Abbott Laboratories Apply Online Recruitment For Executive – QA/QC

Abbott Laboratories is an American multinational medical devices and health care company with headquarters in Green Oaks, Illinois, United States. The company was founded by Chicago physician Wallace Calvin Abbott in 1888 to formulate known drugs; today, it sells medical devices, diagnostics, branded generic medicines and nutritional products. 

1.Vacancy details:

  • Department: Executive – Quality Control
  • Qualifications:  B.Sc. Microbiology or Biotechnology /M.Sc. Microbiology or Biotechnology
  • Experience: 1-4 years
  • Salary:₹ Not Disclosed

Job Description: Greeting from Abbott India Limited, . ..!!!!

Important Details :

  • Location: GOA
  • Post of date:13/05/2024
  • Selection Process: The selection will be on the basis of Interview.
  • Mode of Interview: Face to face
  • Interview Rounds of Interview: HR

Job title: Post Graduate Trainee- QC

Experience: B.Sc. Microbiology or Biotechnology /M.Sc. Microbiology or Biotechnology (1-4 years)

Job Responsibilities

1. To follow current GMP, safety & GLP norms in the laboratory testing areas respectively.

2. Awareness on current guidelines, policies, procedures, and techniques of quality control

3. Upkeep of Laboratory with respect to compliance and safety.

4. To maintain cleanliness and its records in the laboratory.

5. To perform analysis, recording and release of the Raw materials, Packing Materials, Intermediate samples, finished product, Stability Samples and other miscellaneous incoming samples.

6. Sampling and analysis of Water and Environmental Monitoring.

7. Preparation and Maintenance of media.

8. Preparation of autoclave load and operation of autoclave.

9. Responsible to maintain lab stock cultures for evaluative testing and make dilutions of stock cultures as required by procedure.

10. Maintains adequate inventory of media and materials required for testing.

11. Observing, monitoring and identifying in-house microorganisms.

12. To participate in the method validation and method transfer activities.

13. To perform timely calibration, validation, qualification, and preventive maintenance of instrument/ equipment in Laboratory.

14. To perform OOS, laboratory error and exception investigation.

15. To prepare SOPs, Protocols, Trends and other QC related documents.

16. Handling, Operation and maintenance of all computerized system software associated with instruments and documentation.

17. Responsible for receipt and inward of incoming materials.

18. Any other work assigned by the Manager/ Section Head. 1 of 1

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2.Vacancy details:

Department: Executive – Quality Assurance


  • Ensure compliance of all procedures, practices and system to cGMP with respect to Schedule M., WHO guidelines, Abbott Quality guideline and Standard operating procedures at site.
  • Responsible for Line clearance and in process checks.
  • Participate in Investigation of Exceptions and deviations of shopfloor.
  • Responsible for process validation and cleaning validation sampling.
  • Responsible for User management, Audit trail review of QC and Production instruments.
  • To deliver the training at site on GMP topics, SOPs and other technical topics.
  • Any other activities/support as instructed by the superiors as and when required.

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