What are the responsibilities and job description for the Quality Assurance Engineer position at PL Developments?
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
PLD is a proud employer offering many corporate benefits, including:
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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
- 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
- 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
PLD is a proud employer offering many corporate benefits, including:
- 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
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