You haven't searched anything yet.
The Role:
Moderna is seeking a Quality Assurance Specialist for a position based at their Norwood, MA manufacturing site and will directly support the growing area of Individualized Neoantigen Therapy (INT). The main responsibility for this position is to provide batch record review and disposition of products to patients. Strong decision-making skills and independent thinking will be paramount for candidate success. The individual will work closely with Manufacturing and Quality teams.
This position is 2nd shift, Sunday – Wednesday or Wednesday – Saturday.
Here’s What You’ll Do:
Review executed batch record documentation and perform batch disposition activities
Enforce adherence to current good manufacturing practices, standard operating procedures, and manufacturing documentation
Demonstrate general knowledge of standard manufacturing compliance, quality disposition, quality system review
Perform review of environmental monitoring data
Identifying risks and communicating gaps for quality and GMP process/systems
Partner with manufacturing and support teams to initiate and triage new deviation events
Support review and approval of deviations and CAPAs
Support quality functional groups on as needed basis
Authors and/or review SOPs, policies, and other GMP documentation to ensure compliance and adherence to regulations/cGMP operations
Practice safe work habits and adhere to Moderna’s safety procedures and guidelines
Utilize knowledge to improve operational efficiency.
Here’s What You’ll Bring to the Table:
2-5 years of experience in a GMP biopharmaceutical GMP manufacturing environment
Moderna is pleased to provide you and your family with a comprehensive and innovative suite of benefits, including:
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Moderna is a smoke-free, alcohol-free and drug-free work environment.
Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com. (EEO/AAP Employer)
-
Full Time
Durable Manufacturing
$104k-124k (estimate)
01/21/2023
04/01/2024
modernatx.com
CAMBRIDGE, MA
1,000 - 3,000
2010
Public
NOUBAR B AFEYAN
$500M - $1B
Durable Manufacturing
Moderna is a biotechnology company that researches & markets mRNA therapeutics for genetic disorders, oncology treatments & a COVID-19 vaccine.
The job skills required for Specialist, Quality Assurance include Quality Assurance, SOP, Quality Control, Planning, Chemistry, Coordination, etc. Having related job skills and expertise will give you an advantage when applying to be a Specialist, Quality Assurance. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Specialist, Quality Assurance. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Specialist, Quality Assurance positions, which can be used as a reference in future career path planning. As a Specialist, Quality Assurance, it can be promoted into senior positions as a Quality Assurance Specialist IV that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Specialist, Quality Assurance. You can explore the career advancement for a Specialist, Quality Assurance below and select your interested title to get hiring information.