Associate Analyst Quality Control (2nd Shift)

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:

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

We are searching for the best talent for Associate Analyst Quality Control to be in Raritan, NJ.

Purpose: Entry to developing individual contributor, who works under close supervision.

Assists staff in various processes in the Quality Control function.

Supports day-to-day laboratory activities such as sample management, supply ordering and receipt, and general housekeeping.

Assists with analysis, qualification/validation activities, and lab investigations.

Supports data review and metrics reporting.

Executes continuous improvement projects with supervision.

May execute testing under supervision.

You will be responsible for:


* Ensure testing is completed in compliance with all applicable procedures, standards, and current Good Manufacturing Practices regulations.


* Conduct analytical testing of final product samples submitted to the QC laboratories.


* Perform peer review/approval of laboratory data.


* Use electronic systems (LIMS, iLAB) for execution and documentation of testing.


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

Qualifications / Requirements:

Education:


* Minimum of a Bachelor’s or equivalent University Degree required; focused degree in Biology, Biochemistry, Microbiology, or related scientific field is preferred

Experience and Skills:

Required:


* 0 - 2 years of relevant work experience


* Knowledge and understanding of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP)


* Experience performing one or more of the following cellular and/or molecular based techniques: qPCR, ELISA, Cell Culture, and/or Potency assays


* Experience with Manual Sample Processing


* Excellent written and verbal communication skills

Preferred:


* Experience in a Quality Control settin...