Experienced Analyst, QC

• Job title Experienced Analyst, QC
• Function Quality
• Sub function Quality Control
• Category Experienced Analyst, Quality Control (P5)
• Location Titusville / United States of America
• Date posted Jun 04 2026
• Requisition number R-080099
• Work pattern Fully Onsite

This job posting is anticipated to close on Jun 15 2026. We may however extend this time period, in which case the posting will remain available on www.careers.jnj.com to accept additional applications.

Description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

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Job Description:

We are searching for the best talent for a Experienced Analyst, QC to be based in Titusville, NJ.

Purpose: We are seeking a highly skilled and experienced analyst whose primary responsibilities will include conducting comprehensive data reviews and approvals on stability testing in accordance with analytical methodologies. Additionally, this individual should be prepared to perform select analytical tests independently, adhering to established testing schedules to ensure seamless and efficient workflow. We require a candidate who demonstrates both exceptional productivity and meticulous attention to accuracy across all tasks

You will be responsible for:

• Review / Approve laboratory data in compliance with all applicable procedures, standards and GMP regulations as well as all local, state, federal and international regulations and guidelines (FDA, EPA, DEA, OSHA, etc.).
• Maintain a safe work environment align with environmental, health, and safety regulations.
• Demonstrate a high level of understanding of analytical test methods with ability to independently implement and troubleshoot methods where required.
• Use electronic systems (LIMS, MES, LES, Empower, etc.) for execution and documentation of testing.
• Complete analytical method qualification, validation, and transfer with mentorship.
• Assist the execution of internal audits.
• Maintain individual training completion in a compliant state.
• Complete corrective and preventative actions (CAPA) as assigned.
• Support investigations and resolution of laboratory nonconformances.
• Make contributions to, and occasionally lead, continuous improvement teams. Interaction and involvement with global project teams.
• Provide input to functional laboratory meetings and take actions as a QC representative at cross-functional meetings.
• May occasionally assist the supervisor in prioritizing for the functional QC laboratory.
• Support the development and execution of CREDO action plans and initiatives.
• Trend analytical data generated by other analysts

Qualifications/Requirements:

• Bachelor's degree and/or equivalent degree required; preferably in Science or related field.
• A minimum four (4) years of experience in a GMP-regulated, science-related field.
• Detailed knowledge of analytical technologies used in the QC laboratory.
• Skilled in performing intermediate and advanced testing within the functional laboratory, using HPLC and/or UPLC, using the Empower software.
• Knowledge and understanding of current Good Manufacturing Practices (cGMP) related to QC laboratory.
• Knowledge of compendial (USP, EP, JP, etc.) requirements.
• Skilled technical writing skills.
• Ability to manage an individual project with mentorship from supervision/management.
• Ability to review testing documentation, daily testing, method transfer protocols
• Ability to read and interpret documents such as SOPs, work instructions, test methods and protocols.
• Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint).
• Ability to make GMP laboratory decisions both independently and with occasional mentorship from QC Supervisor.
• Performs independent troubleshooting and root cause analysis skills. Works directly with supervision for resolution of complex issues.
• Demonstrates a high level of efficiency and proficiency in performing analytical testing in compliance with all regulations
• Experience with Karl Fischer analysis preferred.
• Experience with Dissolution apparatus and UV preferred.
• Experience authoring Standard Operating Procedures preferred.
• Utilize electronic systems (LIMS, MES, LES, Empower, etc.) for execution and documentation of testing preferred.
• This position will be located in Titusville, NJ and may require up to 10% domestic or international travel.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.

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The anticipated base pay range for this position is :

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