Alcon

Site MS&T Head

Alcon$138K — $257K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Master's degree in Science, Pharmacy, Chemical Engineering, Pharmaceutical Technology, or equivalent experience
  • Minimum 6 years of experience in pharmaceutical manufacturing, with a preference for RLT experience
  • Specialist experience in pharmaceutical formulation, process development, or related technical disciplines is preferred
  • Demonstrated experience in driving quality and compliance within an organization
  • Strong working knowledge of quality systems and regulatory requirements across multiple health authorities
  • Understanding of standard pharmaceutical analytical testing

Responsibilities

  • Lead scientific oversight of manufacturing processes for product reliability and compliance
  • Drive product stewardship and technical oversight during the product lifecycle
  • Own and execute the site Validation Master Plan
  • Maintain process knowledge and monitor critical process parameters in manufacturing
  • Lead technology transfers and commercial scale-up activities with global teams
  • Act as the primary technical interface for regulatory authorities
  • Develop and build a high-performing MS&T organization that emphasizes excellence and innovation

Benefits

  • Comprehensive health, life, and disability benefits
  • 401(k) with company contribution and match
  • Generous time-off package including vacation, personal days, and holidays
  • Performance-based cash incentives
  • Eligibility for annual equity awards
Full Job Description

Band

Level 5

Job Description Summary

Location: Millburn, NJ

Relocation Support: This role is based in Millburn, NJ. Novartis is unable to offer relocation support: please only apply if accessible.

Are you ready to shape the future of pharmaceutical manufacturing and scientific innovation? As the Site MS&T Head, you will play a pivotal leadership role in ensuring the technical excellence, robustness, and continuous improvement of manufacturing processes that deliver life-changing medicines to patients. Leading a high-performing Manufacturing Science & Technology (MS&T) team, you will drive product stewardship, validation strategy, technology transfers, process optimization, and compliance excellence while partnering across functions to advance innovation, quality, and operational performance at the site.


#LI-Onsite


Job Description

Key Responsibilities
  • Lead scientific oversight of manufacturing processes to ensure robust, compliant, and reliable product performance.
  • Drive product stewardship and technical oversight throughout the commercial lifecycle of site products.
  • Own the site Validation Master Plan and ensure execution of validation and revalidation activities.
  • Maintain process knowledge, monitor critical process parameters, and sustain validated manufacturing processes.
  • Lead technology transfers, technical changes, and commercial scale-up activities in partnership with global teams.
  • Serve as the primary technical interface for regulatory authorities and cross-site product-related initiatives.
  • Build and develop a high-performing MS&T organization that advances technical excellence, quality, and innovation.

Essential Requirements
  • Master of Science degree in Science, Pharmacy, Chemical Engineering, Pharmaceutical Technology, or equivalent experience.
  • Minimum 6 years experience within pharmaceutical manufacturing; RLT experience preferred.
  • Additional specialist experience in pharmaceutical formulation, process development, manufacturing technology, or related technical disciplines is preferred.
  • Proven experience driving quality and compliance within an organization.
  • Strong working knowledge of applied statistics, quality systems, and regulatory requirements across multiple health authorities.
  • Fundamental understanding of standard pharmaceutical analytical testing.

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.


Salary Range

$138,600.00 - $257,400.00


Skills Desired

Applied Statistics, Leadership, Manufacturing Production, Manufacturing Technologies, Operational Excellence, Process Control, Quality Compliance, Regulatory Compliance, Technical Leadership, Technology Transfer

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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