Chemist II

PL Developments LLC; Miami (FL); On-site; USD 55,000 - 75,000; 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 <

Company

Job summary

PL Developments LLC, a leading manufacturer, packager, and distributor of OTC pharmaceutical products, seeks a Chemist II to perform routine QC testing and support instrument-based analyses in a regulated lab environment, ensuring compliance with cGMP.

Work schedule is Monday–Friday 11am–7:30pm, on-site at our Miami facility. Responsibilities include method validation support, OOS investigations, and maintaining accurate lab records while contributing to efficient QC operations.

Qualifications

• Bachelor’s degree in Chemical or Biological discipline.
• 3-5 years of industry experience.
• Experience in regulated/cGMP environment is preferred.
• Knowledge of current SCM concepts and principles.

Responsibilities

• Perform routine quality control testing on raw materials, intermediates, and finished products.
• Prepare test solutions, compounds, or reagents for laboratory personnel.
• Evaluates and develops methods and instrument-operations for accuracy and precision, including participation in method validation studies.
• Performs analytical testing in accordance with USP/NF, EP, BP and JP Pharmacopeias, compendiums or other Standard Testing Methods (STMs).
• Conducts qualitative and quantitative chemical and physical testing.
• Evaluates materials for compliance to standards and specifications.
• Creates proper laboratory records in accordance to cGMP and company SOPs and Policies.
• Reviews and analyzes test results for reliability.
• Operates laboratory equipment, such as analytical balances, pH meters, HPLC, GC, UV, IR, Dissolution equipment, Disintegration apparatus, etc.
• Issues Certificate of Analysis for finish products, bulk and raw materials, as assigned.
• Participates in the training of new personnel in the laboratory, as assigned.
• Conducts investigations of Out of Specification (OOS) or unexpected results.
• Maintains the laboratory clean and organize.
• Perform all other tasks oriented by QC management as required.

Skills

Organized

Multitasking

English communication

Computer skills

Education

Bachelor's degree in Chemical or Biological discipline

Tools

HPLC

GC

UV

IR

Dissolution equipment

Disintegration apparatus

Job description

10400 NW 29th Terrace
Miami, FL 33172, USA

• On-site
• Associate
• Full-Time
• Requisition #: CHEMI002708

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 Chemist II performs routine and moderately complex analytical testing to support quality control activities in a regulated laboratory environment. This role evaluates raw materials, intermediates, and finished products for compliance with established specifications, conducts testing using a variety of analytical instruments, and maintains accurate laboratory documentation in accordance with cGMP requirements. The Chemist II supports method validation activities, investigates out-of-specification results, assists in training laboratory personnel, and contributes to the efficient operation of the Quality Control laboratory.

Work Schedule: Monday - Friday 11am-7:30pm

JOB QUALIFICATIONS:

• Bachelor’s degree in Chemical or Biological discipline.
• 3-5 years of industry experience.
• Experience in regulated/cGMP environment is preferred.
• Knowledge of current SCM concepts and principles.
• Highly organized and flexible with the ability to multitask and meet changing deadlines.
• Good written English and verbal communication skills.
• Proficient in computer applications.

POSITION RESPONSIBILITIES:

• Perform routine quality control testing on raw materials, intermediates, and finished products.
• Prepare test solutions, compounds, or reagents for laboratory personnel.
• Evaluates and develops methods and instrument-operations for accuracy and precision, including participation in method validation studies.
• Performs analytical testing in accordance with USP/NF, EP, BP and JP Pharmacopeias, compendiums or other Standard Testing Methods (STMs).
• Conducts qualitative and quantitative chemical and physical testing.
• Evaluates materials for compliance to standards and specifications.
• Creates proper laboratory records in accordance to cGMP and company Standard Operating Procedures and Policies.
• Reviews and analyzes test results for reliability.
• Operates laboratory equipment, such as analytical balances, pH meters, HPLC, GC, UV, IR, Dissolution equipment, Disintegration apparatus, etc.
• Issues Certificate of Analysis for finish products, bulk and raw materials, as assigned.
• Participates in the training of new personnel in the laboratory, as assigned.
• Conducts investigations of Out of Specification (OOS) or unexpected results.
• Maintains the laboratory clean and organize.
• Perform all other tasks that will be oriented by QC management as required.

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: PLD is a proud equal opportunity 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

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.

3-5 years: 3-5 years of industry experience