1 Opening(s)
5.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 12.00 LPA
Position: Executive/Asst. Manager - QC(P)
Location: Vapi
Experience: 5 - 12 Years
Industries: Pharma
Responsibilities:
Analytical Operations:
Perform and supervise analysis of Raw Materials (RM), Packing Materials (PM), and Finished Goods (FG).
Operate and maintain analytical instruments:- HPLC, GC, UV-Vis, FTIR, Dissolution Apparatus
Ensure compliance with ...
1 Opening(s)
4.0 Year(s) To 8.0 Year(s)
7.00 LPA TO 9.00 LPA
Position: ADL Executive
Location: Paria - Vapi
Experience: 4 - 8 Years
Industries: Pharma
Responsibilities:-
Develop and validate analytical methods for raw materials and finished products.
Operate instruments like HPLC, GC, UV, IR, and dissolution testers.
Prepare method validation protocols and reports as per ICH ...
2 Opening(s)
7.0 Year(s) To 15.0 Year(s)
9.00 LPA TO 12.00 LPA
Position: Executive/Asst. Manager - QA
Location: Pariya - Vapi
Experience: 7 - 15 Years
Industries: Pharma
Responsibilities:
Monitor manufacturing and packaging processes, including line clearance and in-process checks (IPQA)
Manage documentation activities, including DOC-QMS systems, SOP preparation, deviation handling, and change control
Support Technology Transfer ...
2 Opening(s)
5.0 Year(s) To 10.0 Year(s)
10.00 LPA TO 12.00 LPA
Position: Asst. Manager - Operation Excellence
Location: Ahmedabad
Experience: 5 - 10 Years
Industry : Pharma
Responsibilities:
Classification of Inventories.
Understanding and implementation of lean manufacturing work practices including 5S, AM and problem solving (including root cause analysis), to drive continuous improvement activity throughout the site.
Ensure all training for direct reports is ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
Not Disclosed by Recruiter
Bank GL Reconciliation – Review accounts, clear transactions in SAP, ensure accuracy, maintain ledgers.
Customer Sub-Ledger & Open Items – Analyze accounts, clear/match transactions, escalate issues, coordinate with GBSS/third parties, maintain ongoing clearing.
Open Sales Orders – Monitor/manage SOs and delivery status in SAP.
Fixed Assets – Review/update records, correct errors, coordinate for ...
1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 6.00 LPA
Responsibilities:
Operate and monitor capsule filling machines as per SOPs.
Perform line clearance, changeover, and basic machine maintenance.
Ensure accurate capsule weight, sealing, and batch output.
Maintain GMP compliance, documentation, and safety standards.
Coordinate with QA/QC for in-process checks.
Requirements:
ITI/Diploma/Graduate with 2–5 years’ experience in pharma capsule filling.
Knowledge of cGMP, SOPs, and machine troubleshooting.
Attention to detail ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.50 LPA TO 3.50 LPA
Position: Officer/Executive - QA
Location: Pariya - Vapi
Experience: 1 - 3 Years
Industries: Pharma
Responsibilities:
Review and approve batch records, laboratory data, and other relevant documents related to the manufacturing process.
Ensure all operations comply with GMP guidelines, FDA documentation requirements, and internal quality ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 6.00 LPA
Position: Officer/Executive – RA
Location: Paria - Vapi
Experience: 2 - 5 Years
Industries: Pharma
Responsibilities:
Compilation and review of regulatory dossiers (CTD, ACTD, eCTD) for CIS, LATAM (especially Brazil & Mexico), African, and EU regions.
Handle full lifecycle of product registration including new submissions, renewals.
Review technical documentation: ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
Not Disclosed by Recruiter
Support OE Head in driving Operational Excellence and site performance.
Facilitate manufacturing excellence initiatives across all departments.
Identify process improvement opportunities to enhance Productivity, Quality, Cost, Delivery & Safety.
Lead Focused Improvement & Daily Management Teams; deliver KPI improvements.
Train teams on structured problem-solving techniques.
Implement daily management tools (Fishbone, Pareto, 5 Why, FMEA); build ...
1 Opening(s)
11.0 Year(s) To 18.0 Year(s)
23.00 LPA TO 50.00 LPA
jD:
Serve as the company’s subject matter expert on drug safety and pharmacovigilance
Ensure compliance with Local & Global PV-relevant Heath Authority requirements
Oversee PV Contracts, vendor management and PV system audits/inspections
Have good understanding of signal management and benefit-risk evaluation activities
Develop and implement Risk Management Plans (RMPs) and additional Risk mitigation measures
Act as the primary safety liaison with country regulatory authorities ...