Quality Assurance Lead, Plant Operations
Lead QA plant operations at RoslinCT, guiding GMP oversight, batch review, and team performance to help deliver life-changing cell and gene therapies.
WHO WE ARE
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.
THE ROSLINCT WAY
Here at RoslinCT, our team can contribute 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. At RoslinCT we focus on developing our corporate culture, people’s development, growth, and the ability to impact patients.
ACCELERATING YOUR FUTURE
The, Quality Assurance Lead, Plant Operations, is responsible for leading QA plant operations and expertise in manufacturing plant operations. This includes batch review, product disposition, review and approval of GMP documentation including but not limited to QC test methods and Work Order Records. The candidate will lead product receipt, shipment and disposition, line clearance and quality system review/ approval in the QA role. This is a full-time, on-site role at our Hopkinton, MA location. Weekends and holidays may be required.
How You Will Make an Impact:
Supervise and lead Quality Assurance team, including coaching and mentoring.
·Coordinate day-to-day operations for the Quality Assurance team. This includes but is not limited to oversight of batch record review, QC data review, deviations, CAPA, Change Control, and training.
Provide QA support to manufacturing operations and ensure compliance with cGMP requirements.
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
Other duties as assigned.
What You Will Bring:
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.
Qualifications:
7+ years of relevant Quality Assurance experience in a pharma/biotech company with internal manufacturing. Cell therapy experience preferred.
Previous leadership or supervisory experience
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 be quality lead within agreed timelines to support plant start up activities
Ability to resolve issues and make decisions independently and escalate complex decisions as needed.
Partner cross functionally and provide quality support within agreed timelines to support plant start up activities.
Well versed in cGMP and ICH regulations / guidelines
Strong verbal and written communication skills
Final compensation will be based on a variety of factors, including education, experience, technical expertise, specialized skill sets, market demand, internal equity, and business needs.
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, a 401(k) program, and a variety of additional resources to help you thrive both personally and professionally.
OUR COMMITMENT
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.
- Department
- Quality Assurance
- Location
- Hopkinton
- Yearly salary
- $85,000 - $125,000
- Employment type
- Full-time
About RoslinCT US
RoslinCT is a global CDMO focused on Advanced Cell and Gene Therapies. It was established in 2006, built upon the ground-breaking cloning technology of Dolly the Sheep. RoslinCT is one of the first to produce clinical-grade human pluripotent stem cells and developed the first CRISPR-edited cell therapy product for a major inherited disorder, taking it from early development to commercialization.