1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
7.00 LPA TO 8.50 LPA
) Develop, implement and maintain QMS, EMS, OH&S
2) New customer specification feasibility report
3) Maintaining customer technical specification, drawings records and documents
4) Preparing techno commercial offer
5) Conducting internal ISO audits
6) Preparing agenda and minutes for MRM
7) Monitoring departmental KPI
8) Develop and maintain ISO manual, sop, work instructions, process flow chart, QAP
9) ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
2.40 LPA TO 3.60 LPA
MANAGER - QC: ONEBudget – 20-30 k Gender : Male Age : 30 to 45JOB DESCRIPTION;Responsible for ensuring that the quality management system (QMS) is fully implemented and followedDevelop test procedures with the help of R&D and upgrade all test facilities as per demanding requirementof customersCoordinate with external agencies for ...
1 Opening(s)
7.0 Year(s) To 10.0 Year(s)
10.00 LPA TO 12.00 LPA
Position: Regional Manager
Location: Pune
Experience: 7 - 10 Years
Industry: Solar
Responsibilities:
Your job is to manage various projects running with the customer & ensure success on deliverables and commercial front.
You are solely responsible for achieving commercial success on the project by controlling the operational costs and ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: QA Officer
Location: Vapi
Experience: 3- 5 Years
Industries: Pharma API
Responsibilities:
Preparation, Review and Issuance of Departmental Sops, Guidelines and Policies.
LNB's and Logbooks Issuance and Checking for daily entries in Logbooks.
To Review various Documents like Change controls, Incident Reports, CAPA, OOS Results, Deviations, Issuance Records and ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
Not Disclosed by Recruiter
Job Description:
We are seeking a dedicated QMS professional to oversee and maintain the Quality Management System in compliance with cGMP and regulatory requirements. The role involves managing documentation, handling quality events, and supporting internal and external audits in an API manufacturing environment.
Key Responsibilities:
Implement and maintain QMS processes in line with ...
1 Opening(s)
15.0 Year(s) To 22.0 Year(s)
15.00 LPA TO 25.00 LPA
Experience in implementing departmental policies, goals, objectives, and procedures; conferring with managing director, departmental in-charge and factory staff
Proficient in modern methodical quality systems, production tools & techniques ? Proficient in taking corrective action for any negative trends related to product quality, customer service, machine capacity, labor efficiency, resource utilization, and ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
4.80 LPA TO 6.00 LPA
Responsibilities:
Perform initial inspection and raise report.
Coordinating between all sites of the company for Quality Control.
Review the process of construction at the site periodically & profess changes to adhere to quality norms.
Following ISO procedures.
Updating ISO documents.
Formulate & Implement Quality Systems in the company.
Review and final approval of the Construction Record Book ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
2.16 LPA TO 2.40 LPA
Perform initial inspection and raise report.
Coordinating between all sites of the company for Quality Control.
Review the process of construction at the site periodically & profess changes to adhere to quality norms.
Following ISO procedures.
Updating ISO documents.
Formulate & Implement Quality Systems in the company.
Review and final approval of the Construction Record Book ...
10 Opening(s)
4.0 Year(s) To 6.0 Year(s)
5.00 LPA TO 7.00 LPA
b Description:
Experience in designing UI web applications, HTML websites, Flash Websites, Logos and Icons.
Translate designs and style guides into functional user interfaces, ensuring cross browser compatibility, performance and robustness.
Ability to quickly turn around detailed wireframes, mock-ups, or visual comps in an iterative environment.
Work on module players and upgrade the versions ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
6.00 LPA TO 8.00 LPA
Provide leadership planning and work assignment.
Drug licence application and renewable of licence in State Drug Authority for different type of Formulation.
Monitoring & Maintaining Quality Systems in the plant to meet State GMP requirements.
To organize inspection & testing of Raw Material, In-Process & Finished Products.
Planning and carrying out self-inspection of all ...