Job Description

About Enlaza Therapeutics

Enlaza Therapeutics is a biotech company developing an innovative synthetic biology platform to create a disruptive new class of biologic therapeutics. We are dedicated to the development of these novel therapies to help patients suffering from cancer and other serious diseases.

Role Description:

We are seeking a highly motivated and skilled analytical development scientist to join our team at our site in San Diego. The successful candidate will leverage their expertise in a range of analytical techniques to support the characterization and development of protein- and antibody-based therapeutics in Enlaza’s covalent biologics platform. The scientist will be responsible for hands-on work to develop, optimize, and execute analytical methods for deployment to support discovery and pre-clinical research through early-stage manufacturing development. They will also provide technical support of analytical development and method transfer and qualification/validation, review of DS/DP release and stability data, and contribute to analytical content in regulatory communications.

Key Responsibilities:

· Independently design, develop, and optimize analytical methods for release, stability, and characterization of biologics, such as antibodies, ADCs, and bispecifics

· Perform routine physicochemical analytical testing to support biologics drug discovery research and early-stage process development, including HPLC (SEC, HIC, IEX), CE (icIEF, CE-SDS), physical testing (UV-Vis, pH, osmolality), and impurities (HCP)

· Analyze and interpret complex analytical data, identifying trends and correlations to inform project decisions and support process development

· Maintain detailed and accurate records in electronic laboratory notebooks, and author and review technical documents including protocols, reports, and method procedures

· Propose continuous improvement in analytical sciences in alignment with industry advances and trends

· Represent the analytical development function in cross-functional CMC and research project teams

· Contribute to oversight of external analytical development activities, including method development, analytical life cycle management, and stability programs

Requirements:

· Advanced degree in analytical chemistry, biochemistry, or closely related field, with 3+ years of industry experience in analytical development for protein-based biopharmaceutical products (equivalent combined education and experience will be considered for the role)

· Subject-matter expertise in analytical separation sciences and proven track record of successful method development and validation

· Demonstrated skill in hands-on operation of modern analytical instruments

· Strong understanding of protein chemistry and degradation pathways

· Comfort operating on a small, dynamic team and open to providing and receiving cross-training opportunities

· Excellent written communication skills

· Previous exposure or participation in authoring regulatory submission content

· Understanding of early-stage biopharmaceutical development manufacturing unit operations, manufacturing science and technology, and GxP quality control

· Previous experience with analytical support of process development, formulation, or drug product groups is preferred

Compensation:

In addition to a competitive compensation package with stock options, the company also offers a comprehensive benefits package for our employees and their families, which includes medical, dental, vision, and supplemental disability insurance.

Job Type:

Full-time

Annual Salary:

$130,000-150,000

Supplemental Pay Types:

Bonus pay

Benefits:

• 401(k)
• Dental insurance
• Employee assistance program
• Flexible schedule
• Flexible spending account
• Health insurance
• Life insurance
• Paid time off
• Parental leave
• Relocation assistance
• Retirement plan
• Vision insurance
• Year-end shutdown

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