Alcon

Sr Manufacturing Technical MES Specialist

Alcon$103K — $192K *
Manufacturing & Automotive
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree or higher, or equivalent relevant work experience.
  • 2 to 5 years of Manufacturing Execution System experience, including Master Batch Record design.
  • 5 years of experience in a regulated current Good Manufacturing Practice environment, preferred.
  • Expertise in technical Manufacturing Execution System Master Batch Record design, testing, implementation, and maintenance.
  • Knowledge of Manufacturing Execution System interfaces and integrations.

Responsibilities

  • Own end-to-end Manufacturing Execution System processes for commercial and clinical programs.
  • Design, configure, and implement electronic Master Batch Records and workflows.
  • Provide production support for Manufacturing Execution Systems and resolve operational issues.
  • Collaborate with cross-functional teams to optimize manufacturing processes.
  • Manage updates, change controls, and documentation to ensure compliance.
  • Support system integrations and master data management across platforms.
  • Coach and train key users on batch record design and best practices.

Benefits

  • Health, life, and disability benefits.
  • 401(k) plan with company contribution and match.
  • Generous time-off package including vacations and holidays.
  • Performance-based cash incentives and eligibility for annual equity awards.
Full Job Description
Job Description Summary
Location: Morris Plains, New Jersey

Imagine helping bring life-changing cell and gene therapies to patients by transforming how manufacturing operations are executed and documented. As a Sr Manufacturing Technical MES Specialist at Novartis, you will play a critical role in advancing digital manufacturing capabilities through the design, implementation, and optimization of Manufacturing Execution Systems. Working closely with manufacturing, quality, supply chain, and technical teams, you will drive paperless manufacturing solutions, enhance operational efficiency, and ensure the compliant execution of complex production processes. This is an opportunity to shape the future of advanced therapy manufacturing while making a meaningful impact on patients worldwide.

Job Description

Key Responsibilities
  • Own end-to-end Manufacturing Execution System processes supporting commercial, clinical, and future manufacturing programs.
  • Design, configure, test, implement, and continuously improve electronic Master Batch Records and manufacturing workflows.
  • Provide Manufacturing Execution System production support and resolve system issues to ensure uninterrupted operations.
  • Collaborate with manufacturing, supply chain, quality, technical development, and validation teams to optimize processes.
  • Manage Manufacturing Execution System updates, change controls, corrective actions, and documentation revisions to maintain compliance.
  • Support system integrations and master data management across enterprise platforms, including laboratory and enterprise resource planning systems.
  • Coach and train key users and subject matter experts on batch record design, execution, and best practices.


Essential Requirements
  • Bachelor's degree or higher, or equivalent relevant work experience.
  • Minimum 2 to 5 years of Manufacturing Execution System experience, including Master Batch Record design and creation.
  • 5 years of experience in a regulated current Good Manufacturing Practice environment, preferred.
  • Demonstrated expertise in technical Manufacturing Execution System Master Batch Record design, testing, implementation, and maintenance.
  • Knowledge of Manufacturing Execution System interfaces and integrations, including enterprise resource planning and laboratory information management systems.
  • Strong business requirements gathering, project management, communication, and documentation skills with exceptional attention to detail.


The salary for this position is expected to range between $98,700 and $183,300 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.

Salary Range
$103,600.00 - $192,400.00

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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