Director, Quality Audit Management

3 weeks ago


Boston, United States Ironwood Pharmaceuticals Full time

Ironwood Pharmaceuticals is a leading global gastrointestinal (GI) healthcare company on a mission to advance the treatment of GI diseases and redefine the standard of care for GI patients. We are pioneers in the development of LINZESS (linaclotide), the U.S. branded prescription market leader for adults with irritable bowel syndrome with constipation or chronic idiopathic constipation. Ironwood is also advancing apraglutide, a next-generation, long-acting synthetic GLP-2 analog being developed for rare gastrointestinal diseases, including short bowel syndrome with intestinal failure, as well as several earlier stage assets. Building upon our history of GI innovation, we keep patients at the heart of our R&D and commercialization efforts to reduce the burden of GI diseases and address significant unmet needs.

Position Summary:

As the head of a new global GxP Quality audit management function reporting directly to the Head of Quality, this individual will be responsible for leading and managing Ironwood's global self-inspection and external GxP audit programs. This Quality professional is a resourceful self-starter and team player, who acts with a sense of urgency and operates independently with minimal oversight. This member of the Quality team is a subject matter expert in managing internal and external GxP audits/self-Inspections and is familiar with US, UK, EU and other international GxP regulations/requirements. This individual is expected to collaborate with internal and external stakeholders and peers in a professional and respectful manner.

Responsibilities: Lead the Quality Audit Management group. Manage the internal self-inspection and external GxP audit programs by performing or overseeing the following activities:

Establish a contract auditor network and process contracts. Maintain annual audit schedules. Coordinate audit logistics. Ensure the proper documentation is produced in a timely manner and in accordance with Ironwood's internal procedures (e.g., Agenda, Report, Responses, CAPA, etc.) Providing feedback to stakeholder groups Measure and evaluate audit performance (business and compliance) using standard metrics, and report periodically to Quality and our business partners. Manage and/or conduct periodic review audits of GxP computer systems. Documenting all audit-related activities using the Ironwood eQMS

Attend meetings with stakeholders. Lead and facilitate all Inspection Readiness (IR) activities. Continuous process improvement through procedural updates, developing and maintaining a set of audit tools and databases, internal and external networking, corporate promotion, etc. Build and maintain a high performing team. Promote the Quality culture via Quality Awareness Campaign initiatives. Establish the annual budget for the AIM group and maintain costs within the budget. Recruit and hire additional resources (i.e., contract and FTE) Performing and processing investigations, deviations, and CAPA using the Ironwood eQMS

Requirements: Bachelor's degree in a scientific discipline (or equivalent) 15 years' experience in the pharmaceutical industry; the last 10 years in a lead auditor/ senior Quality role Knowledge of FDA, MHRA, and EMA GxP regulations, guidelines, and industry standards as a minimum Proficient in the use of MS Office applications and experience operating within an electronic QMS. Strong organizational, prioritization, planning, project management and communication skills Proficient in performing risk and impact assessments, including implementation of mitigation actions and risk monitoring. Ability to perform various tasks in a disciplined, consistent manner under minimal supervision. Effectively presents information in a 1-1 or group setting. Comfortable working in a fast paced, dynamic environment. Able to work remotely in an efficient and effective manner. Minimum 10% travel time

Ironwood Pharmaceuticals is an equal opportunity employer welcoming diversity in our workforce.

Ironwood currently anticipates that the initial base salary for this position could range from between $197,000 to $229,320. The actual base salary will depend, in part, on the successful candidate's qualifications for the role, including education and experience. Ironwood offers a comprehensive compensation and benefits program to eligible employees, including Restricted Stock Unit awards; eligibility to participate in either a bonus or sales incentive program; company-sponsored 401(k) with matching contributions; eligibility for medical, dental, vision and prescription drug benefits; wellness stipends; and a generous vacation/holiday schedule.

#LI-Hybrid #J-18808-Ljbffr



  • Boston, United States Ironwood Pharmaceuticals Full time

      Ironwood Pharmaceuticals is a leading global gastrointestinal (GI) healthcare company on a mission to advance the treatment of GI diseases and redefine the standard of care for GI patients. We are pioneers in the development of LINZESS® (linaclotide), the U.S. branded prescription market leader for adults with irritable bowel syndrome with constipation...


  • Boston, United States Ironwood Pharmaceuticals Full time

    Ironwood Pharmaceuticals is a leading global gastrointestinal (GI) healthcare company on a mission to advance the treatment of GI diseases and redefine the standard of care for GI patients. We are pioneers in the development of LINZESS (linaclotide), the U.S. branded prescription market leader for adults with irritable bowel syndrome with constipation or...


  • Boston, United States Ironwood Pharmaceuticals Full time

    Ironwood Pharmaceuticals is a leading global gastrointestinal (GI) healthcare company on a mission to advance the treatment of GI diseases and redefine the standard of care for GI patients. We are pioneers in the development of LINZESS (linaclotide), the U.S. branded prescription market leader for adults with irritable bowel syndrome with constipation or...


  • Boston, United States HireMinds Full time

    Associate Director, Supplier Quality & AuditingBoston, MA (Remote)Our pharmaceutical client here in Boston, MA is growing and looking to add an Associate Director, Supplier Quality & Auditing (Boston Hybrid or East Coast REMOTE) to their team! This role will perform as a Quality system owner for Supplier Qualification and Auditing systems, including...


  • Boston, United States HireMinds Full time

    Associate Director, Supplier Quality & AuditingBoston, MA (Remote)Our pharmaceutical client here in Boston, MA is growing and looking to add an Associate Director, Supplier Quality & Auditing (Boston Hybrid or East Coast REMOTE) to their team! This role will perform as a Quality system owner for Supplier Qualification and Auditing systems, including...


  • Boston, United States HilleVax, Inc. Full time

    HilleVax is a clinical-stage biopharmaceutical company focused on developing and commercializing novel vaccines. Our initial program, HIL-214, is a virus-like particle (VLP) based vaccine candidate for the prevention of moderate-to-severe acute gastroenteritis (AGE) caused by norovirus infection. It is estimated that norovirus causes nearly 700 million cases...


  • Boston, United States Northern Trust Full time

    About Northern Trust: Northern Trust, a Fortune 500 company, is a globally recognized, award-winning financial institution that has been in continuous operation since 1889. Northern Trust is proud to provide innovative financial services and guidance to the world's most successful individuals, families, and institutions by remaining true to our enduring...


  • Boston, United States The Bank of New York Mellon Full time

    At BNY, our culture empowers you to grow and succeed. As a leading global financial services company at the center of the world's financial system we touch nearly 20% of the world's investible assets. Every day around the globe, our 50,000+ employees bring the power of their perspective to the table to create solutions with our clients that benefit...


  • Boston, United States Vertex Pharmaceuticals Full time

    Job Description General Position Summary: The Audit and Inspection Management Manager is responsible for the execution of audit and inspection management assigned activities, inclusive of internal and external processes, contributing to and executing audit plans, supporting inspection readiness activities, on-site and remote inspection support, and overall...


  • Boston, United States BNY Mellon Full time

    At BNY, our culture empowers you to grow and succeed. As a leading global financial services company at the center of the world’s financial system we touch nearly 20% of the world’s investible assets. Every day around the globe, our 50,000+ employees bring the power of their perspective to the table to create solutions with our clients that benefit...


  • Boston, United States BNY Mellon Full time

    Overview At BNY, our culture empowers you to grow and succeed. As a leading global financial services company at the center of the world's financial system we touch nearly 20% of the world's investible assets. Every day around the globe, our 50,000+ employees bring the power of their perspective to the table to create solutions with our clients that benefit...


  • Boston, United States Bank of America Full time

    **2025 Corporate Audit Summer Analyst Program - Automation, Data Quality, Technology** - What would you like the power to do?_ - At Bank of America, we value being a Great Place to Work®. We recognize that talented, engaged, and satisfied employees are the foundation to help make the financial lives of our customers and clients better._ - Bank of America...


  • Boston, United States Commonwealth Care Alliance Full time

    Why This Role is Important to Us The Sr. Director of Internal Audit position is a key member of the Commonwealth Care Alliance's Internal Audit team responsible for the successful completion of external regulatory compliance audits including, external regulatory compliance audits. The position advises the Audit and Compliance leadership on key risks,...


  • Boston, United States Third Rock Ventures Full time

    Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer. Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at critical targets...


  • Boston, United States Tango Therapeutics Full time

    Company Overview Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer. Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at...


  • Boston, United States Walker Cole International Full time

    Walker Cole International have been engaged on a confidential search for a Director of Quality Assurance to join a Gene Therapy company based on the East Coast, USA.As the Director of Quality Assurance, you will be responsible for:Leadership of entire QA function including QA Systems, Quality Ops and Validation Participation in internal/external audits and...


  • Boston, United States Monte Rosa Therapeutics, Inc Full time

    Overview: Monte Rosa Therapeutics is seeking a passionate Associate Director/Director of Quality Systems is responsible for maintaining and maturing Monte Rosa Txs GxP Quality System, which includes, but is not limited to documentation, training, supplier quality, internal audits, product complaints, risk management, change controls, deviations and CAPAs....

  • Associate Director

    2 weeks ago


    Boston, United States Monte Rosa Therapeutics Full time

    Associate Director – Quality Systems Location: Boston, MA Role Summary: Monte Rosa Therapeutics is seeking a passionate Associate Director/Director of Quality Systems is responsible for maintaining and maturing Monte Rosa Tx’s GxP Quality System, which includes, but is not limited to documentation, training, supplier quality, internal audits, product...


  • Boston, United States Monte Rosa Therapeutics Full time

    Associate Director Quality Systems Location: Boston, MA Role Summary: Monte Rosa Therapeutics is seeking a passionate Associate Director/Director of Quality Systems is responsible for maintaining and maturing Monte Rosa Txs GxP Quality System, which includes, but is not limited to documentation, training, supplier quality, internal audits, product...


  • Boston, United States Monte Rosa Therapeutics Full time

    Associate Director – Quality SystemsLocation: Boston, MA Role Summary:Monte Rosa Therapeutics is seeking a passionate Associate Director/Director of Quality Systems is responsible for maintaining and maturing Monte Rosa Tx’s GxP Quality System, which includes, but is not limited to documentation, training, supplier quality, internal audits, product...