Sr QA Specialist and Quality Engineer FL

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 :

Seeking an experienced QA professional to lead quality systems, support regulatory compliance, and drive continuous improvement in a fast-paced, cGMP-regulated environment. Requires 7+ years in QA, strong knowledge of FDA regulations, and expertise in root cause analysis and validation processes. Work Schedule : Monday-Friday 8 : 00 am - 4 : 30 pm JOB QUALIFICATIONS :

• BS on Science, Engineering or related field from an accredited college or university
• CQE certification, preferred
• Minimum of 7 years of relevant experience, preferably in a pharmaceutical Quality Assurance environment or a similar regulated industry
• Strong knowledgeable of cGMP’s, FDA regulations, and guidance
• Experience with regulatory inspections (e.g., FDA, DEA)
• Proficient in investigations techniques for determining root cause, implementing corrective / preventive actions, and assessing their effectiveness
• High attention to detail
• Excellent interpersonal and communication skills
• Strong written and verbal communication skills
• Effective organizational and time management skills
• Ability to work in a fast-paced, dynamic environment and meet deadlines
• Proficient in Microsoft Word, Excel and Power Point
• Self-starter with the ability to work independently
• Familiarity with Quality System software such as Agile, TrackWise, and SAP

POSITION RESPONSIBILITIES :

PHYSICAL REQUIRMENTS :

BENEFITS :

PLD is a proud employer offering many corporate benefits, including :

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.