Johnson & Johnson

Quality Assurance Specialist

Johnson & Johnson$70K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Associate Degree or higher required.
  • 4+ years experience in regulated manufacturing industry.
  • Preferred 2+ years experience in Quality Assurance.
  • PC literacy with MS Office and relevant software.
  • Bilingual in English and Spanish essential.
  • Knowledge of QSR's and ISO Standards mandatory.
  • ASQ CQT and CQA certifications preferred.
  • Willingness to work various shifts and overtime, including weekends.

Responsibilities

  • Handle non-conformant material effectively.
  • Maintain control of materials in hold cage by placing and removing items as needed.
  • Lead the Stop shipment process for materials in Distribution Centers.
  • Coordinate and provide training on product inspection and disposition.
  • Perform audits and contribute to the internal audit program.
  • Analyze data to make decisions on material disposition.
  • Train and support new Quality Specialists in their roles.

Benefits

  • Dynamic work environment focused on innovation in medical technology.
  • Opportunity to contribute to impactful surgical solutions globally.
  • Engagement in continuous improvements and process enhancements.
  • Potential for career growth within a leading industry company.
Full Job Description
Job Function:
Quality

Job Sub Function:
Quality Control

Job Category:
Professional

All Job Posting Locations:
San Lorenzo, Puerto Rico, United States of America

Job Description:

About MedTech

Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

About Surgery

Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

Are you passionate about improving and expanding the possibilities of surgery? Ready to join a team that's reimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the world's most prevalent conditions such as obesity, cardiovascular disease and cancer. Patients are waiting.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

We are searching for the best talent for Quality Assurance Specialist.

Purpose: Reports to Quality Team Leader, Quality Operations Leader, Quality Operations Lead or designee and with the objective of maintaining high quality standards for the product manufacturing process and the compliance with the regulatory requirements, supports and maintain OPCERT program, performs data analysis to support process improvements and decision making and performs other functions to support the Quality Assurance Department at Ethicon LLC. Engage in the Quality Assurance operation in accordance with the QSR, ISO and Ethicon written specifications and quality standards. Support cost improvement projects at plant level and prepare reports (using the computer system) as assigned.

You will be responsible for:
  • Handling of non-conformant material or potential non-conformant material.
  • In charge of maintaining all material inside the hold cage on control. Placing and removal of material on hold.
  • Lead of Stop shipment process for material in the Distribution Centers or Interplants. Place and remove material on hold as applicable.
  • OPCERT PROGRAM:
    • Coordinate and provide training to associates on inspection and disposition of product.
    • Update and maintain training material for inspection and disposition of product.
    • Coordinate and perform practical evaluation for inspection and disposition to associates.
    • Update and maintain material for practical evaluation and auto-monitoring.
    • Verifies completion of operator certification requirements for associates and request operator certification.
    • Perform audits and support the internal audit program.
    • Maintain knowledge of all procedures, changes to specifications and new regulations related to the area of responsibility.
    • Support associates on defect awareness and specification requirements.
  • Data Analysis, Process Improvements and Decision Making:
    • Exercise initiative, leadership and decision making to solve quality-related issues with other departments' organization members and other Ethicon sites' organization members.
    • Perform data analysis and recommend disposition of material.
    • Use of Statistical Process Control knowledge to make decision on the acceptance/rejection of the product/process.
    • Perform batch record review for product release.
    • Evaluate and make decisions on day-to-day manufacturing QA related issues.
    • Participate in non-conformances' investigations and root cause analysis.
    • Evaluate and approve product control and disposition to determine if product is according to the requirements and Quality Systems Regulations.
    • Responsible for coordination of hold material and track and report of hold trends.
    • Support Engineering and QA Departments in projects and validation activities.
    • Submit changes and support implementation of changes in the documentation system.
    • Support the effective implementation of programs that help improve the overall quality of product and process within area of responsibility.
    • Utilize quality and statistical tools to recommend process improvements.
    • Train new Quality Specialist at the manufacturing area and QA Specialist duties and responsibilities
  • Perform particle count monitoring, per applicable procedures.
  • Coordinate dose audit monitoring samples, per applicable procedures.
  • Support Finished Goods Lab as back up, when necessary, for specific duties of QA Finished Goods Technician as required.


Qualifications / Requirements:
  • A minimum of an Associate Degree is required.
  • A minimum of four (4) years of experience in the regulated manufacturing industry is required.
  • At least two (2) years of experience in Quality Assurance is preferred.
  • PC literacy including MS Office and use of other software and applications is required.
  • Verbal and written communication skills in English and Spanish are required.
  • Knowledge of QSR's and ISO Standards is required.
  • ASQ CQT is preferred.
  • ASQ CQA is preferred.
  • Availability to work overtime, various work schedules, which may include 1st, 2nd, 3rd shifts and/or 12-hour daily shifts, including weekends and holidays is required.


#LI-Onsite

Required Skills:

Preferred Skills:
Analytical Reasoning, Business Behavior, Compliance Management, Continuous Improvement, Controls Compliance, Data Analysis, Execution Focus, ISO 9001, Persistence and Tenacity, Quality Control (QC), Quality Control Testing, Quality Standards, Quality Systems Documentation, Report Writing, Sample Testing, Technologically Savvy

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

Johnson & Johnson Careers

Joining Johnson & Johnson provides an unparalleled opportunity to be a part of a global team of professionals dedicated to blending care, science, and innovation to profoundly change the trajectory of health for humanity.

Work You’ll Do

At Johnson & Johnson, you will engage in work that matters. Join our community of professionals in health care to drive significant and impactful changes across the globe. Our team at Johnson & Johnson leads with science and heart in sectors from pharmaceuticals to medical devices and consumer health products.

Transform Health Care

Leverage Johnson & Johnson’s culture of innovation to transform health care and improve the lives of people around the world. Our collaborative environment encourages leadership and growth, allowing you to pioneer new strategies for health care solutions with a diverse team of experts.

Innovative Work

Engage in groundbreaking work that enhances how care is delivered on a global scale. Johnson & Johnson’s commitment to innovative health solutions results in dynamic career paths filled with opportunities for professional growth and development.

Be Part of a Great Team

Our team at Johnson & Johnson thrives on collaboration and diversity. You will work alongside over 130,000 employees globally who are committed to making a lasting impact. With a culture that values diversity training and leadership, you are supported in both personal and professional growth.

Future-Proof Your Career

Johnson & Johnson offers a myriad of job opportunities and employment benefits designed to help you meet your career and personal goals. Our employees enjoy comprehensive benefits, including health insurance, retirement plans, and family-friendly policies that pave the way for a fulfilling career and life balance.

Explore Job Opportunities and Internships

Whether you’re looking to start your career or take it to the next level, Johnson & Johnson offers positions ranging from internships to leadership roles across various sectors. Enhance your skills through hands-on experience and our extensive networking and mentorship programs.

Johnson & Johnson Leadership and Development

Our commitment to leadership and continuous learning is at the core of our employment philosophy. Every position offers chances to lead, learn, and innovate. We provide extensive training programs and development courses that prepare you for the future of health care.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
NASDAQ

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