QA Coordinator
IconmaLos Angeles, CA
Automate your job search with Sonara.
Submit 10x as many applications with less effort than one manual application.1
Reclaim your time by letting our AI handle the grunt work of job searching.
We continuously scan millions of openings to find your top matches.

Job Description
Our Client, a Pharmaceutical company, is looking for a QA Coordinator for their Los Angeles, CA location.Responsibilities:
- 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.
- 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.
- Bachelor's 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.
- Health Benefits
- Referral Program
- Excellent growth and advancement opportunities
Automate your job search with Sonara.
Submit 10x as many applications with less effort than one manual application.

FAQs About QA Coordinator Jobs at Iconma
What is the work location for this position at Iconma?
This job at Iconma is located in Los Angeles, CA, according to the details provided by the employer. Some roles may also include multiple work locations depending on the requirement.
What pay range can candidates expect for this role at Iconma?
Employer has not shared pay details for this role.
What employment applies to this position at Iconma?
The employer has not provided this information. This may be discussed during the hiring process.
What is the process to apply for this position at Iconma?
You can apply for this role at Iconma either through Sonara's automated application system, which helps you submit applications 10X faster with minimal effort, or by applying manually using the direct link on the job page.