Johnson & Johnson

Analyst Quality Systems

In short

This role manages quality system execution at a Johnson & Johnson manufacturing site in Raritan, NJ, covering document/records management, data integrity, audits, investigations, and change control. The company is a large healthcare and pharmaceutical corporation, and the position is fully onsite Monday-Friday with occasional off-shift support required. It demands a bachelor's degree in engineering or science plus at least 2 years of experience in Quality Assurance/Quality Systems and knowledge of cGMP regulations.

# Analyst Quality Systems
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.
Job Function: Quality
Job Sub Function: Quality Documentation
Job Category: Professional
Location: Raritan, New Jersey, United States of America
Johnson & Johnson is currently recruiting for an Analyst Quality Systems! This position will be located in Raritan, NJ and performed fully onsite Monday-Friday.
Key Responsibilities
•Complete quality system execution activities, including but not limited to Document/Records Management and Data Integrity.
•Act as a liaison between site and above site activities.
•Support document lifecycle and perform site superuser activities.
•Identify improvement opportunities and elevate potential risks to management.
•Actively assist in Audit, Investigation and Change Control related activities.
•Participate in department optimization efforts.
•Take the lead on selected projects assignments following them through closure.
•Update Standard Operating Procedures and related documents.
•Drive alignment and efficiencies between local and global processes.
•Perform tasks in a manner consistent with the safety policies, quality systems and cGxP requirements.
•Provide occasional support at off-shift hours with little or no prior notice.
•Other duties can be assigned to support business continuity.
Education
•Minimum of a bachelor's degree in engineering, Science or equivalent technical subject area.
Required Experience
•Minimum 2 years of work experience in Quality Assurance/Quality Systems/Quality Control/Quality related activities.
•Knowledge of cGMP regulations.
Preferred Experience
•Experience in a highly paced manufacturing environment.
Skills
•Strong written and verbal communication skills in English.
•Strong Collaboration and time management skills.
Pay & Benefits
The anticipated base pay range for this position is: $65,000.00 - $104,650.00
Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
•Vacation – 120 hours per calendar year
•Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado – 48 hours per calendar year; for employees who reside in the State of Washington – 56 hours per calendar year
•Holiday pay, including Floating Holidays – 13 days per calendar year
•Work, Personal and Family Time - up to 40 hours per calendar year
•Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
•Bereavement Leave – 240 hours for an immediate family member; 40 hours for an extended family member per calendar year
•Caregiver Leave – 80 hours in a 52-week rolling period
•Volunteer Leave – 32 hours per calendar year
•Military Spouse Time-Off – 80 hours per calendar year

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