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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! 

Summary: 

The North Creek Manufacturing Facility at Seagen is seeking a highly motivated Manufacturing Associate II that desires the opportunity to significantly contribute to the development and commercialization of transformative cancer therapies. The Manufacturing Associate will use their training and knowledge of biopharmaceutical manufacturing to execute operations in a cGMP Facility. 

Principal Responsibilities: 

  • Utilize standard operating procedures and documents cGMP activities within batch records and logbooks applying good cGMP documentation and data integrity practices 
  • Complete setup, use, and cleaning (as necessary) of cGMP production equipment 
  • Proactively works with senior associates, subject matter experts, and management to achieve training competency in production operations 
  • Maintains a clean and orderly production area. Positively engages and collaborates with other team members to ensure daily production tasks are completed promptly 
  • Ensure work executed in compliance with company and regulatory quality policy and systems 
  • Participates and supports a culture of continuous improvement. Effectively collaborates with cross functional partners such as Quality Assurance, Quality Control, Supply Chain, and Facilities 

Job Duties May include: 

  • Media and buffer compounding, assembly and movement of materials and equipment into staving and production areas, wipe-down and sanitization of equipment/materials prior to and post-transfer, preparation and sterilization of parts and assemblies (including manual wash, equipment wash, and autoclave), stocking of materials, gowning, and supplies, and ensuring cleanliness and audit -readiness of the GMP Manufacturing areas 
  • Performs cell culture operations safely and compliantly in accordance with OSHA and cGMP guidelines. Cell Culture operations include but are not limited to; dispensing and sampling of raw materials, media preparation, small scall passaging, set-up and operation of single use bioreactor, product sampling, and depth filtration harvest set-up and operations 
  • Performs Downstream and Conjugation operations safely and compliantly with OSHA and cGMP guidelines. Operations include but are not limited to, dispensing and sampling of raw materials, buffer preparation, column packing, UF/DF, chromatography, viral inactivation and filtration, product sampling, and formulation of bulk drug substance and intermediate 
  • Performs oversight of process operations and monitors equipment and critical process parameters. Escalates any issues or abnormalities to management. Participates in troubleshooting activities as necessary 
  • Creates and revises SOPs (standard operating procedures) and MBRs (master batch records) as appropriate 

Expected Qualifications: 

  • Bachelor’s degree, preferably in Life Sciences or Engineering, or Associate degree, preferably in Life Sciences or a technical program, or High School Diploma with Biotech certificate from an approved program desirable 
  • Required 2+ years related experience 
  • Must be able to work off-shifts, and overtime as required. Applicant must be willing and able to work reliably on a flexible schedule, some off shift work, to meet the project's demands 
  • Assigned shift will depend on the group to which the Manufacturing Associate is assigned 
  • Must be able to don gowning in the form of hospital scrub, gloves, safety glasses/goggles, head and beard covers, coveralls and safety toe footwear with shoe covers multiple times per shift 
  • Ability to handle and work with hazardous materials and chemicals per standard operating procedures and OSHA guidelines 
  • Good organizational and communication skills, both written and verbal, and the ability to prioritize competing tasks 
  • Excellent interpersonal skills with the ability to work well with others in a dynamic and highly collaborative environment. Ability to interact constructively with peers and support groups 

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.  

The hiring pay range for this position is $69,000 - $89,100 per year based on skills, education and experience relevant to the role. Other components of total compensation include a competitive equity grant at the time of hire and an annual bonus. 

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.  

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