7689 Job openings found

1 Opening(s)
7.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
Position:          Manager/Dy.Manager -QC (Reviewer) Location:          Daman Experience:      7-10 Years Industries:       Pharma formulation  Responsibilities: Review and evaluate QC test results, analyse data and related records generated by QC Team, identify discrepancies and deviations, analyse and resolve deviations, compliance with regulatory requirement, handle OOS, OOT, Have handled HPLC  preventive maintenance of lab equipment, take ...
1 Opening(s)
8.0 Year(s) To 12.0 Year(s)
7.00 LPA TO 12.00 LPA
Position:          Manager/Asst. Manager - QC Location:         Silvassa Experience:     8- 12 Years Industries:      Pharma - Formulation Responsibilities: Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards. To approve or reject, as he sees fit, raw materials, packing materials, semi-finished product ...
1 Opening(s)
10.0 Year(s) To 12.0 Year(s)
13.00 LPA TO 15.00 LPA
Position:           QC Manager Location:          Vapi Experience:       10 - 12 Years Industries:        Pharma - API Responsibilities:         Ensuring/Monitoring of GLP, GMP, GDP, Quality Management System in Quality Control Laboratory and identify the gaps and setup the Quality Control laboratory. Ensuring the Reviews of the Standard ...
1 Opening(s)
10.0 Year(s) To 25.0 Year(s)
10.00 LPA TO 15.00 LPA
Experience between 10 to 25 year in field of inspection of Automobile/Engineereing Industry like Raw Material,Welding,Heat Treatment,Griding,Machining,CNC/VMC,Assembly & Final Inspection etc. 1)Quality Control Management 2)Quality Assurance 3)Quality Audit 4)Quality Check 5) Process Enhancement 6) QC Production 7) Control Quality Management 8)Quality Assurance Quality Control 9)Checking of the raw material as per the quality norms 10) Conduct and review Internal Quality ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
Job Description: The person will  look after jewellery coming from factory. co ordinate for orders from office to jewellery factory.  Check for QC. Should have a good knowlege in jewellery Production. Must be taking the whole responsibility of production.  Creating and overseeing production calendar, following up on deadlines at every process touchpoint. Sourcing all materials for production from current ...
3 Opening(s)
10.0 Year(s) To 15.0 Year(s)
5.00 LPA TO 10.00 LPA
S.NO ACTIVITIES RESPONSIBILITIES 1 TESTING Maintain each Lab Instrument operations as per SOP.   Ø    Arrange & check raw materials testing as per received supplier.  Check the RM description on bags/ drums, in case of any doubts.   Ø    Any deviation found, is to be immediately reported to Asst. Manager / Deputy Manager Quality Control.   Ø    Release the Material in system & clear ...
3 Opening(s)
5.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 6.00 LPA
S.NO ACTIVITIES RESPONSIBILITIES 1 TESTING Maintain each Lab Instrument operations as per SOP.   Ø    Arrange & check raw materials testing as per received supplier.  Check the RM description on bags/ drums, in case of any doubts.   Ø    Any deviation found, is to be immediately reported to Asst. Manager / Deputy Manager Quality Control.   Ø    Release the Material in system & clear ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
15.00 LPA TO 20.00 LPA
Position:          QC Manager Location:         Daman Experience:     15 - 20 Years Industries:       Pharma - Formulation Responsibilities: Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards. To approve or reject, as he sees fit, raw materials, packing materials, semi-finished product and finished products ...
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)
6.0 Year(s) To 7.0 Year(s)
8.00 LPA TO 10.00 LPA
Position:           AM/Dy. Manager -QC (Reviewer) Location:          Vapi Experience:      6- 7 YEARS Industries:       Pharma formulation  Responsibilities: Review and evaluate QC test results, analyse data and related records generated by QC Team, identify discrepancies and deviations, analyse and resolve deviations, compliance with regulatory requirement, handle OOS, OOT, Have handled HPLC  preventive ...

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