5 Opening(s)
1.0 Year(s) To 6.0 Year(s)
Not Disclosed by Recruiter
Responsibilities
Perform and supervise In-Process Quality Assurance (IPQA) OR QA checks during API manufacturing operations.
Conduct on-line review of Batch Production Records (BPR) and ensure adherence to approved procedures.
Ensure sampling, line clearance, and process compliance as per GMP/cGMP norms.
Identify, record, and support resolution of deviations, non-conformances, and quality incidents during manufacturing.
Support quality investigations and prepare required ...
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: IPQA (In-Process Quality Assurance): Hands-on experience in monitoring manufacturing and packaging processes, line clearance, ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 4.50 LPA
Position: QC Chemist
Location: Vatva - Ahmedabad
Experience: 4 - 5 Years
Industry: Chemical
Responsibilities:
Perform quality testing and analysis of raw materials, in-process samples, and finished products.
Conduct chemical analysis using laboratory instruments and testing equipment.
Ensure products meet defined quality specifications and standards.
Prepare and maintain test reports, COA, and ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 3.60 LPA
Plans and directs activities concerned with the development, application, and maintenance of quality standards for industrial processes, materials, and products: Develops and initiates standards and methods for inspection, testing, and evaluation, utilizing knowledge in engineering fields such as chemical, electrical, or mechanical.
Devises sampling procedures and designs and develops forms and ...
3 Opening(s)
0 To 3.0 Year(s)
1.80 LPA TO 4.80 LPA
Perform incoming raw material inspection and finished goods evaluation.
Ensure compliance with customer specifications and international quality standards.
Review and maintain COAs, Specifications, SOPs, Batch Manufacturing Records, and quality documentation.
Coordinate product testing with NABL-accredited laboratories.
Monitor GMP, GHP, HACCP, sanitation, and hygiene practices.
Conduct in-process quality checks during production.
Handle customer quality questionnaires and technical ...
10 Opening(s)
2.0 Year(s) To 8.0 Year(s)
6.00 LPA TO 6.50 LPA
Position: Executive/Sr. Executive - QA
Location: Vapi
Experience: 2 - 8 Years
Industries: Pharma - API
Responsibilities:
Develop, implement, and maintain quality assurance procedures and documentation.
Conduct routine inspections, audits, and quality checks.
Monitor compliance with company policies, industry standards, and regulatory requirements.
Investigate quality issues, deviations, customer complaints, and ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
2.00 LPA TO 3.50 LPA
All Quality Activities and UT Testing
Job Details
Participate in team projects and project/technology transition
Develops and initiates standards and methods for inspection, testing and evaluation.
Devises sampling procedures and designs and develops forms and instructions for recording, evaluating and reporting quality and reliability data.
Develops and implements methods and procedures for disposition of discrepant ...
1 Opening(s)
0 To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: Officer/Executive - Production
Location: Silvassa
Experience: 0 - 5 Years
Industries: Pharma
Responsibilities:
Execute daily production activities as per the approved production plan and batch schedule.
Ensure manufacturing of cosmetic and pharmaceutical products in compliance with GMP, SOPs, and quality standards.
Supervise dispensing, manufacturing, filling, packing, and batch changeover ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 5.00 LPA
Responsible for ensuring sheet metal press components meet strict automotive standards.
Core duties include conducting first-piece inspections, performing process/ Pokayoke audits, monitoring in-house rejections (IHR), and managing documentation for IATF requirements.
Specific responsibilities and requirements for this role often include:
Core Responsibilities
Inspections: Conduct 1st piece inspections against samples and ensure components meet drawing ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
14.00 LPA TO 14.00 LPA
Total Experience Required: Min 8 to 10 years ofexperience in R&D. in any polymer processingindustry having large varieties of product, whichare technically enriched.
Travel Required: Yes
Position would be reporting to: General Manager – Technical
Job Description:1) To Develop New Products as per the market & Business requirement2) Modification of the existing product ...