Canada, Upton, Quebec.

Fulltime: 40 hrs a week

Experience: 2 years

Closing: 17 January 2025

Apply Now

Introduction

We are hiring for our client who operates in the pharmaceutical industry, and we are seeking a Validation Specialist who will be responsible for carrying out all the steps leading to the validation of manufacturing, packaging equipment, processes, and systems associated with the production of pharmaceutical products in a sterile environment.

What are you going to do

Develop validation protocols to meet regulatory expectations from the FDA and Health Canada.
Execute validation protocols according to the validation schedule, requalification, and the site master plan (including validation of equipment, cleaning, processes, and the computer system).
Improve validation systems to comply with global and industry standards.
Draft corresponding validation reports.
Identify opportunities for improvement.
Provide technical support to operations.
Ensure the integrity and traceability of the information produced and reported, making necessary corrections in compliance with GMP and the company's internal standards.
Perform document review, including revising and correcting internal documents (SOPs, IT, etc.).

Essential skills and knowledge

Bachelor's degree, ideally in the sciences.
Over three years of experience in validation within a GMP-regulated environment (pharmaceutical or food industries).
One-plus years of experience in sterile pharmaceutical environments.
Strong knowledge of GMP (Good Manufacturing Practices) and Good Documentation Practices.
Good problem-solving abilities.
Excellent ability to meet deadlines and manage priorities.
Strong technical and documentation rigor.
Foundational knowledge of Microsoft Office Suite (Word, Excel).
Proficiency in written and spoken French.
Strong proficiency in written and spoken English.

What we offer

What We Offer

Why apply through Brunel? Finding the next step in your career can be a full-time job in itself. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with onboarding. We'll get you going while you get on with the job.

About Us

Brunel has a reputation for working with some of the best in the business. That's what we continually strive for. Over 45 years, we've created a global network of interesting clients and talented individuals working together through a vast array of services.

Application process

First Contact

We carefully review your application and in the coming weeks, you will be notified for an interview session if you are selected. Only shortlisted candidates will be contacted within 7 days.

Scheduling an Interview

After being shortlisted, you will be contacted via email or telephone to arrange for a date on your availability for the qualification interview.

Phone/ Qualification Interview

During the interview, you will be assessed on your level of experience and skills, work history, availability, and the qualifications the company is seeking for the position.

Meeting in Real Life

After successfully making through the phone interview, a face to face interview will be scheduled between the candidate and recruiter. This session can be a more in-depth interview to review your communication and interpersonal skills.

Application for the Position

Submission of candidates resume for client’s approval and screening.

Do you have questions?

Cristiano Forezli

contact via tel.+1 403 539 5009

all related jobs

Principal - Maintenance Reliability Data Specialist

Saskatoon, Canada

Parttime: 0 hrs a week

Closing: 18 January 2025

Pharmacovigilance Specialist

Toronto, Canada

Fulltime: 37.5 hrs a week

Closing: 10 March 2025

Technical Sales Specialist

Greater Toronto Area, Canada