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Senior Expert - Good Manufacturing Practices

4+ years
$118,000–$177,600 Annually
10 Dec. 5, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Here’s a concise and organized summary of the job description:


Analytical Operations Specialist – Gene Therapy (GMP)

Location: East Hanover, New Jersey, USA

About Novartis:
Join a passionate community striving for breakthroughs in healthcare. Novartis combines innovative science and collaboration to improve lives and advance quality care.

Role Overview:
The Analytical Operations Specialist supports GMP activities to enable gene therapy delivery, including analytical testing, method development, and process monitoring. This role emphasizes teamwork, innovation, and continuous improvement, with a focus on serving patients and advancing gene therapy development.

Key Responsibilities:

  • Shift Schedule: Flexible shift work (4 days/week, 10 hours/day).
  • Technical Expertise: Acts as SME for GMP assays such as AUC, cell-based potency, ELISA, PCR, flow cytometry, next-generation sequencing, and separations-based assays.
  • Lab Operations:
    • Routine sample testing (in-process, release, and stability) under GMP or non-GMP modes.
    • Participation in method qualification, validation, transfer, and improvement.
    • Lab equipment procurement, maintenance, and system management.
  • Documentation:
    • Drafts/revises SOPs, validation/transfer protocols, and technical reports.
    • Reviews and trends test results.
  • Problem Solving: Leads investigations of deviations and implements corrective/preventative actions.
  • Innovation: Introduces technologies to enhance GMP operations’ efficiency and compliance.
  • Collaboration: Represents GMP in cross-functional teams (e.g., Quality Assurance, Analytical Development).
  • Compliance: Ensures adherence to GMP/GLP regulations, FDA/EMEA requirements, and Novartis guidelines.

Essential Requirements:

  • Education: Bachelor’s degree in Biology, Biochemistry, Molecular Biology, Immunology, or a related field.
  • Experience:
    • 4+ years in GMP laboratory operations, with expertise in assays such as AUC, ELISA, PCR, and flow cytometry.
    • Proficient in GMP testing, problem-solving, and managing lab investigations.
  • Skills: Strong collaboration, technical adaptability, and effective communication in fast-paced environments.

Compensation and Benefits:

  • Salary Range: $118,000–$177,600/year (subject to market and performance factors).
  • Total Compensation Package: Includes potential sign-on bonuses, stock units, medical benefits, 401(k), and paid time off.
  • Growth Opportunities: Comprehensive training and retraining programs to support professional development.

Why Novartis:

Novartis believes in creating a brighter future through collaboration and passion for innovation. Be part of a diverse, inclusive workplace that values individuality and fosters bold innovation.

Diversity & Inclusion Commitment:

Novartis is an Equal Opportunity Employer, dedicated to fostering an inclusive environment that reflects the world around us.

Accessibility & Accommodations:

Novartis provides reasonable accommodations for individuals with disabilities. For assistance, contact us.reasonableaccommodations@novartis.com or call +1(877)395-2339.

Division: Development
Business Unit: Innovative Medicines
Functional Area: Quality
Job Type: Full-Time, Regular

For more information about Novartis benefits and opportunities, visit:


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