1 Opening(s)
7.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 12.00 LPA
Role Purpose:Customer focus - Delivering products well within customer’s expectations on delivery, service, communicationsetcSafety- Building a safer work environment through People centric actionsQuality- Relevant Product quality acceptable to the customer without any defectsDelivery- Delivering on committed timelines to the customer. Deliver in terms of overall improvements inoperations (OTIF)Cost- Developing and ...
1 Opening(s)
10.0 Year(s) To 20.0 Year(s)
10.00 LPA TO 25.00 LPA
A. Organization Context
PositionTitle: Plant Quality HeadEmployeeName: Grade :Department: Location:
Reports to: Unit Head Reported by:
Mgr. QualityChemists(Physical/Chemical/Microbiologist)
B. Job Objective• Develop and ensure Quality Management systems as per regulatory guidelines andquality standards within plant in order to ensure customer satisfaction and businesssustainability.• Develop and sustain Quality culture across the plant• Review product quality ...
1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
8.00 LPA TO 9.00 LPA
Role Purpose: Contributing to the development and handling of Integrated Management System (IMS) at A1 Fencefor meeting the product characteristics to deliver best quality product to the customer and helping organization inmoving towards Goal, vision and adherence to the organization policies.Smooth execution of order from shop floor to customer. Timely ...
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)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 6.00 LPA
M. Sc. / B. Pharm / M. Pharm: 4 - S yrs. of Exp. in QA Documentation, SOP preparation, Change Control, and CAPA, possess knowledge of production prcuzess, experience on activiEes (Analytical'O, handling ISO audits.Doc
M. Sc. / B. Pharm / M. Pharm: 4 - S yrs. of Exp. in QA ...
1 Opening(s)
4.0 Year(s) To 10.0 Year(s)
Not Disclosed by Recruiter
QUALIFICATION : BE in Mechanical, Production or Electronics or Business Proven technical skills on product and processExperience 4 to 10 years experience from Automobile industry.
Gender: MaleWork location: Vasai East in Mumbai
Keyskills: Quality, NPD, New product development, GD&T, PPAP, CFT, PFMEA, DFMEA, CAPA, "customer complaint", "supplier Quality", PDIR
Job profile:Able to handle overall Quality activities like NPD, ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
Not Disclosed by Recruiter
The Analyst role will be a change maker to support various aspects of our systems (QMS, ISMS,and Continual Improvements) to increase the standardization and effectiveness of ouroperations; with direct responsibilities in areas of implementation, and monitoring, of Systemsand continual improvements, and to accelerate technology adaptions in quality management,associated reporting analytics; ...
1 Opening(s)
4.0 Year(s) To 7.0 Year(s)
8.00 LPA TO 10.00 LPA
Position: Sr. Quality Engineer
Location: Sanjan Nearby Vapi
Experience: 4 -7 Years
Industries: Engineering
Responsibilities:
Coordinate with Certifying bodies for conducting External Audits within the timeline.
Ensuring Internal Audits are conducted timely.
Ensuring all the NCs (Internal/External) are closed within the timeline.
Adding new certification in the interest ...
1 Opening(s)
0 To 2.0 Year(s)
1.44 LPA TO 1.80 LPA
Position: Quality Shift Inspector
Location: Daman
Experience: 0 -2 Years
Industries: FMCG
Responsibilities:
In Process Quality control compliances as per quality control plan. - IPQC Report
Destructive tests as per Product Specification - Destructive Test Report.
In Process FG sampling as per ISO sampling or customer standards - IPQC Report.
Helping Quality shift ...
1 Opening(s)
16.0 Year(s) To 20.0 Year(s)
Not Disclosed by Recruiter
Inward Quality Inspection:
Inspection Planning: Develop a daily inspection plan based on material receipts, prioritize inspections according to urgency, and ensure all transactions are accurately recorded in the ERP system.
Sampling Plan Decisions: Design and implement an inspection sampling plan to ensure quality standards.
Rejection Reporting & Management: Report rejections promptly, and coordinate ...