12 QC Analyst – Finished Products
2025-05-09T09:12:18+00:00
Dei BioPharma
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https://deibiopharma.com/
FULL_TIME
Matugga
Uganda
00256
Uganda
Healthcare
Healthcare
2025-05-12T17:00:00+00:00
Uganda
8
Job Summary:
The QC Analyst Finished Products is responsible for performing the analytical testing of finished pharmaceutical products to ensure they meet predefined specifications and regulatory standards before batch release. This includes executing physical, chemical and instrumental tests (e.g., HPLC, UV-Vis, IR, dissolution) in accordance with pharmacopeial monographs (USP, BP, Ph. Eur.), validated analytical methods, and internal quality control procedures. The role also involves preparing test reports, maintaining data integrity, managing laboratory documentation and ensuring compliance with current Good Manufacturing Practices (cGMP) and Good Laboratory Practices (GLP). The ideal candidate should possess strong analytical skills, attention to detail, and proficiency with pharmaceutical testing instrumentation in a GMP-regulated environment.
Key Duties and Responsibilities:
- Perform physical and chemical testing of finished pharmaceutical products in accordance with approved specifications and validated methods.
- Conduct analysis using analytical instruments such as HPLC, UV-Vis spectrophotometers, FTIR, dissolution testers and other QC laboratory equipment.
- Ensure timely and accurate reporting of test results in line with cGMP, GLP and internal SOPs.
- Prepare and review Certificates of Analysis (CoAs) and release documents for batch release purposes.
- Identify and document any out-of-specification (OOS) or out-of-trend (OOT) results and participate in investigations and corrective actions.
- Maintain accurate records and documentation of all test procedures, raw data, results, and observations.
- Prepare reagents, reference standards and solutions used in testing ensuring correct labeling, storage and traceability.
- Participate in routine calibration, maintenance and qualification of laboratory instruments.
- Ensure samples are handled, stored, and disposed of in accordance with regulatory and environmental guidelines.
- Support regulatory inspections and internal audits by ensuring data integrity and audit readiness at all times.
Academic Qualifications:
Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Industrial Chemistry, Analytical Chemistry or a related scientific field from a recognized institution.
Experience and Competencies:
- Minimum of 3–5 years of relevant experience in a pharmaceutical or regulated manufacturing environment.
- Demonstrated experience working with controlled environmental chambers (stability or incubation) and understanding of ICH stability requirements.
- Familiarity with GDP, cGMP, and basic laboratory operations related to sample handling and documentation.
- Ability to read and interpret temperature/humidity monitoring charts, and to respond appropriately to deviations.
- Basic understanding of Good Laboratory Practices (GLP) and internal documentation control systems.
- Attention to detail, reliability, and the ability to work independently with minimal supervision.
- Prior experience supporting audits and inspections will be an added advantage
Perform physical and chemical testing of finished pharmaceutical products in accordance with approved specifications and validated methods. Conduct analysis using analytical instruments such as HPLC, UV-Vis spectrophotometers, FTIR, dissolution testers and other QC laboratory equipment. Ensure timely and accurate reporting of test results in line with cGMP, GLP and internal SOPs. Prepare and review Certificates of Analysis (CoAs) and release documents for batch release purposes. Identify and document any out-of-specification (OOS) or out-of-trend (OOT) results and participate in investigations and corrective actions. Maintain accurate records and documentation of all test procedures, raw data, results, and observations. Prepare reagents, reference standards and solutions used in testing ensuring correct labeling, storage and traceability. Participate in routine calibration, maintenance and qualification of laboratory instruments. Ensure samples are handled, stored, and disposed of in accordance with regulatory and environmental guidelines. Support regulatory inspections and internal audits by ensuring data integrity and audit readiness at all times
Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Industrial Chemistry, Analytical Chemistry or a related scientific field from a recognized institution. Experience and Competencies: Minimum of 3–5 years of relevant experience in a pharmaceutical or regulated manufacturing environment. Demonstrated experience working with controlled environmental chambers (stability or incubation) and understanding of ICH stability requirements. Familiarity with GDP, cGMP, and basic laboratory operations related to sample handling and documentation. Ability to read and interpret temperature/humidity monitoring charts, and to respond appropriately to deviations. Basic understanding of Good Laboratory Practices (GLP) and internal documentation control systems. Attention to detail, reliability, and the ability to work independently with minimal supervision. Prior experience supporting audits and inspections will be an added advantage
JOB-681dc6f240106
Vacancy title:
12 QC Analyst – Finished Products
[Type: FULL_TIME, Industry: Healthcare, Category: Healthcare]
Jobs at:
Dei BioPharma
Deadline of this Job:
Monday, May 12 2025
Duty Station:
Matugga | Uganda | Uganda
Summary
Date Posted: Friday, May 9 2025, Base Salary: Not Disclosed
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JOB DETAILS:
Job Summary:
The QC Analyst Finished Products is responsible for performing the analytical testing of finished pharmaceutical products to ensure they meet predefined specifications and regulatory standards before batch release. This includes executing physical, chemical and instrumental tests (e.g., HPLC, UV-Vis, IR, dissolution) in accordance with pharmacopeial monographs (USP, BP, Ph. Eur.), validated analytical methods, and internal quality control procedures. The role also involves preparing test reports, maintaining data integrity, managing laboratory documentation and ensuring compliance with current Good Manufacturing Practices (cGMP) and Good Laboratory Practices (GLP). The ideal candidate should possess strong analytical skills, attention to detail, and proficiency with pharmaceutical testing instrumentation in a GMP-regulated environment.
Key Duties and Responsibilities:
- Perform physical and chemical testing of finished pharmaceutical products in accordance with approved specifications and validated methods.
- Conduct analysis using analytical instruments such as HPLC, UV-Vis spectrophotometers, FTIR, dissolution testers and other QC laboratory equipment.
- Ensure timely and accurate reporting of test results in line with cGMP, GLP and internal SOPs.
- Prepare and review Certificates of Analysis (CoAs) and release documents for batch release purposes.
- Identify and document any out-of-specification (OOS) or out-of-trend (OOT) results and participate in investigations and corrective actions.
- Maintain accurate records and documentation of all test procedures, raw data, results, and observations.
- Prepare reagents, reference standards and solutions used in testing ensuring correct labeling, storage and traceability.
- Participate in routine calibration, maintenance and qualification of laboratory instruments.
- Ensure samples are handled, stored, and disposed of in accordance with regulatory and environmental guidelines.
- Support regulatory inspections and internal audits by ensuring data integrity and audit readiness at all times.
Academic Qualifications:
Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Industrial Chemistry, Analytical Chemistry or a related scientific field from a recognized institution.
Experience and Competencies:
- Minimum of 3–5 years of relevant experience in a pharmaceutical or regulated manufacturing environment.
- Demonstrated experience working with controlled environmental chambers (stability or incubation) and understanding of ICH stability requirements.
- Familiarity with GDP, cGMP, and basic laboratory operations related to sample handling and documentation.
- Ability to read and interpret temperature/humidity monitoring charts, and to respond appropriately to deviations.
- Basic understanding of Good Laboratory Practices (GLP) and internal documentation control systems.
- Attention to detail, reliability, and the ability to work independently with minimal supervision.
- Prior experience supporting audits and inspections will be an added advantage
Work Hours: 8
Experience in Months: 36
Level of Education: bachelor degree
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