Your experience includes...- BS/MS in Chemistry, Biochemistry, Chemical Engineering, or related field with 5+ years (BS) or 3+ years (MS) of relevant industry experience
- Experience with upstream and downstream processing of oligonucleotides
- Must have experience with Mermade192 and Mermade12 synthesizers
- Experience with Äkta100 oligonucleotide synthesizer is a plus
- Experience with HPLC purification and analytics of guide RNA preferred
- Experience with enzymatic ligation techniques is a plus
- Experience using ELNs to document experimental results is a plus
You are interested in... - Performing small scale, high throughput internal production of guide RNA to support platform research and pre-clinical activities
- Optimizing synthetic reactions and purification methods of drug candidates to ensure scalable and cost-effective processes for oligonucleotide manufacturing
- Working in collaboration with the Internal Manufacturing team during process transfer
- Participating in cross-functional teams and training to gain familiarity in all stages of oligonucleotide research and manufacturing
About you: You are a skilled and self-motivated individual who can optimize and implement processes for synthesizing and purifying complex oligonucleotides. You can operate in a fast-paced environment, troubleshoot instruments, and document operations independently and as part of a team. You will have the opportunity to organize and present results within the group and interface with other teams, so strong communication skills are critical. You enjoy overcoming challenges in collaboration with colleagues.
Meet your Manager:All inquiries regarding the posted position should be directed to the Talent Partner (see below). Interested individuals must apply directly to be considered for the opening.
Cody Pasko - Senior Scientist, Oligo FoundryCody obtained a Masters in Chemistry at Michigan State University, focusing on organometallic catalysis. He has over 9 years of experience working at CROs and CDMOs, most recently being Nitto Avecia where he served as a project lead in the oligonucleotide process development group. At Tessera, he leads a team involved in the development and production of oligonucleotide drug substances, both internally and externally.
Meet your Talent Partner:Ben Hoogheem - Senior Director, Head of Talent ManagementAs Head of Talent Management at Tessera Therapeutics, Ben leads Tessera's talent strategy across talent acquisition, performance management, and talent mobility.
Ben began his career as an in vivo Pharmacologist, which gave him a lasting appreciation for the rigor, creativity, and collaboration that drive scientific discovery. That foundation continues to shape how he helps build organizations designed to enable science thrive.
Ben is focused on aligning exceptional people with bold science - creating the structure, clarity, and culture that empower teams to scale effectively and achieve meaningful impact.
Compensation:The stated base salary range represents Tessera's good-faith estimate for this role. Actual compensation will be determined based on a number of factors, including but not limited to individual qualifications, years of relevant experience, internal compensation alignment, and external market data.
Tessera offers a competitive package of base and incentive compensation as well as a comprehensive benefits program designed to support the health, wellness, and financial security of our employees and their families. Benefits currently include group medical, vision, and dental coverage; group life and disability insurance; a 401(k) plan with company contribution; tuition reimbursement; and more.
This position is also eligible for an annual incentive bonus and equity grants as part of Tessera's total rewards program.
Per Year Salary Range: $90,000 - $108,000 USD
