560 Job openings found

1 Opening(s)
3.0 Year(s) To 8.0 Year(s)
Not Disclosed by Recruiter
Job Objective Responsible for quality testing, inspection, chemical analysis and process-quality control of hard packaging materials. The role will ensure that incoming raw materials, in-process materials and finished packaging products meet defined quality specifications and customer requirements. 2. Key Responsibilities A. Raw Material Testing Conduct testing and inspection of incoming raw materials. Check COA, specifications ...
2 Opening(s)
3.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
Job Responsibilities: Online quality checking & FG To give feedback to production & Quality Department regarding online deviations and get the corrective actions To maintain all documentations as per IPQA To help operations maintain GMP Preparation of the In Process analysis reports for QC To lead and monitor IPQA activities in the Pre dispatch samples sending, communication ...
2 Opening(s)
2.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 4.00 LPA
Key Responsibilities Manage receipt, storage, and issue of raw materials, packing materials, and finished goods. Ensure proper identification, labeling, segregation, and storage of materials as per GMP guidelines. Maintain warehouse records, stock registers, and inventory documentation. Handle material inward/outward activities and coordinate with Production, QC, and QA departments. Follow FIFO/FEFO practices and ensure proper stock ...
2 Opening(s)
2.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 5.00 LPA
Key Responsibilities Perform testing of raw materials, intermediates, APIs and finished products Handle routine analysis using HPLC, GC, UV, IR, pH meter, KF, etc. Prepare and maintain COA, analytical reports, worksheets and laboratory records Follow GMP, GLP, SOP and data integrity requirements Ensure proper sampling, testing and documentation as per specifications Investigate OOS/OOT results and support ...
1 Opening(s)
2.0 Year(s) To 7.0 Year(s)
0.00 LPA TO 7.00 LPA
Sr. Executive – Quality Control Company: PYG Lifesciences Private LimitedLocation: Sayakha GIDC, BharuchExperience: 2–5 YearsEmployment Type: Full-Time | On-siteNo. of Positions: 01 Role Overview:We are looking for a Sr. Executive – Quality Control with experience in API, API Intermediates, Specialty Chemicals, or Synthetic Organic Manufacturing. The candidate will be responsible for raw ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 5.00 LPA
 Position:        QC Executive Location:         Silvassa Experience:     2 - 6 Years Industries:      Pharma Responsibilities:  Perform sampling and testing of raw materials, in-process and finished products. Conduct chemical/physical analysis as per SOPs and specifications. Maintain QC records, logbooks, worksheets, and test reports. Operate and maintain laboratory instruments and equipment. Handle OOS/OOT investigations and support CAPA activities. Ensure compliance ...
8 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.50 LPA TO 6.00 LPA
Description: Position:       Officer/Sr.Officer - QC Location:         Vapi Experience:     2  – 5  Year Industries:      Pharma Formulation Responsibilities: Perform analysis of Raw Materials, Finished Products, Stability samples, and Method Validation samples as per approved procedures. Operate and handle sophisticated laboratory instruments such as HPLC, Dissolution Apparatus, and UV-Visible Spectrophotometer. Handle QC laboratory ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 6.00 LPA
Shift Incharge / Production Supervisor Jobs in Chemical Manufacturing | Orbit Global HR Consultants Job Title: Shift Incharge / Production SupervisorIndustry: Chemical / Aerosol / Process ManufacturingExperience: 5+ YearsPreferred Experience: 8–10+ Years in relevant manufacturing operationsAge Preference: Around 30 YearsSalary: ₹30,000–₹40,000 per monthEmployment Type: Full-timeShift: Rotational / Shift Duty – Candidate ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
Not Disclosed by Recruiter
Location: Digwal, TelanganaEmployment Type: Full-TimePayroll: Third-Party Payroll (Staffing Partner)Work Schedule: Monday to SaturdayWorking Hours: 9:00 AM – 6:00 PM About the Company Our client is a leading multinational pharmaceutical manufacturing company with a strong global presence. The position will be on the payroll of our organization, which has been the client's trusted ...
4 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 4.00 LPA
Documentation review and reconciliation. Responsible and ensuring following GMP. Granulation Process Management: Oversee all aspects of the granulation process, including equipment setup, operation, and troubleshooting. Ensure that granulation activities are carried out efficiently and in compliance with standard operating procedures (SOPs) and regulatory requirements. Team Leadership: Lead and supervise a team of granulation operators, ...

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