Specialist, Quality Assurance (Master Batch Record)

The Quality Assurance Department is looking for Specialist, QA to join the team. You will be supporting day-to-day Quality Assurance activities in accordance with approved SOPs / Policies for a multi-product, cGxP contract manufacturing facility. Display a good level of problem-solving ability by analyzing and interpreting data and puts forward new ideas based on scientific knowledge or field experience. Detect non-compliance with cGxP and cGDP requirements and provide guidance on GDP corrections.

What you will get:

• An agile career with opportunities to grow your validation and engineering expertise.

• An inclusive, ethical, and safety-first workplace.

• A dynamic site environment supporting advanced biotech manufacturing.

• Collaboration with experienced engineering, quality, and operations teams.

• Compensation programs that recognize performance and contribution.

• Fully paid medical insurance, with options to enroll family members at subsidized rates.

Responsibilities:

• Provide oversight to day-to-day Quality Assurance activities in accordance with approved
• SOPs / Plan / Policies for a large scale, multi-product, GMP biotech contract manufacturing facility.
• Mastery and knowledge of processes is recognized by colleagues as a source of expertise.
• Strategic in Quality Systems or Quality Operations planning.
• Work within the Lonza Global network and establish themself as an industry expert within both Lonza and outside.
• Able to direct appropriate follow-up actions on any compliance issues.
• Participates in policy making.
• Ability to communicate quality operations and compliance perspective effectively to senior management.
• Own and lead special projects, often complex in nature.
• Understands and articulates company business strategy. Maintains a broad view of the business recognizes changes and trends in the appropriate area in which the individual operates.
• Look to assign projects to staff for cost-savings.
• Provide direction to staff and/or lead projects in global harmonization/ efficiency.

Education Experience

• Engineering/Science Diploma/Degree or higher from recognized institution
• 1-4 years working experience within the pharmaceutical manufacturing industry
• Excellent knowledge and adherence to all relevant codes, standards and regulatory requirements

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.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.