Stability Chamber Operator (4 positions)

Announcement Number: DB/05/2025/QC04

Position Title: Stability Chamber Operator (4 positions)

Opening Period: 05/05/2025 – 05/12/2025

Series/Grade: L (3)

Salary: Competitive

Who May Apply: All Interested Applicants

Duration Appointment: Indefinite, subject to successful completion of probationary period

Supervisory Position: None

Job Summary:

The Stability Chamber Operator is responsible for managing the storage and monitoring of pharmaceutical samples under controlled environmental conditions as part of stability studies in compliance with ICH guidelines (Q1A-Q1F), Standard Operating Procedures (SOPs), and current Good Manufacturing Practices (GMP). The role includes sample labeling, placement, withdrawal, documentation and maintenance of inventory for both long-term and accelerated stability studies. The operator will be responsible for ensuring the proper functioning of stability chambers, including temperature and humidity monitoring, alarm response and equipment calibration coordination. The ideal candidate should have experience in stability operations, strong organizational skills and a working knowledge of regulatory and documentation standards applicable to pharmaceutical stability programs.

Key Duties and Responsibilities:

1. Operate and monitor stability chambers in compliance with ICH guidelines (Q1A(R2)) and internal SOPs.

2. Perform regular checks on temperature, humidity and other environmental parameters to ensure chamber conditions remain within validated ranges.

3. Schedule and organize stability pulls based on predefined protocols and study designs.
4. Label and place stability samples in appropriate conditions ensuring traceability and documentation.
5. Conduct preliminary visual inspections of samples at stability intervals and submit them to the analytical lab for further testing.
6. Maintain accurate and up-to-date records of chamber usage, sample log-ins and environmental deviations.
7. Perform routine preventive maintenance and initiate service requests for stability chambers as necessary.
8. Participate in the qualification and requalification of chambers including temperature/humidity mapping.
9. Support audit readiness by ensuring all stability documentation is accurate, traceable and compliant.
10. Collaborate with QC, QA and Product Development teams to ensure the effective execution of stability programs.
Academic Qualifications:

Diploma or Bachelor’s degree in Pharmaceutical Sciences, Industrial Chemistry, Laboratory Technology or a related scientific field from a recognized institution.

Experience and Competencies:

1. Minimum of 2-4 years of relevant experience in a pharmaceutical or regulated manufacturing environment.

2. Demonstrated experience working with controlled environmental chambers (stability or incubation) and understanding of ICH stability requirements.

3. Familiarity with GDP, GMP, and basic laboratory operations related to sample handling and documentation.

4. Ability to read and interpret temperature/humidity monitoring charts, and to respond appropriately to deviations.
5. Basic understanding of Good Laboratory Practices (GLP) and internal documentation control systems.
6. Attention to detail, reliability, and the ability to work independently with minimal supervision.
7. Prior experience supporting audits and inspections will be an added advantage.

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 or marital status.

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 Human Resources Manager)

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

Should you not hear from us within twenty one (21) days from the closing date of this advertisement, you may consider your application to be unsuccessful

Deadline: 12th May 2025 by 5:00PM