1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
12.00 LPA TO 15.00 LPA
Job Overview:
The Manager – Global Statutory Compliance will be responsible for ensuring the company's dental implants and medical devices adhere to international regulatory standards, including ISO 13085, FDA, and other country-specific statutory requirements. This role will involve overseeing the creation and management of Design History Files (DHF), ensuring proper document ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
2.50 LPA TO 3.00 LPA
1.Quality Control functions in Pharmaceutical manufacturing facility.
2.Testing and analysis of various raw materials and finished products.
3.Must be versatile with documentation as per GMP (Good Manufacturing Practice) including preparation of BMR, Analytical documents and other relevant statutory procedures.
4. Should have hands-on experience with statutory compliances, analytical instruments, with good knowledge of ...
1 Opening(s)
15.0 Year(s) To 18.0 Year(s)
15.00 LPA TO 20.00 LPA
JOB DESCRIPTION:• P and ID’s preparation for Utilities (Clean & Black)• Should have experience in Basic & Detail Engineering for Mechanical, Piping, Instruments, pharmaceuticalWater System, Capacity analysis, Sizing and selection of equipment.• Project Planning and control, Project Procurement in Pharmaceutical domain• Preparation of load list.• Preparation of Equipment list for ...
1 Opening(s)
18.0 Year(s) To 25.0 Year(s)
25.00 LPA TO 40.00 LPA
Position: Quality Head
Location: Bhopal
Experience: 18 - 25 Years
Industries: Pharma
Responsibilities:
Lead the QA/QC functions for biological and insulin product lines, ensuring compliance with global regulatory standards (FDA, EMA, etc.) and cGMP requirements.
Develop, implement, and maintain robust quality management systems, policies, and procedures for manufacturing and testing.
Drive cross-functional collaboration ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.50 LPA TO 3.00 LPA
Job Description
23.11.24
HPS/2024/729
Q/A
Male
1
2 to 5
BA/Diploma Plastic/BSc Cipet
Responsible for budgets and financial activities and are involved in approving or negotiating contracts and agreements and hire other managers or department heads.
Executives establish and carry out departmental goals, policies, and procedures and oversee the organization's financial and budgetary activities.
Experience:- 2 to 5 years
Salary : ...
4 Opening(s)
3.0 Year(s) To 16.0 Year(s)
12.00 LPA TO 50.00 LPA
Work with global R&D teams to develop software for new and existing medical device products. • Software design and development of embedded real-time systems, including the development of Software Unit Test & Integration plans and protocols. • Participates in reviews, code inspections and will support the development of documentation ...
5 Opening(s)
2.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 5.00 LPA
Job description
Role & responsibilities
Development of Analytical methods.
Validation of Analytical methods.
Preparing analytical method development reports.
Literature survey for existing analytical methods.
Carry out literature survey by establishing the strategies.
Maintenance of FDA department.
Coordinating various development activities in FDA laboratory.
Maintenance of reference standard, working standards and their standardization.
Co-ordinating the activities in Chemical and Instrumentation.
Analytical Method ...
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 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)
3.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 4.00 LPA
Job Description
12.06.24
HPS/2024/347
Q/A - Sr. Executive
Male
1
3 to 4
B.Parmacy / Diploma Parmacy
Responsible for budgets and financial activities and are involved in approving or negotiating contracts and agreements and hire other managers or department heads.
Executives establish and carry out departmental goals, policies, and procedures and oversee the organization's financial and budgetary activities.
Experience:- 3 ...