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Associate Director, Downstream Process Development

Zymeworks

Bellevue, WA

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JOB DETAILS
SKILLS
Analysis Skills, Antibodies, Autoimmune Disease, Biotech and Pharmaceutical, CMOS, Cancer, Change Control, Clinical Support, Clinical Trial Management, Communication Skills, Continuous Improvement, Contract Manufacturing, Contract Research Organization (CRO), Cross-Functional, Current Good Manufacturing Practice (cGMP), Disease, Drug Development, GMP (Good Manufacturing Practices), Healthcare Quality, ICH Regulations, Interpersonal Skills, Manufacturing, Manufacturing Operations, Manufacturing/Industrial Processes, Multivariate Analysis, Operations Management, Organizational Skills, Pre-Clinical, Presentation/Verbal Skills, Process Development, Process Management, Process Manufacturing, Process Validation, Proposal Development, Quality Assurance, Quality Management, Regulations, Regulatory Compliance, Regulatory Requirements, Regulatory Submissions, Sales Pipeline, Standard Operating Procedures (SOP), Standards of Care, Statement of Work (SOW), Strategic Planning, Team Player, Technical Delivery, Technical Operations, Technical Presentation, Technical Support, Technical Writing, Time Management, Toxicology
LOCATION
Bellevue, WA
POSTED
4 days ago
Company Description
Zymeworks is a publicly listed (NASDAQ:ZYME) clinical-stage biotechnology company developing a diverse pipeline of novel, multifunctional biotherapeutics to improve the standard of care for difficult-to-treat diseases, including cancer, inflammation, and autoimmune disease. Zymeworks' suite of complementary therapeutic platforms and its fully-integrated drug development engine provide the flexibility and compatibility to precisely engineer and develop antibody-based therapeutic candidates. We are a global company headquartered in Vancouver, BC, with operations in Bellevue, WA, Dublin, Ireland, and Singapore.

Why Work With Us

Nothing is more critical to our success than the quality of our team. The work we do is meaningful and impactful - we care about each other as well as the patients we serve. We offer challenging career opportunities, competitive benefits and an environment that recognizes and rewards performance.

This role will be located in Bellevue, WA and is hybrid with a minimum of 3 days per week onsite.

What You'll Do

  • Serves as a strategic manager for the company's downstream process development and production operations to drive program timelines.
  • Directs the strategic planning of downstream process development and manufacturing in support of all phases of clinical development including support of late clinical phase filings.
  • Collaborates within cross-functional teams (Research, Development, Clinical, Quality, Regulatory), to define and execute development strategies for novel biotherapeutics and ADCs.
  • Leads project-specific efforts in process development, scale-up, production and tech transfer of processes within and between CMOs.
  • Participates in the development of RFP's to solicit project specific bids from CMOs/CROs.
  • Develops SOWs defining work to be performed and provide subsequent oversight of experiments and activities conducted at the CMO/CRO.
  • Develops highly productive manufacturing processes in a timely manner for novel antibody, multispecific and ADC therapeutics. Brings issues to the attention of appropriate personnel as necessary.
  • Designs, manages and supports process characterization studies and develops control strategies for process validation.
  • Authors technical documents and deliver presentations to technical and project groups.
  • Contributes to the preparation and submission of CMC portions of regulatory submissions and updates (IND and BLA).
  • Works directly with Analytic Sciences, Manufacturing Sciences and Technology and Quality teams to plan and implement execution of downstream process development and manufacturing operations.
  • Ensures that all developed processes are compatible with quality requirements including regulations, policies, applicable guidelines and procedures.
  • Serves as primary point of contact with contract manufacturing organizations (CMOs) and performs person-in-plant duties as needed to provide technical support for ongoing manufacturing.
  • Provides technical support for all CMC activities, including investigations, CAPAs, Change Controls, technology transfers, operation and lifecycle management of pre-clinical and cGMP manufacturing processes, ensuring all product delivery schedules are met.
  • Authors and reviews technical CMC documentation, including protocols, technical reports, manufacturing batch records, SOPs, change controls and deviations.
  • Drives timely decisions and facilitates active communication and information flow between CMOs and Zymeworks team members.
  • Fosters strong, long-lasting cross-functional working relationships with internal and external CMC, Quality Assurance, Project Management, Clinical Operations, and external manufacturing entities to ensure successful development and manufacture of all products.
  • Promotes a culture of continuous improvement in product quality and productivity.
  • Works closely with all internal and external resources to ensure DS supply availability.
What You'll Bring
  • University degree in science or engineering and a minimum of 8 years related experience in biopharmaceutical process development and GMP operations or an equivalent combination of education and experience.
  • Experience working with contract manufacturing organizations.
  • Proven interpersonal skills with the ability to work collaboratively as a member of a cross-functional team. Ability to establish and maintain effective working relationships.
  • Excellent organizational skills and the ability to work effectively in a high paced, fast changing environment.
  • Consistent analytical reasoning ability.
  • Familiarity with QbD and Control Strategy Development or multivariate analysis and DoE approaches to process development a plus.
  • Strong background in the regulatory compliance requirements for the cGMP production of biologicals for clinical and commercial use.
  • Working knowledge of regulatory guidelines and expertise in CMC, PK or toxicology for the advancement of therapeutics through different phases of development.
  • Proficiency with cGMP and ICH guidelines.
Total Rewards

We offer a comprehensive total rewards package, which includes competitive salaries, generous benefits, an outstanding work environment, and excellent opportunities for professional growth. We regularly benchmark our compensation against leading biotechnology companies in our geographies.

The base salary range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position in the location for which the job is posted and does not include bonus, equity, or benefits. Within the range, individual pay is determined by a variety of factors and the salary offered may vary depending on the successful candidate's location and qualifications (including, but not limited to, job-related knowledge, education, training, skills, and experience).

Our total rewards package that includes:
  • Industry leading vacation and paid time off
  • Exceptional medical, dental and vision benefits by country
  • Zymelife health and wellness benefits
  • Matching RRSP / 401K / Pension program
  • Employee Share Purchase Program
  • Employee Equity Program
  • Paid time off to volunteer in your community


This role is not eligible for relocation or immigration support.

All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin or disability.

NOTE TO AGENCIES: Zymeworks values our relationships with our recruiting partners. We only accept resumes from those partners who have been contracted with us. Zymeworks is not responsible for any fees related to resumes that are unsolicited or are received without contract.

The pay range for this role is:

146,250 - 224,250 USD per year (US)

About the Company

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Zymeworks

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