Associate Analyst Quality Control 2nd Shift

Johnson & Johnson; Raritan (NJ); On-site; USD 59,000 - 86,000; Full time

Job summary

A leading healthcare company is seeking an Associate Analyst in Quality Control in Raritan, NJ. This entry-level role involves supporting laboratory activities, ensuring compliance, conducting testing, and managing documentation. Ideal candidates will have a Bachelor’s degree in a relevant field and some experience with analytical techniques. Join a dynamic team dedicated to healthcare innovation.

Benefits

Bonuses

Retirement plans

Time off

Qualifications

• 0-2 years relevant experience required.
• Experience with qPCR, ELISA, Cell Culture.

Responsibilities

• Ensure testing complies with procedures and regulations.
• Conduct analytical testing of final product samples.
• Perform peer review and approval of laboratory data.

Skills

Communication

Knowledge of cGMP

Cellular/Molecular Techniques

Education

Bachelor’s degree in Biology

Bachelor’s degree in Biochemistry

Bachelor’s degree in Microbiology

Tools

LIMS

SAP

Job 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 https://www.jnj.com

Job Function:

Quality

Job Sub Function:

Quality Control

Job Category:

Professional

All Job Posting Locations:

Raritan, New Jersey, United States of America

Job Description:

We are seeking an Associate Analyst in Quality Control based in Raritan, NJ.

Purpose:

This is an entry to developing individual contributor role, working under close supervision. Responsibilities include supporting laboratory activities such as sample management, supply ordering, analysis, qualification/validation, investigations, data review, and metrics reporting. The role may involve executing testing under supervision.

You will be responsible for:

1. Ensuring testing complies with all applicable procedures, standards, and regulations.
2. Conducting analytical testing of final product samples.
3. Performing peer review and approval of laboratory data.
4. Using electronic systems (LIMS, iLAB) for testing documentation.
5. Building, reviewing, and approving QC documents, SOPs, and WIs.

Qualifications / Requirements:

Education:

• Bachelor’s or equivalent degree, preferably in Biology, Biochemistry, Microbiology, or related field.

Experience and Skills:

Required:

• 0-2 years relevant experience.
• Knowledge of cGMP and GDP.
• Experience with cellular/molecular techniques such as qPCR, ELISA, Cell Culture, or Potency assays.
• Manual sample processing experience.
• Excellent communication skills.

Preferred:

• Experience in a QC setting, Biopharmaceutical or Pharmaceutical industry.
• Experience with Cell and/or Gene Therapy or Biologics.
• Familiarity with LIMS, SAP, or similar systems.

Other:

• Ability to work 10-hour shifts between 4PM - 2AM, Wed-Sat, with flexibility for support shifts.
• Physical ability to lift up to 20 lbs, stand or sit for extended periods, and perform visual inspections.
• Up to 10% domestic/international travel.

Additional Information:

The base pay range is $59,000 to $85,100. Employees are eligible for bonuses, benefits, retirement plans, and time off as detailed in the full description. For more details, visit https://www.careers.jnj.com/employee-benefits.

Johnson & Johnson is an Equal Opportunity Employer. We consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, or veteran status. Accommodations are available for applicants with disabilities upon request.