Surya Payidiparty Email & Phone Number | A progressive, forward-thinking professional in pharmaceutical quality with proven success in managing all aspects of testing, quality systems , manufaturing and personnel. Drive compliance with federal regulations and corporate guidelines at all stages of quality testing and quality systems. Skilled trainer and mentor and able to guide staff in all laboratory,Quality and manufacturing functions. SKILLS • More than 18 years of experience in pharmaceutical Quality Control ( Chemistry, microbiology, Environmental monitoring , Raw Material) Compliance and manufacturing including 7 years of management experience. • Strong knowledge in cGMP, GLP, GXP, USP, EU, 21 CFR, TGA, Data Integrity, Quality systems and change management. • Solid knowledge in CAPAs, Deviations, OOS , OOT, investigations, root cause analysis, customer complaints, internal audits, regulatory agency audits. • Experience in Health Canada, FDA, ICH and USP, BP, ISO regulations • Proficiency in method transfers, new product launches, method development, method validations and equipment qualifications. • Experience in technical quality agreements, recalls, complaints, contract laboratories, supplier qualification, Drug Establish License (DEL) process, Stability management, Annual Product Quality Reviews (APQRs) and 3rd party audits. . Experience CDMO management employing cross-functional collaboration skills. . Hands on experience in solid oral doses, creams, ointments, API, liquid doses, natural products, dietary supplements and cannabis products. • Strong analytical instrumentation skills in HPLC, GC, GC-MS, LC-MS, FTIR, KF, UV-VIS, Dissolution etc. . Excellent knowledge QC data/metrics , global QC standards and regulations. • Excellent interpersonal, communication and organizational and people management skills. • Excellent problem solving and risk based decision-making skills • Strong management skills with integrity and team motivation • Able to work in a fast-paced environment, ability to prioritize and adapt to business and manufacturing needs are required • Excellent knowledge Microsoft office applications, LIMS, EMPOWER, Minitab, OpenLabs, Veeva, TrackWise, SAP,JDE, solabs etc. • Qualified AQPIC • American Society of Quality (ASQ) member • Certified Quality Auditor (CQA). • Six Sigma Green Belt (Pursuing)

Surya Payidiparty

A progressive, forward-thinking professional in pharmaceutical quality with proven success in managi...
Toronto, Toronto, Canada

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Surya Payidiparty’s Email surya.payidiparty@taro.ca

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Surya Payidiparty’s Location Toronto, Toronto, Canada

Surya Payidiparty’s Current Industry The Estee Lauder Companies

Surya Payidiparty’s Prior Industry Medipharm Labs | Purdue Pharma | Taro Pharmaceuticals

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Work Experience

The Estee Lauder Companies

Quality Control Manager

2021-10-01 00:00:00 - Present

Medipharm Labs

Quality Control Manager

2020-08-01 00:00:00 - 2021-10-01 00:00:00

Purdue Pharma

Quality Control Supervisor /operations/Compliance

2017-03-01 00:00:00 - 2020-08-01 00:00:00

Taro Pharmaceuticals

Quality Control Supervisor

2015-01-01 00:00:00 - 2017-01-01 00:00:00

Skills

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Languages

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FAQ About Surya Payidiparty

Surya Payidiparty is located at
Toronto, Toronto, Canada

Surya Payidiparty is a A progressive, forward-thinking professional in pharmaceutical quality with proven success in managing all aspects of testing, quality systems , manufaturing and personnel. Drive compliance with federal regulations and corporate guidelines at all stages of quality testing and quality systems. Skilled trainer and mentor and able to guide staff in all laboratory,Quality and manufacturing functions. SKILLS • More than 18 years of experience in pharmaceutical Quality Control ( Chemistry, microbiology, Environmental monitoring , Raw Material) Compliance and manufacturing including 7 years of management experience. • Strong knowledge in cGMP, GLP, GXP, USP, EU, 21 CFR, TGA, Data Integrity, Quality systems and change management. • Solid knowledge in CAPAs, Deviations, OOS , OOT, investigations, root cause analysis, customer complaints, internal audits, regulatory agency audits. • Experience in Health Canada, FDA, ICH and USP, BP, ISO regulations • Proficiency in method transfers, new product launches, method development, method validations and equipment qualifications. • Experience in technical quality agreements, recalls, complaints, contract laboratories, supplier qualification, Drug Establish License (DEL) process, Stability management, Annual Product Quality Reviews (APQRs) and 3rd party audits. . Experience CDMO management employing cross-functional collaboration skills. . Hands on experience in solid oral doses, creams, ointments, API, liquid doses, natural products, dietary supplements and cannabis products. • Strong analytical instrumentation skills in HPLC, GC, GC-MS, LC-MS, FTIR, KF, UV-VIS, Dissolution etc. . Excellent knowledge QC data/metrics , global QC standards and regulations. • Excellent interpersonal, communication and organizational and people management skills. • Excellent problem solving and risk based decision-making skills • Strong management skills with integrity and team motivation • Able to work in a fast-paced environment, ability to prioritize and adapt to business and manufacturing needs are required • Excellent knowledge Microsoft office applications, LIMS, EMPOWER, Minitab, OpenLabs, Veeva, TrackWise, SAP,JDE, solabs etc. • Qualified AQPIC • American Society of Quality (ASQ) member • Certified Quality Auditor (CQA). • Six Sigma Green Belt (Pursuing)