Associate I, Quality Control Labs (2nd Shift)

Alcon; Fort Worth (TX); On-site; USD 42,000 - 52,000; Full time

Job summary

Alcon, a global leader in eye care, is seeking an Associate I for the Quality Control Labs to support testing, inspection, and analysis of products and raw materials. You will report results and collaborate with cross-functional teams to ensure lab data integrates into manufacturing.

In this para-professional role, you will follow SOPs, adhere to GxP regulations, and complete required training. The shift is second, 40 hours per week, with minimal travel and relocation assistance unavailable.

Qualifications

• Fluently read, write, understand and communicate in English.
• 3 years of relevant experience.
• Work hours: Second Shift - 40 hours per week - 1:30 PM to 10:00 PM.
• Travel: Minimal
• Relocation/Sponsorship Assistance: None

Responsibilities

• Perform business support or clerical tasks in the Quality Control Labs according to procedures, contributing to efficient business operations through accurate task completion.
• Follow established procedures with limited decision-making authority, requiring job-related training, attention to detail, and reliability.
• Conduct inspection, testing, and analysis of products and raw materials to ensure they meet required specifications and standards, utilizing various analytical techniques and lab equipment.
• Report test results accurately and collaborate with cross-functional teams, including production, engineering, and quality assurance, to ensure the seamless integration of lab results into the manufacturing process.
• Adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, ensuring rigorous quality control, and completing all required training.
• Commit to continuous improvement and compliance with regulatory requirements, meeting individual job requirements and contributing to the overall compliance of the organization.

Skills

English fluency

Education

High school diploma or equivalent

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 Quality & Regulatory Affairs function, a team that ensures our products are in compliance with global, local, and internal regulations and meet the strictest standards of quality as we help people see brilliantly. The Associate I, Quality Control Labs (Para-Professional & Support Path), is primarily responsible for performing business support tasks in the Quality Control Labs, including inspection, testing, and analysis of products and raw materials. You will report test results accurately and work with cross-functional teams to ensure seamless integration of lab results.

Specifics Include:

• Perform business support or clerical tasks in the Quality Control Labs according to procedures, contributing to efficient business operations through accurate task completion
• Follow established procedures with limited decision-making authority, requiring job-related training, attention to detail, and reliability
• Conduct inspection, testing, and analysis of products and raw materials to ensure they meet required specifications and standards, utilizing various analytical techniques and lab equipment
• Report test results accurately and collaborate with cross-functional teams, including production, engineering, and quality assurance, to ensure the seamless integration of lab results into the manufacturing process
• Adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, ensuring rigorous quality control, and completing all required training
• Commit to continuous improvement and compliance with regulatory requirements, meeting individual job requirements and contributing to the overall compliance of the organization. All associates must adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, ensuring rigorous quality control, and completing all required training. Associates are responsible for meeting their individual job requirements and contributing to the overall compliance of the organization. Compliance with regulatory requirements and a commitment to continuous improvement are essential to our operations.

WHAT YOU'LL BRING TO ALCON:

• High School Diploma or equivalent
• The ability to fluently read, write, understand and communicate in English
• 3 Years of Relevant Experience
• Work hours: Second Shift - 40 hours a week - 1:30 PM - 10:00 PM
• Travel: Minimal
• Relocation/Sponsorship Assistance: None

HOW YOU CAN THRIVE:

• Work together with colleagues to share standard methodologies and discoveries as work progresses.
• Discover your career in a fresh way through specific growth and development possibilities.
• Join Alcon's mission to provide outstanding, innovative products and solutions to improve sight, improve lives, and grow your career!
• Alcon provides a robust benefits package including health, life, retirement, flexible time off for exempt associates, PTO for hourly associates, and much more!

ALCON CAREERS

See your impact at alcon.com/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.