1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.20 LPA
Experience to prepare and review the documentation required for the ISO 9001:2015, EN ISO 13485: 2016, Quality management System, WHO-GMP, EU MDR 2017/745, IMDR 2017.
Knowledge and preparing documents such as Quality Manual, Site Master File, SOP’s, Change Control, Deviation, CAPA, Incident, and Customer complaint, Management Review Meeting, pdate Harmonized Standards, ...
1 Opening(s)
15.0 Year(s) To 17.0 Year(s)
7.20 LPA TO 8.40 LPA
Preparation of Certificate of Pharmaceutical Product.
Expertise in liaising, coordinating inspections with regulatory agencies (FDA ISO 9000)
Knowledge of Microsoft Office, Microsoft Excel, ERP etc.
Goal Oriented and Results Driven Team Leader.
Expertise in writing, reviewing & approving lab procedures / documentations, Out off Specification reports, batch records, protocols, etc.
Review of QC related ...
1 Opening(s)
7.0 Year(s) To 8.0 Year(s)
7.00 LPA TO 9.00 LPA
Position: Sr. Executive - QA
Location: Bhimpore - Daman
Experience: 7 - 8 YEARS
Industries: Pharma
Responsibilities:
Issuance & Control of all Quality Documents Deviation control, change control, Investigation of OOS, Specification, SOP, and BMR.
Assist to head in ensure the evaluation of ...
1 Opening(s)
5.0 Year(s) To 7.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: Executive/Sr. Executive QA
Location: Ankleshwar
Experience: 5 - 7 Years
Industries: Chemical
Responsibilities:
Quality Analytical Method.
Line Clearance before the start of the Production activities.
Performing & Recording In-Process Checks of Manufacturing & Packing department.
Monitoring dispensing of Raw material and packing materials.
In-house Calibration of IPQC Instruments (as per Frequency).
Checking ...