Quality Control Analyst I (HPLC/UPLC)

Location: Onsite in Titusville, New Jersey, United States of America

Salary: $54,000–$87,400 per year

Company

Johnson & Johnson MedTech develops healthcare solutions and medicines through its Innovative Medicine and MedTech businesses.

What you will do

• Conduct analytical testing of stability samples according to testing schedules.
• Perform testing and documentation in compliance with GMP, FDA, EPA, DEA, OSHA, and other applicable regulations.
• Use laboratory systems including LIMS, MES, LES, and Empower.
• Support analytical method qualification, validation, and transfer with mentorship.
• Support audits, CAPAs, laboratory investigations, nonconformance resolution, and continuous improvement initiatives.
• Participate in laboratory and cross-functional meetings, global project teams, and QC prioritization activities.

Requirements

• At least one year of experience in a GMP-regulated, science-related field.
• Basic knowledge of QC laboratory analytical technologies and current cGMP requirements.
• Experience performing basic and some intermediate testing with HPLC and/or UPLC.
• Knowledge of compendial requirements such as USP, EP, and JP.
• Basic technical writing, document interpretation, project management, troubleshooting, and root cause analysis skills.
• Proficiency with Microsoft Outlook, Excel, Word, and PowerPoint.

Culture & Benefits

• Inclusive work environment focused on individual respect, diversity, and dignity.
• Participation in a retirement pension and 401(k) savings plan, subject to plan terms.
• Eligibility for the long-term incentive program.
• Vacation, sick time, holiday pay, parental, caregiver, bereavement, volunteer, and military spouse leave programs, subject to applicable policies and eligibility.