Skip over navigation
Banner
Directory
Directory Search
Jobs
Job Search Post a Job
Patient
Patient Resources Drug Development
History
Genealogy
Toons & Teasers
About
 Advertising
 Home
Quick Links
 Directory
 Job Search
 Toons & Teasers
 Advertising
 
Advertising
 

EquipNet Auction: Lab & Analytical Instruments from Leading Biotech & Pharma Companies - May 24

Check Out Our New Cartoon Celebrating Asian American & Pacific Islander History Month


Seagen

Associate Director Head of Quality Control - Project Launch Pad

Technical Operations & Process Sciences - Bothell, Washington

Description

Seagen is a global, multi-product biotechnology company dedicated to developing and commercializing transformative cancer medicines. As the industry leader in antibody-drug conjugate (ADC) technology, we pioneered a new generation in the science of harnessing antibodies to deliver cell-killing agents directly to cancer cells. Seagen’s dedication to improving the lives of cancer patients goes beyond science, and we believe that every employee has a role in contributing to this mission. By working together with a shared dedication and diverse perspectives, we are able to reach our full potential and make a real difference in the world. Seagen is a fast-growing company and has an abundance of opportunities available for you to grow your career. Put your passion to work at Seagen and join us!

Position Summary:

The Launch Pad Site Quality Control Head is responsible for developing, implementing, and leading a diverse Quality Control organization from the ground up and throughout the various phases of design, construction, commissioning and qualification, and operationalization of our new greenfield manufacturing site (DS, DP, and Packaging) in Seattle.

The Launch Pad Site Quality Control Head oversees all in-process, release, facility monitoring, and microbiologic testing performed by the Launch Pad QC Laboratory. The QC Head sets the strategic direction for Launch Pad QC function, collaborate with Managers/Supervisors to ensure QC Analysts are trained, and set group goals that align with overall Global Quality objectives. The Launch Pad Site Quality Control Head works cross collaboratively with key stakeholders to understand the testing needs for commercial and clinical products. They ensure key training and testing metrics are within expectations. This position is also responsible for the inspection-ready state of all QC Laboratories and works closely with all appropriate subject matter experts to represent their area of expertise in regulatory inspections/partner audits. Launch Pad Site Quality Control Head is a permanent and active member of the Site Quality Leadership Team.

Principal Responsibilities:

  • Provide leadership, vision, and set strategic direction to the Launch Pad Quality Control Testing Group at the site.
  • Build strong relationships and trust with key stakeholders to understand the site strategy and anticipate future needs from QC to deliver on the strategy.
  • Collaborate with Managers and Supervisors to oversee day-to-day tasks, training, goal setting and career development for direct reports.
  • Make Quality decisions around complex issues associated with sub-function/area of expertise that may impact key program and/or inter-department processes.
  • Ensure Quality Control testing at Seagen is in compliance with corporate policies and procedures, and all federal and applicable international regulations.
  • Ensure in-process, release, facility and microbiologic samples are scheduled appropriately and executed within expected timeframes.
  • Make sure the Quality Control Laboratories is always in an inspection-ready state and key subject matter experts are identified to represent key lab activities.
  • Oversee organization of the execution of test method transfers, qualifications, and validations.
  • Collaborate within individual QC teams, Global Quality and individual functions (i.e. development).
  • Develop, monitor and report on QC activities, establish KPI’s and provide updates to senior leadership.
  • Accountable for the QC part of the site Management Review, and for the APQR sections related to the commercial product manufactured and tested at the site
  • Define expense budget planning and project resourcing schedules.
  • Lead operational excellence activities such as LEAN initiatives across the QC labs to drive efficiencies and optimization of processes and performance.
  • Build a strong team including hiring a diverse QC workforce, workload management, coaching/mentoring, development, and performance management. Developing meaningful sets of Key Performance Indicators (KPI’s) to monitor progress with the various phases of development of the QC lab and site (e.g. from construction to registration)

Required Qualifications:

  • Associates degree in a relevant field with 2 years of experience or a bachelor’s degree in a relevant field
  • At least 16+ years of relevant experience leading analytical activities in a Pharmaceutical or Biotech industry in a GMP environment 5+ years’ experience in line managing people
  • Strong Quality Control mind-set with extensive knowledge and experience of cGMP’s
  • Ability to establish and manage multiple competing priorities and proceed with objectives with minimal supervision
  • Demonstrated ability to build effective and high performing teams
  • Highly collaborative with outstanding relationship building skills
  • Strong organizational skills, attention to detail and be able to effectively handle multiple projects or activities simultaneously
  • Adept at leading people, mentoring, and developing other leaders within the group
  • Excellent communication skills

Preferred Qualifications

  • Experience leading or participating in regulatory inspections
  • Green field experience and building up quality teams from the ground up
  • Hands on experience leading and implementing continuous improvement, operational excellence and six-sigma programs in a QC laboratory environment (e.g. LEAN Lab, Black/Green belt certification) would be an asset

As the leading employer in our industry in the Pacific Northwest, Seagen is proud to offer a competitive total compensation package as well as a comprehensive benefits program designed to support the whole lives of our employees and their families. Benefits include medical, vision and dental coverage, group and supplemental life insurance, 401(k) with company match, tuition reimbursement, relocation assistance and much more. To learn more about Seagen, please visit www.seagen.com.

Seagen is an equal opportunity employer. All qualified applications will receive consideration for employment without regard to race, age, gender identity, sexual orientation, color, religion, sex, marital status, national origin, protected veteran status, disability status, or any other status protected by federal, state, or local law. 

To prevent the spread of COVID-19, and as an integral part of its public health and safety measures, Seagen requires that all newly-hired employees be fully vaccinated against COVID-19 before commencing employment, subject to reasonable accommodation and other requirements of applicable federal, state, and local law.

Apply:


Seagen

Seagen is an Equal Opportunity Employer

Submitted: 11/19/2021

EquipNet Auction: Lab and Analytical Instruments from Leading Biotech and Pharmaceutical Companies - May 24 @ 9 am EST




















 
Email thie page to a friend. Email This Page
to a Friend
Print this page. Print This
Page
© 1997 - 2022 Info.Resource, Inc. All rights reserved.
Privacy Policy . Cookie Policy . Terms of Use . About . Advertising

OregonLifeScience.com, owned and published by Info.Resource, Inc., is a resource
for the life science industry in the state of Oregon.