Qa Jobs in Miramar, FL
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Qa • miramar fl
Last updated: 8 days ago
Bilingual Regulatory Technician – (cGMP / FDA Compliance).This position is responsible for ensuring compliance with .FDA regulations (21 CFR Part 111).
The ideal candidate will have a str...Show moreLast updated: 30+ days ago
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Bilingual QA Regulatory Technician
5th HQMiramar, FLFull-time
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- front end engineer (from $ 71,813 to $ 197,730 year)
- data scientist (from $ 91,250 to $ 182,000 year)
- data engineer (from $ 106,600 to $ 178,880 year)
- freelance (from $ 58,500 to $ 175,500 year)
- business development (from $ 48,750 to $ 175,000 year)
- business development director (from $ 88,518 to $ 175,000 year)
- medical director (from $ 135,000 to $ 172,500 year)
- solutions architect (from $ 157,500 to $ 170,250 year)
- Bridgeport, CT (from $ 82,524 to $ 168,219 year)
- Santa Ana, CA (from $ 74,278 to $ 159,732 year)
- Santa Rosa, CA (from $ 75,166 to $ 159,508 year)
- Santa Clara, CA (from $ 75,860 to $ 159,471 year)
- Fremont, CA (from $ 63,375 to $ 159,400 year)
- San Bernardino, CA (from $ 59,423 to $ 154,536 year)
- Seattle, WA (from $ 62,500 to $ 154,010 year)
- San Mateo, CA (from $ 59,421 to $ 153,946 year)
- San Jose, CA (from $ 59,668 to $ 152,424 year)
- San Diego, CA (from $ 60,109 to $ 152,330 year)
The average salary range is between $ 42,898 and $ 117,763 year , with the average salary hovering around $ 77,798 year .
Bilingual QA Regulatory Technician
5th HQMiramar, FL30+ days ago
Job type
- Full-time
Job description
5th HQ -
Bilingual Regulatory Technician – (cGMP / FDA Compliance)
Location : Miramar, FL
Schedule : Monday - Friday :
6 : 00am - 2 : 30pm
2 : 30pm - 11 : 00pm
Pay Rate : $20.00 - $23.00
About the Role :
We are seeking a detail-oriented and highly organized Regulatory Technician to join our Quality and Compliance team. This position is responsible for ensuring compliance with FDA regulations (21 CFR Part 111) and maintaining all regulatory documentation related to the manufacturing, packaging, labeling, and holding of dietary supplements.
The ideal candidate will have a strong background in technical documentation, regulatory compliance, and cGMP practices , as well as solid knowledge of quality systems in a manufacturing environment.
Minimum Qualifications :
Associate or Bachelor’s degree in Chemistry, Biology, Pharmaceutical Sciences, Food Science, or a related field (from the U.S. or a foreign institution).
Prior experience in pharmaceutical, nutraceutical, or food manufacturing preferred.
cGMP training and / or experience in a controlled manufacturing environment.
Strong technical writing and communication skills (English required; bilingual a plus).
Ability to manage multiple projects and meet deadlines.
Proficiency in Microsoft Office (Word, Excel, PowerPoint) and familiarity with ERP systems .
Key Responsibilities :
Ensure compliance with FDA 21 CFR Part 111 regulations for manufacturing, packaging, labeling, and holding operations.
Maintain and update all regulatory documentation, certifications, licenses, and permits .
Review and approve labeling and packaging materials for regulatory compliance.
Act as Regulatory Intelligence , staying current on FDA regulations and industry updates.
Prepare and maintain customer quality questionnaires and technical documentation.
Collaborate with management and department heads to update procedures and SOPs.
Maintain and control the issuance, storage, and return of labels within the packaging department.
Coordinate and conduct GMP training sessions and maintain training records.
Prepare technical submissions for international product registrations.
Support the management of trademarks, registrations, and patents .
Why Join Us :
Competitive compensation and benefits.
Opportunity to grow within a regulatory and quality-driven environment.
Dynamic, supportive team culture focused on compliance and excellence.