2 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.20 LPA TO 2.30 LPA
Designation: Quality Engineer (M)
Salary: Rs.16,000 to Rs. 18,000/- PM
Qualification: BE Mechanical, ASNT Level-II
Soft skills: computer proficiency, good communication skill
Experience: 1-2 years of experience in Fabrication.
Knowledge in quality standards and inspection as per ASME Sec VIII
Responsibilities
Set detailed guidelines on what needs to be checked and what the quality standards are
Update our ...
1 Opening(s)
0 To 2.0 Year(s)
2.16 LPA TO 2.40 LPA
Job description
HPS/2022/105 02 HPS/2024/147
Quality Cum
Male
1
0 to 2
DME/BE Mech
We are looking for a talented Quality Control to join our team. If you are excited to be part of a winning team, Key-Tech Engineering is a right place to grow your career.
Some of the responsibilities include:
Candidate must be well aware of all types ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 3.60 LPA
Material Inspection: Conduct thorough inspection of all incoming materials during inward processing. Maintain detailed records of material inspections using Excel.
Quality Instruments: Utilize various quality instruments, including Vernier calipers and gauges, to ensure accurate measurements and adherence to specifications.
Calibration Management: Update and maintain calibration reports for all relevant instruments. Ensure the proper ...
1 Opening(s)
14.0 Year(s) To 20.0 Year(s)
Not Disclosed by Recruiter
Qualification: BE in Mechanical, Automobile, Production EngineeringExperience: 14 to 20 years of experience from Press shop, Sheet metal plant, Automobile fabrication assembly plant.Work location: Shirwal in Pune
Job Responsibilities:Manage the quality control processReview and update for PPAP, PFD, PFMEA, Control Plan and Process inspection standards.Ensuring continuous improvement in process and product quality ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
6.00 LPA TO 10.00 LPA
DUTIES & RESPONSIBILITIES: Leading and accessing the Quality Improvement Projects (QIP), lean implementation, continual improvement and six sigma projects across JLL factories. Active team member of quality system design (SOP, Inspection, Safety, QA manual, Analysis. PQP, QFD) and responsible person for implementation of the same. Responsible for factory auditing (Own/3P) ...
2 Opening(s)
8.0 Year(s) To 15.0 Year(s)
0.00 LPA TO 20.00 LPA
Bachelor’s degree in Mechanical Engineering.
8 years’ proven experience as an QA Engineer in a fast-paced environment
He shall be fully familiar with ISO-9001-2015 Quality Management System.
ISO 9001:2015 Lead Auditor Certified.
Expert knowledge of technical design processes, flowcharting techniques, and code compliance.
Ability to balance the scope of large projects while managing.
Welding Knowledge ...
1 Opening(s)
2.0 Year(s) To 8.0 Year(s)
10.00 LPA TO 15.00 LPA
Develop and Implement Quality Systems:
Design and establish a comprehensive quality management system (QMS) to ensure consistent service delivery.
Ensure adherence to both internal standards and external regulatory requirements specific to the banking sector.
Process Optimization & Continuous Improvement:
Analyze current processes to identify areas for improvement and efficiency.
Lead continuous improvement initiatives using methodologies ...
1 Opening(s)
3.0 Year(s) To 8.0 Year(s)
Not Disclosed by Recruiter
Former experience in the following:
Working in Medical Device: Initiate, monitor, and verify the effective implementation of the Quality Management System in all areas of company activities
Regulatory submissions: Regulations requirements of the ISO 13485; FDA; CE (MDD/MDR) and MEDDEV
Composing and maintaining quality manual procedures (i.e., SOP’s), Follow the requirements of GLP/GMP.
Internal ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
Not Disclosed by Recruiter
JD For QARA
Regulatory Compliance:
Stay updated on medical device regulations, standards, and guidelines (e.g., FDA, ISO, CE Marking).
Ensure that products meet all regulatory requirements and maintain relevant documentation.
Quality Assurance:
Develop and implement quality assurance processes and procedures.
Conduct internal audits and assessments to identify areas for improvement.
Collaborate with ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
Description :
Regulatory Compliance:
Stay updated on medical device regulations, standards, and guidelines (e.g., FDA, ISO, CE Marking).
Ensure that products meet all regulatory requirements and maintain relevant documentation.
Quality Assurance:
Develop and implement quality assurance processes and procedures.
Conduct internal audits and assessments to identify areas for improvement.
Collaborate with production teams to establish quality control ...