drjobs QA Operations Specialist

QA Operations Specialist

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1 Vacancy
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Job Location drjobs

Essex County, NJ - USA

Monthly Salary drjobs

$ 81200 - 150800

Vacancy

1 Vacancy

Job Description

Job Description Summary

Our QA Operations Specialist manages Quality aspects and projects within area of responsibility as well as ensuring and supporting overall GxP conformity and Compliance with the Novartis Quality Management Systems for the Millburn manufacturing site.

Location: Millburn #LIOnsite

Shift: Week 1: WedSat AM 6:00am5:30pm)
Week 2: WedFri AM 6:00am6:30pm)



Job Description

Key Responsibilities:

  • Supports the qualification validation and operational readiness of the ongoing expansion in Indianapolis Isotopes manufacturing site.
  • As the project progresses this role will transition to provide shopfloor QA support and oversight of GMP operations during qualification and validation runs and other related job duties as assigned.
  • Once the site is operational the role accountabilities will transition to:
    • Provide shopfloor quality oversight of all production quality control and supply chain departments to ensure their practice fully adheres to cGMP including data integrity. Ensure timely escalation to management of all applicable incidents.
    • Perform live review of manufacturing batch records in preparation for batch release and escalate any discrepancies immediately.
    • Assist functional areas with achieving timely and compliant final product disposition of the product and ensure compliance of site personnel according to current procedures and GMP requirements
    • Review approve and support procedures and production/testing records as required and assist in the training of site associates.
    • Support FDA/Regulatory interactions for the Indianapolis Isotopes site activities and Isotopes products to ensure successful regulatory submissions and inspections.
    • Support QA Operations as a valued business partner with a culture of safety quality delivery to patients cost compliance and data integrity.
    • During the initial project expansion project phase the role will be in daytime. The role will move to shift work once qualification and validation activities start and during the operational manufacturing once the site is approved

Essential Requirements

Education: Bachelors Degree preferably in Life Sciences Chemistry or related relevant degree.

Experience:

  • 2 years of experience in a GxP (Bio)pharmaceutical or API manufacturing operations
  • 1 years of experience in a quality assurance role
  • Collaborating across boundaries
  • Functional Breadth
  • QA and/or QC experience in pharmaceutical industry with environmental monitoring & cleanliness zones

Novartis Compensation and Benefit Summary: The pay range for this position at commencement of employment is expected to be between $81200 and $150800/year; however while salary ranges are effective from 1/1/25 through 12/31/25 fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further final pay determinations will depend on various factors including but not limited to geographical location experience level knowledge skills and abilities. The total compensation package for this position may also include other elements including a signon bonus restricted stock units and discretionary awards in addition to a full range of medical financial and/or other benefits (including 401(k) eligibility and various paid time off benefits such as vacation sick time and parental leave) dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired employee will be in an atwill position and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time including for reasons related to individual performance Company or individual department/team performance and market factors.



EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment hiring training promotion or other employment practices for reasons of race color religion sex national origin age sexual orientation gender identity or expression marital or veteran status disability or any other legally protected status.



Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If because of a medical condition or disability you need a reasonable accommodation for any part of the application process or to perform the essential functions of a position please send an email to or calland let us know the nature of your request and your contact information. Please include the job requisition number in your message.


Salary Range

$81200.00 $150800.00


Skills Desired

Continued Learning Dealing With Ambiguity Gmp Procedures Qa (Quality Assurance) Quality Control (Qc) Testing Quality Standards SelfAwareness Technological Expertise Technological Intelligence

Required Experience:

Unclear Seniority

Employment Type

Full-Time

Company Industry

About Company

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