Christopher Frie Email and Phone Number
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o Manage Day-to-day operations of the Quality Management Systems (QMS’s) in both the manufacturing and services industries.o Able to initiate and implement innovative measures to solve problems and improve efficiency by PDCAo Extensive knowledge of Chemical, Biochemical, and Microbiological Sciences. Extensive knowledge of ISO, IEC, cGMP, GFSI, SQF Certification, OSHA, EPA, FDA, USDA, CPSC, EDQM and other regulatory requirements.o SA8000 Lead Auditor; ACS Member; ASQ Member; ASQ Certified Quality Engineer (CQE), HACCP Auditor; Six Sigma Green Belt Certified; ISO Lead Auditor ISO 9001:2015, 17025 & 13485. Lead ISO and cGMP Auditor of numerous company suppliers.o Extensive experience in Managing QMS of Consumer Product, Medical Device, Cosmetic, Food & Dietary Supplement Manufacturers, Feed, Agriculture, Petroleum and Petrochemical Organizations.o Extensive experience in risk management, managing risk assessment teams and risk-based thinking.o Extensive experience in SPC charting and other manufacturing process controls.o Expertise in 21 CFR 11 and process, computer and equipment Validation and Commissioning DQ/IQ/OQ/PQ.o Very adept in computer applications: ERP’s, CRM’s, LIMS, Windows, Excel, Word, MS Outlook, Lotus Notes, PowerPoint, QMS software etc. (>30wpm) & online training platforms.o Advanced presentation and communication skills both written and verbal including public speaking.o Skillful in time management, ability to handle multiple tasks, positive and professional attitude
Hytorc
View- Website:
- hytorc.com
- Employees:
- 502
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Field Compliance ManagerHytorc Dec 2024 - PresentSouth Hackensack, New Jersey, United States -
Quality Director And Director Hs&E (Health, Safety & Environment)Sgs (Consumer Product/Medical Device Division) Oct 2013 - Mar 2024Fairfield, Nj• Overall Management of QHS&E Programs and Accreditation Scopes under ISO 9001, 17025, 17020, 17065, 13485, 22000, 22716, 14971, FDA, GMP, A2LA, IAS, SCC, OSHA NRTL, CPSC, DEP and DOT for SGS facilities across North America• Facilitated and Chaired Management Review as Management Representative• Provided and oversaw coaching and training of all staff on Quality, Health, Safety, and Environment as well as on Integrity and Confidentiality• Managed continuous improvement processes across the SGS US organization in alignment with global SGS programs• Created the Risk Based Thinking system company wide as per ISO 14971.• Conducted and coordinated due diligence audits of companies under M&A consideration and key member of the M&A assimilation team• Continuously monitored and kept abreast of latest developments in QHS&E management system standards and accreditation body requirements• Managed Audit programs, Internal and External• Investigated and responded with action plan for client complaints and other problems encountered• Member of TAC (Technical Advisory Council) for IAS (International Accreditation Service, Inc.)
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Quality Assurance ManagerRegenity Biosciences Jan 2012 - Aug 2013Oakland, Nj• Overall Management of QMS of Implantable Medical Device Company under ISO 13485, ISO 17025, 21 CFR 820, MD 571836, Regulation (EU) 2017/745, IEC 62304 as well as safety program• Facilitated Management Review Meetings held quarterly• Provided training to all staff on Quality and Safety (ISO, cGMP, GDP, OSHA)• Reviewed/Approved IQ/OQ/PQ commissioning and validations of equipment, devices, and systems• Managed Audit program, Internal and External and FMEA meetings• Created a sophisticated supplier evaluation system and arranged and conducted numerous supplier audits across North America. -
Associate Director Quality AssuranceInnophos Mar 2000 - Jan 2012Paterson, Nj• Implemented the ISO 9001, ISO 22000, GMP 21 CFR 111/110, and FSSC and SQF certified quality systems at the various Innophos Nutritional Supplement manufacturing plants in the US• Facilitated Management Review meetings• Primary individual responsible for FDA regulations and FDA inspections, EU Directive (EDQM) Regulatory Requirements, OSHA safety and other regulatory issues and chief liaison with all government regulatory authorities• Provided guidance and expertise to the Quality Control Laboratory, facilitating the rapid set-up of new in-house instrumentation and testing protocols, which saved significant lab outsourcing costs• Managed Internal Audit program under ISO 9001, 22000, cGMP, GDP and HACCP• Created a custom GMP & Food Safety auditing program for raw material suppliers and conducted numerous Supplier audits across North America.
Christopher Frie Skills
Christopher Frie Education Details
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Biochemistry And Molecular Biology -
Biochemistry -
Biochemistry -
Biochemistry And Molecular Biology
Frequently Asked Questions about Christopher Frie
What company does Christopher Frie work for?
Christopher Frie works for Hytorc
What is Christopher Frie's role at the current company?
Christopher Frie's current role is Quality Director and Director HS&E (Health, Safety & Environment).
What is Christopher Frie's email address?
Christopher Frie's email address is ch****@****sgs.com
What is Christopher Frie's direct phone number?
Christopher Frie's direct phone number is +197398*****
What schools did Christopher Frie attend?
Christopher Frie attended The University Of British Columbia, The University Of British Columbia, The University Of British Columbia, The University Of British Columbia.
What skills is Christopher Frie known for?
Christopher Frie has skills like Quality Control, Quality System, Capa, Quality Management, Iso, Quality Assurance, Iso 13485, Quality Auditing, Root Cause Analysis, Analytical Chemistry, V&v, Fda.
Who are Christopher Frie's colleagues?
Christopher Frie's colleagues are Mukesh Rout, Hamza Cheema, Charles Bisland, Rick Rigdon, Kimberly Reese, Tom Isaacson, Italo Lima.
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