1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
4.00 LPA TO 7.00 LPA
Position Overview:The Global Regulatory Specialist will be responsible for coordinating regulatory documentation to supportManagement of Change projects. Situated in Global Regulatory Affairs, the specialist will prepare, review andfinalize all regulatory documents for defined projects, varying in scope. The specialist will operate in a cross-functional role interfacing between registration teams and ...
1 Opening(s)
6.0 Year(s) To 7.0 Year(s)
6.00 LPA TO 7.00 LPA
Job Description: Experience in handling regulatory affairs for ROW market mainly Central and Latin American, African & Asian countries for Pharma Formulations.
? Preparation, Compilation & Review of Registration documents that include Administrative & Technical.
? Reviewing the technical documents provided by QA, QC, Production providing them the report of shortcomings & ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
10.00 LPA TO 15.00 LPA
Position: Regulatory Manager
Location: Mumbai
Experience: 5 - 8 Years
Industries: Chemical
Responsibilities.
Global Product Registration & Dossier Management
Lead the full registration lifecycle (pre-market research, submission, renewal) for all target export countries.
Compile regulatory dossiers, including 5-batch analysis and efficacy data, ensuring strict adherence to national formats.
Serve ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
5.00 LPA TO 7.00 LPA
Quality Assurance Specialist Responsibilities:
Ensure product quality and conformity to regulatory standards, including Medical Device Regulation (MDR) and Quality Management System (QMS).
Conduct internal quality audits and participate in management review meetings.
Handle investigations of complaints and implement corrective and preventive actions.
Maintain and update quality manuals, formats, and standard operating procedures (SOPs) in ...
1 Opening(s)
0 To 5.0 Year(s)
1.00 LPA TO 4.00 LPA
s.Preparing estimates and budgets.Creating accurate project specifications.Designing engineering experiments.Creating technical reports for customers.Cos.Preparing estimates and budgets.Creating accurate project specifications.Designing engineering experiments.Creating technical reports for customers.Completing regulatory documents concerning
safety issues.mpleting regulatory documents
s.Preparing estimates and budgets.Creating accurate project specifications.Designing engineering experiments.Creating technical reports for customers.Cos.Preparing estimates and budgets.Creating accurate project specifications.Designing engineering ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
6.00 LPA TO 7.20 LPA
Job Title: International Purchase & Supplier Management Executive
Role Objective
To manage end-to-end purchase activities against sales orders, ensuring timely purchase execution, commercial optimization, contractual compliance, and seamless coordination with international suppliers and internal stakeholders. The role is accountable for converting sales demand into accurate, compliant, and cost-effective purchases through SAP. ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
3.00 LPA TO 3.60 LPA
Knowledge of Clinical Evaluation Reports (CER) as per EU MDR, MEDDEV 2.7/1 Rev 4.
Perform the risk benefit analysis as per ISO 14971 to demonstrate the medical device benefits outweighed the residual risk.
Writes and contributes to Clinical Evaluation reporting deliverables including Clinical Evaluation Plans/Reports, PMS and PMCF Plans/Reports, SSCPs, Regulatory Responses ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
Not Disclosed by Recruiter
Job Description:
Lead product certification activities and ensure compliance with national and international standards.
Liaise with external laboratories, certification bodies, and regulatory agencies for product approvals.
Prepare, review, and maintain technical documentation, test reports, and compliance files.
Conduct internal compliance audits and implement corrective & preventive actions (CAPA).
Monitor updates in industry regulations and revise ...
1 Opening(s)
5.0 Year(s) To 12.0 Year(s)
Not Disclosed by Recruiter
Key Job Responsibilities:
Draft, review, and negotiate real estate contracts, agreements, Memorandums of Understanding (MoUs), and notices.
Ensure proper formatting, stamping, and registration of all legal documents.
Maintain an organized central repository of all contracts and agreements.
Ensure transactions and projects comply with all relevant real estate laws and regulations, such as ...
1 Opening(s)
8.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 15.00 LPA
· To supervise and control sampling of raw materials finished products and packaging material as per defined procedures.
· To analyze critical finished products and new products for Active content and impurity profile.
· Develop/Standardize/validate analytical methods for raw materials and finished products.
· To create secondary reference standards for product analysis and maintain depository for primary ...