## Senior Specialist Global Quality Excellence (Stability Programs)Applyremote type: Hybridlocations: NLD - North Brabant - Boxmeer: DEU - Niedersachsen - Friesoythe: AUT - Vienna - Vienna (Siemensstrasse): DEU - Bayern - Unterschleissheimtime type: Full timeposted on: Posted Todaytime left to apply: End Date: June 5, 2026 (13 days left to apply)job requisition id: R396633Job Description*We are looking for an execution-focused professional who works with tact and confidence, brings people together, and turns plans into tangible results in a complex global environment.*For our Animal Health organization, we are currently recruiting a **Senior Specialist Global Quality Excellence (Stability Programs)****Welcome to our team**Our Global Quality organization plays a critical role in ensuring that every material in our products is manufactured, processed, tested, packaged, stored, and distributed in full compliance with our high-quality standards and all regulatory requirements. Our Test & Release Excellence team (13 employees) supports our global manufacturing network in its journey toward excellence in quality and laboratory testing. The team works with sites and global teams to improve quality processes, enable focus on higher-value activities, and reduce manual work to support Cost of Goods optimization. To further strengthen the team behind Quality 31, a global productivity-focused initiative driving sustainable improvements and cost reductions through optimization, standardization, and digitalization, we are recruiting a Senior Specialist Global Quality Excellence (Stability Programs).This position can be based in: Boxmeer (NL), Unterschleissheim, Friesoythe (D), or Vienna (A).**About the role**Reporting into the Associate Director Global Quality Test & Release Excellence (based in Friesoythe, Germany), you will play a key role in advancing stability program optimization across our Global Animal Health Manufacturing network. You will support sites across the world in identifying, justifying, and implementing opportunities to reduce ongoing stability testing in a science-based and risk-based way, fully aligned with GMP and global regulatory expectations. Acting as a key enabler of Quality 31 productivity initiatives, you will help strengthen global standards, improve transparency on progress, and ensure effective implementation across the network. This role requires close collaboration with the global Stability Sub System Owner (based in Boxmeer, NL).*Please note: this role is supported by a project budget secured through the end of 2028.***Tasks and responsibilities*** Act as global point of contact for sites on Stability Program Reduction opportunities within Quality 31.* Support the implementation of lean ongoing stability program strategies aligned with global Health Authority requirements.* Collaborate with site Quality, QC, and Laboratory teams to translate global strategy into practical site-level opportunities.* Support the development of scientific and regulatory justification packages for stability reduction initiatives.* Facilitate risk assessments, including product risk profiles, bracketing approaches, alternative approaches, stability protocol updates, and change controls.* Write technical documents for both global quality manuals and site-level use.* Support sites during execution and implementation to help ensure timely progress against plans.* Identify, escalate, and help resolve obstacles, risks, and delays during implementation.* Track site-level progress and implementation status across the network.* Provide regular reporting on milestones, risks, and implementation status to global stakeholders.* Support transparency and alignment with Quality 31 governance and tracking mechanisms.**Your profile*** Bachelor’s degree in Life Sciences, Chemistry, or related scientific discipline.* Strong knowledge of GMP and pharmaceutical/animal health quality systems.* Relevant experience working in Quality, QC, or Analytical environment.* Demonstrated ability to work cross-functionally and across multiple sites, including influencing without direct authority.* Strong analytical, (technical) documentation, and communication skills.* Excellent command of the English language, oral and written.* Living close to one of the locations mentioned above and willing to travel occasionally within Europe.**What we offer**An opportunity to challenge the status quo, lead meaningful changes and make a direct, measurable impact on company results through a high-visibility global optimization project. A role that involves collaborating with teams around the world. Benefits depend on the job location but are in any case competitive. The minimum annual salary for this position in Austria is €61.300,- and varies according to the qualifications and experience of the successful candidate.**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.**For questions about this vacancy**Please send an email including the vacancy number and job title to the following email address: **RecruitmentNL@MSD.com**Applications can only be submitted via our careers site.**Required Skills:**cGMP Regulations, Change Management, Deviation Management, Good Automated Manufacturing Practice (GAMP), Manufacturing Quality Control, Pharmaceutical Quality Assurance, Quality Auditing, Quality Management Standards, Quality Standards, Regulatory Compliance, Risk Management, Strategic Planning**Preferred Skills:**Current Employees apply HERECurrent 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:**06/5/2026**\*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.**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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