Quality Lead

PL Developments LLC; Miami (FL); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

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 <

Job summary

PL Developments LLC is seeking a Quality Lead to head Quality Control laboratory operations in a cGMP environment in Miami, FL. The role emphasizes analytical testing, stability programs, and documentation, with cross-functional teamwork to ensure product quality and regulatory compliance.

The candidate should have a chemistry/pharma-related degree and 5–10 years of lab experience, plus 3–5 years in leadership. On-site schedule is Monday–Friday, 8am–5pm, with comprehensive benefits.

Qualifications

• Bachelor’s degree in Chemistry, Pharmaceutical Sciences, Biochemistry, Microbiology, Chemical Engineering, or a related scientific discipline.
• 5–10 years of progressive analytical laboratory experience in a pharmaceutical, OTC, medical device, or other regulated cGMP environment.
• 3–5 years of experience in leadership roles and technical experience is preferred.
• Strong knowledge of analytical testing, stability program support, laboratory instrumentation, calibration systems, and troubleshooting.

Responsibilities

• Lead quality control laboratory operations and ensure regulatory compliance.
• Support stability studies, data review, and issuance of stability-related documentation.
• Maintain audit readiness and collaborate with cross-functional teams.
• Oversee laboratory investigations, CAPA, and deviation management.
• Coordinate with Quality Assurance, Operations, and external labs to ensure product quality.
• Ensure secure, accurate, compliant, and inspection-ready records.

Skills

Leadership experience

Strong communication

Education

Bachelor’s degree in Chemistry, Pharmaceutical Sciences, Biochemistry, Microbiology, Chemical Engineering, or a related scientific discipline

Tools

Microsoft Office

Laboratory software systems

Job description

Locations

Showing 1 location 10400 NW 29th Terrace 10400 NW 29th Terrace Miami, FL 33172, USA 10400 NW 29th Terrace 10400 NW 29th Terrace Miami, FL 33172, USA +0 more locations less locations

• On-site
• Lead
• Full-Time
• Requisition #: QUALI002665

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

The Quality Lead is responsible for leading Quality Control laboratory operations and ensuring analytical testing, stability programs, laboratory documentation, and equipment activities are performed in compliance with cGMP requirements and company procedures. This role provides technical leadership, supports laboratory investigations, maintains audit readiness, and collaborates with cross-functional teams to ensure product quality, regulatory compliance, and continuous improvement of laboratory operations.

Work Schedule

Monday - Friday 8am-5pm

JOB QUALIFICATIONS

• Bachelor’s degree in Chemistry, Pharmaceutical Sciences, Biochemistry, Microbiology, Chemical Engineering, or a related scientific discipline, or an equivalent combination of education and relevant experience.
• Minimum of 5–10 years of progressive analytical laboratory experience in a pharmaceutical, OTC, medical device, or other regulated cGMP environment, with demonstrated responsibility in quality control and laboratory operations.
• Minimum of 3-5 years of experience in leadership roles and technical experience is preferred.
• Strong technical knowledge of analytical testing, stability program support, laboratory instrumentation, calibration systems, preventive maintenance coordination, and troubleshooting of routine laboratory equipment.
• Demonstrated experience with stability study set-up, sample management, protocol execution, sample pull scheduling, data review, and issuance of stability-related documentation and summary reports.
• Working knowledge of cGMP requirements, good documentation practices, data integrity principles, laboratory investigations, deviation management, OOS/OOT processes, CAPA systems, and audit readiness expectations applicable to pharmaceutical laboratories.
• Strong analytical, investigative, and organizational skills, with the ability to prioritize multiple activities, manage timelines, and perform effectively with minimal supervision
• Excellent interpersonal, written, and verbal communication skills, with the ability to collaborate across Quality Control, Quality Assurance, Operations, external laboratories, and service providers.
• Proficient in Microsoft Office and laboratory software systems, including the ability to maintain secure, accurate, compliant, and inspection-ready records.

POSITION RESPONSIBILITIES

• Bachelor’s degree in Chemistry, Pharmaceutical Sciences, Biochemistry, Microbiology, Chemical Engineering, or a related scientific discipline, or an equivalent combination of education and relevant experience.
• Minimum of 5–10 years of progressive analytical laboratory experience in a pharmaceutical, OTC, medical device, or other regulated cGMP environment, with demonstrated responsibility in quality control and laboratory operations.
• Minimum of 3-5 years of experience in leadership roles and technical experience is preferred.
• Strong technical knowledge of analytical testing, stability program support, laboratory instrumentation, calibration systems, preventive maintenance coordination, and troubleshooting of routine laboratory equipment.
• Demonstrated experience with stability study set-up, sample management, protocol execution, sample pull scheduling, data review, and issuance of stability-related documentation and summary reports.
• Working knowledge of cGMP requirements, good documentation practices, data integrity principles, laboratory investigations, deviation management, OOS/OOT processes, CAPA systems, and audit readiness expectations applicable to pharmaceutical laboratories.
• Strong analytical, investigative, and organizational skills, with the ability to prioritize multiple activities, manage timelines, and perform effectively with minimal supervision.
• Excellent interpersonal, written, and verbal communication skills, with the ability to collaborate across Quality Control, Quality Assurance, Operations, external laboratories, and service providers.
• Proficient in Microsoft Office and laboratory software systems, including the ability to maintain secure, accurate, compliant, and inspection-ready records.

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

The EEO statement needs to be included in the detailed description... 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.

5-10 years: Minimum of 5–10 years of progressive analytical laboratory experience in a pharmaceutical, OTC, medical device, or other regulated cGMP environment, with demonstrated responsibility in quality control and laboratory operations.

Preferred

3-5 years: Minimum of 3-5 years of experience in leadership roles and technical experience is preferred.

Licenses & Certifications

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.