Ultragenyx

Senior Specialist, Quality Assurance

Posted 2 Days Ago

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Bedford, MA

In-Office

50K-100K

Senior level

Biotech

The Role

The Senior Specialist in Quality Assurance oversees QA activities at a gene therapy manufacturing facility, including reviewing production batch records, managing deviations, and ensuring compliance with GMP regulations.

Summary Generated by Built In

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

As Quality Assurance Drug Substance (DS) Senior Specialist, you will be responsible for Quality Assurance activities at the new gene therapy manufacturing facility located in Bedford, MA. You will provide direct QA oversight and support for the core Drug Substance Manufacturing activities across multiple shifts. Activities will include Production Batch Record review, deviation management, QA Manufacturing walkthroughs, logbook review and room/equipment tag-out for manufacturing use. The site is a multi-product facility which will be used for drug substance manufacturing, and aseptic filling of drug product. QA activities are primarily focused on the drug substance manufacturing areas but could also support Drug Product when required.

Your role will partner with Manufacturing, Engineering, Validation, QC, Quality Systems, and MSAT functions to provide QA approval for various operating procedures, DS manufacturing processes, and batch records required for on-going manufacturing at the facility. You will report to the Associate Director, Quality Assurance at Ultragenyx Gene Therapy

Work Model:

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

Responsibilities:

Review and approve of both Master Batch Records and executed DS Production Batch Records
Perform QA review and approval of DS area shutdowns/restarts after planned or unplanned maintenance/EM events etc.
Perform routine area walkthroughs, logbook reviews, inspection readiness assessments
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
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:

Minimum B.S. degree in scientific field such as microbiology, chemistry or biochemistry. 5+ years of experience in biopharmaceutical, biotechnology, cell or gene therapy industries with Manufacturing and Quality roles
Direct experience working at a biologic or advanced therapy medicinal product (ATMP) manufacturing site. Knowledge and experience with drug substance and aseptic practices
Knowledge of domestic and international GMP regulations and their application in the manufacture of biologics, cell, or gene therapy products
Demonstrated ability to communicate technical information or complex situations to site management and/or health authority inspectors in a concise and clear manner

Physical Demands/Work Environment/Safety Considerations:

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
Certain tasks may require the use of a respirator; medical clearance will be required in advance
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

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 [email protected].

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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: [email protected].