Industrious and meticulous, Lynn Neely combines a solid background in science and pharmacy with exceptional communication skills to consistently produce work of the highest standard. Ms. Neely is flexible, outgoing and positive; she prioritizes and multitasks well; and she performs effectively whether working independently or as part of a team.

Technical Writing

• Wrote and revised set-up, operation and changeover SOPs for filling & packaging lines.
• Completed writing and revision of over 70 production procedures and work instructions to meet tight timeline for drug manufacturer.
• Managed SOP revision project for major pharmaceutical manufacturer.
• Revised numerous SOPs (QA, QC, production) for a major pharmaceutical manufacturer ensuring compliance with GMPs and cGMPs.
• Compiled a fully formatted, homogeneous document, based on submissions by a number of authors, for a large pharmaceutical company.
• Produced a formatting template for a new drug submission for a large pharmaceutical company.
• Produced an index to a body of government regulations for use by the pharmaceutical industry.
• Revised policies and procedures for various pharmaceutical companies.
• Helped reorganize and update policies and procedures for an institutional pharmacy, in support of successful application for government accreditation.
• Wrote a User's Manual for a Personal Information Management application.

ISO Consulting

• Led successful implementation of ISO 9001: 2000 quality system for a consultancy; registered with no audit findings.
• Initiated system improvements and developed policies and procedures; hosted internal audits and official audits by external auditors.
• Maintains ISO quality system for consultancy to ensure continued compliance; 3 year re-registration achieved with no findings.

Project Management

• Managed a team that produced a user-friendly publication of a body of government regulations.
• Managed several direct mail campaigns.

Administration

• Reorganized a mid-sized volunteer organization, defining roles, responsibilities and procedures.
• Restructured and streamlined a corporate invoicing process.
• Implemented document control for a consulting company.

• Honours Bachelor of Science, Lakehead University
• Pharmacy Assistant Diploma, Humber College
• Technical Writing Certificate, Humber College

• Business Writing & Grammar refresher course, SkillPath
• cGMP Overview, Aventis Pasteur
• Change Control, Aventis Pasteur
• Clean Room Controls, Pharmaceutical Sciences Group
• GMP Fundamentals Course, PSG
• GMP Training, Aventis Pasteur
• Instructional Design for New Designers, Langevin
• Introduction to GMPs for Importers/Distributors (Quality Control Overview), Q&C
• Introduction to ISO 9001:2000, Q&C
• Organizing, Writing and Managing SOPs in compliance with GMP Requirements, PSG
• Product Disposition, Q&C
• SOP Writing
• Technical Writing Course, Q&C
• WHMIS certification Level II, Aventis Pasteur