Manufacturing Specialist, Quality Assurance(Night Shift)

About the role

This role offers an exciting opportunity to support quality assurance activities in a dynamic manufacturing environment. You will play a key role in ensuring compliance and helping deliver life-changing therapies to patients. This is a fully site-based role.

Responsibilities

• Perform area clearance activities to ensure production readiness and compliance
• Apply and maintain correct product status labeling, including QA hold and rejected materials
• Review production records for accuracy and compliance with quality standards
• Support quality systems implementation and continuous improvement initiatives
• Maintain accurate and compliant documentation
• Monitor product compliance throughout the manufacturing process
• Absorb and communicate potential non-compliance or quality concerns
• Assist with investigations, including root cause analysis and corrective actions

Requirements

• Experience in pharmaceutical, biotechnology, or a related industry
• Ability to work independently and adapt to changing priorities
• Knowledge of quality assurance processes and FDA regulations
• Strong attention to detail and clear written and verbal communication skills
• Experience supporting investigations or deviation management is preferred
• Willingness to work occasional weekends or be on call as needed
• Ability to work on site regularly and use personal protective equipment when required

Qualifications

• High school diploma or equivalent
• Associate's degree or higher in a relevant field
• Minimum of 2 years of experience in a similar role

Skills

• Quality assurance
• Manufacturing
• Compliance
• Investigations
• Documentation

Benefits

• Compensation programs that recognize high performance
• Medical, dental, and vision insurance
• Career growth and development opportunities
• A collaborative environment where your ideas make an impact

Pay

• $20 - $25 per hour

Schedule

• Four 10-hour shifts, Sunday through Wednesday nights (4:00 PM – 3:00 AM, including a one-hour break)

What we are looking for

• Experience in pharmaceutical, biotechnology, or a related industry
• Ability to work independently and adapt to changing priorities
• Knowledge of quality assurance processes and FDA regulations
• Strong attention to detail and clear written and verbal communication skills
• Experience supporting investigations or deviation management is preferred
• Willingness to work occasional weekends or be on call as needed
• Ability to work on site regularly and use personal protective equipment when required

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.