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Analytical Development Scientist II at Serán BioScience | Swiftcruit
Serán is seeking a Scientist II who will support the development, optimization, and validation of analytical methods used to characterize small molecule drug products for early and late phase clinical R&D to support client GMP Clinical Release and Stability programs. The work performed in this role will help to shape analytical strategy, collaboration across functions, and deliver high‑quality data that enables the success of early/late phase clinical programs
Duties and Responsibilities
Perform analytical testing such as UHPLC/HPLC, KF, Water Activity, Dissolution to support small molecules drug product development in GMP environment
Develop and optimize methods for drug products and APIs across early phase and late phase clinical stages
Execute method transfers to QC or partner labs, ensuring robustness and compliance.
Plan, troubleshoot, and independently execute laboratory studies, generating high‑quality data for CMC decision‑making.
Prepare and review technical reports, analytical methods, and protocols, contributing to regulatory‑ready documentation.
Collaborate with cross‑functional teams (QC, QA, Process Development, Project Management) and communicate results to internal and external stakeholders.
Act as a subject matter expert (SME) in analytical development, providing technical leadership and supporting analytical strategy.
Initiate, draft, and perform testing for discrepancy reports; as necessary.
Maintain GMP training certification to be able to perform work in a GMP laboratory
Provide regular updates to management on projects
Identify opportunities for process improvements and propose solutions
Identifies out of trend data.
Responsibilities may increase in scope to align with company initiatives.
Required Skills & Abilities
Proven analytical method development experience (preferably HPLC) with at least 1-2 years in a cGMP pharmaceutical industry lab
Scientific curiosity and willingness to learn
Demonstrates intermediate expertise with analytical equipment (e.g. disso, KF, GC, LC, XRPD, or mDSC; preferred LC and GC)
Conveys general understanding of USP, ICH, and EP guidance as they pertain to method validation/qualification/transfer and general chapters for relevant instrumentation
Excellent verbal and written communication skills
Excellent organizational skills and attention to detail
Excellent time management skills with a proven ability to meet deadlines
Strong analytical and problem-solving skills.
Ability to function well in a fast-pace work environment
Demonstrated ability to collaborate and work in cross-functional teams
Accepts feedback and constructively manages conflict
Proficient with Empower
Proficient with Microsoft Office Suite or related software
Education & Experience
Bachelor’s degree in chemistry or related field, with 4 years of hands-on lab experience preferred; or
Master’s degree in chemistry or related field, with 2 years of hands-on lab experience preferred.
Requires 1 year of GMP experience.
Physical Requirements
Prolonged periods of sitting or standing at a desk and working on a computer.
Prolonged periods of standing or sitting while monitoring laboratory equipment.
Must be able to lift up to 15 pounds at times.
Adheres to consistent and predictable in-person attendance.
Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
Benefits Summary:
Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
