| Resume alert | Resumes 21 - 30 of 74 |
Data Analyst
Hyderabad, Telangana, India
... Responsibilities: Worked on Classifying the device and document the prototype for the FDA (Food and Drug Administration) clearance. Contributed in validating the Tools based on the SOP standards of the organization. Working on planning and executing ... - 2020 Mar 27
... Responsibilities: Worked on Classifying the device and document the prototype for the FDA (Food and Drug Administration) clearance. Contributed in validating the Tools based on the SOP standards of the organization. Working on planning and executing ... - 2020 Mar 27
Engineer Quality
Hyderabad, Telangana, India
... Ensured protocols, records, and procedures are in compliance with applicable FDA and ISO regulations and current Good Manufacturing Practices (cGMP). TECHNICAL SKILLS: FDA Quality system regulations, 21 CFR Part 11 (210, 211, 50, 820), protocols (IQ ... - 2020 Feb 24
... Ensured protocols, records, and procedures are in compliance with applicable FDA and ISO regulations and current Good Manufacturing Practices (cGMP). TECHNICAL SKILLS: FDA Quality system regulations, 21 CFR Part 11 (210, 211, 50, 820), protocols (IQ ... - 2020 Feb 24
Data Sales
Hyderabad, Telangana, India
... Working knowledge on regulatory compliance such as Food and Drug Administration (FDA) under Title 21 for pre-clinical and clinical trials. Gathered requirements from business by developing static mockups, and dynamic prototypes using HTML and CSS. ... - 2019 Dec 19
... Working knowledge on regulatory compliance such as Food and Drug Administration (FDA) under Title 21 for pre-clinical and clinical trials. Gathered requirements from business by developing static mockups, and dynamic prototypes using HTML and CSS. ... - 2019 Dec 19
Quality Engineer Mechanical
Hyderabad, Telangana, India
... Complied with Food and Drug Administration (FDA) regulations, Company policies, operating procedures, processes, and task assignments. Provided guidelines to production department on the implementation of assurances, process controls to ensure that ... - 2019 Oct 16
... Complied with Food and Drug Administration (FDA) regulations, Company policies, operating procedures, processes, and task assignments. Provided guidelines to production department on the implementation of assurances, process controls to ensure that ... - 2019 Oct 16
Clinical Research Data
Hyderabad, Telangana, India
... Project Trainee Lotus Clinical Research Academy, Bangalore July 2011 – February 2012 (8 months) Bangalore Training on different Regulatory Guidelines pertaining to Pharmaceutical Industry and Clinical Research such as FDA, EMA and ICH (CTD). Hands ... - 2019 Oct 08
... Project Trainee Lotus Clinical Research Academy, Bangalore July 2011 – February 2012 (8 months) Bangalore Training on different Regulatory Guidelines pertaining to Pharmaceutical Industry and Clinical Research such as FDA, EMA and ICH (CTD). Hands ... - 2019 Oct 08
Quality Engineer Medical
Hyderabad, Telangana, India
... engineering studies like TMV (Test Method Validation) and statistical approaches Extensive knowledge in Food and Drug Administration (FDA) regulations, GDP, 21 CFR Part 11, 210/Annex 11, 211, 810, 820, ISO 13485, ISO 9001, ISO 14971 (Safety and Risk ... - 2019 Oct 03
... engineering studies like TMV (Test Method Validation) and statistical approaches Extensive knowledge in Food and Drug Administration (FDA) regulations, GDP, 21 CFR Part 11, 210/Annex 11, 211, 810, 820, ISO 13485, ISO 9001, ISO 14971 (Safety and Risk ... - 2019 Oct 03
Engineer Quality
Hyderabad, Telangana, India
Pratikkumar Patel ■ Phone No: +1-618-***-****■ Email: ac5w8k@r.postjobfree.com Qualifications Summary ●4 years of experience as a Validation Engineer and Quality Engineer with expertise in Test Method Validation, Design Verification Strategy and FDA ... - 2018 Jun 18
Pratikkumar Patel ■ Phone No: +1-618-***-****■ Email: ac5w8k@r.postjobfree.com Qualifications Summary ●4 years of experience as a Validation Engineer and Quality Engineer with expertise in Test Method Validation, Design Verification Strategy and FDA ... - 2018 Jun 18
Data Manager
Hyderabad, Telangana, India
... Actively involved with data management team and statistician to analyze clinical trial data and to program integrated summaries (ISE and ISS), FDA, IND, submissions. In-depth work experience in generating tables, listings, and graphs(TLF) by ... - 2018 Apr 26
... Actively involved with data management team and statistician to analyze clinical trial data and to program integrated summaries (ISE and ISS), FDA, IND, submissions. In-depth work experience in generating tables, listings, and graphs(TLF) by ... - 2018 Apr 26
10 + years experience in QA QC in FOOD FSSC.ISO 9001:2015
Hyderabad, Telangana, India
... Lead Auditor Certification from DNV IRCA approved QMS ISO 9001:2015 Lead Auditor Certification from BSI IRCA approved US FDA Food Safety Modernization Act: Trained Preventive Controls Qualified Individual (PCQI) FSPCA six sigma certificate from ... - 2018 Apr 26
... Lead Auditor Certification from DNV IRCA approved QMS ISO 9001:2015 Lead Auditor Certification from BSI IRCA approved US FDA Food Safety Modernization Act: Trained Preventive Controls Qualified Individual (PCQI) FSPCA six sigma certificate from ... - 2018 Apr 26
Manager Test Cases
Hyderabad, Telangana, India
... Thorough knowledge about pharmaceutical/medical device regulations like FDA 21 CFR Part 11, part 820 and on ISO 13485/Part 820 / ISO 14971 Expertise in various SDLC methodologies such as Agile, Scrum and Waterfall in creating various protocols for ... - 2018 Apr 24
... Thorough knowledge about pharmaceutical/medical device regulations like FDA 21 CFR Part 11, part 820 and on ISO 13485/Part 820 / ISO 14971 Expertise in various SDLC methodologies such as Agile, Scrum and Waterfall in creating various protocols for ... - 2018 Apr 24