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The Role:
Moderna is seeking a Quality Assurance Specialist for a position based at their Norwood, MA manufacturing site. This position is part of Moderna’s Quality Assurance team responsible for ensuring quality oversight of our mRNA platform in cGMP Manufacturing. The main responsibility for this position is to provide quality oversight of Quality Control, with a focus on deviations, change controls, and CAPAs. The individual will work closely with Manufacturing, Quality Control, AS&T, and other teams.
Here’s What You’ll Do:
Identifies, classifies, and reports deviations, as appropriate, and typically works on more complex minor and/or major deviations.
Responsible for providing quality oversight to the change management system for change controls. This includes providing plan creation oversight, verifying that changes adhere to SOPs and regulatory compliance.
Reviews and approves Deviations, Laboratory Events and OOS Laboratory Investigations.
Oversees execution of remediation/CAPA activities required to continue production or move a process to the next milestone.
Works closely with others to determine root cause and potential preventative/correction actions.
Authors and reviews SOPs and policies. Create and establish process and procedures to ensure compliance and adherence to regulations and cGMP operations.
Ensure timely closure of investigation.
Participates in quality oversight of Quality Control and AS&T.
Reviews and approves facility alarms, facility work requests, and return-to-service documentation.
Reviews and approves Quality Control method qualification protocols and reports.
Work closely with others to recognize opportunities for improvement and drive change through the use of Quality systems.
Participate in internal audits for compliance with SOPs, GMPs, and regulations.
Other activities as deemed necessary e.g. logbook reviews
Here’s What You’ll Bring to the Table:
5 – 7 years of experience in a GMP manufacturing environment, within Quality (combination of Quality Assurance and Quality Control preferred), with a Bachelor’s Degree in Biology, Microbiology, Chemistry, Biochemistry, Engineering, or related field.
Proven track record of success in a fast-paced production environment at a GMP biotech/pharmaceutical company.
Working knowledge of relevant FDA, EU, ICH guidelines and regulations.
Outstanding communication skills (verbal and written).
Ability to manage multiple projects in a fast-paced environment.
Ability to effectively collaborate effectively in a dynamic, cross-functional matrix environment.
Moderna is pleased to provide you and your family with a comprehensive and innovative suite of benefits, including:
About Moderna
In over 10 years since its inception, Moderna has transformed from a research-stage company advancing programs in the field of messenger RNA (mRNA), to an enterprise with a diverse clinical portfolio of vaccines and therapeutics across seven modalities, a broad intellectual property portfolio in areas including mRNA and lipid nanoparticle formulation, and an integrated manufacturing plant that allows for rapid clinical and commercial production at scale. Moderna maintains alliances with a broad range of domestic and overseas government and commercial collaborators, which has allowed for the pursuit of both groundbreaking science and rapid scaling of manufacturing. Most recently, Moderna’s capabilities have come together to allow the authorized use and approval of one of the earliest and most effective vaccines against the COVID-19 pandemic.
Moderna’s mRNA platform builds on continuous advances in basic and applied mRNA science, delivery technology and manufacturing, and has allowed the development of therapeutics and vaccines for infectious diseases, immuno-oncology, rare diseases, cardiovascular diseases and autoimmune diseases. Moderna has been named a top biopharmaceutical employer by Science for the past seven years. To learn more, visit (url removed).
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 (url removed). (EEO/AAP Employer)
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