Senior Validation Engineer, GxP & Sterility

Socket.dev; Fort Worth (TX); On-site; USD 80,000 - 110,000; Full time

Benefits offered by this job

Health benefits

Life insurance

Retirement plan

Flexible time off for exempt

Job summary

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

Key duties include planning and documenting validation studies, supporting aseptic validation, and ensuring compliance with regulatory requirements while collaborating with cross-functional teams to drive quality and innovation.

Qualifications

• Bachelor’s Degree or equivalent years of directly related experience.
• Ability to fluently read, write, understand and communicate in English.
• 2 years of relevant experience.
• Work hours: Exempt.
• Travel: None; Relocation: No; Sponsorship: No.

Responsibilities

• Plan, execute, and document validation studies to ensure equipment, systems, and processes operate effectively and comply with regulations.
• Prepare, review and rectify validation protocols; provide technical support and manage department expenses.
• Review and approve change control documentation; provide audit support.
• Collaborate with cross-functional teams to drive problem-solving and innovation through scientific principles.
• Perform or oversee risk assessments for validation and participate in transfers and launches.
• Ensure adherence to GxP and SOPs with thorough documentation.

Skills

Cross-functional collaboration

Project management

Data analysis

Statistical methods

Education

Bachelor’s Degree or equivalent

Tools

Minitab

Job description

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

Key duties include planning and documenting validation studies, supporting aseptic validation, and ensuring compliance with regulatory requirements while collaborating with cross-functional teams to drive quality and innovation.