Associate Director, Technical Operations - Small Molecule Drug Product

Job DescriptionWe have an exciting opportunity for an Associate Director, Technical Operations – Small Molecule Drug Product at our Elkton Site in Virginia, USA.At our company, we aspire to be the premier research-intensive biopharmaceutical company, using the power of leading-edge science to save and improve lives around the world. We are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals.Join a purpose-built, agile small molecule manufacturing site where your work will help bring important medicines to patients in the U.S. This facility is designed to move quickly and reliably, receiving technology transfers from commercialization sites and fast-following into production with a focus on quality, safety, and operational excellence.At our site, you’ll be part of a team committed to creating a safe, environmentally responsible, and compliant workplace where people can do their best work. We are building deep small molecule expertise in the U.S., and we want team members who are excited to grow their skills, help improve how we operate, and contribute to a site positioned for future growth.The successful candidate will provide technical leadership and operational support for the startup, technology transfer, validation, and ongoing commercial manufacture of oral solid dosage forms.This role is responsible for leading technical activities across assigned processes and projects, supporting the capital project and facility startup phase through to commercialization and lifecycle management. The Associate Director will ensure safe, compliant, and reliable process performance, while driving continuous improvement and technical excellence.Key ResponsibilitiesTechnical LeadershipRecognized subject matter expert in Drug Product process support, and commercial manufacturingProvide technical oversight and hands-on leadership for oral solid dose manufacturing processes, including:Blending and granulation (where applicable)Roller compaction (dry granulation)Tablet compressionFilm coating and finishing operationsSupport the Capital Project Team, contributing to design, commissioning, qualification, and startup readinessLead process scale-up, technology transfer, and validation (pre-PPQ, PPQ) activities for assigned processesDrive improvements in process performance, yield, robustness, and impurity controlAnalyse technical data and support decision-making for process performance and improvementsIdentify and escalate risks, proposing practical, science-based solutionsTechnology TransferLead and execute technology transfer activities for assigned processes across internal sites and external partnersSupport development and execution of tech transfer plans aligned with project timelinesProvide technical support for:Process fit assessmentsScale-up strategy from development to commercial scaleEquipment capability and process comparability assessmentsEnsure accurate process documentation, knowledge transfer, and batch record readinessSupport process validation and continued process verificationOperational ExcellencePartner with Manufacturing to ensure safe, efficient, and reliable plant performanceProvide direct technical support to:Campaign preparation, execution, and follow-upProcess troubleshooting during manufacturingLead and support deviation investigations, OOS, and CAPA, applying structured root cause analysisMonitor process performance and cycle times, identifying improvement opportunitiesDrive continuous improvement initiatives for yield, cycle time, and costSupport process optimisation and debottlenecking activitiesRegulatory & ComplianceEnsure assigned processes operate in compliance with cGMP and regulatory expectationsSupport inspection readiness and audit activitiesContribute to regulatory submissions and responses, including data generation and technical inputEnsure data integrity and adherence to quality and safety standardsMaintain compliance from startup through commercial operationsCross-functional LeadershipCollaborate with Engineering, Capital Projects, R&D, Quality, Supply Chain, and ManufacturingAct as a technical representative for assigned processes within cross-functional teamsSupport technology transfer and process improvements across the networkParticipate in interactions with external partners and CMOs as requiredContribute to technical reviews and governance forumsPeople, Capability & Business LeadershipLead and develop a team of technical specialists and engineersProvide coaching, technical guidance, and performance feedbackSupport resource planning and execution of departmental prioritiesContribute to budget tracking and departmental administrationSupport recruitment, onboarding, and capability development initiativesQualificationsDegree (BSc/BEng/Masters) or higher in Chemical Engineering, Pharmaceutics, Pharmaceutical Sciences, or related disciplineSignificant experience (typically 10+ years) in:Oral solid dose manufacturing, formulation, or process developmentStrong background in:Process engineering and scale-upProcess, equipment, and cleaning validationWorking knowledge of:cGMP manufacturing operationsRegulatory expectations and inspection readinessExperience with:Deviation management and investigationsElectronic batch records and process systems (e.g., DeltaV)Exposure to capital projects, CQV, and facility startupStrong analytical, problem-solving, and communication skillsAbility to work effectively across cross-functional teams and multiple prioritiesOur CultureWe keep the patient at the heart of everything we do and strive to deliver solutions for some of the world’s most challenging healthcare needs. We believe breakthrough innovation happens when experienced leaders empower talented teams in an inclusive environment. So, if you are ready to:Support delivery of new Drug Product manufacturing capabilityDrive operational and technical excellence in Oral Solid Dose productionDevelop your leadership capability in a high-impact environment…we encourage you to apply.#ELKVACOERequired Skills: Adaptability, Adaptability, Automation Systems, Biopharmaceutical Industry, Biopharmaceuticals, Business Management, Capability Development, Capital Project Management, Change Management, Chemical Engineering, Clinical Manufacturing, Data Analysis, Decision Making, Drug Product Manufacturing, Interpersonal Relationships, Leadership, Lean Manufacturing, Manufacturing Scale-Up, Operational Excellence, Organizational Performance Management, Pharmaceutical Sciences, Process Scale Up, Regulatory Compliance, Root Cause Analysis (RCA), Strategic Thinking {+ 2 more}Preferred Skills: Current Employees apply HERECurrent Contingent Workers apply HEREUS and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:EEOC Know Your RightsEEOC GINA Supplement​We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.Learn more about your rights, including under California, Colorado and other US State ActsThe salary range for this role is$142,400.00 - $224,100.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at .You can apply for this role through (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance OrdinanceLos Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring OrdinanceSearch Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: RegularRelocation:DomesticVISA Sponsorship:NoTravel Requirements:10%Flexible Work Arrangements:Not ApplicableShift:Not IndicatedValid Driving License:NoHazardous Material(s):n/aJob Posting End Date:08/15/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. SummaryLocation: USA - Virginia - ElktonType: Full time