Method Transfer Liaison (Bioassays) at Merck Sharp & Dohme Corp. /Netherlands

Boxmeer, North Brabant, Netherlands -

Full Time

Start Date

Immediate

Expiry Date

31 Jan, 26

Salary

0.0

Posted On

02 Nov, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Accountability, Adaptability, Analytical Problem Solving, Assay Development, Data Analysis, Decision Making, ELISA Development, Empathy, Management Process, Personal Initiative, Process Improvements, Stakeholder Management, Statistics, Virus Titrations

Industry

Pharmaceutical Manufacturing

Description

Job Description Act at the interface of R&D and QC and use your commercial pharma experience to support robust method transfers, minimize supply risk, and support on-time product releases. For our Animal Health location Boxmeer, we are currently recruiting a Method Transfer Liaison (Bioassays) Welcome to our team Our Global Science & Technology (S&T) division applies science, technology and innovation to support new product commercialization and ensure supply continuity for animal health manufacturing. S&T continuously improves processes and analytics to meet customer needs through manufacturing excellence. Within S&T, Global Analytical Technology Solutions (ATS) covers Small and Large Molecules and oversees analytical activities across the Animal Health network. The ATS-Bio EU/APAC team provides bio-analytical test support to QC laboratories in Europe and APAC, handling technical investigations, data analysis, troubleshooting, method transfer/validation, and development and production of biomaterials and new test methods. A new Large Molecule Analytical Transfer sub team will support the transfer of analytical methods from R&D and QC into Animal Health QC labs. Purpose of the role Reporting to the Director ATS-Bio EU/APAC, you will serve as a strategic partner and subject matter expert in the coordination and execution of ATS-Large Molecule analytical transfer priorities. You will support planning, organizing, and coordinating analytical method transfers to meet business goals and customer needs. You will collaborate closely with R&D teams, providing expert advice and support in the development of robust bio-analytical methods during the pre-development and development phases of new product commercialization (NPC) programs. Your involvement involves assay problem-solving and will ensure smooth and efficient analytical method transfers between R&D and QC sites, fostering alignment and mutual understanding. Additionally, you follow the change control process to ensure any product changes after method validation are checked for impact and any required corrective actions. Main tasks and responsibilities Supporting Site-to-Site and R&D-to-Site method transfers to ensure method robustness, compliance, quality and efficiency in QC processes as part of network restructuring and new product commercialization. Continuously prioritize and balance activities to reflect organizational strategic goals and customer demands, maintaining close coordination with QC laboratories and R&D Boxmeer and promptly escalating issues to senior management. Ensure the robustness of analytical methods through proactive efforts and involvement as subject matter expert during early NPC test development. Lead/support complex investigations, conduct complex data and trend analyses to identify root causes, drive resolution of analytical technical issues, and design hypothesis testing for QC laboratories. Analytical technical and multi-project oversight working directly with QC EU/APAC laboratories, R&D Boxmeer and internal cross-functional stakeholders to support analytical testing of large molecule products. Build and maintain strong relationship with among others ATS, BTS, Data Science, (G)RA, IT, R&D, QC and Quality organizations. Drive continuous improvement initiatives to enhance the quality and robustness of method performance through implementation of proactive tools, corrective actions, after action reviews, and best practices. Train and mentor junior ATS-Bio colleagues to enhance their skills and knowledge in biological method transfer activities and ensure method transfer-related analytical knowledge transfer into QC. Present project updates to sponsors and relevant stakeholders, summarizing findings and significant achievements, recommendations, business challenges and act as a representative for concerns related to QC biological method transfers. Author and/or review documents including memo’s, protocols, reports and technical gap & risk assessments related to method performance/execution, development, validation and transfer. Your profile A completed Bachelor of Applied Science (BSc) or Master of Science (MSc) degree in Biochemistry, Biology, Molecular Biology, or a related field. Extensive hands‑on experience with large‑molecule biological QC methods (e.g., ELISA, PCR, cell culture, virus titration, and other relevant bio-analytical techniques), including development, validation, transfer, and troubleshooting/remediation to ensure robust assay performance. Proven experience working within commercial pharmaceutical manufacturing environments, including familiarity with GMP production workflows, batch release processes, and QC release timelines to ensure timely method transfers that support product launch and supply continuity. Strong data analysis skills, including experience with statistical software (e.g., Minitab, Aera), and a demonstrated ability to identify root causes and implement solutions. Proven negotiation skills to harmonize competing priorities while maintaining excellent cross‑team relationships. Good command of the Dutch and English language. Living at a reasonable distance from Boxmeer. What we offer The opportunity to play a key role in method transfers and product launches that affect the whole network, partnering closely with multidisciplinary teams to broaden your influence and expertise. Our 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. Animal Health Our Animal Health Division is a trusted global leader in veterinary medicine, dedicated to preserving and improving health, well-being, and performance of animals and the people who care for them. We are a global team of professionals working together to make a positive difference in animal care and the world’s food supply and have a deep sense of responsibility towards our customers, consumers, animals, society, and our planet. Through our commitment to The Science of Healthier Animals®, we offer veterinarians, farmers, pet owners and governments one of the widest ranges of veterinary pharmaceuticals, vaccines and health management solutions and services as well as an extensive suite of digitally connected identification, traceability and monitoring products. We invest in dynamic and comprehensive R&D resources and a modern, global supply chain. We are present in more than 50 countries, while our products are available in some 150 markets. Do you have questions about this job vacancy? Send your question, including the job number and job title, to the following email address: RecruitmentNL@MSD.com Applications can only be submitted through our career site. Required Skills: Accountability, Adaptability, Analytical Problem Solving, Assay Development, Data Analysis, Decision Making, ELISA Development, ELISA Test, Empathy, Management Process, Personal Initiative, Process Improvements, Stakeholder Management, Statistics, Virus Titrations Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE Search 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: Project Temps (Fixed Term) Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Hybrid Shift: Valid Driving License: Hazardous Material(s): Job Posting End Date: 11/12/2025 *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. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

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Responsibilities

Support method transfers between R&D and QC to ensure compliance and efficiency. Collaborate with teams to develop robust bio-analytical methods and troubleshoot any issues that arise.