Scientist I

Job Description

Salary Range: $78,000 - $82,000/yr DOE

JOB QUALIFICATIONS:

• BS or MS in Chemistry or related Scientific Discipline with a minimum of 4 years of pharmaceutical experience in a QC laboratory analyzing Finish Goods and Raw Materials via HPLC and GC analysis.
• Entry Level experience with Method Verification, Validations and Method Transfers (1-2 years).
• Understanding of the fundamentals of analytical chemistry and instrumentation.
• Knowledge of current Good Manufacturing Practices (cGMP).
• Comprehension and ability to follow procedures of various pharmacopeias (USP, EP, JP).
• Comprehension of regulated guidance (WHO,FCC, FDA, and ICH)
• Demonstrate ability to work well in a fast-paced setting with excellent organizational skills.
• Excellent written and verbal communication skills, problem solving skills and basic computer skills.
  
  

POSITION RESPONSIBILITIES:

• Performs testing on raw material, in-process & finished product samples.
• Executes method transfer, verification and validation protocols with guidance.
• Documents all data in corresponding laboratory notebook and files documentation according to approved SOP and data integrity guidelines.
• Evaluate and interpret the test results and other related technical documentation.
• Mentor, training and transferring analytical methods to QC Chemists.
• Writes analytical method verifications/validations, reports, and analytical test methods.
• Performs routine lab maintenance including equipment calibration, glassware cleaning, chemical and supplies inventory management (includes ordering, cleaning and organization).
• Other duties may be assigned as deemed appropriate by management.
  
  

PHYSICAL REQUIREMENTS:

• Employees are required to wear eye protection and lab coats while in the lab.
• Work safely and follow all OSHA regulations and company safety policies and procedures.
• Ability to frequently lift and/or move up to 25 lb.
• Ability to occasionally lift and/or move up to 35 lb.
• 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.