Senior Validation Engineer

Alcon MX; Fort Worth (TX); Hybrid; USD 85,000 - 130,000; Full time

Benefits offered by this job

Health insurance

Retirement plan

Flexible time off

Paid time off

Job summary

Alcon is seeking a Sr. Associate, Validation to support validation and qualification activities for processes, equipment, systems, and facilities. You will prepare, review, and rectify validation protocols, provide technical support, and help manage department expenses.

The role emphasizes executing validation studies, risk assessment, and collaboration with cross-functional teams to drive compliant, efficient outcomes. Strong technical knowledge and English fluency are required.

Qualifications

• Bachelor’s Degree or equivalent years of directly related experience.
• English fluency in reading, writing and speaking.
• Minimum 2 years of relevant experience.

Responsibilities

• Plan, execute, and document validation studies for equipment, systems and processes.
• Support validation activities in aseptic process management.
• Review and approve change control documentation.
• Provide audit support and collaborate with cross-functional teams.

Skills

Validation studies

Risk assessment

Regulatory compliance

Statistical analysis

Cross-functional collaboration

Education

Bachelor’s Degree or Equivalent

Tools

Minitab

Temperature mapping

Thermocouple data loggers

Job description

At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before. Together, we make a difference in the lives of our patients and customers. Are you ready to join us?

This role is part of Alcon's Engineering function, a team focused on improving quality, processes, products, packaging and materials across our business to help deliver brilliant outcomes. The Sr. Associate, Validation (Science/Tech/Engineering Path) is primarily responsible for supporting and completing validation and qualification activities for processes, equipment, systems, and facilities. You will prepare, review, and rectify validation protocols, provide technical support, and help manage department expenses.

Specifics Include:

• Handle technical tasks, supporting operations and contributing to efficiency within defined procedures.
• Plan, execute, and document validation studies to ensure equipment, systems, and processes operate effectively and comply with regulations.
• Conduct risk assessments, design protocols, analyze data, and prepare validation and qualification reports.
• Support validation activities in aseptic process management.
• Review and approve change control documentation.
• Provide audit support and collaborate with cross-functional teams to drive problem-solving and innovation through scientific principles.
• Make decisions within the scope of assigned tasks, requiring advanced technical knowledge and analytical skills.
• Perform assigned validation activities on time.
• Handle deviations associated with these activities, if required.
• Author complex validation protocols and technical reports (e.g. launches, transfers, weak point remediation).
• Perform process qualification for new equipment and new technologies.
• Participate in transfers and launches by providing data obtained during related validation activities which are needed for the registration documentation.
• Perform or oversee risk assessments for Validation.
• Participate in improvement and remediation of products.
• Update documents on an as needed basis.
• Provide Validation oversight review and approval of change control documentation.
• Adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation.
• Ensure rigorous quality control, complete all required training, and meet individual job requirements to contribute to overall organizational compliance.
• Commit to continuous improvement and compliance with regulatory requirements.

WHAT YOU'LL BRING TO ALCON:

• Bachelor’s Degree or Equivalent years of directly related experience (or high school +10 yrs; Assoc.+6 yrs; M.S.+0 yrs)
• The ability to fluently read, write, understand and communicate in English
• 2 Years of Relevant Experience
• Work hours: Exempt
• Travel Requirements: None
• Relocation assistance: No
• Sponsorship available: No

PREFERRED QUALIFICATIONS/SKILLS/EXPERIENCE:

• Experience working in a regulated pharmaceutical, biologics, medical device, or aseptic manufacturing environment.
• Experience with change control, deviation investigations, CAPA, and quality management systems.
• Proficiency in data analysis, statistical methods, and trending of validation data.
• Experience using statistical analysis software such as Minitab.
• Experience with temperature mapping, thermocouple data loggers, and thermal validation studies.
• Experience with sterilization validation, including E-Beam, EO, steam, or other sterilization technologies.
• Demonstrated project management, organizational, and cross-functional collaboration skills.
• Ability to independently manage multiple validation projects and meet established timelines.

HOW YOU CAN THRIVE AT ALCON:

Join Alcon’s mission to provide outstanding, innovative products and solutions to improve sight, improve lives, and grow your career! Collaborate with teammates to share standard processes and findings as work evolves! See your career like never before with focused growth and development opportunities! Alcon provides a robust benefits package including health, life, retirement, flexible time off for exempt associates, PTO for hourly associates, and much more! This position may be offered at the Associate I or Associate II Engineering level, depending on the candidate’s qualifications and experience. Alcon Careers

ALCON IS AN EQUAL OPPORTUNITY EMPLOYER AND PARTICIPATES IN E-VERIFY. Alcon takes pride in maintaining an inclusive environment that values different perspectives and our policies are non-discriminatory in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to [e-mail] and let us know the nature of your request and your contact information.

At Alcon, we are committed to helping people see better. We believe patients should have access to quality eye care regardless of their economic circumstances; however, barriers to good eye health exist for patients in both developed and emerging markets. Alcon develops and manufactures innovative devices to serve the full life cycle of eye care needs. Its surgical group is one of the largest makers of equipment used for cataract removal and laser vision correction. Its consumer products include the well-known Opti-Free line of contact lens solutions and related products. Alcon, which was founded in 1945, sells its products in 180 countries worldwide.

At Alcon, we are committed to helping people see better. We believe patients should have access to quality eye care regardless of their economic circumstances; however, barriers to good eye health exist for patients in both developed and emerging markets. Alcon develops and manufactures innovative devices to serve the full life cycle of eye care needs. Its surgical group is one of the largest makers of equipment used for cataract removal and laser vision correction. Its consumer products include the well-known Opti-Free line of contact lens solutions and related products. Alcon, which was founded in 1945, sells its products in 180 countries worldwide.