mRNA QC Lab Coordinator

Work Schedule

Environmental Conditions

Job Description

As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.

DESCRIPTION:

Joining the mRNA QC Lab you will be included in a dynamic environment and you will gain and in-depth experience of a GMP Quality control lab passionate about new projects and technology transfers.

In this role you will be responsible for overseeing the day-to-day operations of the Quality Control laboratory ensuring compliance with cGMP requirements and company quality standards. You will coordinate laboratory activities and ensure the timely review and approval of laboratory documentation.

A key aspect of the role will be the management of QC quality systems including the handling of laboratory events as analytical not conformities laboratory deviations OOS investigations CAPAs change controls and laboratory documentation. You will be responsible for maintaining and updating SOPs analytical methods protocols reports and other GMP-controlled documents ensuring data integrity and regulatory compliance.

You will support the qualification calibration and maintenance of laboratory instruments oversee laboratory procedures and ensure adherence to established quality and safety addition you will lead and mentor QC laboratory personnel fostering a culture of quality continuous improvement and operational excellence.

The role requires close collaboration with cross-functional teams to support inspections audits process improvements and overall laboratory compliance.

REQUIREMENTS:
Minimum 4 years of experience in quality control within a regulated environment (pharmaceutical/medical device preferred)
Preferred Fields of Study: Chemistry Biology or related scientific field
Demonstrated proficiency with analytical testing equipment and techniques (HPLC GC spectrophotometry)
Strong understanding of cGMP requirements and quality systems
Experience with quality documentation and data review
Proven ability to lead and mentor others while maintaining quality standards
Excellent attention to detail and organizational skills
Strong verbal and written communication abilities
Proficiency with standard office software and LIMS systems
Ability to work in cleanroom environments and follow gowning procedures
Physical ability to stand for extended periods lift up to 25 lbs occasionally
Flexibility to work various shifts as needed
Problem-solving skills and ability to troubleshoot technical issues
Experience writing and reviewing SOPs and technical documentation

ThermoFisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race creed religion color national or ethnic origin citizenship sex sexual orientation gender identity and expression genetic information veteran status age or disability status.

Join Us!

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process to perform essential job functions and to receive other benefits and privileges of employment. Please contact us to request accommodation.