Join a fast-paced environment where your expertise will significantly contribute to vital validation projects in the healthcare manufacturing sector. Our client is looking for a dedicated professional who is excited about ensuring compliance and excellence in regulatory practices.

As an ideal candidate, you are a skilled Validation Specialist focused on delivering high-quality results and driving improvements in regulatory compliance. If you have a keen eye for detail and a passion for operational integrity, this role could be the right fit for you.

• You develop, implement, and execute URS, SIA, DQ, IQ, OQ, PQ, RV, and TM activities for small scale equipment, including related software.
• You perform qualification of systems while interpreting standards according to specific cases in alignment with cGMP, cGLP, and internal procedures.
• You ensure that the qualified status of systems remains compliant with cGMP at all times.
• You support projects by adhering to all required cGMP regulatory standards.
• You keep up-to-date on emerging validation regulations and testing practices to not only meet but exceed cGMP requirements.
• You are responsible for validation documentation throughout its approval and implementation phases.
• You provide input in reviewing and assessing changes to determine their impact on qualified status and validation documentation.