Job Summary :
Seeking a Quality Systems Specialist II to implement global processes for Change Control & Document Control in a Plan Change implementation project.
Job Requirements :
Associate degree or equivalent in Biology, Chemistry, or related field
Knowledge of device, drug, or biotech manufacturing processes
Preferred Skills :
Experience in implementing global Change Control & Document Control processes
Familiarity with regulatory requirements and standards in the biotech, pharmaceutical, or medical device industries
Job Responsibilities :
Implement and manage global Change Control & Document Control processes
Support the Plan Change implementation project by ensuring compliance with regulatory standards and company policies
Collaborate with cross-functional teams to ensure proper documentation and control of changes in manufacturing processes
Develop and maintain quality system documentation related to Change Control and Document Control
Provide training and guidance to staff on quality system processes and best practices
Pay Details : $33.00 to $42.00 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan.
Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs.
In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer / Veterans / Disabled
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