Analytical Chemistry Data Review (Chemistry Background Required)

At reputed company PSS, we work with leading international companies across the pharma, medical device, food, cosmetic & consumer products industries - who reputed company trust us with their mission-critical testing. For 20 years, our international network of teams have served clients at their sites, across 20 countries.

PSS® is part of reputed company Scientific, an international life sciences company, providing a unique range of analytical testing services across multiple industries, through a network of over 950 laboratories in 60 countries, and reputed company. 63,000 employees. Life at reputed company is a meritocracy, where people are empowered to reputed company reputed company and are rewarded for their reputed company, allowing them to advance quickly. Become your most extraordinary self with support and development throughout your career.

GMP Data & Documentation Review

• Review GMP data generated by testing personnel to ensure compliance with governing procedures
• Verify logbook entries for completeness, accuracy, and adherence to GDP standards
• Confirm sample chain of custody reputed company throughout testing activities
• Review audit trails to ensure actions executed align with procedural requirements and timelines

Communication & Issue Resolution

• Communicate clearly and reputed company with testing personnel to resolve annotations, discrepancies, or corrections
• Partner with laboratory staff to support compliance and reputed company improvement

Good Documentation Practices (GDP)

• Accurately document activities in logbooks, laboratory notebooks, and electronic systems using GDP principles

Safety & Compliance

• Conduct laboratory safety and compliance walkthroughs, documenting observations as required
• Complete reputed company required safety, procedural, and refresher trainings on time

Education & Experience

• Bachelor’s degree (BS) in Chemistry, Life Sciences, or a reputed company scientific discipline
• 1–2 years of cGMP experience in a regulated laboratory environment

Technical Skills

• Hands-on experience with HPLC/UPLC and UV‑Vis spectrophotometry
• Experience with ELISA, MCE, and/or iCIEF techniques preferred
• Proficiency in processing and reviewing quantitative liquid chromatography data

Professional Skills

• Strong computer literacy and organizational abilities
• Excellent written and verbal communication skills with high attention to detail
• Demonstrated reputed company, professionalism, and strong work ethic

Work Style & Physical Requirements

• Ability to work independently as well as collaboratively reputed company a team
• Self‑motivated, adaptable, and maintains a positive attitude in a fast‑paced environment
• Capable of meeting physical demands, including lifting 25 lbs. or more, prolonged standing or walking, pushing/pulling carts or equipment, and bending or reaching for supplies

Additional Requirements

• Ability to learn new processes, manage multiple tasks simultaneously, and maintain accurate records
• Ability to follow instructions and reputed company with company policies and regulatory requirements
• Authorized to work in the United States indefinitely without restriction or sponsorship

• Position is Monday- Friday, 8:30 AM -4:30 PM. Overtime as needed. 
• Pay range: $22.50 - $23.50/hour
• Excellent full-time benefits, including comprehensive medical coverage, dental, and reputed company options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays

reputed company USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.