Product Quality Lead

ESSENTIAL AREAS OF RESPONSIBILITY:

QA support for onsite Phase I/II oral dosage drug product manufacturing and analytical activities, maintaining knowledge of industry standards and regulatory requirements to ensure all drug product manufacturing, testing, storage and shipping activities are compliant. These activities may include:

• Provide QA oversight of analytical lifecycle activities, including:

• Review and approval of analytical instrument qualification and method validation documents

• Review and approval of stability protocols, reports and ongoing stability data review

• Ensure data integrity, completeness and compliance of analytical data supporting batch release.

• Collaboration with Analytical Development to resolve discrepancies and provide QA support for lab investigation.

• Provide QA oversight and ownership of the Cleaning Validation and Cleaning Verification program, including strategy, protocol development, execution, and reporting.

• Lead and/or support execution of cleaning verification activities, including collection of rinse and swab samples, protocol authoring and report generation.

• Ensure compliance with regulatory expectations for cross-contamination control and product changeover.

• Establish and perform GMP operational activities in support of Phase I/II manufacturing, including:

• Sampling and disposition of incoming raw materials and finished products.

• Sampling and monitoring of the USP Water System.

• Development and oversight of the Environmental Monitoring Program.

• Operational training programs, such as gowning, sampling, and GMP fundamentals.

• Creation and maintenance of operational SOPs and programs as required.

• Issuance of Control records

• Manufacturing QA Oversight

• Provide QA support for GMP manufacturing, including line clearances and on-floor QA oversight.

• Ensure compliance with cGMP behaviors, SOPs, and batch records.

• Batch Disposition Support and Data review:

• Perform batch records, supporting documentation and analytical data packages

• Compile data required for QP disposition

• Support trending and KPIs for batch disposition performance

• Provide QA review and approval of other GMP documentation, such as:

• Master and executed batch records

• Quality risk assessments

• SOPs and work instructions (related to all functional areas)

• Raw material/API release documentation

• Deviations, CAPAs and change controls

• Provide support to the regulatory/CMC group in support of regulatory filings as required.

• Provide support for complaints as applicable.

• Support internal and external audits as required.

POSITION SUMMARY:

Provide onsite Quality Assurance (QA) support for the establishment and operation of Phase I/II oral solid dosage (OSD) manufacturing and analytical activities, with primary focus on analytical lifecycle oversight (instrument qualification, method validation, stability, and data review), cleaning validation for manufacturing equipment, and QA support batch manufacturing. Ensure all activities are executed in full compliance with FDA/EU cGMP requirements and internal quality standards, and support batch disposition through robust data review and cross-functional collaboration.

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 BioPharma 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.