Associate Scientist II; HPLC Method Validation

Associate Scientist II role at Pace Labs

Location:

Lebanon, NJ (onsite). Monday – Friday, 8:30 a.m. – 5:00 p.m.

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The Associate Scientist II is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished formulations, and stability samples.

• Perform complex Liquid Chromatography (LC), UPLC, and other testing; troubleshoot issues as needed.
• Participate in or assist with test method validations.
• Perform analytical testing for incoming, in-process, final products, and stability samples using laboratory equipment (balances, pipettes, pH meter, UV/Vis spectrophotometer, TOC analyzer, viscometers, polarimeter, IR, Pycnometer, etc.).
• Onsite sampling of Natural Gases for customers; cylinder prep and leak checks as needed.
• Perform wet chemistry assays.
• Back up QC analytical instrument maintenance and calibration.
• Maintain QC general laboratory equipment, housekeeping, and prepare the laboratory for audits.
• Assist QC Management with OOS, deviations, and CAPA investigations as needed.
• Backup for QC analytical sample receipt, test results processing, and related tasks.

• Bachelor’s degree in chemistry or related field.
• Liquid Chromatography method validation experience is required.
• Minimum 4–7 years’ pharmaceutical experience or an equivalent combination of education and experience.
• Experience in a cGMP or GLP pharmaceutical environment is preferred.

• Excellent verbal and written communication skills; able to present information and respond to questions from managers, clients, and customers.
• Ability to meet deadlines and work under pressure with limited supervision.
• Strong time management and organizational skills; able to multi-task and manage multiple projects independently.
• Ability to read, analyze, and interpret technical procedures and governmental regulations.
• Ability to write reports, business correspondence, and procedure manuals.
• Proficiency with Microsoft Office and instrument-specific software.
• Knowledge of FDA GMPs (21 CFR parts 211, 820, and/or 600); ISO 9001 and 13485 a plus.

The physical demands described herein are representative of those that must be met to perform the essential functions. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

Mobility to work in a lab and office setting; ability to lift up to 50 pounds occasionally and up to 40 pounds frequently; vision to read printed materials and computer screens; hearing and speech to communicate in person or over the telephone.

Work is performed in a lab and office setting with exposure to chemicals, fumes, gases, and related items.

Full-time roles are eligible for our comprehensive benefits program, including medical, dental, vision, 401(k) with employer match, life and disability benefits, paid time off, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage, and  protection.

Equal Opportunity Employer
Pace provides equal employment opportunities to all employees and applicants and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by law.