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QC Analyst—Microbiology( 03 Positions)

Full time @Abacus Parenteral Drugs Limited posted 2 hours ago in HealthCare Email Job

Job Detail

  • Job ID 20733
  • Career Level  Officer
  • Experience  3 Years
  • Gender  Both
  • Industry  Administration
  • Qualifications  Degree Bachelor
  • Job Type  Full time

Job Description

DESIGNATION: QC Analyst—Microbiology( 03)

JOB IDENTIFICATION:

Department: Quality Control         

Reporting to: Team Leader, Microbiology

POSITION PURPOSE:

To carry out microbiological analysis of finished products, raw materials, primary packaging materials, water and environment monitoring.

 

JOB ROLES AND EXPECTATIONS:

Key Result Area Key Roles / Duties
Quality 1.     To ensure compliance with current Good Laboratory Practices as laid down in the Quality Control procedures

2.   Compliance with regulatory requirements & cGMP.

3.    Ensure that all work undertaken is compliant with all relevant internal standards, quality systems, procedures, accreditations, and methodologies and in line with customer expectations.
Technical Work 1.  Sampling of finished products, packaging, and raw material and data entry in logbooks.

2.  Validate/verify the test methods, qualify equipment, and clean room personnel.

3.     Preparation and quality control of media and diluents used in the lab.

4. Perform a bacteria endotoxin test of raw materials, stability study samples and finished products

5.     Perform a sterility test of finished products, stability study samples and raw materials

6.     Perform bioburden test on pre-sterilized samples

7.     Perform Particulate matter count test of finished products and stability study samples

8.     Perform  disinfectant efficacy test

9.    Environmental monitoring of cleanrooms and supporting areas & trend analysis.

10.  Identification of microorganisms using selective media and microscopy

11.  Microbial water analysis analysis as in the SOP

 

12.  Good housekeeping to ensure cleanliness and proper organization of the laboratory at all times.

13. Reception of standard cultures, preparation of in-house isolates, identification and maintenance.

14. Attending trainings and training of staff.

15. Proper management of equipment and consumable resources to meet KPI’s in line with company targets.

16.  Perform microbiological assays of antibiotics.

17. Calibrate equipment and liaise with supervisors to ensure all equipment calibrations/service/maintenance requirements are fully up-to-date.

18.  Microbial examination of non-sterile pharmaceutical samples.

19. Daily monitoring of sample under incubation & updating reports.

20. Daily monitoring of consumables like media & reagents.

21. Fulfilling the tasks according to the daily work plan.

22. Participate in quality management systems like the following:

·       OOS Investigation

·       OOT Investigation.

·       Deviation handling.

·       Change control

·       Quality risk management.

·       CAPA Closure.
Reporting & Communication 1.    Update of records on time.

2.   Timely and proper communication with staff at all levels.

3.    Reporting critical escalation on time.
Safety 1.     Use of provided Personal protective wear (overall, gas masks, Head cap, gloves.)

2.     Identify possible sources of incidents and accidents.

AUTHORITIES:

 

  • Sampling & microbial analysis of all samples.
  • Signing work reports.
  • Request reports & logbooks.
  • Access to the cleanroom.

COMPETENCIES:

Technical Knowledge/Skills:

  1.  Report Writing Skills
  2.  Analytical Skills
  3. Presentation skills
  4. Good communication & interpersonal Skills
  5. Computer Skills (PowerPoint, Excel and MS Word)
  6. Able to learn and adapt to change.
  7. Innovative / creative skills.
Behavioral / Attitude Competencies:

  1. Respect for others
  2. Sociable
  3.  Result-oriented
  4. Open and Decisive.
  5. Business Acumen
  6. Teamwork
  7. Responsible
  8. Mature & assertive.

MINIMUM QUALIFICATIONS / REQUIREMENTS:

  1. BSc Microbiology or Biochemistry
  2. Experience in a pharmaceutical/healthcare industry is an advantage

TRAINING REQUIREMENTS:

  • Basic safety training
  • Basic GMP training
  • Leadership training

Application Procedure

If you are ready to grow your career with one of East Africa’s leading pharmaceutical manufacturers, we encourage you to apply today.

Deadline: 20/05/2026

Apply Now and become part of a team committed to quality, innovation, and excellence.

CLICK HERE TO SEE DETAILS AND APPLY

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