Senior Scientist II, Process/Flow Chemistry

Department
53 - Process Chemistry

Employment Type
Full Time

Location
Redwood City, CA

Workplace type
Onsite

Compensation
$150,000 - $180,000 / year

Description

Codexis, a biotech enzyme engineering company, is looking to hire a Senior Scientist II, Process/Flow Chemistry!  This position is part of the Senior Scientist II, Process/Flow Chemistry and will be located in Redwood City, CA. 
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 biotherapeutic discovery & development. The enzymes we produce aim to solve real-world challenges associated with small molecule pharmaceuticals manufacturing, nucleic acid synthesis and genomic sequencing, and - as biotherapeutic candidates - they have the potential to treat challenging diseases.

To meet this goal, we look for individuals who are driven, eager to grow and ready to embrace meaningful challenges. We empower employees to be authentic, ambitious, agile and have the courage to take action where they can make a positive impact. Whether you are driven by science, or a different area of expertise, we need you to help us create a brighter future.

Come join us on this journey and mission of making the world a safer, healthier, and better place!

About the Opportunity:

This position is a member of the Process Chemistry team, adding critical experience and expertise in flow chemistry and immobilization to develop processes are technically feasible, transferrable, and economically viable at scaled process targets. To achieve these goals, the candidate works cross-functionally with research teams and manufacturing. The successful candidate will play an integral role in both the day to day and long-term strategic success of our Life Sciences business, and in particular the Nucleic Acid Synthesis segment.

This business segment encompasses the engineering, development, commercialization, and manufacture of new enzymes and process technologies for the manufacture of nucleic acid, with a focus on GMP production of therapeutics.

If any of the below describes you, we would love to meet you!

• Background in (bio)chemistry or (bio)chemical engineering
• Experience of process development and/or scale-up for GMP production of pharmaceuticals
• Able to envision, extrapolate, and convey the transition of lab-developed flow processes to manufacturing scales, while being able to anticipate and address obstacles.
• Strong collaboration and communication skills, both written and verbal.

In this role you will be responsible for:

• Working closely with research teams to establish enzyme performance indicators for meeting process development scope and deliverables.
• Leading gap analysis around oligonucleotide synthesis processes in flow and develop strategies for mitigating technical and process risks.
• Establishing methods for process control and ensuring products meet quality and consistency requirements.
• Identifying and managing technical project risks, issues, and opportunities to deliver programs on time and in scope.
• Proactively reporting on status and progress to internal stakeholders.

The essential requirements of the job include:

• Master’s or Bachelors 6+ years in the pharmaceutical or related industry.
• Self-starter with a graduate background in (bio)chemistry or (bio)chemical engineering 
• Practical experience in developing and scaling up flow chemistry processes for pharma manufacturing.
• Thrives in a dynamic and diverse environment, driven to deliver results, while also looking for continuous improvement opportunities.
• Able to envision, extrapolate, and convey the transition of lab-developed flow processes to manufacturing scales, while being able to anticipate and address obstacles.

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

• Experience in solid phase oligonucleotide synthesis methods desirable.
• Detailed understanding and experience of process development and/or scale-up for GMP production of pharmaceuticals with flow process steps desired.

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.