- Responsible for coordinating engineering change notifications (ECNs), facilitating review,
- Coordinates and supports change control activities for labeling, specifications, artwork,
- Assigns unique identification numbers to documents, parts, and components in accordance
- Maintains laboratory notebooks and associated log sheets.
- Coordinates record retention processes, ensuring compliance with company policies and
- Supports Quality System training and maintains training records and training effectiveness
- Performs self-checks/self-audits on document control and training activities and
- Serves as global administrator of electronic Quality Management System, QT9.
- Supports user requests for documentation.
- Identifies and implements opportunities for process enhancements and efficiency
- Other duties as assigned.
- Experience in document control, ideally in regulated industries like manufacturing,
- Proficient in communication and working with teams that consist of diverse personnel and
- Technical proficiency and competence in document control software and other relevant
- Exceptional organizational skills and attention to detail, with the ability to manage multiple
- Strong aptitude for learning, with a growth mindset and eagerness to acquire new skills.
- Understanding of best practices for record retention, storage, and archiving, along with
- Prefer Bachelor of Science or equivalent with at least 2 years' experience in documentation
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Document Control Specialist - Ventura, United States - Administrative and Accounting - Quest Staffing Services
Description
Job DescriptionJob Description
POSITION DESCRIPTION Position Title:
Document Control
SpecialistReports To:
Supervisor,
Document ControlDivision:
Quality Review:
Annual
Primary Function
Coordinates, implements, and maintain Document Control and Training System (eQMS).
Follows established procedures and policies to meet the demands of document control in a
regulated medical device company.
Duties/Responsibilities
Advanced English skills:
writing, grammar, proofreading, redlining.
and data entry/typing.
Skills
Education/Training.
administration of systems within FDA QSR/ISO regulated industry
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