5 Opening(s)
15.0 Year(s) To 20.0 Year(s)
12.00 LPA TO 14.00 LPA
About Company
This company provides metal Tech Factory is a state-for the art manufacturing branch in Dammam, Where our highly skilled workforce design, Fabricate, assemble, test Gas Modular skids, oil modular skids, chemical injection skids, pressure deduction skids, multiphase flow meter skids, atmospheric vessels, all type of metallic piping spools and ...
2 Opening(s)
2.0 Year(s) To 9.0 Year(s)
Not Disclosed by Recruiter
Job Description:
As a Gemologist, you will play a crucial role in ensuring the quality assurance of gemstones and providing gemological inputs for sourcing purposes.Your expertise will help take our gem division to the next level by enhancing our formal understanding of gemstones.
Responsibilities: -
? Conduct quality assurance (QA) assessments of gemstones ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
6.00 LPA TO 7.00 LPA
Position: Head Coordinator - Customer Centricity
Location: Mumbai
Experience: 3 - 5 Years
Industries: Pharma - API
Responsibilities:
Order Receipt & Verification :
Receive and verify customer orders and supporting documents from the Sales/Marketing Team (including product specifications, customer-specific specifications, PO, delivery instructions and packing instructions).
Validate ...
2 Opening(s)
3.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 6.00 LPA
Production Management: Supervise and coordinate all shift production activities, ensuring adherence to the planned schedules and achieving production targets. This includes monitoring process parameters, raw material usage, yields, and overall operational efficiency.
Quality and Compliance Assurance: Ensure strict compliance with cGMP (current Good Manufacturing Practices), Standard Operating Procedures (SOPs), and other regulatory guidelines ...
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 ...
5 Opening(s)
1.0 Year(s) To 6.0 Year(s)
Not Disclosed by Recruiter
We're hiring for the following position for one of our reputed clients. Kindly find details.
Role: QA
Location: Bangalore
Job Description / Responsibilities:
Interfacing with other dept./CSE/Customers in case of issues
Attending the production meetings
Proof checking and clearing from concern person.
Shade matching on proofing machine
Sorting out queries from machine personnel if any.
Maintaining MIS as per current system
Preparing ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 4.00 LPA
WorksAsInward Quality Engineer & MonitoringChild Part Quality.
ConductingAuditsAt Supplier Endsi e.Projection WeldingAudits,MIGWelding& Head
PipeMfgAudits,System Audits.
AdherenceTo InwardsGaugesCalibration Plan & CorrectingIf NCObserved ,
Maintaining Supplier PPM Records& CommunicatingWith Concern Also Preparing Vendor
Meet Presentation
MonitoringRaw Material TestingPlan (Monthly) & CommunicatingTo Concern If NC’s
Observed Also Sending Special Raw Material For TestingAt CustomersEnd (BAL).
MonitoringAnd SolvingQuality Related ...
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 ...
3 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 4.00 LPA
Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards.
To approve or reject, as he sees fit, raw materials, packing materials, semi finished product and finished products as per agreed/approved Specification.
To review and approve analytical reports, validation protocols, calibration reports, environmental monitoring planner and other documents of ...
1 Opening(s)
4.0 Year(s) To 8.0 Year(s)
Not Disclosed by Recruiter
JOB RESPONSIBILITIES:
Monitoring & co-ordinate with all QA Activities & maintained all documentations require for IATF 16949, Feedback analysis (QPCR), MIS & KPI
Manage & track 8D & QPCR report for customer complaint, ensuring closure within defined deadline dates.
Conducting Morning Meeting, Red Bin meeting, Dock Audit, Process Audit & Part Audit regularly or as per Agenda
Monitoring Performance Charts on Quality Board. & prepare Presentations on various topics for Performance review ...