Director, Program Management - Nucleic Acid Synthesis - Life Sciences

Department
31 - Performance Enzyme Commercial Ops

Employment Type
Full Time

Location
Redwood City, CA

Workplace type
Onsite

Compensation
$190,000 - $240,000 / year

Reporting To
Elisa Calimano

Description

Codexis, a Redwood City, CA based company is looking to hire a Director of Program Management for our Nucleic Acid Synthesis business.  

This role is part of the Project & Product Operations team and will be located in Redwood City, CA with the opportunity for hybrid working or remote for the right candidate. This position is critical to the strategic success of Codexis’ Life Sciences business unit, and in particular the Nucleic Acid Synthesis segment for the successful conception and execution of projects to develop differentiated enzyme products for nucleic acid synthesis (including DNA, mRNA and siRNA). 

Codexis is a leading enzyme engineering company leveraging our proprietary CodeEvolver® technology platform to discover and develop novel, high performance enzymes for three healthcare industry pillars: pharmaceutical manufacturing, life sciences and biotherapeutics discovery & development. The enzymes we produce aim to solve for real-world challenges in manufacturing RNA and small molecule pharmaceuticals, in genomic sequencing, and in drug discovery & development. 

Come and join us on this journey of making the world a safe, healthier, better place!
About the OpportunityThe Director of Program Management for Nucleic Acid Synthesis is responsible for leading Codexis’ programs in the development, commercialization and lifecycle management of enzyme products and technologies within the Life Sciences Business Unit. 

In Life Sciences, we use our CodeEvolver® platform technology to develop enzymes for a variety of customers using next generation sequencing and/or PCR/qPCR for in vitro molecular diagnostic and molecular biology research applications, as well as for the synthesis and manufacture of nucleic acids, which is the core focus of this role. 
If any of the below describes you, we would love to meet you!

• Self-starter with a background in (bio)chemistry or (bio)chemical engineering, and experience of program management and/or new product introduction within the GMP manufacturing space – preferably with experience in RNA production. 
• Exceptionally strong collaboration and communication skills to drive clarity and focus across commercial, research, development and operational teams.
• Adaptable, highly accountable, result-oriented and strong in analytical and critical thinking, as well as having a market-oriented mindset, where meeting customer needs is the overarching goal.

If any of the below describes you, we would love to meet you!
Self-starter with a background in (bio)chemistry or (bio)chemical engineering, and experience of program management and/or new product introduction within the GMP manufacturing space – preferably with experience in RNA production. 

• Exceptionally strong collaboration and communication skills to drive clarity and focus across commercial, research, development and operational teams.
• Adaptable, highly accountable, result-oriented and strong in analytical and critical thinking, as well as having a market-oriented mindset, where meeting customer needs is the overarching goal.

In this role you will be responsible for:

• Manage a portfolio of programs for nucleic acid synthesis enzymes, reagents and process technologies, in collaboration with business and functional leaders, ensuring appropriate prioritization, resourcing, risk mitigation, tracking, reporting, and issue escalation. 
• Work closely with business leaders, product marketing, research, product- and process-development, manufacturing and quality/regulatory, the job holder will lead and oversee all of Codexis’ programs in the commercialization and lifecycle management of enzyme products and technologies in the Nucleic Acid Synthesis segment.
• Engage with Business Development and with customers during opportunity ID & qualification, business case analysis and negotiation, with a particular focus on project and operational strategy and cost/margin analysis. 
• Lead multiple complex product commercialization projects, operating as the critical liaison between the commercial team and the functional organizations in research, development, operations & QA/regulatory, including: 
  • Definition, stakeholder alignment on, and documentation of deliverables for product development & commercialization programs, and leadership of successful execution of those outcomes. 
  • Ensuring that technical and quality/regulatory requirements are addressed as early as possible in programs and are spec’d in and monitored throughout projects.
• Oversee successful technology transfer of processes and products to manufacturing (internal or external) in support of successful commercialization, with seamless handover to commercial and operational teams to enable steady state supply.

The essential requirements of the job include:

• Minimum of a Bachelor’s degree in (bio)chemistry or (bio)chemical engineering, or related discipline, with a post-graduate degree preferred. 
• 8+ years of project or (operational) product management or related industrial experience.
• Demonstrated exceptional time management skills and a ‘can do’ approach.
• Familiarity with stage-gated product development and portfolio management processes.

To be successful in this role, your preferred background and experience should include: 

• Detailed understanding and experience of process development &/or scale up for GMP production of pharmaceuticals; experience with RNA manufacturing highly desirable.
• Demonstrated excellent project management skills; a PMP certification, or similar, is desirable.
• Experience in a multi-project, customer-facing organization (e.g. a Contract (Development) & Manufacturing Organization [C(D)MO]) is desirable but not essential.

Pay TransparencyThe anticipated salary range for candidates who will work in Redwood City, CA is $190,000 to $240,000. And competitive bonus. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Codexis is a multi-state employer and this salary range may not reflect positions that work in other states​.



What can Codexis offer you?

• Full benefits on your first day
• 100% match on 401k (up to 4%)
• Life insurance 3x your salary
• Company equity program – stock and RSU’s offered for new hires and annually
• Generous PTO 
• 15 company paid holidays in addition to PTO
• Fitness reimbursement
• Back up child/dependent care
• Commuter vouchers
• Student loan assistance and student debt program
• Schedule that works for you as we support an onsite, hybrid and remote workforce for certain positions
• Internal mobility 
• Volunteer time off
• Health and wellness programs
• Legal and tax support program 

About Codexis Inc

Why join Codexis?

At Codexis we offer a very competitive compensation package and beyond excellent benefits! We foster career growth, continued education and upskilling through our mentorship program and learning and development opportunities. You will learn and work alongside inspirational leaders and colleagues who are equally passionate about our mission and committed to fostering an inclusive, growth-centered, and rewarding culture. Diversity is valued and mutual trust is of paramount importance to the ethos at Codexis. The people, the culture and working with others with a common goal is what makes Codexis a great place to work.

For more information, visit www.codexis.com.

NO AGENCIES OR THIRD PARTIES

Codexis is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status.