93 Job openings found

1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.50 LPA TO 3.00 LPA
Review and approval of artwork. Validate, Checking, analysis and maintain data for samples before final dispatch of each product. Vendor audit and online proof verification and personal visit if required. Prepare document of Export Po, Product information sheet, finished product specification. Follow up from Party for approval of finished goods sample before dispatch. Sample approved ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
3.50 LPA TO 4.50 LPA
Description: Position:          Officer - QA Location:         Vapi Experience:     2 - 3 Years Industries:       Pharma Responsibilities: Process Validation Cleaning Validation Equipment Qualification DQ, IQ, OQ, PQ Hold Time Study QMS Handling Deviation, Change Control, Market Complaint, CAPA IPQA Document Issuance & Control Required Skills Logical thinking. Organizing. Good in communication. Required Qualification: - B.Pharm/M.Pharm/M.Sc - Chemistry Salary :- 4.50 LPA If you ...
2 Opening(s)
3.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 5.00 LPA
Designation : QA Qualification : M.sc/ B.sc/ M.pharm/B.pharm          Total experience : 2 - 5 years            Total Position : 2          Gender : Male          Location : Sachin, GIDC          Salary Range : Upto 4 LPA 1. To perform all the ...
2 Opening(s)
3.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 5.00 LPA
Designation : QA Qualification : M.sc/ B.sc/ M.pharm/B.pharm          Total experience : 2 - 5 years            Total Position : 2          Gender : Male          Location : Sachin, GIDC          Salary Range : Upto 4 LPA 1. To perform all the ...
2 Opening(s)
3.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 5.00 LPA
Designation : QA Qualification : M.sc/ B.sc/ M.pharm/B.pharm          Total experience : 2 - 5 years            Total Position : 2          Gender : Male          Location : Sachin, GIDC          Salary Range : Upto 4 LPA 1. To perform all the ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
1.00 LPA TO 3.00 LPA
Job responsibilities are to Assist Regulatory manager: Preparation, Compilation and review of registration dossier of tablet /capsule/injection in CTD, ACTD as well as country specific format for countries Preparation, Compilation and review of registration dossier of capsule/syrup/balm in a Herbal products for country specific format in countries of African Region, Cambodia, Myanmar, CIS To manage ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Position Junior Executive - IPQA CTC Range Up to 4 LPA Educational Qualification B.Sc., B.Pharm, D.Pharm, M.Sc. Total Experience 1 to 2 Years Preferred Industry Pharmaceutical (Parenteral Manufacturing unit) Job Description Batch Manufacturing record review Batch manufacturing record issuance. Line clearance Calibration activity Operation of Viable / Non-Viable monitoring Preparation of annual product quality review.
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
1.80 LPA TO 3.60 LPA
Job Responsibilities :   Qualification:- Bsc/Msc/B.pharm/M.Pharm Job profile: 1. Coordinate with various outsourced manufacturing sites for QA related work on daily basis 2. Maintain control samples as per SOP's 3. Coordinate artwork with designer and manufacturing site. 4. Artwork designing as per countries requirements 5. Coordination with FDCA liasoining agent for approvals Job Types: Full-time, Permanent   
1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 5.50 LPA
B Position : Sr. Executive BE Mechanical Required Skills : Experience in Validation and Calibration activities, candidate from calibration laboratory or from pharm industry is suitable CTC Maximum 5 to 5.5 Lakh Max Minimum Experience 3 years     B Position : Sr. Executive BE Mechanical Required Skills : Experience in Validation and Calibration activities, candidate from calibration laboratory ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
2.50 LPA TO 3.60 LPA
    Regulatory Affairs Officer (RA) Qualification: B.Pharm/ M.Pharm Experience: Minimum 3 years in regulatory affairs for the ROW (Rest of the World) market, with a total of 3 to 5 years of experience. Job Description: Preparing dossiers as per country-specific guidelines. Compiling and reviewing documents. Coordinating with QA for documentation. Addressing queries raised by respective countries' FDA. Bond: 18-month ...

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