1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: QA Officer
Location: Panoli - Ankleshwar
Experience: 3 - 5 Years
Industries: Pharma
Responsibilities:
Preparation, Review and Issuance of Departmental Sops, Guidelines and Policies.
LNB's and Logbooks Issuance and Checking for daily entries in Logbooks.
To Review various Documents like Change controls, Incident Reports, CAPA, OOS ...
1 Opening(s)
4.0 Year(s) To 8.0 Year(s)
6.00 LPA TO 10.00 LPA
Roles and Responsibility
1. Visual & Physical Inspection of PM as per company and regulatory standard.2. Clearence of Packing material as per AQL plan and supplier quality improvement in coordination with purchase for noncompliance and ensure proper RCA & CAPA from vendor.3. Vendor audits for Existing & New Vendor Development.4. Must ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 6.00 LPA
Position: Maintenance Engineer
Location: Silvassa
Experience: 5 - 10 years
Industries: Pharma
Responsibilities:
Maintenance of Manufacturing & Packing Equipment’s.
Support to JH - CLIT Preparation, review & trainins.to operator.
Support to JH - Yellow Tag Mitigation & Weekly Update
why-why analysis of ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
3.60 LPA TO 4.80 LPA
A Manager of QC/QA/NABL is responsible for developing, implementing, and maintaining a company's quality management system to ensure compliance with industry standards, such as NABL accreditation. Key responsibilities include overseeing quality control processes, conducting internal and external audits, ensuring product quality through testing and inspections, resolving quality issues, managing documentation, and ...
2 Opening(s)
5.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 3.60 LPA
Position: Sr. Executive - Production
Location: Vapi
Experience: 5 - 6 Years
Industries: Plastics
Responsibilities:
Analyze Plan vs Actual Production and conduct gap analysis to identify variances.
Schedule and reschedule machines and equipment to optimize production flow.
Ensure line clearance before production start-up and after batch completion.
Plan resources efficiently, including manpower, ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
9.00 LPA TO 10.00 LPA
Position: QC Manager
Location: Daman
Experience: 10 - 15 Years
Industries: Pharma
Responsibilities:
Oversee day-to-day QC operations including sampling, testing, and release of raw materials, in-process, and finished products.
Conduct Process Capability Analysis (Cp/Cpk) and implement Statistical Process Control (SPC) to maintain consistent product quality.
Ensure adherence to Risk-Based Approach to ...
1 Opening(s)
5.0 Year(s) To 7.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: QA Executive
Location: Vapi
Experience: 5 - 7 Years
Industries: Pharma
Responsibilities
Preparation, Review and Issuance of Departmental Sops, Guidelines and Policies.
LNB's and Logbooks Issuance and Checking for daily entries in Logbooks.
To Review various Documents like Change controls, Incident Reports, CAPA, OOS Results, Deviations, Issuance Records and Internal Audit Reports.
Prepare, Review ...
1 Opening(s)
7.0 Year(s) To 8.0 Year(s)
8.00 LPA TO 10.00 LPA
Position: Shift Incharge - Production
Location: Ankleshwar
Experience: 7 - 8 Years
Industries: Chemical
Responsibilities.
Ensure the Plant Operation with Full Safety.
Ensure the Production, Yield Targets are achieved with specified Quality Parameters.
Ensure the Employees skill upgradation time to time for various job rotation.
Ensure the plant follows ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
12.00 LPA TO 15.00 LPA
Position: QC Manager
Location: Ankleshwar
Experience: 8 - 10 Years
Industries: Chemical
Responsibilities:
Supervise quality control operations for raw materials, intermediates, and finished agrochemical products.
Ensure compliance with ISO, GLP, and regulatory standards such as FAO, WHO, and EPA guidelines.
Oversee analytical testing using instruments like HPLC, GC, UV-Vis, and FTIR.
Develop, ...
2 Opening(s)
3.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 5.50 LPA
Position: QA Officer
Location: Saykha near by Bharuch
Experience: 3 - 6 Years
Industries: Chemical
Responsibilities:
Ensure current versions of all GMP documents are in use across departments.
Prepare, revise, and control SOPs and related quality documents.
Implement and enforce Good Documentation Practices (GDP).
Prevent retention of ...