Executive Quality Control

2 months ago


Baddi, India Abbott Laboratories Full time

Followings will be the Core Job Responsibilities of the position holder:
1. Responsible for sampling of Raw material and packing material along with their documentation.
2. Responsible for testing or review of Raw material, Packing Material, Finished Goods, stability & GLP Analytical method verification, Analytical method validation and AVD samples of OSD & Haemaccel as per defined Protocol and procedure.
3. Well versed with latest analytical technique and instrumentation like HPLC, GC, AAS, Dissolution, Potentiometric analysis, Wet analytical methods etc.
4. To ensure the completion of activity documentation as per their current procedure, cGMP, cGLP, ALCOA+ and right first time approach.
5. Well versed with laboratory QMS investigation.
6. Logbook verification for their completeness and compliance.
7. To perform the activity in the laboratory as per respective procedure.
8. Responsible for STP, Specification, SOP and Data management.
9. Preparation of volumetric solution, standardization, preparation of reagent, test solution and indicator as and when required.
10. To ensure the compliance of the requirement of cGDP/cGLP and Data integrity while performing all activities in the laboratory.
11. Co-ordinating and aligning the practices and procedures in line with the COBC requirements.
12. Ensuring compliance to the EPD global guidelines.
13. Ensuring the timely updation in the documents as per the Pharmacopoeial amendments.
14. Handson experience of Software like SAP, Starlims, Darius, Soltraqs etc.
In absence of the position holder, the sub-ordinate Executive / Manager working in the section or the authorized designee (as applicable) shall be responsible for day to day working.



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