Job Description
Roles and Responsibilities
Authorizing & reviewing medical device Design History File (DHF/DMR/DHR) according to relevant requirements(MDR/FDA/ISO 13485)
PIP making as per their controlled document & updating periodically & upload on SAP.
Prepare & provide technical documents to regulatory team.
Compiling & updating risk management documentation(ISO 14971).
Documentation & distribution of controlled design, controlling of change control note (ECR) & update DHR.
Compiling new SOPs, formats & updating existing SOPs & formats & updating existing SOPs & formats as needed.
Desired Candidate Profile
- Any Graduate from Science background only.
- Only Female candidates.
- Good hand on MSWord, Excel and internet explorer.
- Local candidates preferred.
If interested please share your updated CV with the below details to hrd7@polymedicure.com
Current Location -
Current Salary -
Expected salary -
Notice Period -
Regards,
HR
Poly Medicure Limited
Education
UG:B.Sc in Any Specialization
Company Profile
Polymed
Contact Company:Polymed
Address:Plot No.104 105,,HSIIDC Industrial Area,Sector-59,, Ballabgarh, FARIDABAD, Haryana, India
Salary:
Not Disclosed by Recruiter
Industry:
Department:
Role Category:
Pharmaceutical & Biotechnology
Role:
Medical Writer
Employment Type:
Full Time, Permanent