QUALITY & REGULATORY COORDINATOR Position Available In Pinellas, Florida
Tallo's Job Summary: The Quality & Regulatory Coordinator position at S.S. White Technologies Inc. in St. Petersburg, FL, offers a full-time role with a salary range of $45,000 to $60,000 per year. The role requires a Bachelor's or Master's degree in Engineering or related field, strong analytical skills, and experience with Microsoft Office. Responsibilities include managing product and quality documentation, coordinating regulatory submissions, and ensuring compliance with customer and government requirements.
Job Description
QUALITY & REGULATORY COORDINATOR 2.5 2.5
out of 5 stars 8300 Sheen Drive, Saint Petersburg, FL 33709
Company:
S.S. White Technologies Inc.
Location:
8300 Sheen Drive, St. Petersburg, FL 33709
Job Type:
Full-time, Regular Business Hours:
8:00 AM – 4:30 PM, Monday –
Friday Career Level:
3+ Years of Experience About Us S.S. White Technologies Inc. / SHUKLA Medical is a globally recognized manufacturer of aerospace products, automotive parts, and orthopedic surgical tools , headquartered in St. Petersburg, FL. With a rich history of innovation, we are seeking a skilled and driven Sales Engineer to join our team and play a critical role in driving our sales strategy forward. Position Overview We are seeking a detail-oriented and organized Quality & Regulatory Coordinator to support product compliance and quality documentation for our advanced manufacturing operations. This role will manage document control, coordinate regulatory submissions, and ensure alignment with customer and government requirements. Key Responsibilities Manage and maintain product and quality documentation to ensure regulatory and customer compliance Implement and oversee document control procedures for engineering and quality teams Prepare and package documentation for customer and regulatory submissions (e.g., manuals, certifications, work instructions) Review engineering change orders and ensure documentation reflects current configurations Track and coordinate responses to quality-related documentation with internal teams, vendors, and customers Collaborate with departments like Engineering, Planning, and Operations to gather required data Report compliance issues and delays to the Director of Quality & Regulatory Affairs Represent regulatory functions in process meetings and maintain communication with regulatory agencies Qualifications Bachelors or Master’s degree in Engineering or related field Strong analytical skills Working experience of Microsoft Office, especially excel Ability to read technical prints Understanding of regulatory requirements in the medical devices field is desired What We Offer
- Opportunity to work with innovative and industry-leading products.
- Professional development and growth opportunities.
- Competitive salary and comprehensive healthcare benefits.
- A collaborative and supportive work environment.
What We Value We are looking for candidates who bring a sense of curiosity, a willingness to learn, and strong computer skills. Ideal candidates possess qualities such as integrity, analytical thinking, and a sense of humor. If you have these traits, we’ll provide training and resources to help you succeed. How to Apply If you are ready to join a dynamic team and make an impact, please submit your resume and a cover letter detailing your relevant experience and career goals. We look forward to hearing from you!
Job Type:
Full-time Pay:
$45,000.00 – $60,000.00 per year
Benefits:
401(k) 401(k) matching Dental insurance Health insurance Life insurance On-site gym Paid parental leave Paid time off Vision insurance
Schedule:
8 hour shift Day shift Ability to
Commute:
Saint Petersburg, FL 33709 (Required) Ability to
Relocate:
Saint Petersburg, FL 33709: Relocate before starting work (Required)
Work Location:
In person