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RoslinCT US

Manager Environmental Monitoring QC Microbiology

Career Insights for Quality Control Manager

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What they do

A Quality Control Manager focuses on detection of mistakes and defects in manufacturing products. Develops procedures and tests to identify any irregularities and error in the output. Manages and oversees all steps related to quality control as part of the quality management strategy of a company. May involve leadership of a team of quality control technicians and other associated staff members.

$115,443 / year median in Massachusetts

+3% projected growth

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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.
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 Environmental Monitoring QC Manager oversees cleanroom and controlled environment testing in a cell and gene therapy CDMO. The Manager is responsible for leadership and oversight of the environmental monitoring team. They will manage monitoring staff, track microbial data trends, handle investigations and CAPAs (Corrective and Preventive Actions), and ensure compliance with cGMP and FDA standards. Responsible for writing/revising standard operating procedures (SOPs) and supporting equipment qualification and test method validation in compliance with all applicable quality systems and current cGMPs. How You Will Make an
Impact:
Manage routine viable/total particulate, air, surface, and gas testing in cleanrooms. Supervise, train, and mentor EM analysts and contractors. Review data tracking, trending reports, and environmental excursions in a timely manner. Lead investigations for environmental excursions, results, deviations, and write CAPAs. Host and support internal and external regulatory inspections (FDA, cGMP). Ensure data is accurate and up to date. This includes timely review of documents and cross functional coordination to meet timelines. Investigation and troubleshooting of equipment and associated test methods. Interact with various support departments to assist with scheduling of services performed in QC Microbiology. Identification and implementation of process improvements. Development of processes that will support staff and department evaluation and growth Ensure that work is completed in accordance with requirements including but not limited to CFR's, cGMPs, SOPs, and company policies. Support implementation of information technologies that support documentation and data management systems.
What You Will Bring:
Excellent/Effective written and verbal communications skills. Prepare technical data and present to senior leadership. Escalate issues professionally and on a timely basis. Ability to adhere to timelines for testing and reporting of data Ability to function in a team-oriented environment A highly organized work style that ensures timely execution of tasks. A mindset that ensures accurate results. Effective problem-solving capabilities.
Qualifications:
Bachelor's degree in Biology (Microbiology) 5 to 10+ years of cGMP pharmaceutical experience, 2 to 5 years of leadership experience, and expertise in cleanroom aseptic processing and global regulatory standards (FDA, EU Annex 1). Experience in a cGMP QC laboratory environment performing environmental monitoring, contamination control and investigation writing. 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.