Summary

Job Context

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Job Responsibilities

1. To work as per cGMP and ensure its compliance as per current guideline and SOPs.
2. Responsible to take training before execution of allotted work & maintaining the training file.
3. Responsible to follow safety precaution as per laboratory procedure.
4. Responsible to escalate any issue / incident to reporting manager for prompt corrective action.
5. Responsible for method development studies of Drug Product & In process material.
6. Responsible for method Validation studies of Drug Product & In process Material.
7. Responsible for stability studies of Drug Product & In process Material. Responsible to align with organization goal.
8. Other responsibilities assigned by reporting authority.
9. Responsible to follow Quality Management Document procedure.
10. Responsible to perform the calibration of instrument.
11. Responsible to prepare Study Protocol and Study Reports.
12. Responsible to maintain instrument/equipment as per SOPs.
13. Responsible for timely archival of documents as per SOP.
14. Responsible to follow safety precaution as per laboratory procedure. Responsible to ensure proper Handling and Disposal of waste.
15. Responsible to qualification reference standard / working standard/chemical reference standard samples as per approved and valid procedure.

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Experience Requirements

• 2 - 3 years

Educational Requirements

• Masters

Skills

• asperiores ut

Age

• 22 - 36 Age

Additional Requirements

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Compensation & Other Benefits

• - Tour , Medical , Holidays , Performance Bonus
• - Salary Review: Half Yearly

Work place

• Work At Office

Employment Status

• Full Time

Gender

• Male

Job Location

• Taiwan