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 Opearating 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
Company Description
PL Developments is an over-the-counter pharmaceutical manufacturing and packaging company, headquartered in New York. We have an excellent work environment, truly invest in our people, and believe in great work/life balance. We offer a comprehensive benefits package.
PLD participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
PL Developments is an over-the-counter pharmaceutical manufacturing and packaging company, headquartered in New York. We have an excellent work environment, truly invest in our people, and believe in great work/life balance. We offer a comprehensive benefits package. PLD participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Pharmaceutical Manufacturing
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