PL Developments, Inc.
10400 NW 29th Terrace
Miami, FL 33172, USA
Description PL Developments, also known as PLD, is a leading manufacturer, packager, and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goods.
SUMMARY:
We are seeking a detail-oriented QA Engineer to join our Pharmaceutical Quality Assurance. In this role, the Quality Assurance Engineer plays a key role in maintaining FDA and cGMP compliance for OTC pharmaceutical manufacturing operations. This position supports quality systems, investigations, and process improvements to ensure consistent product quality.
Work Schedule: Monday - Friday 8:00 AM - 4:30 PM
JOB QUALIFICATIONS:
Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biology, Engineering, or a related field
2–5+ years of experience in Quality Assurance within pharmaceutical or OTC manufacturing
Strong knowledge of cGMP, FDA regulations, and quality systems
Experience with deviation investigations, CAPA management, and change control
Familiarity with OTC drug manufacturing and labeling requirements
Excellent written and verbal communication skills
Strong attention to detail and documentation skills
Ability to work cross-functionally in a regulated environment
POSITION RESPONSIBILITIES:
Ensure compliance with FDA regulations (21 CFR Parts 210, 211), cGMPs, and company quality systems
Review and approve batch records, deviations, investigations, CAPAs, and change controls
Provide quality oversight for manufacturing, packaging, labeling, and testing operations
Investigate nonconformances, deviations, and complaints, and lead root cause analyses
Support internal audits, FDA inspections, and third-party regulatory audits
Review and approve SOPs, protocols, validation documents, and quality records
Collaborate with Manufacturing, QC, Regulatory, and Engineering teams to resolve quality issues
Ensure proper implementation of process validation, cleaning validation, and equipment qualification
Monitor quality metrics and support continuous improvement initiatives
Provide QA guidance and training to manufacturing and support staff
Support product releases and ensure documentation accuracy and completeness
PHYSICAL REQUIREMENTS:
Work safely and follow all OSHA regulations and company safety policies and procedures Works frequently in a lab environment, handling of chemicals. Employees are required to wear eye protection and lab coats while in the lab area. Ability to frequently lift and/or move up to 25 lbs. Ability to occasionally lift and/or move up to 35 lbs. Ability to regularly stand, sit, and walk to perform tasks
BENEFITS:
Medical and Dental Benefits
Vision
401K with employer match
Group Life Insurance
Flex Spending Accounts
Paid Time Off and Paid Holidays
Tuition Assistance
Corporate Discount Program
Opportunities to Flourish Within the Company
PL Developments is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
#J-18808-Ljbffr
Description PL Developments, also known as PLD, is a leading manufacturer, packager, and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goods.
SUMMARY:
We are seeking a detail-oriented QA Engineer to join our Pharmaceutical Quality Assurance. In this role, the Quality Assurance Engineer plays a key role in maintaining FDA and cGMP compliance for OTC pharmaceutical manufacturing operations. This position supports quality systems, investigations, and process improvements to ensure consistent product quality.
Work Schedule: Monday - Friday 8:00 AM - 4:30 PM
JOB QUALIFICATIONS:
Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biology, Engineering, or a related field
2–5+ years of experience in Quality Assurance within pharmaceutical or OTC manufacturing
Strong knowledge of cGMP, FDA regulations, and quality systems
Experience with deviation investigations, CAPA management, and change control
Familiarity with OTC drug manufacturing and labeling requirements
Excellent written and verbal communication skills
Strong attention to detail and documentation skills
Ability to work cross-functionally in a regulated environment
POSITION RESPONSIBILITIES:
Ensure compliance with FDA regulations (21 CFR Parts 210, 211), cGMPs, and company quality systems
Review and approve batch records, deviations, investigations, CAPAs, and change controls
Provide quality oversight for manufacturing, packaging, labeling, and testing operations
Investigate nonconformances, deviations, and complaints, and lead root cause analyses
Support internal audits, FDA inspections, and third-party regulatory audits
Review and approve SOPs, protocols, validation documents, and quality records
Collaborate with Manufacturing, QC, Regulatory, and Engineering teams to resolve quality issues
Ensure proper implementation of process validation, cleaning validation, and equipment qualification
Monitor quality metrics and support continuous improvement initiatives
Provide QA guidance and training to manufacturing and support staff
Support product releases and ensure documentation accuracy and completeness
PHYSICAL REQUIREMENTS:
Work safely and follow all OSHA regulations and company safety policies and procedures Works frequently in a lab environment, handling of chemicals. Employees are required to wear eye protection and lab coats while in the lab area. Ability to frequently lift and/or move up to 25 lbs. Ability to occasionally lift and/or move up to 35 lbs. Ability to regularly stand, sit, and walk to perform tasks
BENEFITS:
Medical and Dental Benefits
Vision
401K with employer match
Group Life Insurance
Flex Spending Accounts
Paid Time Off and Paid Holidays
Tuition Assistance
Corporate Discount Program
Opportunities to Flourish Within the Company
PL Developments is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
#J-18808-Ljbffr