Why Join Us?

Be a hero for our rare disease patients

At Ultragenyx, we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to do. To achieve this goal, our vision is to lead the future of rare disease medicine. For us, this means going where other biopharma companies won’t go – challenging the status quo and creating a new model that advances our field so more patients and caregivers can benefit from life-changing treatments. We do this by following the science, applying a novel rapid development approach, making innovative medicines at fair and reasonable prices, and creating a collaborative ecosystem to reach patients in ways that are most meaningful for them.

Our commitment and care for patients extends to our people, so culture is an essential cornerstone for Ultragenyx. We remain continuously focused on creating a supportive and inclusive environment of profound learning and growth – so employees can thrive in all areas of their lives, in and outside of work. Ultimately, we want to be an organization where we would be proud for our family, friends and children to work.

If you want to have a meaningful impact, do the best work of your career, and grow a lot, both professionally and personally, come join our team.

Position Summary:

ultrafocused – Work together to fearlessly uncover new possibilities

The Senior Manager of Quality Assurance Operations Drug Substance will be responsible for Quality oversite of the Gene Therapy Manufacturing Facility (GTMF) Drug Substance manufacturing area. This individual will operate with a quality mindset and provide "on the floor" oversite of manufacturing activities which includes but is not limited to "on the floor" guidance during unexpected events, batch record review, line clearance, and deviation and change control management. You will partner with Manufacturing, Engineering, Facilities, MSAT, Validation, and Quality Control teams to support manufacturing and product release activities as well as ongoing projects, initiatives and reports. You will provide quality expertise to ensure compliant manufacture of GMP material (clinical or commercial). In this role, operational excellence initiatives must be supported and driven. Supervision and mentoring of junior level team members to clarify goals and priorities may be required. You will be required to set goals for your team and ensure the team is supported and trained to meet those goals.

Work Model:

Core Lab & Ops: This role typically requires that the majority of the work be conducted on-site.

Responsibilities:

Must demonstrate the ability to manage deviation/CAPA records and may be required to function as a deviation/CAPA manager for minor or major deviations as needed.
Will be required to review Change Control Records as needed.
Will be required to own various Quality procedures and ensure the systems/processes are deployed effectively. Will contribute to Quality Assurance program policies and procedures related to their area.
Review/Approval of Master Batch Records and review/approval of executed DS Production Batch Records.
Perform QA review/approval of Drug Substance area shutdowns/restarts after planned or unplanned maintenance/EM events etc.
Responsible for writing, reviewing and/or approving documents such as SOPs, work instructions, policies, and standards to enable the execution of GMP manufacturing.
Work with various functions to resolve deviations and assess potential product and compliance impact. Escalate significant events to Quality Management and drive timely completion of effective investigations.
Perform routine area walkthroughs, logbook reviews, inspection readiness assessments.
Drive or support continuous improvement activities to support elimination of waste to enable an effective and efficient manufacturing site/process. Champion process improvement where applicable.

Requirements:

Advanced technical and regulatory understanding of Drug Substance manufacturing, (Formulation, Filling, Aseptic Operations, Vial Inspection/AQL, Packaging & Labeling).
Strong experience with various root cause analysis techniques such as 5-why, Kepner-Tregoe, force-field analysis, DMAIC, fault tree analysis.
Capable of interpreting and adapting various technical reports in support of Investigations/Deviations.
On the floor Biologics experience in a GMP environment required
Strong understanding of industry regulations such as CFR, USP.
BS/BA Degree (Biological or Chemical Science Preferred) with 7+ years of relevant experience preferred or Master's Degree (Biological or Chemical Science) with 5+ years of relevant experience preferred
4+ years of leadership/management experience in a Technical or Quality professional role and experience managing contingent employees

Physical Demand Requirements:

General Manufacturing: Drug Substance/Central Services:

Stand for extended periods of time with periodic stooping / bending / kneeling

Able to lift, push, pull up to 50lbs.

Climb ladders and stairs of various heights.

Work in a controlled environment requiring GxP gowning and wear protective clothing over the head, face, hands, feet, and body. This requires the ability to change clothes into appropriate gowning and personal protective equipment.

Must remove all make-up, jewelry, and contact lenses while in the manufacturing environment.
Working in temperature-controlled environments (cold rooms).

#LI-CS1 #LI-Onsite

The typical annual salary range for this full-time position is listed below. This range reflects the characteristics of the job, such as required skills and qualifications and is based on the office location noted in this job posting. The range may also be adjusted based on applicant's geographic location.

This position is eligible for annual bonus and equity incentives. Actual individual pay is determined by demonstrated experience and internal equity alignment.

Pay Range

$163,700—$202,200 USD

Full Time employees across the globe enjoy a range of benefits, including, but not limited to:

· Generous vacation time and public holidays observed by the company

· Volunteer days

· Long term incentive and Employee stock purchase plans or equivalent offerings

· Employee wellbeing benefits

· Fitness reimbursement

· Tuition sponsoring

· Professional development plans

* Benefits vary by region and country

Ultragenyx Pharmaceutical is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital and veteran status, and any other status or classification protected by applicable federal, state, and/or local laws. Reasonable accommodation will be provided for all protected statuses or classifications protected by applicable law, including individuals with disabilities, disabled veterans, for pregnancy, childbirth, and related medical conditions, and based on sincerely held religious beliefs. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or in any part of the recruitment process, you may contact Talent Acquisition by emailing us at talentacquisition@ultragenyx.com.

See our CCPA Employee and Applicant Privacy Notice.

See our Privacy Policy.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Note to External Recruiters: All candidate activity and open positions are managed strictly through our Human Resources Department. Our Human Resources Department kindly requests that recruiters not contact employees/hiring managers directly in an attempt to solicit business and present candidates. Please note that failure to comply with this request will be a factor in determining a professional relationship with our organization. Submission of unsolicited resumes prior to an agreement set in place between the Human Resources Department and the recruiting agency will not create any implied obligation. Inquiries on developing a recruiting relationship with us, may be directed to: talentacquisition@ultragenyx.com.

Senior Manager QA Operations Drug Substance (M-F, 2:30 pm - 10:00 pm)

Position Summary:

Work Model:

Responsibilities:

Requirements:

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