Job Summary: We are seeking an organized, team-oriented operator for the FPU packaging of sterile pharmaceutical products, ensuring quality and regulatory compliance. Key Highlights: 1. Sterile pharmaceutical product manufacturing and packaging 2. Working in a pharmaceutical production/laboratory environment 3. Focus on quality, safety, and GMP compliance Job Description INTERNAL APPLICANT NOTICE: Please review the Global Job Posting and Employee Mobility Policy for more information about considerations prior to applying for a position. It is important that interested individuals self-assess whether they meet the criteria before proceeding with the application process. Job Description The Sterile Production IPT, part of the Animal Health plant in Salamanca, is responsible for the manufacturing and packaging of sterile pharmaceutical products, including bulk manufacturing, aseptic filling, and FPU packaging. The plant operates integrated within our global manufacturing network to ensure the highest quality of intermediate biological and finished products, adhering to the “Safe by Choice – Quality Always” principles and mindset in all activities performed. To strengthen our Packaging team at the Salamanca plant, we are seeking an organized, team-oriented individual as a full-time operator to perform the necessary tasks for FPU packaging of products manufactured by the Sterile Production IPT. **Responsibilities:** * Perform required FPU packaging activities (weight control, visual inspection, vial loading into cartons, and verification of correct identification) for various products, complying with GMP regulations, local standards and procedures, and production planning across different areas of the IPT. * Follow instructions outlined in the corresponding batch documentation and related procedures, contacting the supervisor in case of discrepancies identified therein. * Clean and disinfect FPU packaging rooms and equipment according to established procedures. * Receive and inspect packaging materials; verify their proper condition. * Prepare the work area and equipment, verify machines and available materials for product packaging in accordance with current procedures. * Regularly monitor required parameters during the packaging process. * Monitor environmental conditions and equipment status per established monitoring protocols. * Collect and identify product samples, when required during the FPU packaging process, for quality control. * Perform necessary SAP administrative transactions to ensure batch manufacturing and material stock updates (if SAP access is granted). * Participate in updating procedures and methodologies aimed at aligning the Salamanca plant with Company objectives, and participate in deviation investigations or CAPA implementation. * Report any incidents occurring during processes; identify, prevent, and report safety risks. * Work organization. * Ability to build relationships and work effectively in a team. **Profile:** * Relevant vocational training. * Minimum 1 year of work experience in a pharmaceutical production/laboratory environment. * Knowledge of GMP and quality systems. * Proficiency in Microsoft Office (Excel, Word, PowerPoint). * Basic written and spoken English. * Batch documentation in compliance with GMP. * SCADA knowledge. * SAP knowledge. Shift work from Monday to Sunday, based on production needs. **Required Skills:** Accountability, Accountability, Analytical Thinking, Biopharmaceutical Industry, Cleanroom Gowning, Communication, Computer Literacy, Equipment Set Up, Fabrication Processes, GMP Environments, GMP Operations, Good Manufacturing Practices (GMP), In\-Process Control (IPC), Materials Handling, Microsoft Excel, Microsoft Office, Operations Management, Packaging Management, Pharmaceutical Manufacturing, Pharmaceutical Microbiology, Problem Resolution, Production Scheduling, Quality Assurance Monitoring, Quality Control Management, Quality Standards {\+ 4 more}**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:** Regular**Relocation:** **VISA Sponsorship:** **Travel Requirements:** **Flexible Work Arrangements:** Not Applicable**Shift:** **Valid Driving License:** **Hazardous Material(s):** **Job Posting End Date:** 04/21/2026* **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.** **Requisition ID:**R391602