Validation Engineering Specialist III - Equipment Engineering

How will you make an impact?

Provide specialized validation knowledge and information, which is directly required to support operations and clients. Finish the protocols related to the validation of equipment and facilities processes and review all finished reports prior to final approval. Ensure documents conform to all SOPs, client requirements and Good Manufacturing Practices.

What will you do:

• Provide leadership to Validation Engineering Specialist I&II by supporting problem solving and solution generation on projects, training/mentoring, and supporting project progression.

• Prepare and execute process validation protocols and reports.

• Review documents from team members.

• Provide guidance to junior members on various validation requirements (through team meetings and individual interactions).

• Lead complex URS, FS, DS, HS, FAT, SAT document generation, review, and approval.

• Develop and lead project timelines, resources, and budgets for both minor and major projects.

• Review and approve vendor documentation, change controls and maintenance reports.

• Lead risk assessment, HAZOP, FMEA’s and Validation plans for Equipment, Systems & Facilities for unique processes and equipment procured in Processing, Packaging & PPT areas.

• Attend client meetings as validation representative (as required)

• Update assigned Master Validation Plans (MVPs) as per validation policy.

• Act as Subject Matter Expert during audit and regulatory inspections. Lead audit responses and assessment.

• Lead/ facilitate technical investigations, deviations, and Corrective Action Preventative Action (CAPA) implementation.

• Lead with a continuous improvement attitude and actively participate in and initiate practical process improvement initiatives.

• Support special projects (as required).

• Maintain a safe working environment and report potential hazards.

• Flexibility to work outside regular work hours (as required).

How will you get here:

Education:

Minimum High School Diploma.

Post secondary diploma in Engineering, Science, or related field is an asset.

Experience:

Minimum 5 years experience in validation within the pharmaceutical industry. Previous experience in project management.

Equivalency:

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

Knowledge, Skills, and Abilities:

Strong written and oral skills. Detail oriented and organized, with a high degree of accuracy and thoroughness. Excellent interpersonal skills, communication, and organizational skills. Strong judgment, decision making and trouble shooting skills. Ability to multi-task, meeting tight deadlines in a fast-paced environment. Mini-T and data analysis knowledge an asset. Proven computer proficiency with Microsoft Office programs and Project Management tools. 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 Standard Operating Procedures (SOPs) and Good Manufacturing Practice (GMP). Maintain workspace in a clean and orderly fashion. Effectively engage in and adhere to departmental systems 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 system improvements and engage in problem solving. Model positive thinking and is open to change, motivating the team to adapt to shifts in priorities and new ways of working. Proactively identify areas for improvement in the execution of procedures. Communicate risks to timelines in a proactive manner. Consistently strives to improve skills and knowledge in related field.