Tim Camp Email & Phone Number

Cambridge, Ontario, Canada

Ontario, Canada

Equipment Qualification and Computer System Validation Consultant

Brantford, Ontario, Canada

- Equipment Qualification and Computer System Validation (CSV)- Global Systems implementation and validation- Protocol preparation and execution IQ, OQ, PQ Validation Protocols and Reports)- OOSs, CAPA, Complaints- Quality Investigations- SOP Editing and Creation

Ontario, Canada

- Equipment and Computer System Validation/Qualification (CSV)- Global Systems implementation and validation - Protocol preparation and execution (DQ, IQ, OQ, PQ Validation Protocols and Reports)- Standard Operating Procedures- System Remediation

Montreal, Canada

- QCL SGS Montreal facility RoyalmountFacility setup and preparation for regulatory inspection (National Research Council (NRC))- Laboratory Equipment Validation and Calibration including CSV/Metrology- Coordinate raw material testing/finished product testing - Vendor/Contractor Qualification - Deviations, OOS investigations, SOP's - Validation Protocol.

Scarborough

- Quality Assurance systems for GLP, Microbiology and Chemistry Laboratories - Part of Health Canada defense team for inspections (Chemistry/Sterility Testing within Micro)- Technical writing; Validation Plans, Validation Protocols and Reports (Microbiology/Chemistry/Computer Systems), SOP's

Markham

- QCL SGS Markham-Maintain adherence to Good Manufacturing Practice regulations (cGMP) for Health Canada, FDA and EU- Manage supervisors and analysts within the chemistry and microbiology laboratories. - Quality systems management including equipment validation/qualification(metrology) and computer systems validation (CSV).- Manage testing of materials.

North York

- US, Canada, Japan, British and European GMP regulations pertaining to pharmaceutical manufacturing and Quality Management Systems Lecture and illustration * Difficult compendial testing techniques * Software (CSV) and equipment validation/calibration * Technical writing, SOP's, protocols and reports * Quality systems implementation * Quality systems.

Whitby, Ontario

Patheon purchased the Novartis Whitby facility in 2001.-Method Development and Validation- Vendor Qualification- Validation Protocol and Report authoring - SOP authoring - Approval of Microbiology and Chemistry Testing (Quality Control)- Deviations, OOS investigations, CAPA - Coordinate raw material testing with production needs - SOP evaluation and.

Richmond Hill, Ontario, Canada

Finished Product Formulation/Accelerated Stability

Bachelor’S Degree, Chemistry

Certificate, Network Admistration (Nt4)