Alcon

Process Engineer III

Alcon$98K — $183K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s degree in Chemical, Electrical, or Mechanical Engineering or related technical field
  • Minimum 5 years pharmaceutical or biopharmaceutical GMP manufacturing experience
  • Strong knowledge of FDA regulations and GMP systems
  • Demonstrated experience in a regulated pharmaceutical or biotechnology environment
  • Proven ability to lead cross-functional teams in dynamic settings
  • Strong project management skills
  • Excellent written and verbal communication skills

Responsibilities

  • Ensure new equipment is designed, qualified, and maintained throughout its lifecycle
  • Manage equipment changes to maintain a validated and compliant state
  • Investigate equipment and process deviations; implement corrective actions
  • Serve as subject matter expert during audits and regulatory observations
  • Develop compliant equipment reliability and maintenance strategies
  • Lead/support capital projects with technical guidance
  • Collaborate with operations for new product introductions

Benefits

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

Band

Level 3

Job Description Summary

Step into a pivotal engineering role where your expertise directly shapes the future of advanced manufacturing. As a Process Engineer III, you will provide engineering, validation, and maintenance support for process manufacturing equipment, facilities, and utilities at the site. In this hands-on position, you will ensure systems operate in a compliant, reliable, and efficient manner throughout their lifecycle—helping to drive operational excellence and deliver high-quality therapies to patients.


 

Job Description

Location:

  • This position will be located in Durham, NC and will be an onsite role.
  • Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

Key Responsibilities:

  • Ensure new equipment is appropriately designed, qualified, and maintained across the equipment lifecycle
  • Own and manage equipment changes to maintain a validated and compliant state
  • Investigate equipment and process deviations; implement corrective actions to prevent recurrence
  • Serve as subject matter expert during audits and respond to regulatory observations
  • Develop and implement compliant and effective equipment reliability and maintenance strategies
  • Lead or support capital projects, providing subject matter expertise and technical guidance
  • Collaborate with operations to support new product introductions and facility fit evaluations
  • Establish equipment specifications including user requirements, functional, and design specifications
  • Evaluate and implement new technologies and equipment platforms for manufacturing operations
  • Mentor process engineers and lead small teams to optimize engineering systems and processes

Essential Requirements:

  • Bachelor’s degree in Chemical, Electrical, or Mechanical Engineering or related technical field
  • Minimum 5 years pharmaceutical or biopharmaceutical GMP manufacturing experience, or equivalent experience
  • Strong knowledge of FDA regulations and GMP systems
  • Demonstrated experience supporting engineering activities in a regulated pharmaceutical or biotechnology environment
  • Proven ability to lead cross-functional teams in a fast-paced and dynamic setting
  • Strong project management skills with experience in both strategic and long-term planning
  • Excellent written and verbal communication skills with strong technical writing capabilities
  • Ability to analyze complex issues and implement effective, compliant engineering solutions

Novartis Compensation and Benefit Summary:

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

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

$98,700.00 - $183,300.00


 

Skills Desired

Business Continuity, Change Control, Cost Management, Data Analytics and Digital, Engineering Technical Expertise, GDP Knowledge, gmp knowledge, HSE Knowledge, Knowledge Of Relevant Tools And Systems  , Manufacturing Process (Production), Operational Excellence, Quality Compliance, Resilience and Risk Management, Total Productive Maintenance

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

Similar Jobs

More Jobs at Alcon

More Pharmaceuticals & Biotech Jobs

Find similar Process Engineer III jobs: