Lykan Bioscience - Now RoslinCT
Sr. QA Specialist - Plant Ops
Lykan Bioscience - Now RoslinCT, Hopkinton, Massachusetts, us, 01748
Overview
Join to apply for the
Sr. QA Specialist - Plant Ops
role at
Lykan Bioscience - Now RoslinCT . RoslinCT is a world-leading cell and gene therapy contract development and manufacturing organization creating cutting-edge therapies that change peoples 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 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, peoples development, growth, and the ability to impact patients. ACCELERATING YOUR FUTURE The Senior QA Specialist Plant Operations is responsible for providing QA support and expertise in manufacturing plant operations, including developing QA procedures related to product disposition, line clearance, and review and approval of GMP documentation (Batch Records, Validation Protocols/Reports, Calibration/Work Order Records). The ideal candidate has startup experience with internal manufacturing operations. Specialists will also assist with 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. Responsibilities
Develop and implement QA specific procedures required for review and approval of GMP documentation, line clearance, and product disposition 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 Support product disposition and shipping Support internal audits and GMP readiness Support Health Authority Inspections and Client Audits Mentor personnel within QA and cross functionally on GMP compliance, promote quality culture Other duties as assigned. What You Will Bring
Add as required 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
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 Strong verbal and written communication skills 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. Seniority level
Mid-Senior level Employment type
Full-time Job function
Quality Assurance
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Join to apply for the
Sr. QA Specialist - Plant Ops
role at
Lykan Bioscience - Now RoslinCT . RoslinCT is a world-leading cell and gene therapy contract development and manufacturing organization creating cutting-edge therapies that change peoples 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 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, peoples development, growth, and the ability to impact patients. ACCELERATING YOUR FUTURE The Senior QA Specialist Plant Operations is responsible for providing QA support and expertise in manufacturing plant operations, including developing QA procedures related to product disposition, line clearance, and review and approval of GMP documentation (Batch Records, Validation Protocols/Reports, Calibration/Work Order Records). The ideal candidate has startup experience with internal manufacturing operations. Specialists will also assist with 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. Responsibilities
Develop and implement QA specific procedures required for review and approval of GMP documentation, line clearance, and product disposition 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 Support product disposition and shipping Support internal audits and GMP readiness Support Health Authority Inspections and Client Audits Mentor personnel within QA and cross functionally on GMP compliance, promote quality culture Other duties as assigned. What You Will Bring
Add as required 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
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 Strong verbal and written communication skills 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. Seniority level
Mid-Senior level Employment type
Full-time Job function
Quality Assurance
#J-18808-Ljbffr