Alcon

Head Quality Systems and Compliance (Assoc Dir)

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

Qualifications

  • Bachelor or Master's in Life Sciences, Pharmacy, Chemistry, Biotechnology, or a related field; advanced degree preferred.
  • 8-10 years of pharmaceutical manufacturing experience, ideally in oral solid dose processes.
  • Proven leadership in managing teams and fostering a culture of accountability.
  • Experience with FDA inspections and audit readiness is essential.
  • Strong background in Quality Systems, including data integrity and compliance oversight.

Responsibilities

  • Lead the implementation of the Quality Management System to ensure compliance with all regulatory standards.
  • Drive continuous readiness for inspections and audits, representing the site in external evaluations.
  • Oversee all quality system components, including corrective actions and change controls.
  • Collaborate with multiple departments to facilitate site operations and validation activities.
  • Investigate and resolve deviations and compliance issues effectively and timely.
  • Manage supplier quality and risk management programs to maintain inspection readiness.
  • Lead and develop the QA Compliance and Systems team through coaching and performance management.

Benefits

  • Comprehensive health, life, and disability benefits.
  • 401(k) plan with company contributions and matching.
  • Generous time-off package including vacation and personal days.
  • Eligibility for a performance-based cash incentive and annual equity awards.
Full Job Description

Band

Level 5

Job Description Summary

Location: Morrisville, NC

Join Novartis as our QA Compliance and Systems Head and help shape the quality foundation that enables the delivery of medicines to patients worldwide. This is a unique opportunity to join our new Small Molecule manufacturing site in Morrisville, playing a critical leadership role in building and advancing the site's quality culture, systems, and compliance programs from the ground up. You will oversee Quality Systems, Compliance, Audit and Inspection Readiness, Data Integrity, Supplier Quality, and Validation programs while partnering across Quality, Manufacturing, Engineering, and Regulatory functions. As a key member of the site Quality leadership team, you will drive a culture of compliance, continuous improvement, and operational excellence while ensuring inspection readiness and supporting the site's long-term growth and transformation journey.


 

Job Description

Key Responsibilities

  • Lead the site Quality Management System and ensure compliance with Novartis Quality Manual, current Good Manufacturing Practice requirements, and regulatory standards.
  • Drive continuous inspection readiness and lead preparation for corporate audits, customer audits, external audits, and Health Authority inspections.
  • Provide oversight of quality systems including deviations, corrective and preventive actions, exceptions, change controls, data integrity, eCompliance, key performance indicators, and key quality indicators.
  • Partner with Manufacturing, Quality Control, Validation, Technical Operations, Engineering, and Regulatory teams to support site operations, technology transfers, qualifications, and validation activities.
  • Lead investigations of deviations, out-of-expectation events, complaints, and compliance issues, ensuring timely and effective resolution.
  • Oversee supplier quality, regulatory compliance, training governance, and risk management programs that support sustainable inspection readiness.
  • Lead, coach, and develop the QA Compliance and Systems team through effective resource planning, performance management, talent development, training governance, and sustained training compliance.
  • Promote a strong quality culture built on accountability, collaboration, continuous improvement, employee development, and proactive risk management.
  • Advance digital enablement and continuous improvement initiatives that strengthen quality performance, simplify processes, and support site transformation.

Essential Requirements

  • Bachelor of Science or Master of Science in Life Sciences, Pharmacy, Chemistry, Biotechnology, or related scientific discipline; advanced degree preferred.
  • Minimum 8-10 years of experience in pharmaceutical manufacturing, which may include expert roles in Production, Manufacturing Science and Technology, Quality, or Engineering. Prior experience in oral solid dose manufacturing preferred.
  • Demonstrated leadership experience managing teams, developing talent, driving performance, fostering training compliance, and building a culture of accountability and collaboration.
  • Significant experience leading FDA inspections, regulatory interactions, audit readiness activities, and inspection remediation efforts.
  • Strong experience leading Quality Systems programs, including deviations, corrective and preventive actions, change control, data integrity, validation, and compliance oversight.
  • Proven ability to lead risk management, continuous improvement, and compliance initiatives in highly regulated manufacturing environments.

Desirable Requirements

  • Previous involvement with facility start-ups, qualifications, validations, transfers
  • Qualifications or certification in Lean Management, Operational Excellence, or comparable continuous improvement methodologies.

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.

#LI-Onsite


 

Salary Range

$138,600.00 - $257,400.00


 

Skills Desired

Business Acumen, Collaboration, Data Integrity, Decision Making, Leadership, Risk Management, Strategic Planning

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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