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Director, Drug Product Development, Biologics
Evommune · Palo Alto, CA, United States · On Site · Active · $220,000–$260,000 / year · Rippling ATS
Job facts
| Field | Value |
|---|---|
| Company | Evommune |
| Title | Director, Drug Product Development, Biologics |
| Normalized title | - |
| Department / team | Technical Operations |
| Location | Palo Alto, CA, United States |
| Work model | On Site |
| Employment type | Full Time |
| Salary | $220,000–$260,000 / year |
| Status | active |
| ATS provider | Rippling ATS |
| Posted / first seen | 2026-06-05 / 2026-06-06 |
| Changed / last seen | 2026-06-06 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Evommune. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Rippling ATS. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Palo Alto. | Open |
| Department jobs | Active postings in Technical Operations. | Open |
| Work model jobs | Active On Site postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Evommune |
| Source | 5665251b-50f1-44d5-ac90-0fb9a1585cba |
| ATS provider | Rippling ATS |
Description
company
About Evommune, Inc.
Evommune, Inc. (NYSE: EVMN) is a clinical-stage biotechnology company focused on developing innovative therapies for immune-mediated inflammatory diseases. Headquartered in Palo Alto, California, with additional operations in New York, NY, Evommune is advancing a differentiated pipeline designed to address the underlying drivers of disease.
Our scientific approach integrates deep immunology expertise with disciplined clinical development to deliver potentially best-in-class therapies for patients with significant unmet medical need. For more information, visit www.Evommune.com .
Work Location: This hybrid position is currently expected to be in the office two days per week, with the option to work remotely up to three days per week. Occasional additional onsite presence may be required based on business needs or operational priorities.
Our Core Values
Before we dive into the specifics of the role, it's important to highlight the core values that are integral to being a member of the Evommune team. Our values are not just words; they shape our culture, guide our decision-making, and define what it means to be part of our team.
Together We Win: We champion teamwork, celebrating every achievement as a shared success. Guided by Insight: We make data-driven decisions, using our collective experience to shape the future of our business. Every Day Matters: We act with urgency to bring transformative therapies to patients by being nimble, decisive, and effective. Driven By Excellence: We set a high bar and hold ourselves accountable to deliver exceptional results in everything we do. Empowered To Act: We invest in our team and value transparency, fostering trust and a sense of ownership. We seek individuals who resonate with these principles, as they are essential for thriving in our collaborative, innovative, and dynamic work environment.
role
The Position
Evommune is seeking a Director, Drug Product Development to manage formulation, process, and delivery-device development for protein therapeutic programs in our clinical pipeline. The Director, Drug Product Development will be responsible for all aspects of biologics drug product development, including formulation optimization, manufacturing process oversight, and container closure system changes such as vials, prefilled syringes, and autoinjectors, as necessary during the product lifecycle. This individual will accomplish these activities through the management of external development labs and contract manufacturers. This individual must be able to make phase-appropriate development-related recommendations based on a thorough knowledge of formulation/device fundamental principles, cGMP requirements, and regulatory guidelines. In this role, the ability to operate effectively in a fast-moving, resource-disciplined biotech environment is essential for the successful candidate.
Key Responsibilities
Formulation, Process, and Device Development
Coordinate phase-appropriate drug product development activities for protein therapeutics, including formulation, process, container closure, and delivery-device considerations. Support development and implementation of delivery devices for clinical stage biologics, including prefilled syringes, autoinjectors, and other combination product presentations as applicable. Drive development of phase-appropriate drug product manufacturing processes, including fill-finish process development, scale-up, technology transfer, and manufacturing readiness. Support development/optimization of formulations that meet clinical and commercial needs, including stability, compatibility, and manufacturability considerations. Contribute to phase-appropriate control strategies, in partnership with CMC leadership, Analytical Development, Quality Assurance, and Regulatory. Identify drug product, formulation, device, and manufacturing risks and recommend practical mitigation options.
CDMO and Manufacturing Oversight
Participate in external vendor and CDMO screening and selection Ensure technical content/scope of contracts meets program needs Manage external development labs and CDMOs responsible for formulation development, fill-finish process development, scale-up, technology transfer, and GMP manufacturing activities. Provide technical oversight for drug product manufacturing activities, including person-in-plant support as needed. Coordinate with Quality Assurance to ensure cGMP compliance Review and approve key technical documents including batch records, development reports, protocols, stability reports, manufacturing records, deviations, investigations, and change controls. Identify and troubleshoot drug product manufacturing, formulation, device, vendor, and process-related issues in partnership with CDMOs and internal stakeholders.
Cross-Functional Collaboration
Partner cross-functionally with other process and analytical leads as well as QA, Regulatory, and project management to ensure execution of drug product deliverables as part of the larger program. Identify drug product and device risks and proactively develop mitigation plans Forecast drug product manufacturing needs to meet clinical milestones Author and review relevant CMC sections for amendments and briefing packages to support regulatory filings in all relevant territories
Budget & Timeline Management
Partner with other functional leads and project management to ensure drug product timelines are aligned with broader program timelines. Be able to provide scenarios for paths forward and an assessment of associated technical risk. Work with the Executive Director, CMC Biologics to ensure timely access to appropriate resources for drug product-related activities Support vendor planning, budget forecasting, and resource prioritization for drug product development, manufacturing, device, and clinical supply activities. Qualifications
Degree in Chemical Engineering, Biochemistry, Pharmaceutical Sciences, or related field. 8+ years of relevant industry experience with PhD, 10+ years with MS, or 12+ years with BS in biologics drug product development, formulation, process development, or CMC technical operations. Demonstrated experience in formulation development and drug product process development Experience with parenteral biologic drug products, including liquid and/or lyophilized formulations. Experience with fill-finish process development, technology transfer, GMP manufacturing, and CDMO oversight. Demonstrated experience in development and implementation delivery devices (PFS, autoinjectors, etc.) Demonstrated strong knowledge of FDA and ICH CMC requirements for biologics Experience with monoclonal antibodies and fusion proteins Strong technical judgment and ability to make phase-appropriate recommendations in a lean biotech environment. Compensation
The salary range for this position is $220,000-$260,000 and the position may be eligible for performance-based bonuses and/or equity-linked compensation. Salary ranges are determined by role, level and location and additional factors, including job-related skills, experience, and relevant education or training. We offer Company-sponsored benefits, which include comprehensive health, dental and vision plans, and pet insurance. In addition, we provide a 401(k) plan, ample time off programs, paid parental leave, life insurance, disability insurance and an employee referral bonus program.
Evommune is proud to be an equal opportunity employer and will consider all qualified applicants for employment.
Full job record
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| Org ID | 3db8c4fe-2cdb-4dd0-9ebb-2c0532003cdf |
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| Board ID | 5665251b-50f1-44d5-ac90-0fb9a1585cba |
| Provider | rippling |
| Provider Job Key | 0e32f433-32c8-44ac-8889-a4af5af739b4 |
| Title | Director, Drug Product Development, Biologics |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Palo Alto, CA, United States |
| Department | Technical Operations |
| Team | — |
| Employment Type | full_time |
| Workplace Type | on_site |
| Remote Policy | — |
| Country | United States |
| Region | CA |
| City | Palo Alto |
| Salary Raw | salary range for this position is $220,000-$260,000 and the position may be eligible for performance-based bonuses and/or equity-li |
| Salary Min | 220,000 |
| Salary Max | 260,000 |
| Salary Currency | USD |
| Salary Period | year |
| Source URL | https://ats.rippling.com/evommune/jobs/0e32f433-32c8-44ac-8889-a4af5af739b4 |
| Apply URL | https://ats.rippling.com/evommune/jobs/0e32f433-32c8-44ac-8889-a4af5af739b4 |
| First Seen At | 2026-06-06 08:43:53Z |
| Last Seen At | 2026-06-06 20:20:19Z |
| Last Checked At | 2026-06-06 20:20:19Z |
| Last Changed At | 2026-06-06 20:20:19Z |
| Inactive At | — |
| Source Posted At | 2026-06-05 00:43:08Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=rippling/board=evommune/date=2026-06-06/2026-06-06T20-20-19-270Z-781c9793b1dc50daa3e4ec9fc5ba6b87c600f7448b464a8d26d5ebb9265dc42d.json |
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"role": "<meta><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><b><strong style=\"color:rgb(54,80,124);font-size:18pt;white-space:pre-wrap;\">The Position</strong></b></p><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><span style=\"color:rgb(32,33,36);background-color:white;font-size:11pt;white-space:pre-wrap;\">Evommune is seeking a Director, Drug Product Development to manage formulation, process, and delivery-device development for protein therapeutic programs in our clinical pipeline. 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Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;\"><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Coordinate phase-appropriate drug product development activities for protein therapeutics, including formulation, process, container closure, and delivery-device considerations.</span></li><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Support development and implementation of delivery devices for clinical stage biologics, including prefilled syringes, autoinjectors, and other combination product presentations as applicable.</span></li><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Drive development of phase-appropriate drug product manufacturing processes, including fill-finish process development, scale-up, technology transfer, and manufacturing readiness.</span></li><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Support development/optimization of formulations that meet clinical and commercial needs, including stability, compatibility, and manufacturability considerations.</span></li><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Contribute to phase-appropriate control strategies, in partnership with CMC leadership, Analytical Development, Quality Assurance, and Regulatory.</span></li><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Identify drug product, formulation, device, and manufacturing risks and recommend practical mitigation options.</span></li></ul><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><br></p><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><b><strong style=\"color:rgb(32,33,36);background-color:white;font-size:11pt;white-space:pre-wrap;\">CDMO and Manufacturing Oversight</strong></b></p><ul data-pattern=\"discCircleSquare\" data-depth=\"1\" style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;\"><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Participate in external vendor and CDMO screening and selection</span></li><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Ensure technical content/scope of contracts meets program needs</span></li><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Manage external development labs and CDMOs responsible for formulation development, fill-finish process development, scale-up, technology transfer, and GMP manufacturing activities.</span></li><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Provide technical oversight for drug product manufacturing activities, including person-in-plant support as needed.</span></li><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Coordinate with Quality Assurance to ensure cGMP compliance</span></li><li style=\"--listitem-marker-color:#202124;--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"color:rgb(32,33,36);background-color:white;font-size:11pt;white-space:pre-wrap;\">Review and approve key technical documents including batch records, development reports, protocols, stability reports, manufacturing records, deviations, investigations, and change controls.</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Identify and troubleshoot drug product manufacturing, formulation, device, vendor, and process-related issues in partnership with CDMOs and internal stakeholders.</span></li></ul><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><span style=\"color:rgb(32,33,36);background-color:white;font-size:11pt;white-space:pre-wrap;\"> </span></p><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><b><strong style=\"color:rgb(32,33,36);background-color:white;font-size:11pt;white-space:pre-wrap;\">Cross-Functional Collaboration</strong></b></p><ul data-pattern=\"discCircleSquare\" data-depth=\"1\" style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;\"><li style=\"color:rgb(32,33,36);--listitem-marker-color:#202124;--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"color:rgb(32,33,36);background-color:white;font-size:11pt;white-space:pre-wrap;\">Partner cross-functionally with other process and analytical leads as well as QA, Regulatory, and project management to ensure execution of drug product deliverables as part of the larger program.</span></li><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Identify drug product and device risks and proactively develop mitigation plans</span></li><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Forecast drug product manufacturing needs to meet clinical milestones</span></li><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Author and review relevant CMC sections for amendments and briefing packages to support regulatory filings in all relevant territories</span></li></ul><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><span style=\"color:rgb(32,33,36);background-color:white;font-size:11pt;white-space:pre-wrap;\"> </span></p><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><b><strong style=\"color:rgb(32,33,36);background-color:white;font-size:11pt;white-space:pre-wrap;\">Budget & Timeline Management</strong></b></p><ul data-pattern=\"discCircleSquare\" data-depth=\"1\" style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;\"><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Partner with other functional leads and project management to ensure drug product timelines are aligned with broader program timelines.</span></li><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Be able to provide scenarios for paths forward and an assessment of associated technical risk.</span></li><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Work with the Executive Director, CMC Biologics to ensure timely access to appropriate resources for drug product-related activities</span></li><li style=\"color:rgb(32,33,36);--listitem-marker-background-color:white;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Support vendor planning, budget forecasting, and resource prioritization for drug product development, manufacturing, device, and clinical supply activities.</span></li></ul><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><b><strong style=\"color:rgb(54,80,124);font-size:18pt;white-space:pre-wrap;\">Qualifications</strong></b></p><ul data-pattern=\"discCircleSquare\" data-depth=\"1\" style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;\"><li style=\"color:rgb(32,33,36);font-size:12pt;--listitem-marker-background-color:white;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Degree in Chemical Engineering, Biochemistry, Pharmaceutical Sciences, or related field. 8+ years of relevant industry experience with PhD, 10+ years with MS, or 12+ years with BS in biologics drug product development, formulation, process development, or CMC technical operations.</span></li><li style=\"color:rgb(32,33,36);font-size:12pt;--listitem-marker-background-color:white;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Demonstrated experience in formulation development and drug product process development</span></li><li style=\"color:rgb(32,33,36);font-size:12pt;--listitem-marker-background-color:white;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Experience with parenteral biologic drug products, including liquid and/or lyophilized formulations.</span></li><li style=\"color:rgb(32,33,36);font-size:12pt;--listitem-marker-background-color:white;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Experience with fill-finish process development, technology transfer, GMP manufacturing, and CDMO oversight.</span></li><li style=\"color:rgb(32,33,36);font-size:12pt;--listitem-marker-background-color:white;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Demonstrated experience in development and implementation delivery devices (PFS, autoinjectors, etc.)</span></li><li style=\"color:rgb(32,33,36);font-size:12pt;--listitem-marker-background-color:white;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Demonstrated strong knowledge of FDA and ICH CMC requirements for biologics</span></li><li style=\"color:rgb(32,33,36);font-size:12pt;--listitem-marker-background-color:white;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Experience with monoclonal antibodies and fusion proteins</span></li><li style=\"color:rgb(32,33,36);font-size:12pt;--listitem-marker-background-color:white;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"background-color:white;font-size:11pt;white-space:pre-wrap;\">Strong technical judgment and ability to make phase-appropriate recommendations in a lean biotech environment.</span></li></ul><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><b><strong style=\"color:rgb(54,80,124);font-size:18pt;white-space:pre-wrap;\">Compensation</strong></b></p><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:justify;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">The salary range for this position is $220,000-$260,000 and the position may be eligible for performance-based bonuses and/or equity-linked compensation. Salary ranges are determined by role, level and location and additional factors, including job-related skills, experience, and relevant education or training. We offer Company-sponsored benefits, which include comprehensive health, dental and vision plans, and pet insurance. In addition, we provide a 401(k) plan, ample time off programs, paid parental leave, life insurance, disability insurance and an employee referral bonus program.</span></p><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:justify;\"><span style=\"font-size:11pt;white-space:pre-wrap;\"> </span></p><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Evommune is proud to be an equal opportunity employer and will consider all qualified applicants for employment.</span></p>",
"company": "<meta><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><b><strong style=\"color:rgb(54,80,124);font-size:18pt;white-space:pre-wrap;\">About Evommune, Inc.</strong></b></p><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Evommune, Inc. (NYSE: EVMN) is a clinical-stage biotechnology company focused on developing innovative therapies for immune-mediated inflammatory diseases. Headquartered in Palo Alto, California, with additional operations in New York, NY, Evommune is advancing a differentiated pipeline designed to address the underlying drivers of disease.</span></p><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Our scientific approach integrates deep immunology expertise with disciplined clinical development to deliver potentially best-in-class therapies for patients with significant unmet medical need. For more information, visit </span><a href=\"http://www.Evommune.com\" target=\"_blank\" class=\"css-173makr-linkStyle\" style=\"color:rgb(30,74,169);cursor:pointer;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">www.Evommune.com</span></a><span style=\"font-size:11pt;white-space:pre-wrap;\">.</span></p><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><br></p><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><b><strong style=\"color:rgb(0,31,95);font-size:11pt;white-space:pre-wrap;\">Work Location: </strong></b><span style=\"font-size:11pt;white-space:pre-wrap;\">This hybrid position is currently expected to be in the office two days per week, with the option to work remotely up to three days per week. Occasional additional onsite presence may be required based on business needs or operational priorities.</span></p><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><br></p><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><b><strong style=\"color:rgb(54,80,124);font-size:18pt;white-space:pre-wrap;\">Our Core Values</strong></b></p><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><span style=\"color:black;background-color:white;font-size:11pt;white-space:pre-wrap;\">Before we dive into the specifics of the role, it's important to highlight the core values that are integral to being a member of the Evommune team. Our values are not just words; they shape our culture, guide our decision-making, and define what it means to be part of our team.</span></p><ul data-pattern=\"discCircleSquare\" data-depth=\"1\" style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;\"><li style=\"font-size:11pt;--listitem-marker-color:#36507c;--listitem-marker-background-color:white;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><b><strong style=\"color:rgb(54,80,124);background-color:white;font-size:11pt;white-space:pre-wrap;\">Together We Win:</strong></b><span style=\"color:black;background-color:white;font-size:11pt;white-space:pre-wrap;\"> We champion teamwork, celebrating every achievement as a shared success.</span></li><li style=\"font-size:11pt;--listitem-marker-color:#36507c;--listitem-marker-background-color:white;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><b><strong style=\"color:rgb(54,80,124);background-color:white;font-size:11pt;white-space:pre-wrap;\">Guided by Insight:</strong></b><span style=\"color:black;background-color:white;font-size:11pt;white-space:pre-wrap;\"> We make data-driven decisions, using our collective experience to shape the future of our business.</span></li><li style=\"font-size:11pt;--listitem-marker-color:#36507c;--listitem-marker-background-color:white;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><b><strong style=\"color:rgb(54,80,124);background-color:white;font-size:11pt;white-space:pre-wrap;\">Every Day Matters:</strong></b><span style=\"color:black;background-color:white;font-size:11pt;white-space:pre-wrap;\"> We act with urgency to bring transformative therapies to patients by being nimble, decisive, and effective.</span></li><li style=\"font-size:11pt;--listitem-marker-color:#36507c;--listitem-marker-background-color:white;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><b><strong style=\"color:rgb(54,80,124);background-color:white;font-size:11pt;white-space:pre-wrap;\">Driven By Excellence:</strong></b><span style=\"color:black;background-color:white;font-size:11pt;white-space:pre-wrap;\"> We set a high bar and hold ourselves accountable to deliver exceptional results in everything we do.</span></li><li style=\"font-size:11pt;--listitem-marker-color:#36507c;--listitem-marker-background-color:white;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><b><strong style=\"color:rgb(54,80,124);background-color:white;font-size:11pt;white-space:pre-wrap;\">Empowered To Act:</strong></b><span style=\"color:black;background-color:white;font-size:11pt;white-space:pre-wrap;\"> We invest in our team and value transparency, fostering trust and a sense of ownership.</span></li></ul><p style=\"font-family:"Basel Grotesk",Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><span style=\"color:black;background-color:white;font-size:11pt;white-space:pre-wrap;\">We seek individuals who resonate with these principles, as they are essential for thriving in our collaborative, innovative, and dynamic work environment.</span></p>"
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