Letap Pharmaceuticals Limited Quality Control/Assurance Jobs in Ghana
1. Patiently scroll down and read the job description below.
2. Scroll down and find how to apply or mode of application for this job after the job description.
3. Carefully follow the instructions on how to apply.
4. Always apply for a job by attaching CV with a Cover Letter / Application Letter.
This Quality Control (QC) Analyst position is a non-supervisory role. The applicant will mainly conduct laboratory testing of pharmaceutical raw materials, in-process, finished products and packaging materials. The incumbent will spend about 85 % of his/her time on the bench and 15 % in the development of QC relevant documentation. He/she will:
- Do sampling and conduct tests on raw materials, in-process, finshed pharmaceutical products and packaging materials.
- Ensure that safety standards and cleanliness of laboratory are maintained
- May provide training to other analysts to perform key laboratory tests
- Participate in self-inspection and/or audits where necessary
- Indentify and troubleshoot equipment problems when the need arises
- Assist in the development and review of quality control processes, policies, standard oprating procedures, test methods and specifications
- Participate in the conduct and reporting of investigation on non-conforming work
- Participate in the conduct of equipment/device periodic calibration/verification and preventive maintenance
- Undertake any other work assigned as required by the management
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Required Skills or Experience
The incumbent should meet the following requirements:
Education
- Bachelor’s degree in Chemistry, Biochemistry, Microbiology, Biology, Pharmacy or in any relevant scientific discipline
Experience
- At least three (3) years of experience in the use of the following key equipment for evaluating the quality of pharmacopoeial articles: UV-Vis, DT, Sieve Analyzer, Dissolution tester, TLC, HPLC, GC, Karl Fischer Titrator, Oven, Moisture Analyzer, FTIR, AAS etc. Should also have appreciable troubleshooting experience in the above techniques.
- Communication skills:Candidate should have the ability to follow verbal and written instructions as well as excellent written and oral communication skills for documentation purposes and an effective work relationship
- Organizational skills: He/she is expected to have the ability to prioritize, manage multiple tasks, and meet deadlines; as well as to organize and maintain data or information
- Apt for learning: Candidates must be willing and able to learn through research, observation and hands-on experience
- Integrity: QC work is very sensitive and affects lives; the candidate must have the ability to maintain integrity, honesty and transparency at all times.
- Self-starter/team player: He/she must possess the ability to work both independently and as part of a team
- Drive for quality: Applicant must have a drive to continuously improve processes for improved performance
- Computer skills: Should have a basic working knowledge of Microsoft Office tools, especially Word, Excel, Visio and PowerPoint
1. Patiently scroll down and read the job description below.
2. Scroll down and find how to apply or mode of application for this job after the job description.
3. Carefully follow the instructions on how to apply.
4. Always apply for a job by attaching CV with a Cover Letter / Application Letter.
This Quality Control (QC) Analyst position is a non-supervisory role. The applicant will mainly conduct laboratory testing of pharmaceutical raw materials, in-process, finished products and packaging materials. The incumbent will spend about 85 % of his/her time on the bench and 15 % in the development of QC relevant documentation. He/she will:
- Do sampling and conduct tests on raw materials, in-process, finshed pharmaceutical products and packaging materials.
- Ensure that safety standards and cleanliness of laboratory are maintained
- May provide training to other analysts to perform key laboratory tests
- Participate in self-inspection and/or audits where necessary
- Indentify and troubleshoot equipment problems when the need arises
- Assist in the development and review of quality control processes, policies, standard oprating procedures, test methods and specifications
- Participate in the conduct and reporting of investigation on non-conforming work
- Participate in the conduct of equipment/device periodic calibration/verification and preventive maintenance
- Undertake any other work assigned as required by the management
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Required Skills or Experience
The incumbent should meet the following requirements:
Education
- Bachelor’s degree in Chemistry, Biochemistry, Microbiology, Biology, Pharmacy or in any relevant scientific discipline
Experience
- At least three (3) years of experience in the use of the following key equipment for evaluating the quality of pharmacopoeial articles: UV-Vis, DT, Sieve Analyzer, Dissolution tester, TLC, HPLC, GC, Karl Fischer Titrator, Oven, Moisture Analyzer, FTIR, AAS etc. Should also have appreciable troubleshooting experience in the above techniques.
- Communication skills:Candidate should have the ability to follow verbal and written instructions as well as excellent written and oral communication skills for documentation purposes and an effective work relationship
- Organizational skills: He/she is expected to have the ability to prioritize, manage multiple tasks, and meet deadlines; as well as to organize and maintain data or information
- Apt for learning: Candidates must be willing and able to learn through research, observation and hands-on experience
- Integrity: QC work is very sensitive and affects lives; the candidate must have the ability to maintain integrity, honesty and transparency at all times.
- Self-starter/team player: He/she must possess the ability to work both independently and as part of a team
- Drive for quality: Applicant must have a drive to continuously improve processes for improved performance
- Computer skills: Should have a basic working knowledge of Microsoft Office tools, especially Word, Excel, Visio and PowerPoint
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