Senior Process Engineer, Technical Operations - Small Molecule Drug Product (Oral Solid Dose)

Job DescriptionWe have an exciting opportunity for a Senior Process Engineer, Technical Operations – Small Molecule Drug Product (Oral Solid Dose) to join our growing team.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 process ownership supporting facility design, commissioning, qualification, and startup through to technology transfer, validation, and ongoing commercial manufacture of oral solid dosage forms.In this role, you will work as a key member of a cross-functional team, initially supporting the capital project and transitioning into process lead responsibilities across technology transfer and commercial manufacturing, driving technical excellence and operational performance.Key ResponsibilitiesTechnical & Process LeadershipProvide technical leadership for oral solid dose manufacturing processes, including:Blending and granulation (where applicable)Roller compaction (dry granulation)Tablet compressionFilm coating and finishing operationsAct as process owner / SME for assigned unit operations, equipment, or product processesProvide technical input to the Capital Project Team, supporting:Equipment selection and design reviewsCommissioning and qualification (CQV)Startup readiness for OSD manufacturing linesLead or coordinate process scale-up, technology transfer, and validation activities (e.g. process performance qualification – PPQ)Analyze and interpret process and product data (e.g. blend uniformity, tablet properties, coating performance) to drive data-driven decision-making and performance improvementsProvide advanced troubleshooting support for compression, compaction, and coating issues (e.g. weight variability, hardness, sticking/picking, coating defects)Technology Transfer & CommercializationLead or play a key role in execution of technology transfers for oral solid dose products into the facilityPartner with global R&D and network sites to ensure robust transfer of formulation and process knowledgeDrive:Process fit assessmentsScale-up strategy from development to commercial scaleEquipment capability and process comparability assessmentsOwn or guide development and optimization of:Master batch records (MBRs)Process descriptions and control strategiesSupport integration and industrialization of new formulations and technologies (e.g. continuous manufacturing, advanced granulation approaches where applicable)Process Optimization & Operational ExcellencePartner with Manufacturing to ensure safe, efficient, and reliable OSD plant performanceIdentify, prioritize, and implement improvements in:Content uniformity and tablet qualityProcess robustness (e.g. compaction consistency, compression stability)Yield, throughput, and cycle timeLead or drive continuous improvement initiatives aligned with operational excellenceUse structured problem-solving approaches (e.g. RCA, DOE where applicable) to resolve:Compression issues (e.g. capping, lamination)Compaction variabilityCoating defects (e.g. color variation, twinning, roughness)Monitor process trends and product quality attributes to proactively identify risks and opportunitiesContribute to line optimization, changeover reduction, and debottlenecking activitiesCompliance & DocumentationEnsure all activities are conducted in compliance with cGMP, safety, and environmental standardsProvide technical leadership in campaign preparation, execution, and post-campaign reviewOwn and approve batch record updates, process specifications and control strategiesSupport regulatory inspections and audits, providing technical input and ensuring inspection readinessEnsure high standards of data integrity and technical documentationCross-functional Collaboration & InfluenceAct as a technical representative across Manufacturing, Quality, Engineering, Supply Chain, and R&DProvide clear technical direction and influence decision-making across product introductions and commercial operationsLead or contribute to cross-functional initiatives, ensuring alignment to timelines and site objectivesSupport knowledge sharing and best practice transfer across internal and external networksQualificationsTo excel in this role, you will have:Degree in Chemical Engineering, Pharmaceutics, Pharmaceutical Sciences, or related disciplineTypically 5+ years’ experience in oral solid dose manufacturing, formulation, or process development(PhD may offset experience)Strong experience in OSD manufacturing operations, particularly:Roller compaction (dry granulation)Tablet compressionFilm coating processesExperience in process scale-up and commercialization of solid oral dosage formsDemonstrated involvement in:Technology transferProcess validation (PPQ)Manufacturing supportGood understanding of cGMP manufacturing and regulatory expectationsExperience troubleshooting tableting and coating processes in a commercial environmentKey Skills:Strong analytical capability with ability to interpret process and product performance dataDemonstrated ability to lead technical workstreams or projectsExcellent problem-solving skills with structured, science-based approachEffective communicator with ability to influence cross-functional stakeholdersProven ability to manage multiple priorities in a dynamic manufacturing environmentProactive, self-driven mindset with strong focus on continuous improvement and ownershipOur 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 innovation happens when empowered individuals collaborate in an inclusive, high-performing environment.So, if you are ready to:Play a key role in delivering oral solid dose manufacturing capabilityTake ownership of formulation and process performance at commercial scaleDevelop as a technical leader in a high-impact manufacturing environment…we encourage you to apply.#ELKVACOERequired Skills: Adaptability, Biopharmaceutical Industry, Change Control Processes, Chemical Engineering, Customer-Oriented, Deviation Management, Engineering Standards, Equipment Selection, Good Manufacturing Practices (GMP), Maintenance Engineering, Manufacturing Process Validation, Operational Excellence, Oral Solid Dosage, Pharmaceutical Sciences, Process Optimization, Regulatory Compliance, Root Cause Analysis (RCA), Strategic Thinking, Teamwork, Technical Leadership, Technical Support, Technical Transfer, Technology Transfer, Vibratory RollersPreferred 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$117,000.00 - $184,200.00This 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:09/8/2026*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