We are seeking a Validation Specialist to support validation activities within the Molding area. The selected candidate will assist in the execution documentation and completion of validation projects while ensuring compliance with quality standards and applicable regulatory requirements.
Key Responsibilities
Support the execution of validation protocols for Molding processes and equipment.
Collect analyze and document validation data and results.
Collaborate with Manufacturing Engineering Quality and Validation teams to ensure project objectives are met.
Assist in the investigation and resolution of validation-related issues deviations and corrective actions.
Maintain accurate documentation in compliance with cGMP requirements and internal procedures.
Participate in continuous improvement initiatives and provide technical support as needed.
Ensure assigned activities are completed within established timelines and quality standards.
Requirements
Requirements
Bachelors degree in Engineering Life Sciences or a related technical field.
Previous experience in validation activities within a regulated environment preferred (Medical Device Pharmaceutical or Manufacturing).
Required Skills:
risk assessments SOPs and cross-functional collaboration
Required Education:
Bachelors degree in a technical field and experience in pharmaceutical safety or regulated environments.
We are seeking a Validation Specialist to support validation activities within the Molding area. The selected candidate will assist in the execution documentation and completion of validation projects while ensuring compliance with quality standards and applicable regulatory requirements.Key Respons...
We are seeking a Validation Specialist to support validation activities within the Molding area. The selected candidate will assist in the execution documentation and completion of validation projects while ensuring compliance with quality standards and applicable regulatory requirements.
Key Responsibilities
Support the execution of validation protocols for Molding processes and equipment.
Collect analyze and document validation data and results.
Collaborate with Manufacturing Engineering Quality and Validation teams to ensure project objectives are met.
Assist in the investigation and resolution of validation-related issues deviations and corrective actions.
Maintain accurate documentation in compliance with cGMP requirements and internal procedures.
Participate in continuous improvement initiatives and provide technical support as needed.
Ensure assigned activities are completed within established timelines and quality standards.
Requirements
Requirements
Bachelors degree in Engineering Life Sciences or a related technical field.
Previous experience in validation activities within a regulated environment preferred (Medical Device Pharmaceutical or Manufacturing).
Required Skills:
risk assessments SOPs and cross-functional collaboration
Required Education:
Bachelors degree in a technical field and experience in pharmaceutical safety or regulated environments.