**Job Opportunity:** Quality Assurance Professional
We are seeking an experienced QA Validation Engineer to join our team. As a key member of our quality assurance department, you will be responsible for ensuring the validation and qualification of equipment, utilities, processes, and software comply with regulatory standards.
Responsibilities:
* Develop and execute project validation plans and schedules.
* Create and maintain validation protocols and reports in accordance with GMP standards.
* Support validation investigations and implement corrective actions.
* Manage validation, exception event, and change control processes.
* Document all activities in line with GMP requirements.
* Cross-train within the team and train new members.
* Participate in continuous improvement programs to enhance manufacturing, quality, safety, and training systems.
* Coordinate activities to maximize team effectiveness.
* Communicate with peers and management regarding activities and concerns.
Requirements:
* 2+ years of experience in validation/quality assurance, preferably in sterile/aseptic environments.
* Knowledge of GMP and regulatory requirements in the pharmaceutical/medical device industry.
* Strong communication, presentation, and troubleshooting skills.
* Effective interpersonal and organizational skills.
* Ability to work independently and in a team environment.
* Capability to prioritize work and multitask.
Work Requirements: