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DOCUMENT CONTROL SPECIALIST
Job Field: Legal Jobs
Location: San Diego, CA
Salary: $Not stated
Location: San Diego, CA
Salary: $Not stated
JOB SUMMARY:
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<tr><td valign="top" width="450"><b>Document Control SpecialistCategory: QualityDescription: This person will be responsible for processing change control documentation related to Quidel products within the document control system and within defined company policies, procedures, and regulatory requirements. This includes creating, editing, maintaining and, as necessary, collaborating on manufacturing and quality system documentation. This person must be self-motivated, capable of directing multi-functional users in the timely processing of document changes and able to prioritize responsibilities with minimal supervision. Must be confident and able to define, develop and implement departmental policies, procedures, and decisions regarding document structure, compliance etc. This person must lead the effort in developing systems and resources in screening document changes for noncompliance, lack of clarity, spelling/grammar errors, etc., and implementing the required actions to resolve the problems to an acceptable conclusion. Likewise, this person needs to take the lead effort in developing and implementing solutions to document originators, and work with the originators to create and accurate document.Requirements: • BS or equivalent experience required. • 3-5 years experience in documentation control systems, with preference in coordinating administration of systems within QSR/ISO and high volume manufacturing work environment. • Advanced English skills: writing grammar, proofreading, redlining • Advanced computer skills: data entry/typing, Word, Excel, Access, Flowcharts, or other “Office” software • Technical experience and knowledge in developing and coordinating documentation systems. • Full understanding of documentation control systems and configuration management systems within a medical device or ISO, and high-volume manufacturing environment, with experience in developing and implementing system improvements • High degree of attention to detail to assure high quality documentation.Location San Diego , CAMinimum Experience (yrs): Required Education: Not SpecifiedBenefits:
</tr>
<tr><td valign="top" width="450"><b>Document Control SpecialistCategory: QualityDescription: This person will be responsible for processing change control documentation related to Quidel products within the document control system and within defined company policies, procedures, and regulatory requirements. This includes creating, editing, maintaining and, as necessary, collaborating on manufacturing and quality system documentation. This person must be self-motivated, capable of directing multi-functional users in the timely processing of document changes and able to prioritize responsibilities with minimal supervision. Must be confident and able to define, develop and implement departmental policies, procedures, and decisions regarding document structure, compliance etc. This person must lead the effort in developing systems and resources in screening document changes for noncompliance, lack of clarity, spelling/grammar errors, etc., and implementing the required actions to resolve the problems to an acceptable conclusion. Likewise, this person needs to take the lead effort in developing and implementing solutions to document originators, and work with the originators to create and accurate document.Requirements: • BS or equivalent experience required. • 3-5 years experience in documentation control systems, with preference in coordinating administration of systems within QSR/ISO and high volume manufacturing work environment. • Advanced English skills: writing grammar, proofreading, redlining • Advanced computer skills: data entry/typing, Word, Excel, Access, Flowcharts, or other “Office” software • Technical experience and knowledge in developing and coordinating documentation systems. • Full understanding of documentation control systems and configuration management systems within a medical device or ISO, and high-volume manufacturing environment, with experience in developing and implementing system improvements • High degree of attention to detail to assure high quality documentation.Location San Diego , CAMinimum Experience (yrs): Required Education: Not SpecifiedBenefits:
KEY REQUIREMENTS:
Not stated
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