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 of experience in pharmaceutical or biopharmaceutical GMP manufacturing
  • Strong understanding of FDA regulations and GMP systems
  • Experience with both automated and manual visual inspection systems
  • Proven leadership in cross-functional teams
  • Strong project management skills and strategic planning experience
  • Excellent communication skills with an emphasis on technical writing

Responsibilities

  • Support design and lifecycle management for manufacturing equipment
  • Validate and maintain manufacturing facilities and utilities
  • Ensure reliable and compliant GMP operations
  • Lead engineering activities in a regulated environment
  • Analyze complex engineering issues to implement solutions
  • Collaborate with cross-functional teams in fast-paced settings
  • Manage projects strategically and long-term

Benefits

  • Comprehensive health, life, and disability benefits
  • 401(k) plan with company contribution and matching
  • Generous time off policy including vacation and personal days
  • Performance-based cash incentives and equity awards eligibility
  • Work environment fostering growth in the pharmaceutical industry
Full Job Description

Band

Level 3

Job Description Summary

Step into a pivotal engineering role where your expertise directly shapes advanced manufacturing operations. As a Process Engineer III, you will support the design, validation, maintenance, and lifecycle management of manufacturing equipment, facilities, and utilities. This role requires hands-on experience with automated and manual visual inspection systems and drug product/fill-finish equipment to ensure compliant, reliable, and efficient GMP operations.


 

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:

  • 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
  • Experience with automated and manual visual inspection equipment, as well as general drug product / fill-finish production equipment
  • 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

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

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