×
Register Here to Apply for Jobs or Post Jobs. X

Senior Director​/Vice President, Site Operations

Job in Seal Beach, Orange County, California, 90740, USA
Listing for: Dendreon
Full Time position
Listed on 2026-01-30
Job specializations:
  • Business
    Operations Manager
Job Description & How to Apply Below

Overview

Who We Are
:
At Dendreon, we’re transforming the battle against cancer with personalized immunotherapy. Our flagship product,
PROVENGE® (sipuleucel-T), was the first FDA-approved immunotherapy for metastatic castrate-resistant prostate cancer, utilizing a patient’s own immune cells to fight the disease.

If you’re driven by the opportunity to make a meaningful impact on cancer patients' lives, we invite you to join our team. With Immunotherapy Manufacturing Facilities in Seal Beach, CA, and Union City, GA, a strong Research & Development group in Seattle, WA, and a highly skilled Commercial team across the nation, Dendreon is at the forefront of cancer treatment innovation.

Core Values

  • Put Patients First:
    Every day is an opportunity to improve the lives of those living with cancer.
  • Act with Integrity:
    We commit to transparency, honesty, and always doing what’s right.
  • Build Trust:
    Trust is earned through candid, open communication and a collaborative approach.
  • Raise the Bar:
    We embrace continuous improvement and innovation, always striving to elevate our people.
  • Drive Results:
    We are accountable to each other and deliver success together.
Your Role

The Senior Director or Vice President of Site Operations is responsible for leading PROVENGE manufacturing at Dendreon’s commercial immunotherapy facilities. This strategic role provides oversight and direction across U.S. site operations to ensure alignment with product and project objectives, while working collaboratively with the Operations Leadership Team to meet production goals, uphold quality standards, and enhance overall business performance. The position defines and drives the strategic and operational direction of manufacturing and support functions, including planning, implementation, and continuous improvement of processes.

The ideal candidate is a strong, influential leader capable of guiding directors and senior managers across multiple functional areas to deliver results and advance organizational goals.

Responsibilities
  • Ensures the relevant business processes, procedures, and resources are in place to compliantly, safely and effectively produce PROVENGE and other biotech products.
  • Represents technical operations at the Steering Committee level when interfacing with external clients.
  • Manages technical operations at Dendreon’s commercial IMFs (Seal Beach / Union City) and contract manufacturing facilities (CMFs), as appropriate.
  • Leads site EHS&S teams at each Dendreon facility to maintain Dendreon safety standards and align with corporate EHS&S programs.
  • Works collaboratively with cross-functional departments to ensure strict compliance with cGMP guidelines, understanding phase-appropriate requirements for clinical and commercial manufacturing.
  • Interfaces with external customers and FDA during audits and inspections.
  • Develops and achieves both enterprise-wide and site performance goals.
  • Leads metric reviews (manufacturing, safety, engineering, quality, materials, etc) across cross-functional site teams on a regular basis
  • Manages review and adherence to department and site budgets, including COGS
  • Leads and facilitates the planning and execution of a broad range of technical programs and projects as assigned (e.g. Corporate EHS&S, PMO, corporate initiatives, etc).
  • Provides leadership that enhances Dendreon’s culture.
  • Able to coach, develop and retain talent across all levels.
  • Proactively builds cross functional relationships – Apheresis Operations, Technical Operations, Supply Chain, Research and Manufacturing Sciences, Regulatory, etc.
  • Other duties as assigned.
Scope
  • Leads or participates with cross-functional and cross-site teams in the development and implementation of policies, procedures and practices associated with all aspects of an FDA licensed drug product.
  • Avoids erroneous decisions that could have a longer-term effect on the company’s success.
  • Working knowledge of cGMP’s, quality systems, aseptic processing and the numerous EHS&S regulations (e.g., EPA and OSHA)
  • Able to assess IMF capabilities and capacities and develop plans to solve problems / improve performance.
  • Provides leadership, directs and controls the activities of multiple functional…
Position Requirements
10+ Years work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary