Quality Control Chemist II: Analytical Lab & cGMP

PL Developments LLC; Miami (FL); Sur place; USD 55 000 - 75 000; Plein temps

Avantages offerts par ce poste

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

Résumé du poste

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.

Responsabilités

• 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.

Connaissances

Organized

Multitasking

English communication

Computer skills

Formation

Bachelor's degree in Chemical or Biological discipline

Outils

HPLC

GC

UV

IR

Dissolution equipment

Disintegration apparatus

Description du poste

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.