Job Posting Title: QA Coordinator
Location: Los Angeles CA 90032
Duration: 6 mOnths
Schedule: 8:00AM to 4:30 PM
Job Summary:
This position will be responsible for workflow management and review of change control documentation and documents in Document management system issuance of production work/support orders tracking pending tasks in electronic quality management system and coordinate/follow up for completion.
Essential Job Duties:
- Responsible for review and workflow management of change control records in electronic Quality Management System (Veeva)
- Responsible for review of change control and associated requirements documentation for accuracy completeness compliance with cGMPs and applicable standards
- Will generate reports on a scheduled basis for the status and tracking of open change control records
- Responsible for follow-up on status/open items related to change control
- Responsible for issuance of tag-outs for equipment/facilities as required by change control
- Generate reports and data for Key Performance Indicator reporting
- Coordinate and follow up to ensure timely completion of change control requirements for shutdown projects including authorization of area back to production and product release
- Responsible for processing and maintenance of documents in Document Management System managing workflows of review approval issuance and effective.
- Assist as needed for projects related to document management systems and change control
- Familiar with Microsoft Excel eQMS Access to utilize for tracking trending and data entry.
- Communicate effectively with multiple departments in order to provide customer service.
Job Requirements:
- Bachelors degree and a minimum of 2 years of related experience; or an advanced degree without experience; or equivalent work experience. Related cGMP industry experience is desirable
- Experience working with eQMS highly desirable
- Ability to keep neat accurate and complete records and logs.
- Must be proactive results oriented with a strong attention to detail.
- Self-starter with good work ethic and ability to work independently with minimum supervision and use good judgment or as a contributing member of a team.
- Ability to manage multiple projects simultaneously meet deadlines and handle an ever changing fast paced critical work environment.
- Strong organizational analytical troubleshooting and problem-solving skills.
- Ability to analyze details and perform structured decision-making on a daily basis.
- Excellent verbal and written communication. Must be able to read write and speak English.
- Strong interpersonal skills with ability to interact with all levels of personnel in a professional manner. Good computer skills with basic knowledge of Microsoft programs particularly Outlook Word Excel Access etc.
Top of Form
Job Posting Title: QA Coordinator Location: Los Angeles CA 90032 Duration: 6 mOnths Schedule: 8:00AM to 4:30 PM Job Summary: This position will be responsible for workflow management and review of change control documentation and documents in Document management system issuance of production work/...
Job Posting Title: QA Coordinator
Location: Los Angeles CA 90032
Duration: 6 mOnths
Schedule: 8:00AM to 4:30 PM
Job Summary:
This position will be responsible for workflow management and review of change control documentation and documents in Document management system issuance of production work/support orders tracking pending tasks in electronic quality management system and coordinate/follow up for completion.
Essential Job Duties:
- Responsible for review and workflow management of change control records in electronic Quality Management System (Veeva)
- Responsible for review of change control and associated requirements documentation for accuracy completeness compliance with cGMPs and applicable standards
- Will generate reports on a scheduled basis for the status and tracking of open change control records
- Responsible for follow-up on status/open items related to change control
- Responsible for issuance of tag-outs for equipment/facilities as required by change control
- Generate reports and data for Key Performance Indicator reporting
- Coordinate and follow up to ensure timely completion of change control requirements for shutdown projects including authorization of area back to production and product release
- Responsible for processing and maintenance of documents in Document Management System managing workflows of review approval issuance and effective.
- Assist as needed for projects related to document management systems and change control
- Familiar with Microsoft Excel eQMS Access to utilize for tracking trending and data entry.
- Communicate effectively with multiple departments in order to provide customer service.
Job Requirements:
- Bachelors degree and a minimum of 2 years of related experience; or an advanced degree without experience; or equivalent work experience. Related cGMP industry experience is desirable
- Experience working with eQMS highly desirable
- Ability to keep neat accurate and complete records and logs.
- Must be proactive results oriented with a strong attention to detail.
- Self-starter with good work ethic and ability to work independently with minimum supervision and use good judgment or as a contributing member of a team.
- Ability to manage multiple projects simultaneously meet deadlines and handle an ever changing fast paced critical work environment.
- Strong organizational analytical troubleshooting and problem-solving skills.
- Ability to analyze details and perform structured decision-making on a daily basis.
- Excellent verbal and written communication. Must be able to read write and speak English.
- Strong interpersonal skills with ability to interact with all levels of personnel in a professional manner. Good computer skills with basic knowledge of Microsoft programs particularly Outlook Word Excel Access etc.
Top of Form
View more
View less