a Project Manager Bioprocess Technology Solutions

This job is with MSD, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.Solliciteer snel, bekijk de volledige omschrijving door naar beneden te scrollen om de volledige vereisten voor deze functie te ontdekken.Job DescriptionFor our animal health location in Boxmeer we are currently recruiting aProject Manager Bioprocess Technology SolutionsWelcome to the teamThe global Bio Technology Solutions (BTS) team (~230 employees) drives and executes Bioprocess technology excellence in close alignment with their partners in R&D and Manufacturing to ensure robust product introductions, product transfers and a reliable product supply to customers. BTS has considerable expertise in viral cell culture, bacterial fermentation, downstream processing, purification, freeze drying and vaccine formulation. They are responsible for seed development, new product process development, validation/qualification and commercialization of our animal health large vaccine pipeline.Our global Product Development Team (~75 employees) provides process development, and process improvement of the Large Molecule (LM) vaccine portfolio covering the discovery, pre-development and development phase as well as transfer from R&D to Manufacturing.Purpose of the roleReporting to one of the BTS Leads, you are responsible for driving (part of) the LM process development of the R&D vaccine portfolio for all species in Europe. Projects have low to moderate complexity and cover the discovery, pre-development, development, transfer, regulatory, launch and post-launch phase. This role requires close collaboration with BTS, ATS, Quality departments and Manufacturing at different LM sites, R&D species teams, Discovery & Technology, Regulatory Affairs, Procurement, Global Supply Chain and Network Strategy.Primary responsibilitiesActs as a (Junior) project manager for one or more projects and project teams. This includes, amongst other experimental planning, strategic and (inter)departmental alignment, budget oversight, issue and risk management, stakeholder management, objective setting and reporting.Communication and knowledge exchange between global BTS departments and between Global R&D and Manufacturing to optimize knowledge and technology utilization and benefit from synergies.Writes Statements and Assessments, Subject Protocols / Memos / Reports, and Regulatory documents.Follow external developments / trends in vaccine process development on specific focus areas.Performs subject-related literature searches and publishes and presents technical papers to internal and external audiences.Operational responsibility for development of (improved) processes on one or a couple of focus areas such as upstream, downstream, Vaccine Manufacturing, IPC, FPC, media, bacteriological, viral, monoclonal, expression system).Recommends new areas of technology research and development.Involved in resolving manufacturing and supply issues of our vaccine portfolio according to the needs of Manufacturing.Is open to general tasks with the organization related to lab coordination and global events.Manages interns and students.Consultant of Global Supply Chain (GSC) management, business development and legal on their expertise.YourprofileRelevant BSc/MSc/PhD education and/or experienceFamiliarity and expertise in laboratory operations.Experience with either viral antigen production, bacterial antigen production (Upstream and Downstream processing) or vaccine manufacturing and relevant laboratory techniques.Strong analytical and problem-solving skills, and the ability to work independently and make decisions in a constantly changing (international) environment.Knowledge of and experience with GxP guidelines is a plusUnderstanding of Regulatory/compliance requirements.Excellent command of the English language.Living within reasonable distance from Boxmeer.What we offerOur benefits are very competitive, and the summary below will give you an idea of what you can expect.Competitive salary and a 3% year-end allowance.35,5 days of leave.Attractive collective health care insurance package with considerable reduction rates.Solid Pension Plan.Annual bonus based on own and company performance.Travel allowance for commuting.Numerous training, coaching and e-learning modules for long term job opportunities and development.For questions about this vacancyPlease send an email including the vacancy number and job title to the following email address: Required Skills:Accountability, Analytical Chemistry, Business Development, Cell Cultures, Clinical Data Interpretation, Cross-Functional Teamwork, Detail-Oriented, Downstream Processing, Experimentation, High Resolution Mass Spectrometry (HRMS), Laboratory Techniques, Manufacturing, New Product Introduction Process, Stakeholder ManagementPreferred Skills:Current Employees apply HERECurrent Contingent Workers apply HERESearch Firm Representatives Please Read CarefullyMerck & 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:VISA Sponsorship:Travel Requirements:Flexible Work Arrangements:Not ApplicableShift:Valid Driving License:Hazardous Material(s):Job Posting End Date:01/17/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. xnkfpon Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.Requisition ID: R377366