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(Fixed Term) Specialist, Validation (CQV) at Moderna - ApplyBlast

(Fixed Term) Specialist, Validation (CQV)

Moderna

4 months ago

3.2 on Glassdoor

Canada

Onsite

Full Time

Senior

0 applicants

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About this role

This role involves executing Commissioning, Qualification, and Validation (CQV) activities for GMP systems and equipment within Moderna's mRNA manufacturing facility. As an individual contributor, you will collaborate cross-functionally to ensure operational readiness, compliance with regulatory requirements, and the maintenance of a validated state across facilities and processes.

Responsibilities

Execute commissioning, qualification, and validation activities for GMP systems
Support validation of facilities, utilities, and equipment across the manufacturing site
Manage requalification and periodic reviews to maintain compliant validated state
Lead deviation investigations including root cause analysis and CAPA implementation
Author and review validation protocols, reports, and risk assessments

Skills

Qualifications

B.S. in Chemical EngineeringB.S. in Mechanical Engineering

About Moderna

modernatx.com

Headquarters

Cambridge, Massachusetts, United States

Company Size

1001-5000 employees

Founded

2010

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Moderna is a biotechnology company that is pioneering the use of mRNA technology to develop transformative medicines and vaccines. It gained global prominence for its COVID-19 vaccine, which showcased the potential of mRNA in rapidly addressing public health emergencies. The company is focused on creating innovative therapies to treat a range of diseases, advancing its product pipeline, and exploring new career opportunities in the biotech field. With a commitment to changing the landscape of medicine, Moderna is at the forefront of scientific research and development.