Senior QA Specialist – Plant Operations

About Us

RoslinCT is a world-leading cell and gene therapy contract development and manufacturing organization creating cutting-edge therapies that change people’s lives. Collaborative, dedicated, and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilizing ground-breaking science.

Here at RoslinCT, our team contributes to the development of revolutionary treatments. We live every day by our core values: Partner Focus, One Team, Personal Growth, Integrity, Innovation, and Trust and Respect. We put our employees at the forefront by providing a flexible and empowering work environment, an attractive benefits package, and an emphasis on work-life balance. Our people are the key to our success, and we focus on developing our corporate culture, people’s development, growth, and the ability to impact patients.

Responsibilities

• Support day-to-day operations, including batch record review and review of QC testing records to ensure compliance with approved procedures.
• Support product disposition.
• Assist in deviation investigations, CAPA, and Change Control implementations.
• Develop training materials and deliver training for QA-specific procedures.
• Monitor implementation of QA-specific procedures for compliance and identify opportunities for improvement.
• Work cross-functionally and provide QA support for development, review, and approval of procedures/workflows for manufacturing operations.
• Provide QA review and approval of plant-related SOPs and GMP documentation.
• Mentor personnel within QA and cross-functionally on GMP compliance, promote quality culture.
• Other duties as assigned.

Requirements

• A highly organized work style that ensures timely execution of tasks.
• A mindset that ensures accurate results.
• Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).
• Effective problem-solving capabilities.
• Strong oral and written communication skills.
• 5-8 years of relevant Quality Assurance experience in a pharma/biotech company with internal manufacturing. Cell therapy experience preferred.
• Prior experience in Quality Assurance Operations focused on support of internal manufacturing operations.
• Prior experience working in contract services and interfacing with clients preferred.
• Ability to partner cross-functionally and provide quality support within agreed timelines to support plant start-up activities.
• Ability to work independently to meet objectives and timelines.
• Ability to resolve issues and make decisions of moderate complexity independently and escalate complex decisions as needed.
• Well-versed in cGMP and ICH regulations/guidelines.

Benefits

At RoslinCT, we offer more than just competitive pay. Our comprehensive Total Rewards package is designed to support your health, financial well-being, and professional development throughout your career. Benefits include:

• Medical, dental, and vision insurance.
• Educational assistance.
• 401(k) program.
• A variety of additional resources to help you thrive both personally and professionally.

Commitment to Diversity

All RoslinCT employees embrace the principles of our culture and values and are deeply committed to fostering an environment where diversity and inclusion are not only valued but prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. RoslinCT is proud to be an equal opportunity employer; we seek to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or any other applicable legally protected characteristics.