Manager Document Control

3 weeks ago

Whitby, Canada Thermo Fisher Scientific Full time

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

**Summary**:
Lead the activities of the Document Control & Training team to support compliance of our site to documentation and training requirements. Perform as Site System Owner for the Electronic Document Management System (eDMS) and Learning Management System (LMS) to ensure they meet validated and regulatory requirements at the site. Responsible for GMP document workflows through the respective document lifecycles at Whitby Region Operations (WRO). Ownership of the Corporate Quality Standards alignment process at the site. Perform Good Manufacturing Practices (GMP) Training to employees as part of the new onboarding program. Lead specifications for finished products (FP), intermediates and raw materials, and issuance of Certificates of Analysis. Support client and regulatory audits.

**Essential Functions**:

- Supervise the Document Control & Training team to create a culture of quality awareness, teamwork, compliance, and continuous improvement.
- Mentor and train the Document Control & Training team to provide the best cross functional service through effective communication, leadership, and problem solving.
- Perform as Site System Owner for eDMS and LMS
- Maintain eDMS and LMS in compliance with all applicable regulations, corporate requirements, and site procedures.
- Ownership of eDMS and LMS related Standard Operating Procedures (SOPs), Work Instructions (Wis) and associated training materials.
- Responsible for document lifecycle workflows through eDMS and LMS: review, approval, effective date assignment, assignment of training, inactivation as required, course creation, training verification, curricula maintenance, and curricula removal as required.
- Collaborate cross functionally to support various documentation and training needs to ensure compliance to requirements.
- Deliver training as required in support of eDMS and LMS function.
- Troubleshoot eDMS and LMS issues and provide support to end users
- Manage performance by identification, monitoring, trending, and reporting of metrics.
- Oversee the periodic (triennial) review process of SOPs, WIs, and LMS training curricula.
- Ensure site document alignment to Corporate Quality Standards and Guidelines.
- Manage the archive, retention, and destruction process for GMP documentation in accordance with requirements.
- Lead the creation and revision of specifications for finished products, intermediates, and raw materials.
- Oversee the issuance of Certificates of Analysis for In-Process, Raw Material, Bulk and Finished Product.
- Support vendor change assessments, material gap analysis, and compendial update assessments.
- Initiate Change Controls for Analytical Release Forms, Control Procedures, and Certificates of Analysis.
- Attend Client meetings and internal readiness meetings as required.
- Support regulatory and client audits as site SME for processes and procedures in scope of role.
- Promote a safe working environment, report potential hazards, and ensure all direct reports follow Environmental Health and Safety procedures.

**REQUIRED QUALIFICATIONS**

**Education**:
Bachelor of Science (BSc) in Chemistry, Biology, Pharmacy, Engineering, or related field.

**Experience**:
Minimum 8 years’ experience within the pharmaceutical industry.

Minimum 5 years’ experience in Quality or Compliance within the pharmaceutical industry.

Minimum 3 years supervisory and/or leadership experience.

**Equivalency**:
Equivalent combinations of education, training, and relevant work experience may be considered.

**Knowledge, Skills, and Abilities**:
Demonstrated computer proficiency with Microsoft Office programs. Intermediate Excel proficiency and previous database experience. Detail oriented and organized, with a high degree of accuracy and thoroughness. Excellent organizational skills and ability to prioritize in a face-pace environment. Works well and efficiently with limited supervision. Strong written and oral communication skills. Proficiency with the English Language.

**Standards and Expectations**:
Follow all Environmental Health & Safety Policies and Procedures. Work collaboratively with fellow team members, modelling positive team principles and partnering to meet project and departmental objectives. Carry out all duties within strict compliance to Patheon quality systems SOP's and Good Manufacturing Practice (GMP). Maintain workspace in a clean and orderly fashion. Actively engage in and adhere to departmental systems in order to maintain a smooth and efficient workflow (visual management, scheduling systems, etc.). Be client and patient conscious at all times. Understand Key Performance Indicators and strive to improve the performance of the team by identifying areas for s

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