Sorry, this listing is no longer accepting applications. Don’t worry, we have more awesome opportunities and internships for you.

Quality Control Analyst 1

Learn more about Johnson & Johnson
Johnson & Johnson

Johnson & Johnson

Quality Control Analyst 1

Titusville, FL
Full Time
Paid
  • Responsibilities

    Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Quality Control Analyst 1 to be located in Titusville, NJ.

    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 https://www.jnj.com/. 

    For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.

    We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

    At Johnson & Johnson, we all belong.

    The QC Analyst I conducts analytical testing of stability samples according to testing schedules in a productive and efficient manner.

    Key Responsibilities:

    • Perform analytical testing 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 moderate 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.
    • Provide input to functional laboratory meetings and take actions as a QC representative at cross-functional meetings
    • Support the development and execution of CREDO action plans and initiatives

    Qualifications

    Education

    • Bachelor's degree and/or equivalent degree required; preferably in Science or related field

    Experience and Skills:

    Required:

    • At least 2 years of experience in a GMP-regulated, science-related field
    • Basic knowledge of analytical technologies used in the QC laboratory
    • Skilled in performing intermediate and some advanced testing within the functional laboratory, using HPLC and/or UPLC
    • Knowledge and understanding of current Good Manufacturing Practices (cGMP) related to QC laboratory
    • Basic knowledge of compendial (USP, EP, JP, etc.) requirements
    • Basic technical writing skills
    • Ability to participate in projects with mentorship from supervision/management
    • 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 makes GMP laboratory decisions both independently and with occasional mentorship from QC supervisor
    • Performs basic instrument troubleshooting and has basic root cause analysis skills. Works directly with supervision for resolution of complex issues.

    Preferred:

    • Experience with Karl Fischer analysis
    • Experience authoring Standard Operating Procedures
    • Experience in HPLC or UPLC

    Additional Information:

    The anticipated base pay range for this position is $50,000 to $80,500.

    • Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
    • Employees may be eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).
    • This position is eligible to participate in the Company’s long-term incentive program.
    • Employees are eligible for the following time off benefits:
      • Vacation – up to 120 hours per calendar year
      • Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar year
      • Holiday pay, including Floating Holidays – up to 13 days per calendar year of Work, Personal and Family Time - up to 40 hours per calendar year
    • Additional information can be found through the link below. https://www.careers.jnj.com/employee-benefits

    The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market.

    Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.

    For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.

  • Industry
    Hospital and Health Care
  • Fun Fact
    We aspire to be the world's healthiest work force, offering group fitness classes, beach volleyball courts, bicycle desks, and more!
  • About Us

    Push the boundaries of science to transform health—and your career.

    Join us and advance life-changing treatments for people who need them most. At Johnson & Johnson, our focus is on improving global health equity and developing MedTech and pharmaceutical innovations that impact the future of health. Using AI and robotics to transform surgery or helping data scientists and clinicians formulate new ways to diagnose and treat disease, this work may sound like sci-fi, but it’s all science, all real, and could be your career. Whatever your background, skills, or career goals, there’s a place for you to help solve some of the world’s most pressing health challenges with us.

    Accelerate your career while changing the world.

    Each of our broadly-based family of companies offers an inclusive and empowering culture and employee benefits (like paid time off to volunteer, transgender-inclusive and same-sex partner health insurance coverage, and more) designed to help you live your best life, however you define it. And our best-in-class learning and development approaches, mentorship, and access to innovators across the world will help you grow your skills and reach your career goals. Because when you're at your best, nothing stands between you and your next breakthrough.