2 Opening(s)
5.0 Year(s) To 10.0 Year(s)
25.00 LPA TO 40.00 LPA
Minimum 5 year of experience, should have experience in Implementation and support both.
IDM /SSO Specialist to perform the below activities:
IDM Implementation
Sanity check & Environment Validation
Base OIM Configuration
Firewall opening requests for OIM to connect to AD, OID, HCM
OID
Complete pre-reqs
Connector installation
Connector configuration
Reconciliation configuration
Provisioning Configuration
Technical Validation
AD
Complete pre-reqs
AD Connector installation
AD Connector configuration
AD Reconciliation configuration
Provisioning ...
1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 5.50 LPA
B Position : Sr. Executive
BE Mechanical
Required Skills : Experience in Validation and Calibration activities, candidate from calibration laboratory or from pharm industry is suitable
CTC Maximum 5 to 5.5 Lakh Max
Minimum Experience 3 years
B Position : Sr. Executive
BE Mechanical
Required Skills : Experience in Validation and Calibration activities, candidate from calibration laboratory ...
1 Opening(s)
4.0 Year(s) To 7.0 Year(s)
5.00 LPA TO 10.00 LPA
Skills and competencies:
? Must have knowledge of Automotive protocols:
? CAN ,
? XCP ,
? SPI , I
? 2C.
? Must have worked on automation test tools:
? Vector CANOe, ? vTestStudio, ? CAPL.
? Worked on requirement management tools like:
? JIRA
? Aware of Defect management.
? Shall have worked in Diagnostic testing based on ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
2.40 LPA TO 2.50 LPA
Job Description• To perform IPQA activities at shop floor in each and every stage of sterile manufacturing and packing.• QA overview for clean room behavior and aseptic activity.• Review of batch processing records.• Review of all documents relating to the manufacturing, Packaging & analysis report prior to batch release.• Review ...
1 Opening(s)
6.0 Year(s) To 7.0 Year(s)
6.00 LPA TO 7.20 LPA
Responsibility- 1. Knowledge of analysis related to process plastic, Rubber, LSR
Able to do all types of trial on machine related to process
Able to make the SOP of all mould
Able to make the setup sheet of new mould after process validation and if any process change in running mould
5.New mould process validation and ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
6.00 LPA TO 7.20 LPA
We have an urgent opening for the position of R&D Engineer for a reputed Manufacturing Company at the Umargam(Gujarat) location.
Job Description:
In-depth understanding of design, development, and validation of Electronics products.
Experience in PCB design and has worked in quality control in the R&D department.
Exceptional knowledge in Design, Development & Validation of analog and ...
4 Opening(s)
0 To 0
0.00 LPA TO 0.00 LPA
Medical Reviewer
we’re creating a culture that enables exceptional outcomes. Forget business as usual. This is about pursuing some of the world’s most exciting, cutting-edge technologies; inspired solutions that enhance the lives of millions across the globe. Our workplace thrives on ideas and opportunities. Everyone is invited to challenge convention, and ...
2 Opening(s)
1.0 Year(s) To 5.0 Year(s)
3.50 LPA TO 4.50 LPA
Position: Officer/Executive - QA
Location: Vadodara
Experience: 1 - 5 Years
Industries: Pharma
Responsibilities:
Review and approve batch records, laboratory data, and other relevant documents related to the manufacturing process.
Ensure all operations comply with GMP guidelines and internal quality standards.
Conduct internal audits to assess ...
5 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 5.00 LPA
System Operation & Monitoring:
Operate, monitor, and troubleshoot purified water, water for injection (WFI), and pure steam generation systems, including but not limited to, reverse osmosis (RO) units, deionization (DI) units, multi-effect stills, and clean steam generators.
Monitor critical parameters such as temperature, pressure, flow rate, conductivity, TOC (Total Organic Carbon), and ...
2 Opening(s)
3.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 5.50 LPA
Position: QA Officer
Location: Sarigam nearby Vapi
Experience: 3 - 6 Years
Industries: Chemical
Responsibilities:
Ensure current versions of all GMP documents are in use across departments.
Prepare, revise, and control SOPs and related quality documents.
Implement and enforce Good Documentation Practices (GDP).
Prevent retention of obsolete ...