1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
10.00 LPA TO 12.00 LPA
About Augrade:At Augrade, our mission is to make AR/VR more accessible & adaptable to how we live, work & play.We’re a wearable tech startup working on AR glasses for B2B industry starting with a niche focus on Architects & interior designers. We enable them to ideate, design & present their ...
77 Opening(s)
3.0 Year(s) To 10.0 Year(s)
Not Disclosed by Recruiter
Software Developer
Hands on experience in development of Linux/Containers/Hypervisor/Boot loader/Linux Device drivers/BSP /IPC/ System Programming. Mandatory: C/C++Hands-on strong experience in C++ coding in embedded software Automotive projects with good knowledge on at least one ECU. Worked on Microservices architectures with strong knowledge on IPCs.Knowledge on vehicle features desired
1 Opening(s)
14.0 Year(s) To 18.0 Year(s)
30.00 LPA TO 35.00 LPA
The preferred working location for this role is the Medtronic facility located in Hyderabad - India
Bring your talents to an industry leader in medical technology and healthcare solutions – we’re a market leader and growing every day. You can be proud to be a part of technologies that are rooted ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
32.00 LPA TO 35.00 LPA
Position: Plant Head (Medical Device)
Location: Daman
Experience: 15- 20 Years
Industries: Pharma - Medical Device
Responsibilities:
To ensure annual production plan and dispatch plan. To prepare manufacturing plan, dispatch plan and material plan so as to meet the customer ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
30.00 LPA TO 35.00 LPA
Job Title: Associate Vice President/ Sr. Manager
Department: Human Resource
Reports to: Vice President- HR
Span of Control: The HR team in the areas of Recruitment, HR Operations, Compliance, PMS, Training, etc.
Required Qualification: - Master's degree in Human Resources/ Business Administration or related field
Experience: 12-15 years’ experience in Generalist HR /HRBP/ HR Operations role in a reputed organization.
Experience in ...
1 Opening(s)
8.0 Year(s) To 12.0 Year(s)
7.00 LPA TO 8.00 LPA
Position: Sr. Executive - RA
Location: Daman
Experience: 8 to 12 Years
Industries: Pharma
Responsibilities:
Maintaining compliance with ISO 13485, MDD, and MDR requirements.
Preparing technical and device master files
Preparing and compiling documents for registration to various countries
Reviewing and updating of documents w.r.t various regulatory requirements
Reviewing and updating ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 6.00 LPA
Sr. No
Details
1
Capex:
1) Collaborate with Users & Buyers to create & implement procurement strategies for CAPEX purchases and categories of spend.
2) Should be responsible for Capex procurement of (To Be Defined)
2
OPEX Purchase:
1) Arranging timely procurement and supply of all Engineering consumables, boiler fuel & utility consumables and spares of specified quantity ...
1 Opening(s)
4.0 Year(s) To 8.0 Year(s)
4.00 LPA TO 6.00 LPA
Position: Sr. Executive/Asst. Manager -QA
Location: Vapi
Experience: 4- 8 Years
Industries: Medical Device
Responsibilities:
Should have experience in Medical Device
Coordinate with Certification body for Certification / Surveillance Audit.
Conduct Internal Quality audit as per define timeline.
Document and Data control by periodic review of SOPs, Formats.
Develop, ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
Not Disclosed by Recruiter
We are hiring for ANZ PDT and Complaints Coordinator (Quality Associate) for Medical Devices Company at Hyderabad
Designation : ANZ PDT and Complaints Coordinator (Quality Associate)
Qualification : BSC/ MSC or Bio Medical Sciences/Engineering
Work Timings :09:30am to 05:30pm
Working Days : Monday to Friday
Experience : Min 2 Years
Location: Hyderabad
Salary: Best in industry
Other Details:- Payroll company - Talisman HR
Industry- Medical Device (MNC Pharmaceutical)
Primary ...
1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 7.00 LPA
Job Description:
Position: Sr. Officer/ Executive - RA
Location: Daman
Experience: 3 to 6 Years
Industries: Pharma
Responsibilities:
Maintaining compliance with ISO 13485, MDD, and MDR requirements.
Preparing technical and device master files
Preparing and compiling documents for registration to various countries
Reviewing and updating of documents w.r.t various regulatory requirements
Reviewing and updating of documents ...