3 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
QMS: Maintain detailed documentation of QMS(change control, deviation, incident, market complaints, product recall)
VMP: maintain and execution of Validation plan as per schedule
Master index: Prepare and maintain of Master index for SOP, STP, Protocols, MFR, BMR/BPR
Document control: Issue and retrieval of documents like BMR/BPR, SOP, Formats, and log books
APQR: Prepare the ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 4.00 LPA
Carry out sampling as per sampling Plan.
Carry out analysis as per documented procedure.
Monitor Control Points in QMS &EMS.
Inform emergency to superiors
Maintain relevant records of QMS &EMS.
Document the analytical results as per statutory requirement
To carry out Quality Control functions as per standard procedure.
Ensure initializing request for & follow up on corrective ...
1 Opening(s)
0 To 1.0 Year(s)
1.00 LPA TO 2.00 LPA
Job Location- Wagholi Pune
JOB DESCRIPTION
Deliver business value through Right and Fast partnershipBe a part of a team of Quality Engineers at the (insert site)
that applies its expertise and knowledge in finding innovative,
cost-effective means to improve quality output and continuous
improvements. You will drive process initiatives that ensures
compliance with customer requirements, regulatory ...
3 Opening(s)
0 To 1.0 Year(s)
1.00 LPA TO 1.44 LPA
Job Description:
1.R&D Dept- 01 Male
Exp: 0-2 Yrs
Job profile and responsibilities:
•New Business case study like technology roadmap meeting / RFQ meeting.
•Competitor product study like design concept, material, Bill of Material and developing new ideas.
•Preparation of Material shortage sheet and make planning accordingly and communicate with the purchasing team.
•Preparation of Proto samples and meeting with customers, sharing all the details, taking the requirement and fulfill accordingly.
•Submission of R&D proto sample report to the customer and taking approval for SOP.
•Arranging and leading pre-handover and handover meetings.
•.Responsible for planning & developing new product as per customer requirement.
•Monitoring PFS, FS, MDS and APQP sheet.
2.QMS Dept- 01 Male
Exp: 0-2 Yrs
Job profile and responsibilities:
Handles TPM , TS & Quality Documents as per Customer Requirement .
Handles Customer Complaints
Preparing Presentations of Rejection Analysis and presents it to the management.
Conducting IPO & Process Audits in order to continually refine the process ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
1.80 LPA TO 2.40 LPA
Designation: Quality inspector (Male or Female)
Education : DME/ITI
Experience : 1-2 years
Job Skill required:
1 Well knowledge about assembly part defects & Child part inspection
2 QMS Documentation Knowledge -IPO, Control Plan, QA/QM Matrix, FPA, SIR, Dimensional inspection, RM report preparation
3 Check ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
6.00 LPA TO 6.50 LPA
Position: Quality Manager
Location: Silvassa
Experience: 3 - 4 Years
Industries: Packaging
Responsibilities:
Ensure all documentations are accurate and complies as per QMS requirement.
Ensure products comply with customer specification and regulatory requirements with supporting documents.
Verify that products adhere to customer specifications ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
Housekeeping & Facility Management
Supervised daily housekeeping across GMP/non-GMP areas, washrooms, corridors, pest control, horticulture, waste disposal, and audits as per pharma hygiene & EHS standards.
Maintenance & Repairs
Coordinated preventive maintenance, civil/electrical/plumbing/carpentry repairs, and maintained documentation for audit readiness.
Inventory & Vendor Management
Managed consumables inventory, vendor manpower, schedules, compliance, and invoice processing.
Audit & ...
3 Opening(s)
3.0 Year(s) To 7.0 Year(s)
3.00 LPA TO 7.00 LPA
Job Summary:We are seeking a detail-oriented and experienced Quality Control (QC) Engineer –Machining & Structural Fabrication with 3–7 years of hands-on experience in qualityinspection for crane components or heavy structural fabrication. The role involves thoroughinspection of machined components and fabricated structures to ensure compliance withquality standards, design specifications, and customer ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 6.00 LPA
We are seeking a detail-oriented and experienced QC Engineer to oversee and improve the quality assurance processes in our coil manufacturing plant. The QC Engineer will be responsible for developing quality standards, conducting inspections, analyzing data, and ensuring compliance with industry standards and customer requirements.
Key Responsibilities:
Develop, implement, and maintain quality control procedures ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 4.20 LPA
Position: Executive/Asst. Manager - QA
Location: Silvassa
Experience: 2 - 10 Years
Industries: Pharma
Responsibilities:
Ensure compliance with GMP, regulatory guidelines, and quality standards in pharmaceutical formulation manufacturing.
Manage quality systems, audits, documentation, validations, and batch release while leading the QA team.
Implement and maintain Quality Management ...