Site Quality Head, Carlsbad (Associate Director)

Job Posted 19 Days Ago Posted 19 Days Ago
Be an Early Applicant
Carlsbad, CA
139K-257K Annually
Senior level
Biotech • Pharmaceutical
The Role
Lead the Quality function for a new pharmaceutical site, ensuring quality assurance, compliance with regulations, and supporting site start-up and operations.
Summary Generated by Built In

Job Description Summary

At Advanced Accelerator Applications, a Novartis company, we are committed to leading innovation in nuclear medicine and delivering the next generation of targeted radioligand therapy (RLT) to cancer patients. We are looking for an experienced pharmaceutical industry professional with experience building teams in start-up environments to lead the Quality function at our new Carlsbad site.
As the Site Quality Head, you will provide quality assurance oversight and be accountable for supporting site start up and Quality operations at the Carlsbad site. You will provide technical and strategic leadership for the Manufacturing site for all quality-related matters and be part of the Site Senior Leadership Team.


 

Job Description

Key Responsibilities:

  • Support plant start up, expansions and product transfers. Create and maintain updated project plans to track progress, and support in informing senior management. Ensure proper preparation and consolidation of the budget for the Quality Unit.
  • Provide leadership for strategic site initiatives and represent site SLT quality in local cross-functional and global projects teams as team member or team leader that represent site quality. Establish Quality as a valued business partner.
  • Provide leadership, direction and support to the people within the Quality Assurance department and ensure that they are qualified, achieve a high level of competence, are motivated and carry out their duties in a safe manner.
  • Work with internal and external personnel to create user requirements and specifications to be used for projects in compliance with company standards for equipment, process and facilities.
  • Ensure all facilities, utilities and equipment are designed and installed to be operated in a safe and effective manner and are compliant with applicable standards
  • Ensure that during project phase planning, construction, commissioning, qualification (IQ, OQ and PQ) including any other validation activity complies with cGMP
  • Timely escalation of risks in meeting timelines and / or budget incorporating site master planning and the long-term strategic plan.
  • Ensure adequate management of product critical quality issues (deviations, out of specifications). Ensure investigations are correctly executed and adequate CAPAs are defined, and proper follow up of CAPAs effectiveness. Review, provide guidance for, escalate where appropriate, and approve Health Authority notifications.
  • Define, implement, monitor, consolidate and analyze Site Quality KPIs. Ensure Site Quality Committee is established, ensure relevant corrective and preventive actions are endorsed and implemented.
  • Drive for Site management team accountability. Coordinate the generation and monitor the execution of the Site Quality Plans, DI Plan, Site Quality Risk Assessments and other relevant gap assessments.

Essential Requirements:

  • BS in Life Sciences and/or related experience in lieu of degree. 10 years of experience in GMP Pharmaceutical Manufacturing (including laboratory operations and Aseptic experience), at least 3 years combined of relevant experience in Quality Control and/or Quality Assurance.
  • Proven track record and practical experience in supporting a Quality Control operations unit and operating in full compliance with global cGMP requirements. Successfully managed inspections from major Health Authorities (e.g. US FDA, EMA)
  • In-depth knowledge of cGMP, FDA regulations (21 CFR Parts 211, 212), and ICH regulations. Understanding of United States Pharmacopoeia (USP), European Pharmacopoeia (EP), American Chemical Society (ACS).
  • Proven ability to manage multiple projects with moderate resource requirements, risk and/or complexity. Highly developed management and communication skills, with experience in working in a matrix organization.
  • Experience in process improvement approaches (Lean Six Sigma, Total Quality Management, 5S, etc.)  Understands economic business impacts of decisions. Defining and implementing productivity improvement measures.

#LI-Onsite

Benefits and Rewards:  Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: novartis-life-handbook.pdf​.

The pay range for this position at commencement of employment is expected to be between $ 138,000 and $ 257,400  per year; however, while salary ranges are effective from 1/1/25 through 12/31/25 fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.


 

EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. 


 

Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.


 

Salary Range

$138,600.00 - $257,400.00


 

Skills Desired

Audit Management, Communication Skills, Continued Learning, Dealing With Ambiguity, Decision Making Skills, Employee Performance Evaluations, Gmp Procedures, Inspection Readiness, Organizational Skills, People Management, People Management and Leadership, Product Release, Qa (Quality Assurance), Self-Awareness, Technological Expertise

Top Skills

Cgmp
Fda Regulations
Lean Six Sigma
Total Quality Management
Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
HQ: Basel
110,000 Employees
Hybrid Workplace
Year Founded: 1996

What We Do

Novartis is an innovative medicines company. Every day, working to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide.

Similar Jobs

ZS Logo ZS

Strategy Insights & Planning Associate Consultant - Strategy/Business Advisory

Artificial Intelligence • Healthtech • Professional Services • Analytics • Consulting
Hybrid
3 Locations
13000 Employees
118K-134K Annually

ServiceNow Logo ServiceNow

Mgr, Systems Engrg Mgmt

Artificial Intelligence • Cloud • HR Tech • Information Technology • Productivity • Software • Automation
Hybrid
San Diego, CA, USA
26000 Employees
147K-258K Annually

Anduril Logo Anduril

Hazard Zone Deployment Lead

Aerospace • Artificial Intelligence • Hardware • Robotics • Security • Software • Defense
Irvine, CA, USA
4500 Employees
108K-162K Annually

Anduril Logo Anduril

Change Manager

Aerospace • Artificial Intelligence • Hardware • Robotics • Security • Software • Defense
Costa Mesa, CA, USA
4500 Employees
150K-225K Annually

Similar Companies Hiring

Takeda Thumbnail
Software • Pharmaceutical • Manufacturing • Healthtech • Biotech • Analytics
Cambridge, MA
50000 Employees
Novo Nordisk Thumbnail
Software • Pharmaceutical • Healthtech
Bagsværd, DK
69000 Employees
Cencora Thumbnail
Pharmaceutical • Logistics • Healthtech
Conshohocken, PA
46000 Employees
By clicking Apply you agree to share your profile information with the hiring company.

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account