What are the responsibilities and job description for the QA Administrator position at Ion Nutritional Labs?
Job Title
QA Administrator
Reports To
Document Control Supervisor
YOUR PURPOSE
The QA Administrative Clerk provides clerical and administrative support to the Quality Department.
POSITION RESPONSIBILITIES
- Provide administrative support to the Quality Department.
- File and organize all Quality documents to ensure proper traceability and retrieval.
- Scan, file, copy, and index training-related documents, ensuring proper traceability and retrieval.
- Scan and electronically maintain Quality and Regulatory documents (this may include data entry).
- Issuance and archiving of all GMP logbooks.
- Electronic filing of GMP documents.
- Document filing, archiving, and destruction.
- Retrieve archived documents upon request.
- Create writable documents of current form revisions, upon request.
- Assist with copying SOPs and related facility documents.
- Utilizes appropriate software for tracking, monitoring and reporting.
- Assist with department projects and related activities.
- Assists the ETC in communicating with Leadership, providing updates, SOP and process changes, training rollouts, scheduling and training concerns.
- Perform periodic inspection/monitoring of training documentation.
- Coordinate training activities with various team members/departments.
- Assist QA Specialists with relevant quality tasks, such as Gemba Walks, GMP and Sanitation Audits, Internal Audits, Complaint Management, and Quality Event monitoring.
- Assist all other departments as needed.
- Participate in Continuous Improvement initiatives.
- Actively participate during audits/inspections/customer visits by providing copies of documents in a timely manner as requested by the auditor.
- Willing to work overtime, holidays, and weekends as requested by management.
MINIMUM QUALIFICATIONS
Education:
High School or equivalent
Experience:
None
Knowledge, Skills and Abilities:
· Must acquire strong knowledge of cGMP, Standard Operating Procedures, and Batch Records, and Industry Regulations
· Ability to operate Microsoft Office (Outlook, Word, PowerPoint, Excel)
· Work flexible hours as required by Management
· Able to correctly type at least 40 words per minute
· Work independently, as well as in team environments
· Must have a good interpersonal and communication skill in English, understand both oral and written instructions and be detail oriented.
Training, Certification or License:
Department cGMP and SOP requirements
Job Type: Full-time
Pay: $18.90 - $22.76 per hour
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Employee assistance program
- Flexible spending account
- Health insurance
- Health savings account
- Life insurance
- Paid time off
- Referral program
- Vision insurance
Compensation package:
- Bonus opportunities
- Hourly pay
- Overtime pay
Experience level:
- No experience needed
Schedule:
- Day shift
- Monday to Friday
- Weekends as needed
Ability to Relocate:
- Largo, FL 33773: Relocate before starting work (Required)
Work Location: In person
Salary : $19 - $23