Engineering Validation Specialist

Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesnt just wait for change but actively creates itwhere your skills and values drive our collective progress and impact.

Job Description

Position Title : Contractor Validation Engineering

Reports to : Specialist Validation Engineering

Number of Direct Reports : 0

1. Primary Responsibilities

The role of the Validation Contractor is to prepare qualification documentation for :

New equipment

Existing equipment undergoing modifications

Utility systems (HVAC compressed air purified water BMS etc.)

The role also includes :

Coordinating and executing tests described in the protocols and coordinating required corrective actions with other departments

Preparing and maintaining all documentation related to equipment qualification

Providing technical expertise on all aspects related to qualification

2. Management Responsibilities

This position has no direct supervisory responsibilities.

3. Key Working Relationships (Internal / External)

Internal Partners : Production Engineering Projects HSE Quality Procurement

External Partners : Service providers and contractors involved in projects

4. Required Knowledge and Skills

a) Education

Bachelors degree in Science or Engineering

b) Languages

French and English

c) Experience and Specific Knowledge

5 years of experience in validation

Knowledge of Canadian and American standards

Knowledge of the pharmaceutical industry

d) Specific Technical Skills

Automation / Industrial IT

Energy and utility systems (air water etc.)

HSE

GMP

Regulations and equipment

We are an Equal Opportunity Employer. We are committed to building diverse teams representative of the patients and communities we serve and we strive to create an inclusive workplace that cultivates collaboration.

Required Experience :

IC

Key Skills

Python,SOC,Debugging,C / C++,FDA Regulations,Minitab,Technical Writing,GAMP,OS Kernels,Perl,cGMP,Manufacturing

Employment Type : Full Time

Experience : years

Vacancy : 1