1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 3.60 LPA
04.12.25
121436
HPS/2025/618
QC Engineer
Male
1
2 to 5
DME/ITI/B.E-Mechanical
8 Hours
GET - QUALITY CHECKER
Develop and maintain a quality management system to achieve qualityobjectives and ensure customer satisfaction. Prepare, revise, and upgrade quality plans, including inspectionprocedures, in accordance with process reliability, stability, and clientexpectations. Implement a robust QA and QC plan and mechanism across the entireoperation ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.40 LPA TO 3.60 LPA
Job Responsibilities:
Maintain QMS documentation, SOPs, training records & audit readiness
Conduct internal audits for clinical, BE & pharmacovigilance operations
Support vendor audits, gap assessments, CAPA tracking, compliance reviews
Ensure adherence to ICH GCP, regulatory guidelines & quality standards
Required Qualification:
B.Pharm/M.Pharm/MSc in Life Sciences
1–3 years experience in QA within CRO/BE/Clinical Trial setup
Understanding of QMS, risk ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
7.00 LPA TO 9.00 LPA
What you’ll do:* Work across all teams and job functions in founders office to organise, schedule, track, past, existing, and upcoming projects* Liaison between the CEO and all teams for arranging meetings, call to actions, and outcomes* Reach out to external and third party stakeholders on behalf of the founder ...
3 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.60 LPA TO 3.60 LPA
Perform routine calibration and maintenance: Conduct periodic preventive maintenance, testing, and calibration of all instrumentation equipment (including sensors, transmitters, and control valves) according to manufacturer specifications and relevant industry standards (e.g., ISO, NABL, cGMP).
Troubleshoot and repair instrumentation systems: Diagnose, analyze, and repair defects or malfunctions in complex control systems, including Programmable Logic ...
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)
15.0 Year(s) To 20.0 Year(s)
40.00 LPA TO 50.00 LPA
Vacmet India LtdReports To: Director - Product Development
A. New Product Development (NPD) Lead development of new BOPET film grades, including:o Metallizable & metalized filmso Heat-sealable filmso Matte, Alox, coated, chemically treated filmso Specialty films (shrink films, label films, insulation-grade films, lamination films) Conduct feasibility studies, lab-scale trials, and pilot/industrial trials. Develop ...
1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
7.00 LPA TO 7.00 LPA
We are looking for a proactive and customer-focused Team Leader – Client Servicing to oversee and manage the client servicing team for our courier aggregation platform. The ideal candidate will ensure seamless customer experience, timely issue resolution, and strong coordination between clients, internal teams, and courier partners.
Team Management
Lead, guide, and ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 3.00 LPA
Key Responsibilities:
* Record and post daily financial transactions accurately in Tally.* Handle Accounts Receivable and Accounts Payable, including invoicing, collections, and vendor payments.* Maintain accurate books of accounts, ledgers, and supporting documentation.* Prepare and manage export-related documentation in standard formats.* Perform bank and ledger reconciliations and resolve discrepancies.* Assist in ...
3 Opening(s)
2.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 4.50 LPA
Process Excellence: Analyze and optimize manufacturing steps (e.g., granulation, blending, compression, coating, filling) to improve yield, throughput, and cycle time using continuous improvement methodologies.
Troubleshooting & RCA: Quickly diagnose and resolve technical issues, equipment malfunctions, and production deviations, performing Root Cause Analysis (RCA) and implementing CAPAs (Corrective and Preventive Actions).
Equipment & ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 8.00 LPA
Oversee day-to-day production activities for formulation batches as per approved BMR/BPR.
Ensure compliance with cGMP, GDP, and regulatory guidelines (WHO, EU, USFDA, MHRA as applicable).
Monitor production planning, batch scheduling, material requirement, and manpower allocation.
Coordinate with QA, QC, Warehouse, Engineering, and RA for smooth production operations.
Review and ensure timely completion of batch ...