QA Training Specialist

RoslinCT

Hopkinton (MA)

On-site

USD 65,000 - 90,000

Full time

14 days+

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Job summary

RoslinCT is a world-leading cell and gene therapy contract development and manufacturing organization. The QA Training Specialist role supports maintenance and ongoing management of the Training Program within the Quality Management System, on-site in Hopkinton, MA.

You will implement and maintain the Learning Management System, review training content, administer users, and collaborate with cross-functional teams to ensure training compliance and continuous improvement.

Qualifications

  • Bachelor’s degree in related discipline.
  • 3-5 years QA experience in pharma/biotech focusing on Training/Training management or Administration.
  • Experience supporting training plans and curricula.
  • Experience serving as Quality reviewer/approver.
  • Experience driving continuous improvement initiatives.
  • Ability to partner cross-functionally and integrate feedback with quality systems.
  • Ability to work independently to meet objectives and timelines.
  • Experience in 21 CFR Part 210/211 and 21 CFR Part 11; familiar with ICH regulations/guidelines.

Responsibilities

  • Support LMS implementation and maintenance in line with health authority guidelines.
  • Review/approve training content.
  • Administer Learning Management System (user management).
  • Review and approve training plans and curricula.
  • Collaborate with cross-functional teams to ensure training compliance.
  • Assess and determine fit-for-purpose training tools and methodologies.
  • Back-up delivery of new hire training and refresher trainings (GMP, eQMS workflows, data integrity).
  • Monitor training compliance rates and reporting metrics to leadership.
  • Support Quality Culture enhancement efforts.
  • Assist health authority inspections and client audits.
  • Update procedures, processes, provide training, and report QMS metrics.

Skills

Training review
Problem solving
Communication
Organized work
Accuracy mindset
Microsoft Office

Education

Bachelor’s degree

Tools

Microsoft 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 QA Training Specialist is a position responsible for supporting maintenance, enhancements, and on-going management of the Training Program within the Quality Management System.

How You Will Make an Impact
  • Support the implementation and maintenance of Learning Management System in in line with applicable health authority guidelines, regulations, key performance indicators and compliance trends, and operational needs.
  • Support review/approval of training content
  • Support user administration of the Learning Management System
  • Support review and approval of training plans and curricula
  • Collaborate with cross functional teams to ensure training compliance based on approved training curricula and periodically review training curricula with functional teams
  • Assess and determine “fit for purpose” training tools and methodologies based on training needs, including (but not limited to) computer-based training, On-the-Job Training (OJT), and Instructor Led Training (ILT)
  • Serve as a back-up to support delivery of new hire training and periodic refresher training such as GMP training, eQMS workflows training, and data integrity training.
  • Support monitor training compliance rates and reporting compliance metrics to the leadership team, including overdue training assignments for individual functional teams as and when requested.
  • Support Quality Culture enhancement efforts
  • Support health authority inspections and client audits, including corrective actions.
  • Support QMS team efforts to update procedures, processes, provide training, and reporting QMS metrics on periodic basis.
  • Complete other responsibilities, as assigned within the Quality Assurance department.
  • Serve as a user administrator for the Quality Management System
What You Will Bring
  • Experience in Training Course and Training Plan/Curriculum review
  • Effective problem-solving capabilities.
  • Strong oral and written communication skills.
  • 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).
Qualifications
  • Bachelor’s degree in related discipline.
  • 3-5 years relevant Quality Assurance experience in a pharma/biotech company working within a Quality with focus on Training/Training management or Administration
  • Prior experience with supporting training plans and curricula
  • Prior experience serving as Quality reviewer/approver
  • Prior experience driving continuous improvement initiatives
  • Ability to partner cross functionally and integrate feedback with quality systems
  • Ability to work independently to meet objectives and timelines
  • Experience in 21 CFR Part 210/211 and 21 CFR Part 11; familiar with ICH regulations/ guidelines

*This is an on-site position

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.

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