QA Compliance Supervisor Position Available In Pinellas, Florida

QA Compliance Supervisor Ion Nutritional Labs – 1.0

Largo, FL Job Details Full-time Estimated:

$45K – $55.4K a year 9 hours ago Benefits Health savings account Health insurance Dental insurance 401(k) Flexible spending account Paid time off Employee assistance program Vision insurance Life insurance Referral program Qualifications Microsoft Powerpoint Microsoft Word CGMP Microsoft Excel English Mid-level Manager Microsoft Office 3 years High school diploma or GED Attention to detail Typing Communication skills Full Job Description

YOUR PURPOSE

The QA Compliance Supervisor is responsible for managing various quality programs and processes to ensure that all product meets required industry regulations.

POSITION RESPONSIBILITIES

: Oversee quality processes, such as: Complaint handling and investigations. Deviation investigations and closures. Corrective and preventative actions. Effectiveness checks. Vendor evaluations and requalification’s. Packaging component specification review and approval. Label Compliance. Actively participate during internal/external audits. Manage all aspects of the daily activities regarding the printed packaging process to ensure label compliance to industry regulations. Serve as a regulatory advisor to other staff members and clients. Develop personnel through daily interactions and coaching of staff, provide guidance to staff in technical and quality matters and in effective partnering with other departments. Actively participate in continuous improvement initiatives to identify opportunities to increase efficiency and effectiveness, and reduce cost. Author and/or review standard operating procedures. Assist Food Safety/Regulatory and Document Control departments as needed. All other duties as assigned by Quality Management.

MINIMUM QUALIFICATIONS

Education:

High School or Equivalent College Degree Preferred Experience:

Minimum of 3 years’ experience in a cGMP environment (drugs, cosmetics, dietary supplements, food, or medical device).

Knowledge, Skills and Abilities:

Must acquire strong knowledge of cGMP, Standard Operating Procedures, and Batch Records. Strong understanding of 21 CFR Part 101 Food Labeling. 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 strong interpersonal and communication skill in English, understand both oral and written instructions and be detail oriented.

Job Type:

Full-time Benefits:

401(k) Dental insurance Employee assistance program Flexible spending account Health insurance Health savings account Life insurance Paid time off Referral program Vision insurance

Schedule:

Day shift

Work Location:

In person