Production Associate O1 (2nd shift, SVLM/Serum, M-F, 2-10:30 pm)

Cytiva; Logan (UT); On-site; USD 35,000 - 45,000; Full time

Job summary

A leading company in life sciences is seeking a Production Associate O1 for the 2nd shift. This role involves following GMP guidelines, performing quality control inspections, and collaborating with team leads for process improvements. Ideal candidates will have a high school diploma and effective communication skills. Join a dedicated team making a difference in human health.

Benefits

Healthcare

Paid time off

Qualifications

• Entry-level position requiring a high school diploma.
• Effective communication skills for collaboration.

Responsibilities

• Follow work policies and perform quality control inspections.
• Comply with production processes and documentation controls.

Skills

Effective communication

Education

High School Diploma/GED

Tools

MS Office

Job description

Production Associate O1 (2nd shift, SVLM/Serum, M-F, 2-10:30 pm)

Join us as a Production Associate O1 (2nd shift, SVLM/Serum, M-F, 2-10:30 pm) at Cytiva.

Overview

Are you ready to accelerate your potential and make a difference in life sciences, diagnostics, and biotechnology? Cytiva, part of Danaher, is dedicated to innovation that saves lives. We foster a culture of belonging and continuous improvement, enabling you to contribute to impactful solutions in human health. Join us to work on challenges that matter alongside caring and dedicated colleagues.

Responsibilities

• Follow work policies, procedures, and GMP guidelines; perform quality control inspections and interpret schematics or verbal instructions.
• Complete all required quality and compliance training and report any concerns promptly.
• Understand and operate within production processes, documentation controls, and quality standards to ensure product conformity. Comply with Stop Order, Concessions, ESD, Calibration, Preventative Maintenance, Material Identification & Segregation, and Good Documentation Practices.

Qualifications

• High School Diploma/GED or equivalent.
• Effective communication skills to collaborate with team leads, engineers, supervisors, and managers for process and quality improvements.

Physical and Environmental Requirements

• Frequent movement, climbing stairs/ladders, lifting up to 50 lbs, and occasional heavier lifts with assistance.
• Ability to squat, kneel, reach, and handle small objects; good vision including depth perception and focus.
• Ability to adhere to ISO5 environment protocols and wear PPE, including cleanroom gowning and chemical-resistant clothing.

Preferred Experience

• Manufacturing or production experience.
• Proficiency in MS Office programs.

Additional Information

Cytiva offers comprehensive benefits including healthcare and paid time off. We are committed to diversity, equal opportunity, and providing reasonable accommodations for individuals with disabilities. For accommodations, contact [e-mail].

Employment Details

• Seniority level: Entry level
• Type: Full-time
• Function: Manufacturing and Production
• Industry: Manufacturing

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