REQ-10031156
12月 04, 2024
USA

摘要

The Compliance Specialist is responsible for supporting the Morris Plains QMS and Inspection Management

This role is required to be on-site in Morris Plains, NJ. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

365 days a year, we aspire to be the best manufacturer of Cell & Gene therapies to ensure our patients have the treatments they need to live longer, healthier lives

About the Role

Key Responsibilities:

 

  • Responsible for management of Technical Compliance Investigations and Signal Review
  • Perform complaint investigations and facilitate escalation as needed
  • Complete and maintain certification through the Investigation Certification Program (ICP) to supporting compliant investigations and site investigations as needed
  • Manage, monitor and coordinate records in1QEM System relating to complaints
  • Contributing and providing report for APQRs for Complaints, BPDR, Recall and FARs
  • Function as Complaint liaison for CGT between Customer Complaint group, CPO QA and Country CPO
  • Support Inspection and Audit Management and Self-inspection program
  • Quality System Ownership for QMR reporting and Support as onsite SME for eDoc Systems
  • Site Master Validation Plan and Sub-Plan Governance and Site Master Files Management
  • QMS Functional Representation Role

 

Essential Requirements:

  • BA/BS in Chemistry, Microbiology or Biological Sciences or related degree.
  • 4+ years of related pharmaceutical experience, preferably to include cell gene therapies
  • Experience with Global systems
  • Experience in Quality Control, Quality Assurance, Documentation Control, Compliance
  • Knowledge of GMPs/Regulatory
  • Knowledge of deviation, CAPA, Compliant, BPDR, Recall, Change Control, manufacturing processes, Packaging process, Regulatory inspection, technical writing
  • Demonstrate Excellent leadership

The pay range for this position at commencement of employment is expected to be between $92,800 and $139,200 per year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including a sign-on 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 “at-will 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.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? http://www.novartis.com/about/strategy/people-and-culture

Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: http://talentnetwork.novartis.com/network

Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: http://www.novartis.com/careers/benefits-rewards

Operations
Innovative Medicines
USA
New Jersey
Morris Plains
Quality
Full time
Regular
No
A female Novartis scientist wearing a white lab coat and glasses, smiles in front of laboratory equipment.
REQ-10031156

QA Compliance Specialist

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