Sr. Specialist, Engineering - Raw Material Planner (Onsite)

Position Summary Applications are sought for a Raw Material Planner Sr. Specialist within Planning and Manufacturing Systems (PAMS) in our Company's Research & Development Bioprocess Clinical Manufacturing and Technology (BCMT). The individual will support pilot‑scale campaigns for the GMP manufacture of bulk biologic (vaccines, therapeutic proteins, monoclonal antibodies) clinical supplies. Primary Responsibilities Establish priorities for raw material (RM) procurement and procure RM internally or externally. Coordinate culture media (CM)/buffer manufacturing. Collaborate and benchmark across the network to influence and execute RM management standards. Coordinate RM/CM deliveries to and from Biological Support Operations (BSO) and VAX Process Research and Development (VAX PR&D) bulk manufacturing suites, including the Biologics Pilot Plant (BPP). Track and manage inventory of RMs and GMP supplies, including single‑use technology. Manage RM/CM storage space. Collaborate with Process Development to determine critical parameters. Perform CM laboratory studies as required. Participate in SOP development, support of new IT initiatives, and supply chain management of RMs and GMP supplies. Excellent understanding of the regulatory guidelines governing GMP manufacture is required. The candidate is expected to work in a team atmosphere in close collaboration with Process Development groups, Facility Engineering, RM/CM Release, and Procurement, and overtime or off‑shift work may be required. Qualifications BS degree in Engineering, Sciences, Business, or a related field with a minimum of 5 years of relevant experience, or a master’s degree with a minimum of 3 years of relevant experience. Required Experience and Skills Ability and desire to work in a fast‑paced and dynamic pilot plant environment that demands out‑of‑box thinking, prioritization, and rapid response to events and situations. Direct experience with SAP/PASX. Strong understanding of manufacturing principles/processes through work experience. Ability to work collaboratively as part of a team across various functions in a challenging and changing global environment. Proven track record of analytical skills, problem‑solving, and attention to detail. High personal integrity, credibility, and energy. Strong written and verbal communication skills. Strong computer skills in Excel. Preferred Experience and Skills Experience in pharma/sterile manufacturing. Required Technical Skills Adaptability Analytical Testing Data Analysis Detail‑Oriented Deviation Management Equipment Qualification Good Manufacturing Practices (GMP) Process Design Process Hazard Analysis (PHA) Process Optimization Root Cause Analysis (RCA) Strategic Thinking Technical Leadership Technical Problem‑Solving Technical Writing Location and Eligibility US and Puerto Rico residents only. Compensation and Benefits Salary range: $117,000.00 – $184,200.00. The successful candidate will be eligible for an annual bonus and long‑term incentive, if applicable. We offer a comprehensive package of benefits, including medical, dental, vision, retirement (401(k)), paid holidays, vacation, and sick days. Equal Employment Opportunity 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. #J-18808-Ljbffr Merck