| Resume alert | Resumes 41 - 50 of 52 |
Manager Pvt Ltd
New Delhi, DL, India
... FDA (SHIMLA) Audit Faced WHO, cGMP, GHANA & CONGO Strengths • Achievement Oriented with an ability to manage change with ease. • Multi task taking ability, good communication, Strong learning and organizing skills. • Ability to manage stress, time ... - 2014 Jul 19
... FDA (SHIMLA) Audit Faced WHO, cGMP, GHANA & CONGO Strengths • Achievement Oriented with an ability to manage change with ease. • Multi task taking ability, good communication, Strong learning and organizing skills. • Ability to manage stress, time ... - 2014 Jul 19
Quality Control Assurance
New Delhi, DL, India
... Job Profile : Quality control technologist in microbiological laboratory, performing routine sea food testing method as per us FDA, EU, guidelines. PROJECT M PHIL RESEARCH PROJECT Screening of salmonellae is culture raised head on shrimps (p.monodon ... - 2014 May 24
... Job Profile : Quality control technologist in microbiological laboratory, performing routine sea food testing method as per us FDA, EU, guidelines. PROJECT M PHIL RESEARCH PROJECT Screening of salmonellae is culture raised head on shrimps (p.monodon ... - 2014 May 24
Cv for the Post of Manager QA/ Deputy Manager QA
Delhi, DL, India
... US-FDA (TRIGEN) 7. UKRAINE AUDIT Details of Experience 1) Experience as an Assistant Quality Assurance Chemist with Brawn Laboratories Limited. N.I.T. Faridabad (An ISO 9001-2000 WHO, GMP Certified) since 7th Sep. 2004 to 18th Oct. 2005. Company ... - 2013 Jun 27
... US-FDA (TRIGEN) 7. UKRAINE AUDIT Details of Experience 1) Experience as an Assistant Quality Assurance Chemist with Brawn Laboratories Limited. N.I.T. Faridabad (An ISO 9001-2000 WHO, GMP Certified) since 7th Sep. 2004 to 18th Oct. 2005. Company ... - 2013 Jun 27
Quality Assurance Manager
NOIDA, UP, 201301, India
... Co-ordination of Regulatory (US-FDA, MHRA etc.), Customers and Internal Audits. Total Manpower Reporting to QA, Manager about 80. Panacea Biotec Ltd., Dy. April 2001 Creation and implementation of New Delhi General to Oct, 2002 Quality Systems as ... - 2013 May 04
... Co-ordination of Regulatory (US-FDA, MHRA etc.), Customers and Internal Audits. Total Manpower Reporting to QA, Manager about 80. Panacea Biotec Ltd., Dy. April 2001 Creation and implementation of New Delhi General to Oct, 2002 Quality Systems as ... - 2013 May 04
Quality Control Training
Delhi, DL, India
... > More than Three and Half Years of experience in SHASUN CHEMICALS AND DRUGS Ltd., (US FDA, ISO 9002:2001,) as an Officer Q.C in Microbiology at Cuddalore Unit from November 2003 to June 2007. > Three Years of experience in Medispan Pharmaceuticals ... - 2013 May 03
... > More than Three and Half Years of experience in SHASUN CHEMICALS AND DRUGS Ltd., (US FDA, ISO 9002:2001,) as an Officer Q.C in Microbiology at Cuddalore Unit from November 2003 to June 2007. > Three Years of experience in Medispan Pharmaceuticals ... - 2013 May 03
Manager Quality Control
Gurgaon, HR, India
... • Worked as Officer in ARD Lab, with Vitalife Laboratories Ltd, (Gurgaon, Haryana) a US FDA Unit, Division of Arch Pharma (Mumbai) from Nov 09 to July10. • Analytical method development and validation as per ICH guidelines by HPLC and UV • Execution ... - 2012 Nov 04
... • Worked as Officer in ARD Lab, with Vitalife Laboratories Ltd, (Gurgaon, Haryana) a US FDA Unit, Division of Arch Pharma (Mumbai) from Nov 09 to July10. • Analytical method development and validation as per ICH guidelines by HPLC and UV • Execution ... - 2012 Nov 04
Project Manager Management
Gurgaon, HR, 122001, India
... Clin Rheumatol DOI 10.1007/s10067- 010-1402- Area of Interest: > Clinical Trials > Pharmacovigilnace > Drug Regulatory Affairs > IPR > P'Ceutical Medicine > P'Co therapeutics > Good Comprehension of FDA and guidelines, Good Clinical Practice (GCP), ... - 2012 Sep 05
... Clin Rheumatol DOI 10.1007/s10067- 010-1402- Area of Interest: > Clinical Trials > Pharmacovigilnace > Drug Regulatory Affairs > IPR > P'Ceutical Medicine > P'Co therapeutics > Good Comprehension of FDA and guidelines, Good Clinical Practice (GCP), ... - 2012 Sep 05
Maintenance Research
Greater Noida, UP, 201308, India
... h Conceptual knowledge of ICH-QSEM topics in reference to individual regulatory markets (US-FDA, EDMQ/EMEA (PDMA).s h A keen communicator with honed problem solving, synthetic design and analytical abilities. CAREER CONTOUR TEVA API India Ltd., ... - 2012 Aug 19
... h Conceptual knowledge of ICH-QSEM topics in reference to individual regulatory markets (US-FDA, EDMQ/EMEA (PDMA).s h A keen communicator with honed problem solving, synthetic design and analytical abilities. CAREER CONTOUR TEVA API India Ltd., ... - 2012 Aug 19
Medical Pharmaceutical
New Delhi, India
... , Defense R & D Organization (DRDO), New Delhi TECHNICAL EXPERTISE Utravoilet visible - spectrophotometer Dissolution studies Gamma Scintigraphy Techniques Acute and Subacute Toxicity Studies in rodents Documentation – for DCGI, FDA, HEC etc . ... - 2012 Jun 27
... , Defense R & D Organization (DRDO), New Delhi TECHNICAL EXPERTISE Utravoilet visible - spectrophotometer Dissolution studies Gamma Scintigraphy Techniques Acute and Subacute Toxicity Studies in rodents Documentation – for DCGI, FDA, HEC etc . ... - 2012 Jun 27
Scientist
New Delhi, DL, 110089, India
... SPE QuChERS & US EPA Technique AOAC and other Contemporary Techniques US FDA Approved Kit Proficient in Agilent UHPLC that include: Setting up and validating the carbohydrates such as Sucrose, Dextose, Fructose, Maltose and Glycerol on RI detector. ... - 2012 Jan 11
... SPE QuChERS & US EPA Technique AOAC and other Contemporary Techniques US FDA Approved Kit Proficient in Agilent UHPLC that include: Setting up and validating the carbohydrates such as Sucrose, Dextose, Fructose, Maltose and Glycerol on RI detector. ... - 2012 Jan 11