Electronic Qc

Product Vertical (Auto/Aero/HE/O&G) Defence Product Domain RF & Microwave Software NA Experience Range (Years) to YEARS Qualification (Minimum) / : ELECTRONICS Notice period / Candidate Availability Months Work days Per Week Shifts (if shifts, Shift allowance) Transportation facility NO Canteen facility NO Number of...

Job Description: · Incoming inspection of components, cables and assemblies in accordance with inspection activity carried out on day-to-day basis.· Reject all products and materials that fail to meet quality expectations with the concurrence of QA as situations raises· Document inspection results and maintain accurate inspection records for...

**Position: Observer** **Job Code: 602 (Forward your profile, mentioning job code in the Subject Line)** **Location : Project sites within India.** **Education**: B.E/B.Tech/B.Sc. Electronics & Electrical **Experience & Skills** - Minumum 5 years experience in seismic industry as an Observer - Should have experience in operation and maintenance of latest...

a)You shall need to prepare and review SOPs, STM, protocols, worksheets, records, reports etc. as per GMP/GLP requirements. b)You need to carry out validations of analytical methods and all other validations related to Microbiology lab and prepare protocols &reports. c)You need to ensure that cultures and standards are maintained properly. d)You need to...

**Summary**: Ensure compliance with internal and external guidelines, to compile and add electronic navigation to clinical and regulatory documents. Support the timely submission of documents to the Health Authorities (HAs) and provide publishing consultancy to the clinical teams and other line functions. **About the Role**: **Major accountabilities**: -...

About the RoleWe are seeking an experienced Digital Transformation Lead to drive innovation and excellence in lab systems implementation within the pharmaceutical sector.Job DescriptionThis is a senior leadership role that requires strategic direction, technical expertise, and people management skills. The successful candidate will lead a global team...

**Company Description** Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because **Good Health Can’t Wait**. We started in 1984 with a modest...

Job Profile Summary The Statistical Programmer II provides technical expertise for the conduct of clinical trials, and works with mínimal supervision to support various programming activities related to the analysis and reporting of clinical study data. In addition, the Statistical Programmer II may fill the Statistical Programming Lead role (or part of...

Looking for a candidate at the level of an ‘Associate Director’ that can drive innovation and excellence in lab systems implementation within pharmaceutical sector Lead and provide strategic direction to a global team accountable for delivering (Opex & Capex), and lifecycle of laboratory information management systems, QC Lab enterprise systems,...

Looking for a candidate at the level of an ‘Associate Director’ that can drive innovation and excellence in lab systems implementation within pharmaceutical sectorLead and provide strategic direction to a global team accountable for delivering (Opex & Capex), and lifecycle of laboratory information management systems, QC Lab enterprise systems,...

Looking for a candidate at the level of an ‘Associate Director’ that can drive innovation and excellence in lab systems implementation within pharmaceutical sector Lead and provide strategic direction to a global team accountable for delivering (Opex & Capex), and lifecycle of laboratory information management systems, QC Lab enterprise systems,...

JOB SUMMARY Responsible for providing statistical programming support for the Biostatistics and Data Management functions for all clinical trials and regulatory submissions. Works closely with Biostatisticians and Data Managers to support creating SAS programs for independently validating tables, listings, and figures produced by programming vendors, for...

JOB SUMMARY Responsible for providing statistical programming support for the Biostatistics and Data Management functions for all clinical trials and regulatory submissions. Works closely with Biostatisticians and Data Managers to support creating SAS programs for independently validating tables, listings, and figures produced by programming vendors, for...

JOB SUMMARYResponsible for providing statistical programming support for the Biostatistics and Data Management functions for all clinical trials and regulatory submissions. Works closely with Biostatisticians and Data Managers to support creating SAS programs for independently validating tables, listings, and figures produced by programming vendors, for...

Responsible for providing statistical programming support for the Biostatistics and Data Management functions for all clinical trials and regulatory submissions. Works closely with Biostatisticians and Data Managers to support creating SAS programs for independently validating tables, listings, and figures produced by programming vendors, for ad-hoc...

Responsible for providing statistical programming support for the Biostatistics and Data Management functions for all clinical trials and regulatory submissions. Works closely with Biostatisticians and Data Managers to support creating SAS programs for independently validating tables, listings, and figures produced by programming vendors, for ad-hoc...

JOB SUMMARY Responsible for providing statistical programming support for the Biostatistics and Data Management functions for all clinical trials and regulatory submissions. Works closely with Biostatisticians and Data Managers to support creating SAS programs for independently validating tables, listings, and figures produced by programming vendors, for...

JOB SUMMARYResponsible for providing statistical programming support for the Biostatistics and Data Management functions for all clinical trials and regulatory submissions. Works closely with Biostatisticians and Data Managers to support creating SAS programs for independently validating tables, listings, and figures produced by programming vendors, for...

**Description** At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, to the partnerships we build, to the conversations we foster, we affirm the crucial value of Diversity, Equity, Inclusion and Belonging in...

**Description** **Brief Job Overview** This is a non-supervisory position in Reference Standard Laboratory responsible for performing the required tests as part of the project and maintaining the GLP environment in the Laboratory. The incumbent will utilize his or her technical expertise, knowledge of pharmaceutical analysis in collaborative testing,...