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Quality Control Finished Products Analyst Jobs – Dei BioPharma Ltd
Job Title: Quality Control Finished Products Analyst
Organisation: Dei BioPharma Ltd
Duty Station: Matugga, Wakiso, Uganda
About the Company:
Dei BioPharma Ltd is a biotech and pharmaceutical research firm duly incorporated in Uganda, specializing in the development and manufacture of innovative medicines and vaccines. Our state-of-the-art manufacturing facility, situated in Matugga, Wakiso district, Uganda, shall produce high-quality medicines across a wide range of therapeutic areas.
Job Summary: Dei BioPharma Ltd., a Drugs and Vaccines Manufacturing Plant is seeking eligible and qualified applicants for the position of Quality Control Finished Products Analyst. The candidate will be responsible for testing of semi-finished, finished products and stability samples in the Quality Control laboratory in an effective, efficient and compliant manner so as to fulfill marketing requirements.
Key Duties and Responsibilities:
- To perform the chemical analysis of samples of Semi-Finished and Finished product in accordance with current approved standard test methods and specifications.
- To perform the chemical analysis of stability samples kept at accelerated and long term conditions in accordance with current approved standard test methods.
- To prepare the stability protocols of samples of products
- To help out the team leader for the management of inventory of lab consumable, like reagents and HPLC columns, to facilitate smooth testing of samples of products.
- To perform analytical method validations.
- To prepare the Standard testing method and specifications for finished products.
- To prepare the standard operating procedures relevant to quality control systems.
- To report monthly KPIs of finished product testing on prescribed format.
Qualifications, Skills and Experience:
Education:
- Bachelor’s degree in Pharmaceutical Sciences or Analytical Chemistry.
- An advanced Degree (master’s) in a relevant field is an advantage but not required.
Experience:
- 2-3 years of experience in a pharmaceutical quality control laboratory, for the testing of finished products.
Job knowledge:
- Understanding of quality control standards and regulatory requirements specific to the pharmaceutical or biopharma industry. Ability to apply regulatory knowledge to ensure compliance in all testing and documentation processes.
- Evaluations: (This may be tested)
- Language: English level IV (Advanced knowledge) Reading/Writing/Speaking is required.
Skills and abilities:
- Proficiency in laboratory techniques and procedures.
- Knowledge of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP)
- Good Documentation Practices (GDP) with regulatory guidelines from agencies such as the FDA, EMA, or WHO.
- Regulatory Knowledge
- Analytical and Problem-Solving Skills
- Software Proficiency (like, MS Office)
- Attention to Details
- Organizational Skills
- Continuous Learning
Qualifications: All applicants under consideration will be required to pass medical and security certifications.
EQUAL OPPORTUNITY EMPLOYER: Dei BioPharma Ltd. provides equal opportunity and fair and equitable treatment in employment to all people without regard to race, color, religion, sex, national origin, age, disability, political affiliation, marital status, or sexual orientation.
How to Apply:
All interested candidates who meet the required qualifications and experience are invited to submit their CVs, Cover Letter & Academic documents (addressed to the Head Human Capital)
All Application documents should be merged as one document in PDF or .DOC / .DOCX, which should not exceed 10MB
Applications should be sent by email to recruitment@deibiopharma.com with the
JOB TITLE IN THE SUBJECT LINE.
Deadline: 21st October 2024 by 5:00PM
NB: Should you not hear from us within fourteen (14) days from the closing date of this advertisement, you may consider your application to be unsuccessful.
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