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Ultragenyx
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Ultragenyx

3.4

Associate Director, Facilities Engineering

Bedford, MA

$158K - $195K (Employer provided)

Is your resume a good match?

Use AI to find out how well the skills on your resume fit this job description.

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 Associate Director, Facilities Engineer candidate will partner closely with GMP Facilities and be responsible for providing engineering support for GMP and non GMP utility systems (including WFI, HVAC, chilled water, electrical systems, condensate systems, gases, etc.) at Ultragenyx Gene Therapy GMP Manufacturing and Laboratory facilities located in Bedford, MA and Woburn, MA. The candidate will be the primary engineering resource for operational support and process improvements related to the facility and utility systems within the sites.

Work Model:

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

Responsibilities:

Provide direction to junior engineers and external service providers to develop scope of work and schedules for execution of physical work on facilities and equipment.

Provides high level of leadership, direction and decision making in the direction of work including design and implementation.

Technical and Quality ownership of facility and utility systems including on site troubleshooting and investigations; provides on-call operational support in the event of any equipment issues.

Improves preventative maintenance program and strategies within the CMMS that maximize system/equipment reliability and availability.

Use reliability-centered maintenance concepts and data to prioritize efforts and system improvements/optimization. Monitor and trend repeat equipment failures and perform root-cause analysis to identify cause and recommend and implement corrective actions, as necessary.

Help establish, monitor, and drive continuous improvements for facility and utility KPI's.

Independently owns tasks and deliverables for projects and will be main Engineering point of contact for facility and utility projects from design through commissioning/validation.

Provide technical ownership of multiple complex projects/changes at a time.

Active training and mentoring of junior team members.

Solutions are expected to incorporate broad experience and input from expert & industry sources.

Subject matter expert for investigations of any facilities or equipment system deviations or failures and drives the development and implementation of CAPAs.

Owns and executes change management for facility and utility systems.

Ensure systems/equipment comply with industry standards and regulations.

Support the development and revision of governing system/equipment SOPs.

Identify and drive opportunities for innovation and efficiency in facility systems

Supports equipment shutdowns and general repairs when necessary.

Requirements:

Minimum of a Bachelor of Science degree in Chemical, Mechanical, or related engineering field preferred.

Minimum of 12 years of experience in technical functions including Utilities/Plant Engineering, or related functions in a cGMP manufacturing environment.

Demonstrated leadership skills in executing projects within an FDA/EMA regulated environment, including direct experience working at a biologic or advanced therapy medicinal product (ATMP) manufacturing site.

Experience and knowledge related to reviewing and approving equipment submittals, functional and configuration specifications, maintenance and calibration, equipment installation, and specifications with facilities, equipment, and utilities related to drug substance and/or drug product manufacturing.

Extensive knowledge of industry standards for cGMP engineering design, commissioning, validation, and operation of bioprocessing equipment and utility systems related to drug substance and/or drug product manufacturing.

Demonstrated experience working with Computerized Maintenance Management Systems (e.g., Blue Mountain RAM, Maximo, EAM, etc).

Proven record with troubleshooting, problem solving, and investigational skills.

Experience with quality systems including change controls, CAPAs, deviations, etc.

Strong interpersonal and communications skills with ability to present to regulatory authorities, key stakeholders, and senior management effectively.

Willingness to work in a dynamic and changing corporate environment. Flexible in the face of shifting needs and/or priorities.

Physical Demand Requirements

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

Ability to climb ladders and stairs of various heights.

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

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 use of a respirator; medical clearance will be required in advance.

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 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.

See company reviews

Base pay range

The minimum salary is $158K and the max salary is $195K.

$158K – $195K/yr (Employer provided)

$176K

/yr Median

Bedford, MA

If an employer includes a salary or salary range on their job, we display it as "Employer Provided". If a job has no salary data, Glassdoor displays a "Glassdoor Estimate" if available. To learn more about "Glassdoor Estimates," see our FAQ page.

Working here doesn’t have to be a secret

3.4

Recommend to a friend
Approve of CEO
CEO: Emil Kakkis
154 Ratings

Ultragenyx

3.4

Associate Director, Facilities Engineering

Bedford, MA

$158K - $195K (Employer provided)

Ultragenyx

3.4

Associate Director, Facilities Engineering

Bedford, MA

$158K - $195K (Employer provided)

Is your resume a good match?

Use AI to find out how well the skills on your resume fit this job description.

Why Join Us?

Be a hero for our rare disease patients

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

Work Model:

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

Responsibilities:

Provide direction to junior engineers and external service providers to develop scope of work and schedules for execution of physical work on facilities and equipment.

Provides high level of leadership, direction and decision making in the direction of work including design and implementation.

Technical and Quality ownership of facility and utility systems including on site troubleshooting and investigations; provides on-call operational support in the event of any equipment issues.

Improves preventative maintenance program and strategies within the CMMS that maximize system/equipment reliability and availability.

Use reliability-centered maintenance concepts and data to prioritize efforts and system improvements/optimization. Monitor and trend repeat equipment failures and perform root-cause analysis to identify cause and recommend and implement corrective actions, as necessary.

Help establish, monitor, and drive continuous improvements for facility and utility KPI's.

Independently owns tasks and deliverables for projects and will be main Engineering point of contact for facility and utility projects from design through commissioning/validation.

Provide technical ownership of multiple complex projects/changes at a time.

Active training and mentoring of junior team members.

Solutions are expected to incorporate broad experience and input from expert & industry sources.

Subject matter expert for investigations of any facilities or equipment system deviations or failures and drives the development and implementation of CAPAs.

Owns and executes change management for facility and utility systems.

Ensure systems/equipment comply with industry standards and regulations.

Support the development and revision of governing system/equipment SOPs.

Identify and drive opportunities for innovation and efficiency in facility systems

Supports equipment shutdowns and general repairs when necessary.

Requirements:

Minimum of a Bachelor of Science degree in Chemical, Mechanical, or related engineering field preferred.

Minimum of 12 years of experience in technical functions including Utilities/Plant Engineering, or related functions in a cGMP manufacturing environment.

Demonstrated leadership skills in executing projects within an FDA/EMA regulated environment, including direct experience working at a biologic or advanced therapy medicinal product (ATMP) manufacturing site.

Experience and knowledge related to reviewing and approving equipment submittals, functional and configuration specifications, maintenance and calibration, equipment installation, and specifications with facilities, equipment, and utilities related to drug substance and/or drug product manufacturing.

Extensive knowledge of industry standards for cGMP engineering design, commissioning, validation, and operation of bioprocessing equipment and utility systems related to drug substance and/or drug product manufacturing.

Demonstrated experience working with Computerized Maintenance Management Systems (e.g., Blue Mountain RAM, Maximo, EAM, etc).

Proven record with troubleshooting, problem solving, and investigational skills.

Experience with quality systems including change controls, CAPAs, deviations, etc.

Strong interpersonal and communications skills with ability to present to regulatory authorities, key stakeholders, and senior management effectively.

Willingness to work in a dynamic and changing corporate environment. Flexible in the face of shifting needs and/or priorities.

Physical Demand Requirements

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

Ability to climb ladders and stairs of various heights.

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

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 use of a respirator; medical clearance will be required in advance.

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

See our CCPA Employee and Applicant Privacy Notice.

See our Privacy Policy.

See company reviews

Base pay range

The minimum salary is $158K and the max salary is $195K.

$158K – $195K/yr (Employer provided)

$176K

/yr Median

Bedford, MA

Working here doesn’t have to be a secret

3.4

Recommend to a friend
Approve of CEO
CEO: Emil Kakkis
154 Ratings

75,989 Associate field manager jobs in United States

Position Summary:

Work Model:

Responsibilities:

Base pay range

Working here doesn’t have to be a secret

Position Summary:

Work Model:

Responsibilities:

Base pay range

Working here doesn’t have to be a secret