Alcon

Head of QA Operations (Assoc Dir level)

Alcon$138K — $257K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Chemistry, Biology, Pharmacy, Biochemistry, Engineering, or related field.
  • Over 10 years experience in Quality Assurance, Quality Control, or operational GxP.
  • Previous leadership experience in Quality Assurance organizations, with team development skills.
  • Experience supporting aseptic pharmaceutical manufacturing operations.
  • Comprehensive knowledge of GMPs and relevant regulatory standards.
  • Direct experience in conducting investigations and root cause analysis.
  • Experience with health authority inspections and audits.

Responsibilities

  • Lead QA Operations with oversight for Drug Product Manufacturing and Quality Control.
  • Ensure timely and compliant product disposition, prioritizing patient safety.
  • Promote quality oversight and operational excellence across manufacturing operations.
  • Manage resource allocation and operational priorities for quality objectives.
  • Lead investigations and corrective actions to address quality issues.
  • Oversee the preparation and delivery of validation plans for manufacturing compliance.
  • Support escalations, FDA interactions, and ensure ongoing inspection readiness.
  • Develop high-performing teams while enhancing the site quality culture.
  • Collaborate with cross-functional teams to achieve production and quality goals.
  • Monitor metrics to drive continuous improvement in compliance and execution.

Benefits

  • Comprehensive health, life, and disability benefits package.
  • 401(k) plan with company contributions and matching.
  • Generous vacation and time-off package including personal days and holidays.
  • Potential for performance-based cash incentives and eligibility for equity awards.
Full Job Description
Job Description Summary
Location: Indianapolis, Indiana

As Head of QA Operations, you will lead the Quality Assurance Operations organization supporting Novartis' Indianapolis Radioligand Therapy (RLT) Drug Product manufacturing site, providing quality oversight for production, quality control operations, and product disposition activities. This is a highly visible leadership opportunity to build and develop high-performing teams, strengthen quality culture, and partner across manufacturing, quality control, engineering, and site leadership to ensure the reliable delivery of innovative therapies to patients who need them most. If you are passionate about operational excellence, regulatory compliance, and developing people while driving continuous improvement, this role offers the opportunity to make a lasting difference every day.

Job Description

Key Responsibilities

  • Lead the QA Operations organization, providing quality oversight for Drug Product (DP) Manufacturing and Quality Control operations, including Shop Floor QA, QA Engineering, and final product disposition.


  • Ensure compliant and timely product disposition decisions while maintaining patient safety and regulatory compliance.


  • Drive quality oversight across manufacturing operations, promoting inspection readiness and operational excellence.


  • Lead resource allocation, capacity planning, and operational prioritization to support quality, compliance, and business objectives.


  • Lead investigations, deviations, corrective actions, and change controls to resolve quality issues effectively.


  • Ensure preparation, review, and delivery of validation plans supporting compliant manufacturing and quality operations.


  • Support escalation management, FDA interactions, and commercial product field actions while maintaining inspection readiness.


  • Build, coach, and develop high-performing leaders and teams while strengthening site quality culture.


  • Partner cross-functionally to achieve production goals, address risks, and support business priorities.


  • Monitor quality performance metrics and drive continuous improvement initiatives to strengthen compliance and execution.


Essential Requirements

  • Bachelor of Science in Chemistry, Biology, Pharmacy, Biochemistry, Engineering, or related experience.


  • 10+ years of experience in Quality Assurance, Quality Control, Quality Systems, Compliance, or operational GxP area (Manufacturing / Development) within the pharmaceutical, diagnostic, or medical device industries.


  • Prior experience leading a Quality Assurance organization, including developing high-performing teams and talent.


  • Prior experience supporting aseptic pharmaceutical manufacturing operations.


  • In-depth knowledge of current GMPs, Quality Assurance, Quality Control, and applicable regulatory requirements and standards.


  • Direct experience conducting investigations and root cause analysis for pharmaceutical or medical device products.


  • Experience reviewing manufacturing and Quality Control validation documents and supporting validation activities in a regulated environment.


  • Proven experience leading Health Authority inspections and audits within a regulated manufacturing environment.


Desirable Requirements

  • Experience in advanced therapy platforms, including Radioligand Therapy, Cell and Gene Therapy, or other novel therapeutic technologies.


  • Experience with continuous improvement methodologies such as Lean, Six Sigma, or 5S and leading projects.


The salary for this position is expected to range between $138,600 and $257,400 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.

Your compensation will include a performance-based cash incentive and, depending on the level of the

role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

To learn more about the culture, rewards and benefits we offer our people click here.

#LI-Onsite

Salary Range
$138,600.00 - $257,400.00

Skills Desired
Collaboration, Data Integrity, Decision Making, Leadership

About Alcon

Alcon is a global medical company specializing in eye care products and services. The company's products include surgical equipment, contact lenses, and eye drops. Alcon was founded in 1945 and is headquartered in Baar, Switzerland. The company operates in over 70 countries and has over 20,000 employees. In 2019, Alcon became an independent publicly traded company after being spun off from Novartis.
Learn more about Alcon
Size
24,389 employees
Market Cap
$33.3 billion
Industry
Founded
1945
NASDAQ

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