QC Scientist: Pharma Analysis (HPLC/UV-Vis)

Actalent; Boca Raton (FL); On-site; USD 40,000 - 54,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

401(k)

Job summary

Actalent is hiring a talented Quality Control Scientist in Boca Raton, FL to perform routine analytical testing on pharmaceutical samples using UV-Vis and HPLC, ensuring compliance with cGMP and SOPs. The Associate Scientist will maintain meticulous documentation and support both first and second shifts, with training on the first shift.

The ideal candidate holds a Bachelor’s or Master’s degree in chemistry or a related field with demonstrated pharmaceutical analysis experience and proficiency

Qualifications

• Requires degree in chemistry with pharma analysis experience.
• Proficiency in HPLC for pharmaceutical analysis.
• Experience with UV-Vis spectroscopy.
• Knowledge of USP methods and SOPs.

Responsibilities

• Perform routine testing of finished products, stability samples, raw materials and process validation samples using UV-Vis and HPLC.
• Conduct assays and chromatographic purity tests, content uniformity analyses and water determinations as per USP methods.
• Evaluate test results and determine sample acceptability based on criteria and analytical outcomes.
• Maintain accurate laboratory notebooks and complete analytical reports and documentation in compliance with SOPs.
• Ensure labs maintain good housekeeping and remain compliant with cGMP requirements.

Skills

HPLC

UPLC

UV-Vis

Pharmaceutical analysis

Education

Bachelor's degree in Chemistry or related field

Master's degree in Chemistry or related field

Job description

Actalent is hiring a talented Quality Control Scientist in Boca Raton, FL to perform routine analytical testing on pharmaceutical samples using UV-Vis and HPLC, ensuring compliance with cGMP and SOPs. The Associate Scientist will maintain meticulous documentation and support both first and second shifts, with training on the first shift.

The ideal candidate holds a Bachelor’s or Master’s degree in chemistry or a related field with demonstrated pharmaceutical analysis experience and proficiency