Executive Director, GMP Quality

Ionis Pharmaceuticals, Inc.

$221K — $288K *
Pharmaceuticals & Biotech
15+ years of experience
Job Overview by Ladders

Qualifications

  • 20+ years of QA or GMP Quality experience in a pharmaceutical or biotech environment.
  • 10+ years in a senior leadership role developing Quality organizations.
  • Strong regulatory inspection and audit experience.
  • Background in biologics, drug substance, and/or drug product manufacturing is essential.
  • Proven ability in stakeholder management and strategic leadership.

Responsibilities

  • Provide strategic leadership for GMP Quality activities across Carlsbad and Faraday facilities.
  • Establish and enhance GMP Quality processes for manufacturing and testing activities.
  • Offer senior QA expertise on quality issues, including investigations and CAPAs.
  • Cultivate relationships with CMOs and other business partners to support quality initiatives.
  • Direct strategic Quality direction for new compounds and manufacturing processes.
  • Oversee audit and inspection readiness and lead responses during health authority inspections.
  • Develop and enhance Quality policies and training to ensure compliance with GMP standards.

Benefits

  • Comprehensive health insurance plans.
  • 401(k) retirement plan with company match.
  • Paid time off and holidays.
  • Support for professional development and training.
  • Flexible work schedule options.
Full Job Description
EXECUTIVE DIRECTOR, GMP QUALITY

SUMMARY:

The Executive Director, GMP Quality is a senior QA leadership position and the senior GMP Quality leader supporting the Carlsbad campus. The position provides strategic direction and leadership for GMP Quality activities and initiatives across the drug development lifecycle through clinical and commercial supply, including internal operations and activities managed through CMOs and other service providers. The position is accountable for ensuring effective GMP Quality oversight and for developing and enhancing QA operations in accordance with applicable cGMP requirements.

The scope of the position includes drug substance and drug product manufacturing support and related GMP Quality activities at the Carlsbad campus and Faraday facility, as well as activities conducted internally by Ionis and externally through CMOs and other service providers. The position is accountable for strategic oversight of Quality relationships with Ionis business partners and serves as a key interface for domestic and international regulatory GMP inspections, audits, and partner communications as they relate to Quality. The position leads audit and inspection readiness activities and serves as the lead QA representative during health authority inspections of the Faraday campus.

The Executive Director, GMP Quality reports directly to the Vice President of GMP Quality.

WORK LOCATION: onsite in Carlsbad, CA

CORE RESPONSIBILITIES:

  • Provide strategic leadership and direction for GMP Quality activities supporting the Carlsbad campus, Faraday facility, and Ionis development lifecycle products manufactured internally or outsourced to CMOs.
  • Lead the establishment and enhancement of GMP Quality processes for clinical supply, drug substance and drug product manufacturing, testing, and release activities in accordance with applicable GMP regulations and guidelines (e.g. EU, FDA, HC, ICH, MHLW, TGA, etc.).
  • Provide senior QA expertise and strategic guidance on quality issues, including manufacturing deviations, investigations, CAPAs, change controls, OOS/OOT results, and other GMP matters.
  • Lead and influence relationships with CMOs, business partners, Technical Operations, Manufacturing, QC, Regulatory, and Ionis leadership to support risk management, issue resolution, continuous improvement, and a culture committed to quality excellence.
  • Provide strategic Quality direction and oversight for Ionis' new compounds, new chemistries, and novel manufacturing processes, as applicable.
  • Lead audit and inspection readiness for the Carlsbad campus, Faraday facility, and external service providers; lead the development of responses to health authority observations; and serve as the lead QA representative during health authority inspections of the Faraday campus.
  • Lead the development and enhancement of Quality policies, programs, procedures, and training to support Ionis business objectives and promote consistent GMP Quality standards.


REQUIREMENTS:

  • Minimum of 20 years of QA, GMP Quality, or compliance experience, with 10+ years of senior leadership experience leading and developing a Quality organization in a pharmaceutical or biotechnology manufacturing setting. Demonstrated success providing strategic direction, developing Quality processes and procedures, and establishing a culture committed to Quality excellence. A degree in a relevant scientific, engineering, pharmacy, or related discipline is preferred.
  • Significant experience with regulatory inspections, audits, investigations, CAPA, change control, risk management, and applicable USA/global GMP requirements.
  • Experience with biologics and drug substance and/or drug product manufacturing is required
  • experience with aseptic products, combination products, or other complex pharmaceutical operations is preferred.
  • Proven record of strong senior-level people, program, communication, stakeholder-management, influencing, and strategic leadership skills, with the judgment to establish priorities, manage risk, and escalate quality issues appropriately.
  • Demonstrated ability to lead cross-functional initiatives; coach and mentor colleagues; represent Quality with internal and external stakeholders; and drive compliant, sustainable improvements aligned with established functional accountabilities.


Please visit our website, http://www.ionis.com for more information about Ionis and to apply for this position; reference requisition #IONIS004102

Ionis offers an excellent benefits package! Follow this link for more details: Ionis Benefits

Full Benefits Link: https://ionis.com/careers#:~:text=Highly%20competitive%20benefits

The pay scale for this position is $221,151 to $288,783

NO PHONE CALLS PLEASE. PRINCIPALS ONLY.

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