Alcon

Manufacturing Unit Lead-Drug Substance

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

Qualifications

  • Bachelor's degree in Engineering, Chemistry, Biology, Pharmacy, or related field.
  • 10+ years of pharmaceutical or life sciences manufacturing experience in a GMP environment.
  • 5+ years of experience in people leadership and managing manufacturing operations.
  • Strong background in quality, compliance, and regulatory audit processes.
  • Expertise in Drug Substance manufacturing processes and commercial operations.

Responsibilities

  • Lead the start-up and commercial production of Drug Substance manufacturing operations.
  • Provide technical leadership for processes, equipment, and validation activities.
  • Ensure compliance with cGMP and maintain reliable manufacturing operations.
  • Build and develop a high-performing manufacturing team while ensuring training compliance.
  • Drive readiness for inspections and support regulatory compliance activities.
  • Lead investigations of deviations and implement effective corrective actions.
  • Champion initiatives for operational excellence and process improvement.

Benefits

  • Comprehensive health, life, and disability benefits.
  • 401(k) plan with company contribution and matching.
  • Generous time-off package including vacation and holidays.
  • Access to performance-based cash incentives and potential equity awards.
Full Job Description

Band

Level 5

Job Description Summary

Location: Morrisville, NC
This is an Associate Director level role.

Imagine leading the launch and long-term success of a state-of-the-art Drug Substance manufacturing organization at Novartis. As Manufacturing Unit Head, you will play a pivotal role in building and leading a high-performing team while shaping the future of manufacturing operations at our new Morrisville site. From facility start-up and operational readiness through commercial operations, you will drive manufacturing excellence, foster a culture of safety and quality, and deliver reliable supply for patients. This is a unique opportunity to make a lasting impact by combining technical expertise, people leadership, and strategic vision to establish world-class manufacturing capabilities from the ground up.


Job Description

Key Responsibilities
  • Lead Drug Substance manufacturing operations from facility start-up through commercial production. Serve as the process owner and end-user representative for Drug Substance (DS) manufacturing, process equipment, and systems throughout the project lifecycle.
  • Provide technical leadership for manufacturing processes, equipment, validation, and operational readiness activities.
  • Ensure safe, compliant, and reliable manufacturing operations aligned with cGMP requirements.
  • Build, lead, coach, and develop a high-performing manufacturing team while maintaining training compliance.
  • Drive inspection readiness and support successful regulatory inspections, audits, and compliance activities.
  • Lead deviation investigations, root cause analysis, and implementation of effective Corrective and Preventive Actions.
  • Champion operational excellence initiatives to enhance productivity, process robustness, and manufacturing performance.
  • Explore and leverage data and technology to support the site's digital transformation journey.

Essential Requirements
  • Bachelors degree in Engineering, Chemistry, Biology, Pharmacy, or related scientific discipline.
  • Minimum 10 years of pharmaceutical or life sciences manufacturing experience in GMP environment.
  • Minimum 5 years of people leadership experience managing manufacturing operations and developing high-performing teams.
  • Demonstrated experience leading quality, compliance, inspection readiness, and regulatory audit activities.
  • Strong knowledge of Drug Substance manufacturing processes, validation, qualification, and commercial operations.
  • Proven ability to drive operational excellence, continuous improvement, and cross-functional collaboration in a regulated environment.

Desirable Requirements
  • Experience with Active Pharmaceutical Ingredients (API), freeze drying (lyophilization), manufacturing skids, and oligonucleotide manufacturing.
  • Lean Management, Operational Excellence certification, or comparable qualifications.

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

Data Analytics

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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