1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
6.00 LPA TO 8.00 LPA
ISO full form is International Organization for Standardization. It is considered as an Independent, non- governmental, non-profitable, the worldwide federation of national standards bodies that can develop and publishes international standards.
ISO full form is International Organisation for Standardization. It is considered as an Independent, non- governmental, non-profitable, the worldwide federation ...
2 Opening(s)
2.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
Greetings from Talisman HR Solution
We are hiring Quality Engineer for Manufacturing industry at Vasai
Designation: Quality Engineer
Experience: Min 2 years
Location: Vasai & Goregaon
Working days: Monday to Saturday (Sunday fixed off)
Working time: 09:30 am to 06:00 pm
Salary: As per company norms
Other Employee benefits: Bonus, PF, ESIC, Medical, Travelling allowance, Paid leaves etc.
Age: up to 35 ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
0.96 LPA TO 1.00 LPA
Job Title: QA/ QC Engineer
Experience: 5 years
Salary: AED 7,000-8,000
Job Location: Dubai, U.A.E
Contract Period: 3 years and renewable
Probation Period: 6 months
Working hours: 10 hours per day
Food and Accommodation has to be arranged by the Employee with the allowance to be provided by the Employer.
Job Summary:
The QA/QC Engineer will be responsible for ...
1 Opening(s)
6.0 Year(s) To 8.0 Year(s)
7.00 LPA TO 8.00 LPA
Position: Safety Officer
Location: Vatva - Ahmedabad
Experience: 6 - 8 Years
Industries: Chemical
Responsibilities:
Legal compliance related to safety health andenvironment of the site.
Knowledge on GPCB consent including monthlyreturn ,annual return, environment audit statement submission, hazardous waste return submission & its compliance, Handling of ETP operation and guide to ETP operator.
Knowledge ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 8.00 LPA
Conduct all ISO 9001:2015 Certification Audits, management review meetings, customer audits anddocument performance toward quality objectives? Improve and update our current ISO 9001:2015 Quality System and will implement ISO 14001 andOSHAS 18001 systems going forward.? Prepare and maintain Quality Checklists, forms, and reports. Review actual procedures whenrequired.? Provide updates to ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
10.00 LPA TO 12.00 LPA
Hiring for PCB Manufacturing Industry.
Position: Quality Manager/GM
Qualification: BE - Electronics/Mech/Electrical
Work Experience: 15-20 years
Work profiles:
Additional Knowledge - IATF Internal Audit , Six Sigma Yellow /Green Belt
Preferably from Mechanical / Automobile/ EMS / Electronics / PCB ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.50 LPA TO 3.00 LPA
Must be Diploma/B.E in Rubber, cipet ,
Should have 02 to 05years of Rubber Industry excluding Tyre and Footwear
Should have Technical knowledge of Silicone
Should have knowledge of ISO:9001, HSE:14001 & OHSAS:
Should be certified ISO
Should have knowledge of Clean Room
Should have knowledge of Rubber Testing
Must have good command over English Language written ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 15.00 LPA
Must be B.E in Rubber
Should have 10 to 15 years of Rubber Industry excluding Tyre and Footwear
Should have Technical knowledge of Silicone
Should have knowledge of ISO:9001, HSE:14001 & OHSAS:
Should be certified ISO
Should have knowledge of Clean Room
Should have knowledge of Rubber Testing
Should have handled a team of 5 to 6
Must ...
1 Opening(s)
5.0 Year(s) To 15.0 Year(s)
4.00 LPA TO 5.50 LPA
Hiring for QMS / MR/ TPM Manager
Experience: Min 5 Years in Experience in operating the quality management system & Integrated Management System (EMS & OHSAS), TPM, Kaizen, Writing procedures and processes to support the QMS development, internal auditing, and QMS documentation.
Salary budget: up to 5.50 LPA
Key Responsibilities :
Preparation and maintenance of the company for IMS (ISO 9001:2015 OHSAS 18001:2007, ...
1 Opening(s)
2.0 Year(s) To 9.0 Year(s)
2.00 LPA TO 5.00 LPA
Responsible for: . Analyzing, collecting data, and providing accurate, documented information abou
t the status of quality . Verifying the correctness of quality related development results in compliance
with the Quality Management Plan & authorize their release for medical devices . Validation of compliance to basic requirements, e.g. ISO standards and
regulations like ...