Research Associate, Drug Product Development
1 week ago
The Role:
We are seeking a highly skilled and motivated Research Associate in Drug Product Development, to work in a team developing Modernas sterile drug product processes and products that enable clinical and future commercial supply. The primary role for this position will be to support product concept development including process development and scale-up work, container development and conditions of use studies. The incumbent will support the development of compositions, aseptic fill/finish unit operations through the development and use of scale-down models, process characterization studies etc. Applicants should have relevant pharmaceutical sciences related experience with various aspects of drug product development. The applicant should have exceptional ability to plan, execute and report, to communicate and collaborate, and requires strong attention to detail while working in a fast-paced, interdisciplinary environment.
Heres What Youll Do:
Conduct studies to support scale-up of drug product manufacturing (e.g. freeze/thaw, mixing, filling, filtration, lyophilization, transport etc).
Develop protocols to evaluate the compatibility of the drug product with processing materials, container closure components, and sterilization processes.
Provide support to drug product development activities executed in collaboration with Modernas Pilot organization, including toxicology fills stability fill operations.
Plan, organize and execute experiments (using DoE where possible) prepare study protocols and summarize the development results with presentations and study reports.
Communicate and collaborate with various groups such as analytical development to execute experiments and compile data.
Support manufacturing with studies for process trouble-shooting and investigations.
Perform a range of routine and non-routine characterization techniques, including opacity testing, microscopy, particle sizing etc.
Develop processes suitable to ensure long-term stability of vialed drug product.
Maintain an up-to-date ELN with good documentation practices
Closely collaborate with multiple groups to generate innovative solutions to challenging formulation and process problems.
Heres What Youll Bring to the Table:
Education Qualifications - Masters or Bachelors Degree in on one of the following fields: Chemical Engineering, Biochemical or Biomedical Engineering, Pharmaceutical Sciences, or any related or sub-disciplines of the above.
Relevant Experience: 0 2 years post Masters Degree or 0 4 years post Bachelors Degree.
Exceptional laboratory skills with ability to work efficiently and productively in a highly dynamic environment
Knowledge of statistical design of experiments (DoE) and analysis
Knowledge of nucleic acid chemistry and biology is a plus
Preferred: Experience in BioPharma, BioPharmaceutical, Pharmaceutical, or Biotechnology industry
Preferred: Experience with nanoparticle formulation technology
Preferred: Knowledge of GMP compliance.
Moderna is pleased to provide you and your family with a comprehensive and innovative suite of benefits, including:
Highly competitive and inclusive medical, dental and vision coverage optionsFlexible Spending Accounts for medical expenses and dependent care expensesLifestyle Spending Account funds to help you engage in personal enrichment and self-care activitiesFamily care benefits, including subsidized back-up care options and on-demand tutoringFree premium access to fitness, nutrition, and mindfulness classesExclusive preferred pricing on Peloton fitness equipmentAdoption and family-planning benefitsDedicated care coordination support for our LGBTQ+ communityGenerous paid time off, including:Vacation, sick time and holidays
Volunteer time to participate within your community
Discretionary year-end shutdown
Paid sabbatical after 5 years; every 3 years thereafterGenerous Paid Leave offerings, including 18 weeks of 100% paid parental leave for all new parents 401k match and Financial Planning toolsModerna-paid Life, LTD and STD insurance coverages, as well as voluntary benefit optionsComplimentary concierge service including home services research, travel booking, and entertainment requestsFree parking or subsidized commuter passesLocation-specific perks and extras
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, theinfrastructure 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 peopleare 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.
As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute and make a meaningful impact.
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. Were 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 contact the Accommodations team at leavesandaccommodations@modernatx.com. (EEO/AAP Employer)
-
-
Research Associate, Drug Product Development
3 weeks ago
Norwood, United States Moderna Full time**The Role**: We are seeking a highly skilled and motivated Research Associate in Drug Product Development, to work in a team developing Moderna’s sterile drug product processes and products that enable clinical and future commercial supply. The primary role for this position will be to support product concept development including process development and...
-
Research Associate, Drug Product Development
1 week ago
Norwood, Massachusetts, United States Moderna, Inc. Full timeThe Role:We are seeking a highly skilled and motivated Research Associate in Drug Product Development, to work in a team developing Modernas sterile drug product processes and products that enable clinical and future commercial supply. The primary role for this position will be to support product concept development including process development and scale-up...
-
Norwood, Massachusetts, United States Moderna, Inc. Full timeThe RoleModerna is seeking a highly skilled and motivated Scientist or Engineer to join our Respiratory Drug Product Development (DPD) team in Norwood, MA. To support Modernas exciting pipeline of products, the DPD team works to develop, characterize, and implement robust clinical/commercial manufacturing processes. From pre-clinical through...
-
Norwood, United States Moderna, Inc. Full timeThe RoleModerna is seeking a highly skilled and motivated Scientist or Engineer to join our Respiratory Drug Product Development (DPD) team in Norwood, MA. To support Modernas exciting pipeline of products, the DPD team works to develop, characterize, and implement robust clinical/commercial manufacturing processes. From pre-clinical through...
-
Scientist, Drug Product Development
3 weeks ago
Norwood, United States Moderna Full timeThe Role Here’s What You’ll Do Design and execute detailed experiments using risk assessments, appropriate scale down models, QbD principles, and process characterization/modeling techniques to develop and troubleshoot specific unit operations. Contribute to establishing and executing integrated development plans for inhalation products, working as...
-
Director, Drug Product Development
1 week ago
Norwood, Massachusetts, United States Moderna, Inc. Full timeThe RoleModernas Drug Product Development team is seeking an experienced, innovative and accomplished leader. Drug product development is responsible for ensuring the translation of mRNA technology into successful dosage forms and commercial products from a pharmaceutical sciences and engineering perspective. The incumbent will be a part of the leadership...
-
Director, Drug Product Development
1 week ago
Norwood, United States Moderna, Inc. Full timeThe RoleModernas Drug Product Development team is seeking an experienced, innovative and accomplished leader. Drug product development is responsible for ensuring the translation of mRNA technology into successful dosage forms and commercial products from a pharmaceutical sciences and engineering perspective. The incumbent will be a part of the leadership...
-
Scientist, Drug Product Development
2 weeks ago
Norwood, United States Moderna, Inc. Full timeThe RoleModerna is seeking a highly skilled and motivated Scientist or Senior Engineer to join our Drug Product Development (DPD) team in Norwood, MA. To support Modernas exciting pipeline of products, the DPD team works to develop, characterize, and implement robust clinical/commercial manufacturing processes. From pre-clinical through commercialization,...
-
Associate Director, QA Operations, Drug Product
3 weeks ago
Norwood, United States Moderna Theraputics Full timeThe Role Reporting to the Director, QA Drug Product, the Associate Director, QA Operations is responsible for leading the quality and compliance readiness for a state-of-the-art Drug Product (Fill Finish) cGMP manufacturing facility. This role involves ensuring operational readiness for production of both clinical and commercial drug products while adhering...
-
Associate Director, QA Operations, Drug Product
4 weeks ago
Norwood, United States Moderna Theraputics Full timeThe Role Reporting to the Director, QA Drug Product, the Associate Director, QA Operations is responsible for leading the quality and compliance readiness for a state-of-the-art Drug Product (Fill Finish) cGMP manufacturing facility. This role involves ensuring operational readiness for production of both clinical and commercial drug products while adhering...
-
Research Associate, Process Development
2 weeks ago
Norwood, Massachusetts, United States Moderna Full timeResearch Associate, Process Development page is loaded Research Associate, Process Development Apply locations Norwood, Massachusetts Technical Development time type Full time posted on Posted 9 Days Ago job requisition id R14693 The Role:Moderna is working to develop first-in-class messenger RNA (mRNA) based medicines. Were seeking a highly...
-
Sr. Engineer I, Drug Product Development
4 weeks ago
Norwood, Massachusetts, United States Moderna, Inc. Full timeThe Role:Moderna is seeking a highly skilled and motivated Scientist or Senior Engineer to join our Drug Product Development (DPD) team in Norwood, MA. To support Modernas exciting pipeline of products, the DPD team works to develop, characterize, and implement robust clinical/commercial manufacturing processes. From pre-clinical through commercialization,...
-
Sr. Engineer II, Drug Product Development
4 weeks ago
Norwood, United States Moderna, Inc. Full timeThe Role:This position is part of Modernas Drug Product Development team responsible for ensuring the translation of mRNA technology into successful dosage form and commercial product from a pharmaceutical sciences and engineering perspective. The incumbent will also provide technical leadership and mentoring to the Drug Product Development (DPD) group,...
-
Associate Director, QA Operations, Drug Product
4 weeks ago
Norwood, United States Moderna, Inc. Full timeThe RoleReporting to the Director, QA Drug Product, the Associate Director, QA Operations is responsible for leading the quality and compliance readiness for a state-of-the-art Drug Product (Fill Finish) cGMP manufacturing facility. This role involves ensuring operational readiness for production of both clinical and commercial drug products while adhering...
-
Associate Director, QA Operations, Drug Product
4 weeks ago
Norwood, United States BioSpace Full timeJob DetailsThe RoleReporting to the Director, QA Drug Product, the Associate Director, QA Operations is responsible for leading the quality and compliance readiness for a state-of-the-art Drug Product (Fill Finish) cGMP manufacturing facility. This role involves ensuring operational readiness for production of both clinical and commercial drug products while...
-
Associate Director, QA Operations, Drug Product
4 weeks ago
Norwood, Massachusetts, United States Moderna, Inc. Full timeThe RoleReporting to the Director, QA Drug Product, the Associate Director, QA Operations is responsible for leading the quality and compliance readiness for a state-of-the-art Drug Product (Fill Finish) cGMP manufacturing facility. This role involves ensuring operational readiness for production of both clinical and commercial drug products while adhering...
-
Associate Director, QA Operations, Drug Product
4 weeks ago
Norwood, United States Moderna, Inc. Full timeThe RoleReporting to the Director, QA Drug Product, the Associate Director, QA Operations is responsible for leading the quality and compliance readiness for a state-of-the-art Drug Product (Fill Finish) cGMP manufacturing facility. This role involves ensuring operational readiness for production of both clinical and commercial drug products while adhering...
-
Associate Director, QA Operations, Drug Product
4 weeks ago
Norwood, United States Moderna Full timeThe Role Reporting to the Director, QA Drug Product, the Associate Director, QA Operations is responsible for leading the quality and compliance readiness for a state-of-the-art Drug Product (Fill Finish) cGMP manufacturing facility. This role involves ensuring operational readiness for production of both clinical and commercial drug products while adhering...
-
Sr. Engineer II, Drug Product Development
4 weeks ago
Norwood, Massachusetts, United States Moderna, Inc. Full timeThe Role:This position is part of Modernas Drug Product Development team responsible for ensuring the translation of mRNA technology into successful dosage form and commercial product from a pharmaceutical sciences and engineering perspective. The incumbent will also provide technical leadership and mentoring to the Drug Product Development (DPD) group,...
-
Norwood, United States BioSpace, Inc. Full timeJob Details The Role Reporting to the Sr. Director of Sterility Assurance, the Associate Director of Sterility Assurance is tasked with leading the development and management of an aseptic and sterility assurance program for a state-of-the-art Drug Product (Fill Finish) cGMP manufacturing facility. This role encompasses overseeing operational readiness for...
