Senior Manager, Analytical Development & QC | Formation Bio · Teeming.ai
Formation Bio
Formation Bio is a tech-driven, AI-native pharmaceutical company focused on accelerating drug development and bringing new treatments to patients faster and more efficiently. They leverage a…
Formation Bio is a tech-driven, AI-native pharmaceutical company focused on accelerating drug development and bringing new treatments to patients faster and more efficiently. They leverage a…
About Formation BioFormation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development.
Advancements in AI and drug discovery are creating more candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of new medicines that can reach patients, Formation Bio, founded in 2016 as TrialSpark Inc., has built technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines to patients. The company is backed by investors across pharma and tech, including a16z, Sequoia, Sanofi, Thrive Capital, Sam Altman, John Doerr, Spark Capital, SV Angel Growth, and others.
You Can Read More At The Following Links
Our Vision for AI in Pharma
Our Current Drug Portfolio
Our Technology & Platform
At Formation Bio, our values are the driving force behind our mission to revolutionize the pharma industry. Every team and individual at the company shares these same values, and every team and individual plays a key part in our mission to bring new treatments to patients faster and more efficiently.
About The Position
We are seeking a highly motivated, self-driven and detail-oriented Sr. Manager/Associate Director of Analytical Development and Quality Control to join our CMC team. This role will provide broad exposure across Formation Bio’s portfolio, requiring the ability to flex between small molecule and biologics programs at different phases of development in an outsourced development model, requiring strong technical skillset, vendor management, and the ability to balance scientific rigor with program timelines.
You will play a key role in providing technical leadership as a subject matter expert for the development, optimization, and validation of drug substance and drug product analytical methods to support outsourced development and manufacturing of small molecule and biologics programs including but not limited to proteins, monoclonal antibodies, and vaccines. In this role you will also oversee all Formation Bio stability programs and closely collaborate with CMC, QA, and Regulatory teams.
Responsibilities
In close collaboration with CDMOs and contract testing laboratories, lead development, optimization and validation of phase-appropriate analytical methods for small molecule and biologics drug substances and drug products.
About You
Formation Bio is prioritizing hiring in key hubs, primarily the New York City and Boston metro areas. These positions will follow a hybrid work model with 1-3 days required at the office. Applicants from the Research Triangle (NC) and San Francisco Bay Area may also be considered.
Please only apply if you reside in these locations or are willing to relocate.Compensation Range:$177,000 - $235,000
Salary ranges are informed by a number of factors including geographic location. The range provided includes base salary only. In addition to base salary, we offer equity, comprehensive benefits, generous perks, hybrid flexibility, and more. If this range doesn't match your expectations, please still apply because we may have something else for you.
You will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
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Manage testing (in-process, release, stability) at CDMOs and contract testing laboratories.
Provide technical oversight for method transfers, comparability assessments, and laboratory readiness.
Support selection, qualification, and ongoing performance management of external analytical vendors.
Oversee and manage Formation Bio’s stability studies across all programs, including review and approval of stability protocols and review and trending of stability data to support shelf-life and retest dating. Track and publish stability program metrics. Act as the primary contact for stability-related inquiries.
Oversee and manage Formation Bio’s critical reagents and reference standards inventory and testing.
Lead investigations of release and stability OOS and OOT results, deviations, CAPAs and change controls.
Author and review analytical sections of CMC documents, including protocols, reports, and regulatory submissions.
Author and review of SOPs and work instructions.
Closely collaborate with CMC, QA, and Regulatory teams.
Analytical Chemistry, Biochemistry, Molecular Biology, or a related discipline Master’s degree with 5+ years or Bachelor’s Degree with 8+ years of relevant small molecule and biologics analytical development and QC experience.
Proven ability to operate effectively in a fast-paced, virtual, and outsourced development environment.
Highly organized with a track record of managing multiple priorities across programs in an outsourced development model.
Strong scientific judgment with the ability to independently assess data quality, identify risks, and recommend mitigation strategies.
Ability to communicate complex analytical concepts clearly to both technical and non-technical stakeholders.
Collaborative mindset with a strong sense of ownership and accountability.
Extensive hands-on experience developing, optimizing, and validating analytical methods for release and stability testing of small molecules and biologics.
Hands-on experience with analytical methods pertinent to bilogics (qPCR, IEF, UHPLC, MS, CE, SDS-PAGE, ELISA, peptide mapping, glycan analysis, etc.) and small molecules (UHPLC, IC, GC, IR, UV, KF, PSD, dissolution, etc.).
Experience with authoring and reviewing technical documents such as test methods, method development reports, validation protocols, validation reports, specification justification reports, retest and shelf-life memos, and SOPs.
Experience with designing stability studies and performing stability data trending according to applicable guidances.
Strong working knowledge of Smartsheet and JMP.
Thorough understanding of ICH, FDA, EMA guidances and GMP requirements governing process development, manufacturing, and stability.
Ability to travel domestically and internationally up to 25% of the time.
