TEMP Manufacturing Operations AssociateDendreon Pharmaceuticals, LLC
TEMP Manufacturing Operations Associate
US-CA-Seal Beach
Job ID: 2026-3232
# of Openings: 1
Category: Dendreon Manufacturing
Seal Beach
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.
Job Summary:
Manufacturing Operations Associates in our Commercial Manufacturing Division are the heart and soul of our organization as they are responsible for the manufacturing of Provenge (Sipuleucel-T) product in a clean room environment. Provenge is manufactured using the patients' blood, personalizing the treatment.
NOTE: This role requires on-site presence at our Seal Beach, CA location.
Responsibilities
- Works with other Manufacturing Operations Associates utilizing current good manufacturing practices (cGMPs) to aseptically manufacture commercial products using Standard Operating Procedures (SOPs).
- Ensures right-the-first-time performance of all process steps specific to the phase or stage of operation. Escalates processing and equipment issues as needed.
- Weighs, measures and checks raw materials to ensure batches manufactured contain proper ingredients and quantities.
- Rigorously adheres to SOPs and cGMP regulations to accurately complete paper and electronic records associated with commercial manufacturing.
- Reviews in-process cGMP documentation for completeness and accuracy.
- Unpacks and checks materials received against specifications, maintains records of materials used and rejects unsatisfactory items when necessary.
- Prepares products for final shipment and maintains records of products shipped.
- Examines, stocks, and distributes GMP and non-GMP materials to inventory and manufacturing lines.
- Helps drive the safety-first culture
- Applies job skills and company policies and procedures to complete a narrow range of tasks.
- Works on assignments that are simple in nature, escalates issues when required, and making routine recommendations.
- Normally receives general instructions on routine work, detailed instructions on non-routine and new assignments.
- Ability to be flexible and support all functions by readily responding to changing circumstances (i.e. shift changes) and business needs.
- Other duties as assigned
Qualifications
- High School Diploma
- Associates/Technical/BA/BS degree in Science.
- No prior industry experience required.
- Experience in medical device, pharma or biotech preferred.
- Must be able to read and understand quality documents.
- Must be able to read, write and communicate fluently in English
Equal employment opportunity, including veterans and individuals with disabilities.
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