Program Manager, Pharma

Skills this role screens for

About the role

About Varda

Low Earth orbit is open for business. Varda is accelerating the development of commercial space infrastructure, from in-orbit pharmaceutical processing to reliable and economical reentry capsules. Varda’s W-Series vehicles are built, designed, and operated by Varda in-house, including the pharmaceutical processing payloads, the capsules, the C-PICA heat shields, and the satellite buses.

From life-saving pharmaceuticals to more powerful fiber optics, there is a world of products used on Earth today that can only be manufactured in space. Varda is accelerating innovation in the orbital economy by creating both the products and infrastructure needed so space can directly benefit life on Earth. Our mission is to expand the economic bounds of humankind.

Our team is uniquely suited to accomplishing this goal, with leadership and staff comprised of veterans from SpaceX, Blue Origin, major pharmaceutical companies and Silicon Valley. Varda was founded in January 2021 by Will Bruey and Delian Asparouhov with significant backing from world class investors including Khosla Ventures, Lux Capital, Founders Fund, Caffeinated Capital, General Catalyst, and Also Capital.

Varda is headquartered in El Segundo, California, where we have offices and a production facility where our vehicles, equipment, and materials are built, integrated, and tested. Varda also has offices in Washington, DC and Huntsville, AL.

Join Varda, and work to create a bustling in-space ecosystem.

About this Role

Our pharmaceutical team is looking for a highly motivated and creative Pharma Program Manager who will manage efforts in driving pharma programs to completion and report to the VP, Pharma Program Management, This is an opportunity in an exciting area of growth for Varda, the role will shape Varda’s product culture and will play a significant role in establishing the low Earth orbit economy.

The work

Responsibilities

• Collaborate with program leads to develop and track schedules and milestones, identifying critical path activities and dependencies.
• Support pharma programs and meetings: set agendas, document decisions, assign owners, and follow up on action items.
• Establish program objectives, define scope, and align with departmental strategy.
• Ensure project deliverables meet expectations for quality, cost, and schedule.
• Partner with technical leads to identify and manage program risks and issues, while also proposing mitigation strategies and maintaining a risk register with mitigation plans.
• Align with technical leads to allocate resources, control costs, and ensure efficient use of personnel and resources.
• Communication of project status via SmartSheet, reports, and dashboards.
• Serve as the operational liaison to CDMOs, CROs, and contract testing laboratories on scheduling, deliverables, and issue escalation.

Who they want

Basic Qualifications

• 2+ years of program management experience, and 6+ years of experience in the biopharmaceutical industry.
• B.S. or M.S. in life sciences such as Chemistry, Biochemistry, or related fields.
• Effective communication (verbal and written), well organized, collaborative with peers.

Nice to have

Preferred Skills and Experience

• 10+ years of experience in the pharmaceutical industry.
• 3+ years of program management experience, PMP / PgMP certification.
• Demonstrated experience managing multiple programs.
• Excellent communication across a diverse group of stakeholders. Must be able to tailor messaging to each audience.
• Experience with program planning and coordination, aligning with organizational strategy.
• Cross-functional team influence. Without direct reports, this role must influence and drive task completion from multiple stakeholders.
• Strong critical thinking and troubleshooting experience to guide cross-functional teams toward achieving program objectives.
• Understanding and implementation of change management during program lifecycle.
• Extensive experience with MS Project and/or SmartSheet.

What you get

Pay Range

ITAR Requirements

Varda, like all employers, must ensure that its employees working in the United States are lawfully authorized to work in the U.S. Additionally, our employees are exposed to and have access to certain export-controlled items. Because our employees are provided access to export-controlled items, our policy is to only hire “U.S. persons” who are permitted to have access to our technology without an export license.

“US person” means: U.S. citizen, U.S. lawful permanent resident, or protected individual as defined by 8 U.S.C. 1324b(a)(3) (i.e., individual admitted to the U.S. as a refugee or granted asylum).

E-Verify Statement

Varda Space Industries, Inc. participates in the U.S. Department of Homeland Security E-Verify program. The E-Verify program is an Internet-based employment eligibility verification system operated by the U.S. Citizenship and Immigration Services. Learn more about the E-Verify program.

E-Verify Notice Right To Work Notice

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Varda Space Industries is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Candidates and employees are always evaluated based on merit, qualifications, and performance. We will never discriminate on the basis of race, color, gender, national origin, ethnicity, veteran status, disability status, age, sexual orientation, gender identity, martial status, mental or physical disability, or any other legally protected status.

• Salary range: $125,000 - $170,000/per year
• This role is on-site in El Segundo, CA
• Leveling and base salary is determined by job-related skills, education level, experience level, and job performance
• You will be eligible for incentives in the form of stock options and/or long-term cash awards