Executive Quality Control

6 months ago


Goa, India Abbott Laboratories Full time

Experience: Minimum 3-5 years in QC Laboratory.

1. Setting the analysis priorities based on the production planning in RM/PM/FP section.
2. Review of analytical documents in QC department.
3. To perform investigations and RCA for OOS/OOT, Laboratory Errors, and deviations.
4. Responsible for review of documents updated as per the changes made to the
pharmacopeias/regulatory documents.
5. Familiar with troubleshooting for Instrumental analysis such as HPLC, FTIR, UV-Vis
Spectrophotometer, Autotitrator, Dissolution Tester etc.
6. Awareness on current guidelines, policies, procedures, and techniques of quality control
7. To follow current GMP, safety & GLP norms in the laboratory testing areas respectively.
8. Review and implementation of compendial changes.
9. To coordinate with cross functional team and stakeholders to ensure smooth functioning.



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