Junior Validation Support

Empresa: Oxford Global Resources
Tipo de empleo: A tiempo completo

We are currently looking for a Junior Validation Consultant for one pharmaceutical client of us located in Waver. Interested in stepping in the industry within Quality Assurance for a first challenge ? Apply now !
Job description Provide QA support and oversight to validation activities according to validation procedures in the framework of the PUPSIT and Point of fill filtration implementation project.
Responsibilities Within the center of excellence in validation at our Client, the responsibilities will be:

  • Support the improvement program regarding filters and filtration management, participate in the documentation review, including validation plans, protocols, reports, and standard operating procedures (SOPs).
  • Perform gap assessment between different documents and between documents and practices in the field. Propose improvement and simplification following observations.
  • Using current procedure and state of the art knowledge, contribute to build educational materials on validation topics (creation of training packages including writing, formatting, illustrating and animating contents).
  • Collect data across different system to build a databases related with validation activities.
  • For a given situation, use available data and statistical tools to calculate operational ranges and min or maximum values as needed.
  • Executing validation protocols for equipment, systems, and processes, documenting each step to provide a comprehensive record.
  • Collaborate closely with cross-functional teams, including Quality Assurance, Manufacturing, and Engineering, to ensure all activities are performed in accordance with current Good Manufacturing Practices (cGMP) and other relevant guidelines.

Stay updated with industry trends, regulatory updates, and technological advancements to contribute to the development of best practices and innovative validation methodologies within the pharmaceutical manufacturing. Requirements

  • Strong understanding of Life Sciences and GMP regulations.
  • Fluency in English and French (documents in both languages).
  • Meticulous and detail-oriented.
  • Excellent communication and writing skills.

Benefits

  • Open to junior profiles.
  • Full-time position.
  • Ability to work from home 1-2 days per week.
  • A balanced salary package based on your capabilities and experience, including extra legal benefits.