Senior Manager, Analytical Development

Harmony Biosciences is recruiting for a Senior Manager, Analytical Development in our Plymouth Meeting Office. This position is a key contributor within Harmony's Technical Operations organization, supporting the analytical development and oversight of drug substance and drug product activities across external manufacturing partners. The individual in this position will play an integral role in coordinating and executing analytical strategies for both clinical and commercial programs, ensuring continuity of supply and adherence to the highest quality standards. Working cross-functionally, this role helps drive the delivery of safe, reliable, and high-quality pharmaceutical products to patients by enabling seamless execution of analytical activities across the development lifecycle.Responsibilities include but are not limited to:Serve as an analytical Subject Matter Expert (SME) for clinical and development programs, including drug substance and drug product (oral solids/liquids and other dosage forms) development and manufacturing at contractor sitesLead and support analytical development activities at multiple contractor sites related to analytical method development, method improvements, product characterization and comparability assessments for Harmony's early and late-stage programsDirect technical oversight of multiple Contract Organizations (COs), with the following responsibilities:Serve as technical resource on drug substance and drug product aspects with particular emphasis in analytical chemistry and associated methodologiesProvide oversight and serve as technical lead for the execution of method development, method improvement and method validation activitiesManage laboratory deviations/investigations to successful closure in a timely manner as product SME in close and seamless collaboration with Harmony's Quality functionOversee and co-manage release testing and stability programs for drug substance and drug product with Quality AssuranceEnsure COs meet Harmony business objectives while meeting quality and compliance standardsDrive uncompromising quality as a fundamental and valued attribute of all output and patient safety as an overarching responsibilityReview and maintain lifecycle product documentation and data files related to analytical activities for early and late-stage development programs, including but not limited to protocols, reports, SOPs, certificates, etc.Work closely with the Project Manager and Contract Organizations (CMOs/CROs) to ensure all analytical deliverables are aligned and meet agreed project timelines. Apply Quality by Design (QBD) principles and Design of Experiments (DoE) to develop robust analytical methods.Trend, analyze, and statistically interpret stability data.Identify degradation pathways and variability drivers.Establish scientifically justified shelf-life projections.Collaborate with other Harmony departments as required to:Achieve corporate goals and mission for uninterrupted clinical and commercial supply to patientsWork closely with teams to define analytical testing strategyDevelop and maintain technical aspects of quality agreementsImplement analytical improvement or analytical aspects of other product lifecycle programsLead the execution of analytical technology transfers, method implementation, qualification/validationPrepare and review dossiers for regulatory filingsDrive fiscal responsibility with the operational budget and cost savings initiativesQualifications:Bachelor's degree in in Analytical Chemistry (or related field) with 8+ years of relevant industry experience; Master's degree with 5+ years of relevant industry experience; or PhD with 2+ years of relevant industry experience.Technical Proficiency in analytical method development, including dissolution testing, chromatographic techniques (such as HPLC, and GC), and spectroscopy methods (such as UV-Vis, NMF, MS, along with expertise in method robustness and qualification/validation requirements. Experience managing a contract manufacturing organization (CMO) is a plus.Knowledge and application of pharmaceutical analytical development principles, concepts, and industry practices to assist during audits or vendor inspections, and offer solutions to troubleshoot technical problemsExperience in developing and transferring analytical methods from R&D to the commercial stage of the product lifecycleKnowledge of regulatory environment (FDA/ICH regulations) and experience with organizing and writing regulatory submissionsKnowledge and demonstrated mastery of current Good Manufacturing Practices (cGMPs) and associated quality guidance and principles (ICH, USP, and ISO standards), with particular emphasis on laboratory techniques and proceduresStrong computer, organizational, and analytical skills requiredPhysical demands and work environment:Travel (both domestic and international) is estimated to be 20% of the time for this position; Candidate must be able to maintain or obtain valid US Passport within 90 days of hire dateWhile performing the duties of this job, the noise level in the work environment is usually quiet.Specific vision abilities required by this job include: Close vision.Manual dexterity required to use computers, tablets, and cell phone.The employee must occasionally lift and /or move more than 20 pounds.Continuous sitting for prolonged periods.What can Harmony offer you?Medical, Vision and Dental benefits the first of the month following start dateGenerous paid time off and Company designated HolidaysCompany paid Disability benefits and Life Insurance coverage401(k) Retirement Savings PlanPaid Parental leaveEmployee Stock Purchase Plan (ESPP)Company sponsored wellness programsProfessional development initiatives and continuous learning opportunitiesA certified Great Place to Work for eight consecutive years based on our positive, values-based company cultureWant to see our latest job opportunities? Follow us on LinkedIn!Harmony Biosciences is a pharmaceutical company headquartered in Plymouth Meeting, PA. The company was established in October 2017 with a vision to provide novel treatment options for people living with rare, neurological disorders who have unmet medical needs. For more information on Harmony Biosciences, visit www.harmonybiosciences.comHarmony Biosciences is an Equal Opportunity, e-Verify Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.Recruitment agencies please note: Harmony Biosciences will only accept applications from agencies/business partners that have been invited to work on a specific role. Candidate Resumes/CV's submitted without permission or directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.#LI-Hybrid