5 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
๐ Documentation & Compliance
Preparation, review, and control of SOPs, BMRs, BPRs, and other GMP documents
Ensure proper documentation practices (GDP compliance)
Handling change control, deviation, and CAPA
๐ญ Shop Floor QA Activities
Line clearance before batch initiation
In-process checks and verification
Monitoring of manufacturing and packing activities
๐งช Validation & Qualification
Support in process validation, cleaning validation
Equipment qualification ...
5 Opening(s)
1.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 7.00 LPA
Position: QA Asst Manager ( OSD , ORAL LIQUID & OINTMENT FACILITY) Position: QA Asst. Manager Vacancy: 01 Location: VAPI- GUJARAT Experience: 10 to 15 Years Qualification: B. Pharma / M. Pharma Core Technical Expertise: ๏ท IPQA (In-Process Quality Assurance): Hands-on experience in monitoring manufacturing and packaging processes, line clearance, ...
2 Opening(s)
3.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
IPQA activities, Plant round, Online BMR review, Line clearance, Samplingof APIs, Analytical data review, Batch release, APQR preparation. People who have faced regulatory audits like EDQM would be givenpreference.
Process & cleaning validation, including cleaning matrix preparation
QMS documentation management; SOP preparation, review, and training
IPQA activities
to ensure GMP compliance during manufacturing.
Regulatory inspection exposure ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
3.00 LPA TO 3.60 LPA
Position: Shift Officer - Production (Pharma API)
Location: Vapi
Experience: 2 - 3 Years
Industries: Pharma API
Responsibilities:
Execute API manufacturing activities as per Batch Manufacturing Records (BMR), SOPs, and GMP requirements.
Operate and monitor reactors, centrifuges, filters, dryers, and other production equipment.
Ensure accurate charging of raw materials and ...
1 Opening(s)
9.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 14.00 LPA
A Quality Assurance (QA) Manager for a Starch Powder Active Pharmaceutical Ingredient (API) or excipient manufacturing plant oversees cGMP compliance, quality management systems (QMS), process validations, and regulatory audits tailored to pharma-grade modified or native starches used as excipients/APIs.
Job Title: Quality Assurance Manager
Industry: Pharmaceutical API, Excipients & Starch Powder Manufacturing
Reporting ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
Not Disclosed by Recruiter
Job Description:
We are looking for an IPQA Executive to monitor and ensure in-process quality during manufacturing and packing operations in our API facility. The ideal candidate will be responsible for real-time quality assurance, GMP compliance, and documentation control throughout the production lifecycle.
Key Responsibilities:
Perform in-process checks during various stages of API ...
2 Opening(s)
1.0 Year(s) To 2.0 Year(s)
3.00 LPA TO 3.60 LPA
Position: Quality Officer
Location: Daman
Experience: 1 - 2 Years
Industries: Plastic
Responsibilities:
Line clearance during manufacturing and packing activities.
Testing of incoming material (RM & PM), Semi-Finished and Finished Goods as per specification.
IN process Inspection.
Redispatch Inspection.
Preparation of dimensional report.
Attending Customer place.
Preparation of COA
Knowledge about system & ...
2 Opening(s)
2.0 Year(s) To 7.0 Year(s)
3.00 LPA TO 7.00 LPA
Generic
Implement Quality Assurance activities for Pharmaceutical at Ankleshwar adhering to standard operating procedures with optimum utilization of resources to ensure consistent good quality of products to meet with customers’ requirements, living Group’s Values and Code of Ethics.
Specific additions (if needed)
KEY ACCOUNTABILITIES
Quality Management/Continuous Improvement
Line Clearance and shop floor compliance
Assisting in Complaint ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
1.00 LPA TO 5.00 LPA
RESPONSIBILITIES:1. To issue the Batch Manufacturing Record, Equipment cleaning record, Logbooks, AnalyticalReport for raw material, finish product and packing material.2. Assistance in preparation of SOP of various departments/ preparation of draft SOPs.3. During plant round QA Executive to verify documents as per cGMP and GLP norms.4. Line Clearance activities for ...
4 Opening(s)
4.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
To issue the Batch Manufacturing Record, Equipment cleaning record, Logbooks, Analytical Report for raw material, finish product and packing material.
Assistance in preparation of SOP of various departments/ preparation of draft SOPs.
During plant round QA Executive to verify documents as per cGMP and GLP norms.
Line Clearance activities for manufacturing and packaging ...