testing methods and activities.
• Operate laboratory equipment safely and effectively to conduct testing.
• Record, analyze and report test results to Quality Assurance Manager.
• Maintain inventory of chemicals and supplies in laboratory.
• Responsible for testing Pharmaceutical raw materials and finished products for quality assurance.
• Keeping up to date with scientific and technical developments.
• Using a range of software, techniques and equipment to carry out research and analysis.
• Responsible for cleaning all lab equipment and the overall lab environment to ensure a safe and clean laboratory environment within the factory premises.

Requirements

• Applicant must possess at least a Bachelor's Degree in Chemistry / Industrial Chemistry
• At least one(1) year of experience in the pharmaceutical manufacturing industry as a Chemical Analyst

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Job Responsibilities

• The In - Process Control Officer will report to the Quality Control / Assurance Manager and will be responsible for carrying out process checks of tablet parameters to ensure the integrity of products' re-hardness, thickness and leakages and documentation in line with GMP.

Key Accountability

• Conduct regular process checks of tablets parameter - hardness and thickness leakages test.
• Documentation and record keeping and lone clearance.
• Ensure GMP in factory operations.

Qualifications / Experience

• A good Bachelor's Degree or HND in any of the Natural Sciences.
• A minimum of five years cognate experience in pharmaceutical manufacturing.
• Good level of computer literacy.