Manufacturing Operator

Description

Job Description Job Description – Manufacturing Operator About the Position We are seeking a candidate with experience in aseptic manufacturing to join the Blending Paracox team. The selected individual will participate in the commissioning and operation of sterile product manufacturing, packaging, and packing processes, contributing to ensuring the highest standards of quality, safety, and compliance with GMP regulations. **Important:** Until the candidate’s formal integration into the Blending Paracox area, they will be assigned to IPT\-Sterile Production, where they will gain familiarity with processes and organizational structure prior to joining the new team. Responsibilities * Perform aseptic manufacturing, aseptic packaging, and packing operations. * Complete manufacturing documentation in accordance with GMP requirements. * Participate in cleaning, preparation, and changeover activities. * Identify, report, and record incidents, deviations, and opportunities for improvement. * Collaborate in qualification, validation, and commissioning activities for the new facility. * Ensure compliance with quality, safety, and risk prevention standards. * Work in coordination with the rest of the team to ensure continuity and efficiency of production processes. Working Hours * Availability to work Monday through Sunday, across three shifts, with 24-hour coverage. Requirements * Proven experience in pharmaceutical aseptic production. * Knowledge and experience in blending, packaging, and packing of sterile products. * Familiarity with GMP regulations and experience working in cleanrooms. * Availability to work rotating shifts. * Teamwork capability, quality orientation, and proactive attitude. * Experience in commissioning new pharmaceutical lines or facilities. * Knowledge of GMP Annex 1. **Required Skills:** Analytical Thinking, Analytical Thinking, Cleanroom Gowning, Computer Literacy, Driving Continuous Improvement, Equipment Set Up, Fabrication Processes, GMP Environments, GMP Operations, Good Manufacturing Practices (GMP), In\-Process Control (IPC), Manufacturing Processes, Problem Resolution, Process Manufacturing, Production Operations, Production Processes, Production Scheduling, Product Quality Assurance, Quality Assurance (QA), Quality Assurance (QA) Standards, Quality Standards, Recordkeeping, Risk Prevention, Safety Protocols, Standard Operating Procedure (SOP) Management {\+ 1 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:** 07/16/2026\*A job posting is effective until 11:59:59PM on the dayBEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFORE the job posting end date. **Requisition ID:** R404528