Job Description

Company Description
Zymeworks is a publicly listed (NASDAQ:ZYME) clinical-stage biopharmaceutical company dedicated to the discovery, development and commercialization of next-generation, biospecific and multifunctional biotherapeutics, initially focused on the treatment of cancer. Zymeworks\' suite of complementary therapeutic platforms and its fully-integrated drug development engine provide the flexibility and compatibility to precisely engineer and develop highly-differentiated product candidates.

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.

Zymeworks is proudly headquartered in our brand new, net-zero facility located in the vibrant Main St biotech hub of Vancouver, BC, with operations in Seattle, WA and Dublin, Ireland. We offer a hybrid work environment with most team members working in-office three days per week.

Key Responsibilities

• Manage the method development and phase-appropriate validation of methods at CDMOs for GMP biotherapeutic manufacturing.
• Serve as Analytical Team Lead (ATL) and Subject Matter Expert (SME) for analytical method development and biochemical characterization for all phases of process development from first-in-human to late-stage clinical and commercial filings.
• Collaborate productively within internal and external cross-functional teams (Research, Development, Clinical, Quality, Regulatory) and provide analytical expertise for biotherapeutics including ADCs.
• Author technical documents and deliver presentations to management, technical, and project groups.
• Contribute to the preparation and submission of CMC portions of regulatory submissions and updates (IND and BLA).
• Organize, maintain, and analyze internal archive of data and reports generated by CDMO partners.
• Ensures that all developed methods are compatible with quality requirements including regulations, policies, applicable guidelines, and procedures.
• Establish and maintain positive working relationships with peers, management, and external partners.

Education and Experience

• Ph.D. degree in biochemistry, analytical science, chemistry, or biophysics (or equivalent industry experience) and 2-5 years\' related experience in the pharmaceutical or biotechnology field.
• Experience with analytical chromatography, capillary electrophoresis, ELISA, cell-based bioassays, protein mass spectrometry, biophysical, and other analytical techniques is desired.
• Excellent oral and writing skills.
• Familiarity with regulatory guidelines for method qualification/validation and experience authoring regulatory sections for IND through BLA filings is preferred.
• The final job title (Scientist or Senior Scientist) will depend on the years of experience and the relevance of experience in the biopharmaceutical industry.

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 US base salary range for this full-time position is $116,000 - $178,000 + bonus + equity + benefits. Our salary ranges are determined by role, level, and location.

The range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position across all US locations. 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).

Please note that the compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits. This role is also eligible for a competitive benefits package that includes:

• Industry leading vacation and paid time off
• Excellent health and wellness benefits
• Zymelife health and wellness benefits
• Paid time off to volunteer in your community
• Matching RRSP / 401K program
• Employee Share Purchase Program
• Employee Equity Program

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

Date: Jul 9, 2023

Zymeworks