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)
3.0 Year(s) To 9.0 Year(s)
14.00 LPA TO 27.00 LPA
Job Description
• Responsible for executing CFD based analysis & design validation of gas turbine combustion systems, development rig and engine test campaigns, planning, monitoring, data reduction and verification, validation. • Execute & lead combustion aero design CFD– 2D/3D analysis, 1D flow, evaluating and propose new solutions to meet design CTQ’s.• ...
1 Opening(s)
10.0 Year(s) To 16.0 Year(s)
15.00 LPA TO 18.00 LPA
Position: Manager/Sr. Manager -QA
Location: Daman
Experience: 10 to 16 Years
Industries: Pharma
Responsibilities:
Qualification of Facility
Approval of URS,SOP, Protocol & Report
Approval of area layouts & equipment positioning layout
Qualification of equipment’s
Process validation
Utility system validation
HVAC system validation
Required Skills
Greenfield Project Experience
Excellent Communication
Required Qualification: - B.pharm/M.pharm
Salary :- Upto 15.00 to 18.00 LPA
If you are interested for this opening ...
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 ...
1 Opening(s)
8.0 Year(s) To 12.0 Year(s)
12.00 LPA TO 14.00 LPA
Vacancy For DGM Production
Experaince in API Production is mandotory
B Pharma/M Pharma/Ph D Pharma is mandotory to apply.
Job location - Ambernath, Dist - Thane, Maharashtra
Age should be less than 40 year
Job Description
To organize, supervise and control the production activity till raw material dispensing to packing.
Monitor constantly the progress of monthly production plan and collaborate with subordinate in dealing with all shop floor problems.
Ensure that the products are manufactured and storage according to appropriate documentation.
Responsible for qualification and validation document review.
Daily monitoring of OAE and reporting to Production head.
Drive the production team to deliver operational excellence with quality and customer service targets.
Preparation of Quality Risk Assessment (QRA), APQR and support to perform Cleaning Validation, Process Validation activity.
Ensure the operations shall perform with documentation integrity.
Handling of Change Control, Audit compliances, Investigation of Deviation, OOS, Market Complaints etc.
Ensure departmental training for effectiveness of CAPA, SOP, HSE.
Provide opportunities for development of product team with particular emphasis on the process.
Develop team to solve day-to-day operational issues and planning of goals, organize and facilitate work team meetings.
1 Opening(s)
8.0 Year(s) To 14.0 Year(s)
8.00 LPA TO 12.00 LPA
Technical Skills :
Design And Development :
Conceptualize, design, and detail precision fixtures, jigs, and gauges specifically for heat exchanger assembly and testing processes.
Technical Analysis And Validation :
Create comprehensive technical layouts, assembly drawings, and detailed part drawings using advanced CAD software.
Production Support And Optimization :
Develop and validate gauge designs for in-process and ...