Alcon

Technical Transfer Lead

Alcon$126K — $234K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's in Pharmacy, Pharmaceutical Technology, Chemistry, or equivalently scientific degree
  • 5+ years' experience in oral solid dosage pharmaceutical manufacturing
  • Experience in technical transfer, process scale-up, and validation activities
  • Strong knowledge of Good Manufacturing Practices (cGMP) and regulatory requirements
  • Proven project management skills and experience leading cross-functional teams
  • Strong technical expertise in pharmaceutical processes and problem-solving

Responsibilities

  • Lead comprehensive technical transfer projects on timelines, scope, and quality
  • Serve as main contact for technical transfer activities, unifying diverse stakeholders
  • Develop and implement transfer and validation strategies for processes
  • Manage technical, regulatory, and validation batches ensuring documentation compliance
  • Establish and guide cross-functional project teams to drive execution and risk management
  • Ensure cGMP compliance and prepare for inspections and audits
  • Pursue process improvements for successful product launches and manufacturing excellence

Benefits

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

Band

Level 4

Job Description Summary

Location: Morrisville, NC

Step into a pivotal role where your expertise drives the successful launch of life-changing medicines. As a Technical Transfer Lead, you will own and lead complex technology transfer initiatives, shaping how innovative therapies move from development to commercial manufacturing. Working at the heart of a highly collaborative environment, you will partner with cross-functional teams to deliver robust, compliant, and efficient processes—ensuring patients receive high-quality treatments, on time and at scale.


 

Job Description

Key Responsibilities

  • Lead end-to-end technical transfer projects, ensuring timelines, scope, and quality objectives are achieved
  • Act as site point of contact for transfer activities, aligning stakeholders across Technical Development, Supply Chain, Manufacturing, Quality, HSE, and other sites
  • Develop and execute transfer and validation strategies, including process, cleaning, packaging and supportive studies. 
  • Coordinate technical, regulatory, and validation batches, ensuring documentation readiness and compliance
  • Establish and lead cross-functional project teams, driving execution, risk mitigation, and decision-making
  • Ensure compliance with cGMP and readiness for inspections and pre-approval audits
  • Drive process improvements and optimization to support successful product launches and ongoing manufacturing excellence

Essential Requirements

  • Bachelor of Science in Pharmacy, Pharmaceutical Technology, Chemistry, or equivalent scientific degree
  • Minimum 5 years of experience in oral solid dosage pharmaceutical manufacturing
  • Demonstrated experience in technical transfer, process scale-up, and validation activities
  • Strong knowledge of current Good Manufacturing Practices and regulatory requirements
  • Proven project management skills with ability to lead cross-functional teams
  • Strong technical expertise in pharmaceutical processes, with ability to solve complex manufacturing challenges

Desirable Requirements

  • Master of Science or equivalent experience

The salary for this position is expected to range between $126,000 - $234,000 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

$126,000.00 - $234,000.00


 

Skills Desired

Applied Statistics, Change Controls, Data Analytics and Digital (Inactive), GDP Knowledge (Inactive), Good Manufacturing Practices (GMP), HSE Knowledge (Inactive), Manufacturing Processes, Manufacturing Production, Manufacturing Technologies, Operational Excellence, Process and Cleaning Validation (Inactive), Process Control, Quality Compliance, Regulatory Compliance, Resilience and Risk Management (Inactive), 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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