{"@context":"https://schema.org","@type":"JobPosting","title":"Analyst Quality Control","description":"

Job Title: Analyst Quality Control

Company Name: Johnson & Johnson

Job Location: Raritan, NJ

Job Street Address: Raritan, NJ

Job Employment Type: FULL_TIME

Job Salary: $65,000 - $104,000 per year

Full Job Description:

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 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.
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Professional
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
A candidate has been pre-identified for consideration. However, all applications will be considered.
We are searching for the best talent for an Quality Control Analyst based in Raritan, NJ.
The Quality Control Analyst is responsible for conducting biochemical, microbiological, and/or general testing of final product samples submitted to the QC laboratories. They are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. They typically work with a team of 5 - 15 other Analysts within the functional laboratory of the Quality Control department.
Key Responsibilities:

Perform analytical testing and maintain a safe work environment in compliance with all applicable procedures, EHS, and GMP regulations.

Perform peer review and approval of laboratory data and logbooks.

Use electronic systems (e.g., LIMS, iLAB) for the execution and documentation of testing.

Build, review, and approve relevant QC documents, SOPs, and WIs.

Complete invalid assay and general laboratory investigation records, CAPAs, and change controls.

Support Health Authority inspections.

Provide input to functional laboratory meetings.

Qualifications:
Education:

A minimum of a Bachelor's degree or equivalent university degree is required; an advanced degree (MSc., Ph.D.) or a focused degree in Biology, Biochemistry, Chemistry, or a related scientific field is preferred.

Experience and Skills:
Required:

A minimum of two (2) years of relevant work experience.

Experience performing one or more of the following cellular and/or molecular-based techniques: qPCR, Flow Cytometry, ELISA, Cell Culture, and/or potency assays.

Experience within the biopharmaceutical or pharmaceutical industry.

Experience with aseptic processing in biosafety cabinets and/or ISO 5 cleanroom environments.

Demonstrated experience successfully working in an analyst role/level and proficiency using analytical methodologies within a functional laboratory.

Knowledge of cGMP regulations and Good Documentation Practices (GDP).

Experience with Quality Control document reviews and regulatory inspection processes.

Proficiency in technical writing (e.g., test methods, SOPs, protocols, etc.).

Excellent written and verbal communication skills.

Preferred:

Work experience in Cell and/or Gene Therapy or Biologics.

Basic knowledge of compendial requirements and standards (e.g., USP, EP, JP, etc.).

Experience with LIMS and SAP or equivalent systems.

Experience, training, or certification with Process Excellence tools and methodologies.

Other:

Requires the ability and flexibility to work 10-hour shifts between the operational hours of 8:00 AM - 6:00 PM (Sunday-Wednesday), and to provide occasional support on weekends or other shifts.

Requires the ability to meet physical demands, including lifting up to 20 lbs, and standing or sitting for extended periods in a laboratory setting; performing visual inspections of materials (e.g., color, appearance, particles); and documenting observations during laboratory testing.

Requires up to 5% domestic travel to other sites/locations.

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

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