Senior Quality Assurance Associate II

Why join Team Alkermes?

Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.

We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts’ Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in Bio Pharma by Fortune Magazine.

Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law.  Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  

Alkermes is an E-Verify employer.

Skills / Qualifications  6+ years of experience in a pharmaceutical quality function

Thorough knowledge of FDA and EU cGMPs and pharmaceutical manufacturing requirements QA Experience in pharmaceutical product development and expectations for early phase clinical trials

Broad quality experience, preferably including manufacturing operations, API and drug product release, method development, method validation and transfer, QP release, process validation.

Strong ability to troubleshoot and problem solve

Demonstrated proficiency in use of risk assessment tools

Ability to effectively plan, organize and prioritize work

Education

Bachelor’s degree in a scientific discipline or related field#LI-RS1#LI-Onsite Responsibilities:

Primary interface with contract manufacturing organizations including oversight of ongoing CMO activities vs. Alkermes Quality policies and cGMPs. Oversight responsibilities include review of batch documentation, deviations, investigations, and change controls

Facilitate and interact with QP for review and release process

Maintenance and enhancement of quality systems to ensure conformance to Alkermes quality practices and international regulatory compliance requirements

Represent department on cross site projects

Monitor quality indicators highlighting trends and risks

Independently lead and/or support investigations into variances and quality issues and able to assure that proper changes are made to guarantee continued and consistent product quality

Proactively promote GMPsProvide quality assurance representation, guidance, leadership, and direction to product development teams for two or more different operations which include; API/drug substance, drug product and labeling/packaging operations

Identify and evaluate quality, technical and product development issues

Provide guidance/mentoring to QA Associates and cross functionally and provide performance feedback to CMO as appropriate

Review of regulatory documentation and submissions

Full time Posting Date: