Alcon

IT/OT Senior Lab Specialist

Alcon$108K — $201K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • B.S. degree in Engineering, Computer Science, IT or related field
  • 8 years of pharmaceutical or biopharmaceutical lab operations experience (or 12 years equivalency)
  • Proficient in oral and written communication
  • Experience in leading teams for lab system installations in GMP environments
  • Proficient in implementing computerized systems within corporate networks
  • Knowledge of FDA regulations, especially 21 CFR part 11 and GMP
  • Familiarity with Quality by Design, six-sigma, and operational excellence tools
  • Experience managing third-party collaborations (in-house and outsourced)

Responsibilities

  • Lead the design, configuration, installation, and maintenance of lab instruments software and hardware
  • Ensure lab instruments have high availability for users by collaborating with vendors
  • Manage work order execution for timely completion of lab maintenance activities
  • Act as a Subject Matter Expert during health authority and internal inspections
  • Track and drive timely completion of corrective and preventive actions (CAPA)
  • Prepare, review, and archive GxP and non-GxP documentation for instruments
  • Facilitate discussions with business partners regarding project priorities and timelines
  • Support operational excellence and compliance, addressing technical issues in lab operations
  • Create and update procedures to improve efficiency and compliance
  • Provide support as a team member for site operations, including on-call responsibilities

Benefits

  • Comprehensive health, life, and disability coverage
  • 401(k) with company contributions and match
  • Generous paid time off including vacation, personal days, and holidays
  • Performance-based cash incentives and eligibility for equity awards
  • Support for employee growth and skill development opportunities
Full Job Description

Band

Level 4

Job Description Summary

Join Novartis and play a critical role in enabling cutting-edge laboratory operations that help bring innovative medicines to patients. As an IT/OT Senior Lab Specialist, you will lead the strategy, implementation, and lifecycle management of computerized laboratory systems across GMP and non-GMP environments, ensuring reliability, compliance, and operational excellence. This is an opportunity to work at the intersection of technology, quality, and science, partnering with cross-functional teams to optimize lab performance, drive continuous improvement, and support a highly regulated manufacturing and development environment where your expertise will directly impact business success and patient outcomes.


 

Job Description

Key Responsibilities:

  • Lead design, configuration, installation, and maintenance of lab instrumentation/equipment software and associated hardware; including interacting with other teams as necessary, e.g., process engineering.
  • Ensure lab instruments/equipment maintain high availability for lab owners. Work closely with vendors to ensure appropriate instrument/equipment architectures and connectivity are designed and implemented.
  • Manage work order execution to ensure on-time completion of all required maintenance related activities on lab equipment (e.g, user reviews, audit trail reviews).
  • Participate as an SME in health authority and internal inspections ensuring full compliance with applicable procedures.
  • Track and drive to on-time completion of corrective and preventive actions (CAPA), including escalation of issues related to closure of CAPA, as appropriate. Lead lab instrument change controls per applicable procedures.
  • Prepare, review, approve, archive GxP and non-GxP instrument/equipment documentation, e.g., User Requirements (URS), Functional Specification (FS) and Detail Design Specifications (DDS/HDS/SDS).
  • Lead discussions with internal business partners on priorities, timelines and transparent sharing of information.
  • Support operational excellence and continuous improvement. Partner with Quality to ensure a quality and compliant lab environment. Problem solve technical related issues impacting lab operations.
  • Create and update procedures to drive operational efficiency and compliance. Implement and revise SOPs to conform with standards and policies. Support investigations of non-conformances related computerized systems.
  • Participate as active IT/OT team member providing support to other functions as necessary. Support 24x7 site-based operations including rotating on-call responsibilities.

Essential Requirement:

  • B.S. degree in Engineering, Computer Science, IT or related technical field.
  • 8 years' work experience in pharmaceutical or biopharmaceutical-based lab operations, or equivalent work experience (12 years) in pharmaceutical or biopharmaceutical-based lab operations.
  • Excellent oral and written communication skills.
  • Experience leading teams installing, configuring and maintaining lab systems in a GMP environment.
  • Experience implementing computerized system in a corporate network environment.
  • Knowledge of FDA regulations particularly 21 CFR part 11 and GMP systems.
  • Knowledge of Quality by Design, six-sigma, and operational excellence tools in creating efficient and high quality processes and end products.
  • Experience working with and leading 3rd parties (both in-sourcing and outsourcing).

Desirable Requirement:

  • Ability to support contingency plans and logically work through complex issues in a pressure filled atmosphere.
  • Provide technical support on computerized system lab instrument issues when driving towards issue resolution. Up to 10% travel may be required.

Novartis Compensation and Benefit Summary:

The salary for this position is expected to range between $108,500 and $201,500.00 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

$108,500.00 - $201,500.00


 

Skills Desired

Business Continuity, Cost Management, Decision Making, Operational Excellence, Problem Solving, Project Management, Quality Compliance, Risk Management, Stakeholder Management, Vendor Management

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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