Job title: Validation Specialist
Company: SIRE Group
Location: Haarlem, Noord-Holland
Job Description: Validation SpecialistThe Company
Our client is a multinational healthcare company whose aim is to provide innovative medicines vaccines and animal health products globally. Will you be their next team member?Role Description
As a Validation Specialist you will be responsible for validation e qualification of Equipment System, you will play a critical role in ensuring compliance with regulatory requirements and industry standards while optimizing operational efficiency and product quality.Responsibilities
– Lead and participate in equipment qualification activities, including Installation Qualification, Operational Qualification and Performance Qualification (PQ).– Support execution of validation protocols/plans for Validations/Re-qualifications of steam.
– Technical expertise and guidance on validation-related issues to project teams and stakeholders.– Collaborate with cross-functional teams to ensure validation activities align with production schedules, project timelines and quality expectations.– Draft, review and assess validation data, deviations, and change controls.
– Ensure adherence to Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) during validation activities.Requirements
– Bachelor’s or higher degree in a relevant scientific or engineering discipline.– Minimum 2 years of experience in validation/CQV within the pharmaceutical industry.
– Knowledge of experience in GMP including V-Model & SDLC methodologies.– Strong analytical, problem-solving, organizational and project management skills.– Team player with attention to detail and strong can-do mentality.Other information
Are you interested? Feel free to contact me!
Only applicants based in The Netherlands and holding a valid work permit.
Salary:
Application:apply for this job.
Curriculum vitae in the database!
