Senior QA Specialist – Plant Operations

RoslinCT; Hopkinton (MA); On-site; USD 110,000 - 140,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

401(k) Plan

Educational assistance

Job summary

RoslinCT is seeking a Senior QA Specialist – Plant Operations to provide QA support for manufacturing operations, review batch records, and ensure GMP documentation aligns with internal procedures. The role focuses on maintaining product quality and regulatory compliance in a fast-paced biotech setting.

The ideal candidate has 5–8 years of QA experience in pharma/biotech with internal manufacturing, and strong communication skills to mentor teams and collaborate across departments.

Qualifications

• 5-8 years of relevant QA experience in pharma/biotech with internal manufacturing.
• Cell therapy experience preferred.
• Strong knowledge of cGMP and ICH guidelines.
• Excellent verbal and written communication skills.

Responsibilities

• Support day-to-day QA operations, including batch record review and QC testing record reviews to ensure compliance with procedures.
• Assist in product disposition and deviation investigations, CAPA and Change Control implementations.
• Develop training materials and deliver training for QA procedures.
• Monitor implementation of QA procedures for compliance and identify opportunities for improvement.
• Provide QA review and approval of plant SOPs and GMP documentation.
• Mentor QA staff and cross-functional teams on GMP compliance and quality culture.

Skills

Quality Assurance

GMP compliance

ICH guidelines

MS Office

Job description

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.

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 Senior QA Specialist – Plant Operations is responsible to provide QA support and expertise to manufacturing plant operations. This includes supporting QA specific procedures related to product disposition, line clearance and review and approval of GMP documentation including but not limited to Batch Records, Quality records, and Calibration/Work Order Records. The ideal candidate has worked in a start up environment with internal manufacturing operations.

How You Will Make an Impact:

What You Will Bring:

Qualifications:

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.

• 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.
• 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 elevate complex decisions as needed.
• Well versed in cGMP and ICH regulations / guidelines
• Strong verbal and written communication skills

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.