Notifications

Ultragenyx
3.4
Executive Director, CMC QA
Novato, CA
$294K - $363K (Employer provided)
Strong quality risk management capability and proficiency with root cause analysis, risk assessment, trend analysis, and decision-making tools.…
18d
Ultragenyx
3.4
Facilities Technician II (GMP) – Pitman Schedule (12:00 AM–10:00 AM)
Bedford, MA
$64K - $79K (Employer provided)
Respond to emergency service calls and resolve identified issues in a timely manner and in accordance with all safety, quality and compliance requirements.…
30d+
Ultragenyx
3.4
Executive Director, CMC QA
South San Francisco, CA
$294K - $363K (Employer provided)
Strong quality risk management capability and proficiency with root cause analysis, risk assessment, trend analysis, and decision-making tools.…
18d
Smart Sand
3.3
Maintenance Tech I
Taylor, WI
$26.00 - $30.00 Per Hour (Employer provided)
Easy Apply
Perform regular preventive maintenance on machines, equipment, and plant facilities using mechanical, electrical, welding, hydraulic, and pneumatic skills.…
30d+
Chick-fil-A Supply
4.0
Fleet Maintenance Technician Class B
United States
$80K - $90K (Employer provided)
Use hand tools such as screwdrivers, pliers, wrenches, pressure gauges, and precision instruments, as well as power tools such as pneumatic wrenches, lathes,……
30d+
Amberwell Health
3.3
Surgical Technician
Hiawatha, KS
$49K - $64K (Glassdoor est.)
Certificates, License, Registrations: Surgical technician certification, preferred. Ensures that management of the Central Sterilization/OR/PAR Department is in……
30d+
Forge
3.5
Licensed Electrician
Auburndale, MA
$35.00 - $50.00 Per Hour (Employer provided)
Valid driver's license required. Active Massachusetts Journeyman Electrician license required. Substantial hands-on experience in electrical work specific to……
10d
The Wine Group
3.2
Enologist - Ripon
Ripon, CA
$70K - $81K (Employer provided)
Assist Winemaking to work up process orders and approve prior to giving to compliance tracker for data entry. Direct lab analysis based on wine needs.…
17d
OSS Health
3.7
Certified Central Sterile Tech - PRN
York, PA
$35K - $45K (Glassdoor est.)
CBSPD or CRCST certification required, or pass within the first 18 months of employment. Responsible for pulling case carts for OR cases per schedule, utilizing……
21d
East Coast Appliance
2.9
Appliance Tech
Richmond, VA
$41K - $55K (Glassdoor est.)
We service all appliance sold at East Coast Appliance ,all major Brands warranty and cash calls, so we are very busy all year round.…
30d+
Lowell General Hospital
3.7
CT Technologist II
Lowell, MA
$42.00 - $51.67 Per Hour (Employer provided)
Radiologic Technologist state license eligible. An experienced level role requiring basic knowledge of job procedures and tools obtained through work experience……
30d+
CHRISTUS Health
3.6
Computed Tomography (CT) Tech - CAT Scan (Up to $10K Sign-on)
Corpus Christi, TX
Easy Apply
Performs examinations/procedures as needed to assist in patient throughput within the scope of the Manager’s license(s), certification(s), and/or documented……
30d+
Critical Process Systems
3.8
Welder - 2nd Shift "Sign-On-Bonus"
Colchester, VT
$26.00 - $34.00 Per Hour (Employer provided)
Easy Apply
Able to read and understand cut sheets and engineering prints thoroughly. Set up the work area, select and verify the material for production, and meet the……
30d+
Penske Truck Leasing
3.3
Diesel Technician Mechanic II
Rochester, NY
$29.50 Per Hour (Employer provided)
Valid driver’s license required. Experienced using tools of the trade (including diagnostic equipment, hand tools, and power tools).…
7d
Koch Trucking
3.7
Diesel Tech II Sun-Wed 7AM to 5:30PM + $7,500 sign on bonus!
Minneapolis, MN
$30.00 - $47.00 Per Hour (Employer provided)
Easy Apply
Reading and interpreting manuals, schematics, blueprints, and technical drawings. Associates degree in Heavy Duty Truck Technology or related field.…
17d
Washington Energy Services
3.8
HVAC Service Manager
Fife, WA
$100K - $125K (Employer provided)
Easy Apply
The Service Manager will conduct site visits, provide real time coaching, training, and mentorship to field technicians, support technical troubleshooting in……
30d+
West 66 Truck & Trailer Repair
SEMI TRUCK MECHANIC / ELECTRICAL SPECIALIST
Joliet, IL
$30.00 - $40.00 Per Hour (Employer provided)
Easy Apply
Perform mechanical repairs and maintenance when electrical work is not available. We need someone who knows how to properly diagnose electrical problems,……
2d
MASOUD KHORSAND-SAHBAIE, M.D.
2.9
Multi-Modality Tec (Radiology, CT, MRI, and/or Nuc Med)
Roswell, NM
$42K - $72K (Glassdoor est.)
Easy Apply
Responsible for explaining imaging procedures to patients and answering any questions. Advanced technical computer skills as required for technical support of……
30d+
Strada Electric
3.0
AC Maintenance Technician
Arden, NC
$44K - $65K (Glassdoor est.)
Degree or Trades School certification in related field preferred. Must have clean driving record. Diagnose malfunctioning systems, apparatus, and components,……
30d+
Scott HR
Senior Civil Engineer Department Manager
Kansas City, MO
$76K - $116K (Glassdoor est.)
Easy Apply
O Work with a multi-discipline team of engineers and technicians in the design of municipal water distribution and sewer collection system pipeline design as……
3d
Bavarian Rennsport
Mercedes Master Technician with Experience On Other Brands (Min. 10 Years Exp)
Jacksonville, FL
$100K - $200K (Employer provided)
Easy Apply
Have a valid and current driver’s license. We provide most Manufacture specialty tools, scan tools and licensed factory diagnostic software.…
7d
Ellis Medicine
3.2
Electrophysiology Technician- CVT
Schenectady, NY
$31.50 - $47.26 Per Hour (Employer provided)
Easy Apply
Accredited certification or be eligible for certification. Should be able to push/pull, lift/move 35 lb., be able to perform moderately difficult manual……
30d+
Critical Process Systems
3.8
Quality Technician 2nd Shift (3:30PM-2:00AM)
Colchester, VT
$20.00 - $24.00 Per Hour (Employer provided)
Easy Apply
High school diploma or equivalent; an associate degree or vocational training in Quality Assurance, Engineering, or a related field is preferred.…
28d
Critical Process Systems
3.8
Blaster Lead- 2nd Shift (3:30pm-2:00am)
Colchester, VT
$57K - $81K (Glassdoor est.)
Easy Apply
Direct supervision of front-line production staff in the assigned production area; work collaboratively with other production supervisors and team-leads on key……
30d+
Hometown Garage
Experienced Auto Tech – Family Owned Shop Over 25 Years (Up to $105k / Weekends Free / 401k Match)
Burlington, MA
$50K - $110K (Employer provided)
Easy Apply
✓ *WE INVEST IN YOU (PAID TRAINING + ASE REIMBURSEMENT)* – We reimburse ASE certification costs and invest in ongoing paid training.…
7d
Vector Surgical
Inside Sales Specialist - Clinical Experience Required (HT, Pathologists' Assistant, Lab Tech)
Menomonee Falls, WI
$67K - $103K (Glassdoor est.)
Easy Apply
Advanced degree or certification in clinical area. Contribute to sales and marketing strategy based on his or her clinical experience.…
30d+
MASOUD KHORSAND-SAHBAIE, M.D.
2.9
Nuclear Med Tech or Nuclear-Med/Multi-Modality Tech
Roswell, NM
Easy Apply
Responsible for explaining imaging procedures to patients and answering any questions. Advanced technical computer skills as required for technical support of……
30d+
Kokosing
4.0
Experienced Electrical Tech - 2nd Shift
Columbus, OH
$45K - $63K (Glassdoor est.)
Easy Apply
Must have a valid driver's license. Electromechanical starters, solid state, VFDs. Install, maintain, and repair all electrical items in our surface limestone……
30d+
Iowa Select Farms
3.1
Maintenance Technician I - N.IA
Riceville, IA
$25.50 Per Hour (Employer provided)
Training farm maintenance staff on proper repair techniques, safety practices, and preventative maintenance. Coordinate and support larger repair needs such as……
4d
East Coast Appliance
2.9
Appliance Tech
Norfolk, VA
$39K - $53K (Glassdoor est.)
We service all appliance sold at East Coast Appliance ,all major Brands warranty and cash calls, so we are very busy all year round.…
30d+

Ultragenyx

3.4

Executive Director, CMC QA

Novato, CA

$294K - $363K (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:

ultraimpact – Make a difference for those who need it most

The Executive Director, CMC QA will provide strategic, operational, and technical quality leadership across all Ultragenyx programs inclusive of biologics, small molecule, gene therapy, and ASO. This leader will oversee CMC QA responsibilities spanning program QA and CMO QA for starting materials, drug substance, and drug product, ensuring phase-appropriate and commercially robust quality oversight from development through lifecycle management. The role will lead and develop a team of approximately 8–12 quality professionals, partner closely with Technical Operations, Product Development, Supply Chain, Regulatory, and Quality stakeholders, and represent CMC QA in governance forums, inspections, regulatory submissions, and external partner interactions.

Work Model:

Flex: This role will typically require onsite work 2-3 days each week, or more depending on business needs. In many locations, the business will set certain days each week that Flex employees are required to be onsite.

Responsibilities:

Set and execute the CMC QA vision, strategy, operating model, and priorities for External Operations across all Ultragenyx programs and modalities, including starting materials, drug substance, and drug product.

Lead, coach, and develop a high-performing team of approximately 8–12 staff members responsible for program QA and CMO QA oversight; establish clear accountabilities, resource plans, succession plans, and performance expectations.

Ensure external partners operate in compliance with FDA, EMA, ICH, and other applicable global regulatory requirements, Ultragenyx Quality standards, approved regulatory filings, quality agreements, and industry best practices.

Drive proactive, risk-based oversight of external manufacturing quality systems, including deviations, investigations, CAPAs, change controls, complaints, product impact assessments, APR/PQR/APQR, CPV, validation, and tech transfer activities.

Own or oversee quality risk management strategies for external operations, including risk profiles, risk controls, escalation pathways, quality metrics, scorecards, trend reviews, and continuous improvement plans for CMOs and critical suppliers.

Ensure robust CMO and supplier qualification, selection, onboarding, ongoing monitoring, and lifecycle governance in partnership with Technical Operations, Supply Chain, Regulatory, Inspection Management, and Quality Systems.

Lead and/or support health authority inspection readiness, pre-approval inspection readiness, CMO inspection support, due diligence assessments, and responses to inspection observations associated with CMC and external operations.

Provide Quality leadership for regulatory submissions and post-approval commitments, including review of relevant CMC sections for INDs, BLAs, MAAs, amendments, supplements, annual reports, and responses to health authority questions.

Develop, implement, and continuously improve CMC QA policies, SOPs, standards, governance processes, and scalable quality infrastructure to support rare and ultrarare disease product development, commercial supply, and portfolio growth.

Model and reinforce a culture of quality, accountability, collaboration, continuous improvement, and patient focus across internal teams and external partners.

Perform other duties as assigned.

Requirements:

Bachelor's degree in life sciences, engineering, pharmacy, chemistry, biotechnology, or a related discipline; advanced degree (MS, PharmD, PhD, or equivalent) preferred.

Typically 15+ years of progressive experience in pharmaceutical, biotechnology, biologics, gene therapy, small molecule, or related regulated industry, with significant experience in CMC Quality Assurance and external manufacturing oversight.

Typically 10+ years of leadership experience within a Quality organization in a FDA/EMA-regulated environment, including experience leading leaders or senior professionals and managing departmental priorities, budgets, and resources.

Demonstrated experience providing quality oversight for CMOs/CDMOs, critical suppliers, and/or outsourced GMP operations across clinical, launch, and commercial lifecycle stages.

Expert knowledge of global GMP requirements and expectations, including FDA, EMA, ICH Q7/Q8/Q9/Q10/Q11/Q12 as applicable, and experience with other regulatory authorities such as MHRA, PMDA, Health Canada, ANVISA, and/or other global agencies.

Strong technical understanding of CMC development and manufacturing across multiple modalities such as biologics, small molecules, oligonucleotides, gene therapy, mRNA, enzymes/proteins, or other advanced/novel therapeutics; direct experience with starting materials, drug substance, and drug product preferred.

Proven ability to lead CMC QA strategy for rapid development, rare disease, ultrarare disease, registration, launch readiness, and commercial operations in a matrixed and/or highly outsourced operating model.

Demonstrated expertise in quality agreements, supplier qualification, deviation/investigation approval, CAPA effectiveness, change control, validation, technology transfer, APQR/PQR, CPV, and quality metrics.

Experience supporting health authority inspections, PAI readiness, regulatory filings, responses to health authority questions, and inspection observation remediation.

Strong quality risk management capability and proficiency with root cause analysis, risk assessment, trend analysis, and decision-making tools.

Executive-level communication, influencing, negotiation, and stakeholder-management skills, with the ability to align senior leaders and external partners around pragmatic, compliant, patient-focused solutions.

Demonstrated ability to build, lead, engage, and develop high-performing teams through ambiguity, growth, and organizational change.

Experience with Veeva or other electronic Quality Management Systems preferred; proficiency with Microsoft Word, Excel, PowerPoint, Teams, and Project or equivalent tools required.

Ability to travel up to approximately 20–30% domestically and internationally to Ultragenyx sites, CMOs/CDMOs, suppliers, and regulatory or inspection-related activities, as business needs require.

Physical Demand Requirements:

Primarily office-based role using a computer, phone, and virtual collaboration tools for extended periods.

Ability to work in a hybrid environment and travel to Ultragenyx sites, external manufacturing partners, contract laboratories, supplier sites, and other business locations as needed.

Occasional entry into GMP manufacturing, warehouse, laboratory, or controlled environments may require use of personal protective equipment and adherence to site-specific gowning, safety, and access requirements.
Ability to sit or stand for extended periods and participate in meetings, inspections, walkthroughs, and partner visits.

#LI-KJ1 #LI-Hybrid

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 $294K and the max salary is $363K.

$294K – $363K/yr (Employer provided)

$329K

/yr Median

Novato, CA

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

Executive Director, CMC QA

Novato, CA

$294K - $363K (Employer provided)

Ultragenyx

3.4

Executive Director, CMC QA

Novato, CA

$294K - $363K (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:

ultraimpact – Make a difference for those who need it most

Work Model:

Responsibilities:

Set and execute the CMC QA vision, strategy, operating model, and priorities for External Operations across all Ultragenyx programs and modalities, including starting materials, drug substance, and drug product.

Lead, coach, and develop a high-performing team of approximately 8–12 staff members responsible for program QA and CMO QA oversight; establish clear accountabilities, resource plans, succession plans, and performance expectations.

Ensure external partners operate in compliance with FDA, EMA, ICH, and other applicable global regulatory requirements, Ultragenyx Quality standards, approved regulatory filings, quality agreements, and industry best practices.

Drive proactive, risk-based oversight of external manufacturing quality systems, including deviations, investigations, CAPAs, change controls, complaints, product impact assessments, APR/PQR/APQR, CPV, validation, and tech transfer activities.

Own or oversee quality risk management strategies for external operations, including risk profiles, risk controls, escalation pathways, quality metrics, scorecards, trend reviews, and continuous improvement plans for CMOs and critical suppliers.

Ensure robust CMO and supplier qualification, selection, onboarding, ongoing monitoring, and lifecycle governance in partnership with Technical Operations, Supply Chain, Regulatory, Inspection Management, and Quality Systems.

Lead and/or support health authority inspection readiness, pre-approval inspection readiness, CMO inspection support, due diligence assessments, and responses to inspection observations associated with CMC and external operations.

Provide Quality leadership for regulatory submissions and post-approval commitments, including review of relevant CMC sections for INDs, BLAs, MAAs, amendments, supplements, annual reports, and responses to health authority questions.

Develop, implement, and continuously improve CMC QA policies, SOPs, standards, governance processes, and scalable quality infrastructure to support rare and ultrarare disease product development, commercial supply, and portfolio growth.

Model and reinforce a culture of quality, accountability, collaboration, continuous improvement, and patient focus across internal teams and external partners.

Perform other duties as assigned.

Requirements:

Bachelor's degree in life sciences, engineering, pharmacy, chemistry, biotechnology, or a related discipline; advanced degree (MS, PharmD, PhD, or equivalent) preferred.

Typically 15+ years of progressive experience in pharmaceutical, biotechnology, biologics, gene therapy, small molecule, or related regulated industry, with significant experience in CMC Quality Assurance and external manufacturing oversight.

Typically 10+ years of leadership experience within a Quality organization in a FDA/EMA-regulated environment, including experience leading leaders or senior professionals and managing departmental priorities, budgets, and resources.

Demonstrated experience providing quality oversight for CMOs/CDMOs, critical suppliers, and/or outsourced GMP operations across clinical, launch, and commercial lifecycle stages.

Expert knowledge of global GMP requirements and expectations, including FDA, EMA, ICH Q7/Q8/Q9/Q10/Q11/Q12 as applicable, and experience with other regulatory authorities such as MHRA, PMDA, Health Canada, ANVISA, and/or other global agencies.

Strong technical understanding of CMC development and manufacturing across multiple modalities such as biologics, small molecules, oligonucleotides, gene therapy, mRNA, enzymes/proteins, or other advanced/novel therapeutics; direct experience with starting materials, drug substance, and drug product preferred.

Proven ability to lead CMC QA strategy for rapid development, rare disease, ultrarare disease, registration, launch readiness, and commercial operations in a matrixed and/or highly outsourced operating model.

Demonstrated expertise in quality agreements, supplier qualification, deviation/investigation approval, CAPA effectiveness, change control, validation, technology transfer, APQR/PQR, CPV, and quality metrics.

Experience supporting health authority inspections, PAI readiness, regulatory filings, responses to health authority questions, and inspection observation remediation.

Strong quality risk management capability and proficiency with root cause analysis, risk assessment, trend analysis, and decision-making tools.

Executive-level communication, influencing, negotiation, and stakeholder-management skills, with the ability to align senior leaders and external partners around pragmatic, compliant, patient-focused solutions.

Demonstrated ability to build, lead, engage, and develop high-performing teams through ambiguity, growth, and organizational change.

Experience with Veeva or other electronic Quality Management Systems preferred; proficiency with Microsoft Word, Excel, PowerPoint, Teams, and Project or equivalent tools required.

Ability to travel up to approximately 20–30% domestically and internationally to Ultragenyx sites, CMOs/CDMOs, suppliers, and regulatory or inspection-related activities, as business needs require.

Physical Demand Requirements:

Primarily office-based role using a computer, phone, and virtual collaboration tools for extended periods.

Ability to work in a hybrid environment and travel to Ultragenyx sites, external manufacturing partners, contract laboratories, supplier sites, and other business locations as needed.

Occasional entry into GMP manufacturing, warehouse, laboratory, or controlled environments may require use of personal protective equipment and adherence to site-specific gowning, safety, and access requirements.
Ability to sit or stand for extended periods and participate in meetings, inspections, walkthroughs, and partner visits.

#LI-KJ1 #LI-Hybrid

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 $294K and the max salary is $363K.

$294K – $363K/yr (Employer provided)

$329K

/yr Median

Novato, CA

Working here doesn’t have to be a secret

3.4

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

109,586 Area tech jobs in United States

Position Summary:

Work Model:

Responsibilities:

Requirements:

Physical Demand Requirements:

Base pay range

Working here doesn’t have to be a secret

Position Summary:

Work Model:

Responsibilities:

Requirements:

Physical Demand Requirements:

Base pay range

Working here doesn’t have to be a secret