QA Validation Engineer
About Arcadis
Arcadis is the world’s leading company in sustainable design, engineering, and consultancy for natural and built assets. With over 36,000 professionals across 70+ countries, we are united in our mission to improve quality of life and solve the world’s most complex challenges.
Be part of something meaningful – join us!
QA Validation Engineer
Position summary:
Reporting to the QA Validation Supervisor, to direct and monitor the validation program on site and to ensure compliance with SII validation procedures by reviewing and/or approving validation documentation across all areas of validation at SII.
Duties and Responsibilities
Key duties and responsibilities may include:
Operational:
* Co-ordinate, execute and report on Process, Transport and Cleaning Validation activity.
* Support equipment/system/facility/utility and laboratory qualifications.
* Protocol preparation and Report writing.
* Assist in the preparation and carry out reviews on qualification/ validation documentation and associated manufacturing/quality documentation.
* Work closely with and co-ordinate the work of the persons responsible for validation in various departments and ensure the Company’s validation policies are respected.
* Ensure all products/processes/equipment/systems are validated/qualified as per site procedures and policy.
* Define the contents and ensure the control of validation documentation.
* Adhere to the schedule and co-ordinate, execute and report on post validation monitoring activity.
* Adhere to the Change Management and Quality Management system procedures.
* Support Industrial Transfers, internal transfers and optimisations.
* Ensure Registration compliance.
* Support Root Cause Problem Solving and Risk Assessments.
* Perform Training for Validation activity execution and implementation.
* Contribute to achievement of the Validation Master Plan Project schedule and site KPI.
* Prepare, review and maintain SOP’s /Policies/Validation Master Plan detailing the company validation strategy.
* Keep up to date on current industry practices and regulatory expectations.
* Ensure that the Company’s policy regarding formal release of processes, equipment, and systems is strictly implemented.
* Support internal and external audit and inspections.
Team work:
* Work co-operatively and flexibly both within your department and with other departments.
* Be prepared to undertake additional tasks as requested to meet Operational, Quality or Business requirements.
Desirable:
* 3-4 years’ experience in the Pharmaceutical Industry.
* Qualification in a GMP regulated discipline.
* Previous validation experience
Why Join Arcadis?
At Arcadis, we empower individuals to excel because your contributions matter. Taking a skills-based approach, we provide opportunities for you to shape your career, maximize your impact, and grow professionally.
By joining us, you’ll engage in meaningful work that drives sustainable solutions for a better planet while leaving a lasting legacy.
Our Commitment to Equality, Diversity, and Inclusion
We are dedicated to creating an environment where everyone can thrive. Through our six ED&I workstreams—Age, Disability, Faith, Gender, LGBT+, and Race—we foster innovation by bringing together diverse perspectives. Together, we strive to improve quality of life while building a more inclusive future
#J-18808-Ljbffr