Sr. Technician, Shared Services Operations (Onsite)

Merck; New Jersey; On-site; USD 70,000 - 90,000; Full time

Job summary

Merck in Rahway, NJ is seeking a Senior Technician, Operations to support sterile pharmaceutical development and GMP clinical supply in the FLEx Center. The role focuses on hands-on sterile processing, packaging, and documentation within a Grade C environment, with opportunities to cross-train in filling and other areas.

Responsibilities include assembling sterile equipment, operating sterilization systems, managing sterile supplies, and performing closed and open aseptic formulations under

Qualifications

• High School Diploma/GED with 5+ years in pharmaceutical manufacturing or processing, or an Associates Degree in Science/Engineering.
• Experience with sterile processing and aseptic formulation.
• Familiarity with GMP guidelines and SOPs.
• Ability to read, understand, and follow drawings.

Responsibilities

• Assemble sterile equipment following drawings for clinical development and manufacturing processes.
• Operate and maintain cleaning and sterilization equipment (parts washers, dry heat ovens, autoclaves).
• Receive, inspect, and store sterile supplies ensuring proper inventory levels.
• Prepare and formulate sterile products per batch records, including closed formulation in isolators.
• Perform visual inspections of products and components for defects and non-conformities.
• Maintain meticulous records of formulation processes, ingredients, equipment used, and environmental conditions.
• Follow GMP procedures and participate in continuous improvement projects.
• Collaborate with formulators, engineers, Quality, Safety, and Facilities teams to drive performance.

Job description

Job Description

Senior Technician, Operations

Pharmaceutical Operations and Clinical Supply is seeking highly motivated individuals for R&D Operations roles in our Rahway, NJ, Formulation, Laboratory, and Experimentation (FLEx) Center to support drug product development and GMP clinical supply of sterile dosage forms. Positions will support development and clinical manufacturing and supply, as part of the FLEx-Sterile team, specifically in Manufacturing Shared Services which supports sterile supply, aseptic formulation and visual inspection.

This position will be responsible for hands‑on processing activities that include equipment assembly and disassembly, sterile processing, inventory management, open aseptic formulation in an isolator and closed formulation activities in a Grade C environment, and manual visual inspection of filled units (i.e. vials or syringes).There is also opportunity to cross‑train in other areas, such as filling. These individuals are expected to partner with and support formulation development colleagues in further understanding and knowledge capture of processes, which could include providing feedback on product and process development.

These roles require adherence to GMP procedures, strong attention to detail in completing GMP documentation, proficiency in electronic systems, and participation in continuous improvement projects. Positions may also support commissioning, qualification, and demonstration of new equipment and technologies. Successful candidates will collaborate closely with team members and partner groups including formulators, engineers, Quality, Safety, and Facilities management to drive overall success and performance of the area and clinical pipeline.

Key Responsibilities

• Assembly: Able to read, understand, and follow drawings to assemble sterile equipment to utilize in clinical development and manufacturing processes.
• Sterilization Processes: Operate and maintain cleaning and sterilization equipment, including parts washers, dry heat ovens, and autoclaves.
• Supply Management: Receive, inspect, and store sterile supplies and equipment, ensuring proper inventory levels and organization within the sterile supply area.
• Sterile Formulation: Prepare and formulate sterile products according to established protocols and batch records, ensuring accuracy and compliance with GMP standards. Able to perform closed formulation activities as well as open aseptic activities inside a Grade A isolator. Experience with operating isolator machines and/or Grade A aseptic experience is required.
• Visual Inspection: Perform visual inspections of products and components to identify defects, inconsistencies, and non‑conformities. Individual should be detailed and organized, and able to manage a large quantity of units.
• Attention to Detail: Maintain meticulous records of formulation processes, including ingredient quantities, equipment used, and environmental conditions.
• GMP Compliance: Follow all GMP guidelines and standard operating procedures (SOPs) to ensure the quality and safety of clinical production lots. Identifies and addresses compliance, environmental, safety, and process deviations as appropriate while notifying management.
• Batch Adaptability: Quickly adapt to changes in batch procedures and production schedules, demonstrating flexibility and problem‑solving skills.
• Cleanroom Environment: Able to gown and work in Grade C conditions, maintaining good aseptic cleanroom behaviors.
• Documentation: Maintain accurate records of sterilization processes, inventory levels, and equipment logs in an electronic system. Knowledge of PAS‑X is preferable.
• Collaboration: Able to communicate clearly with team and work closely with other teams to ensure on time delivery of supplies.
• Training and Compliance: Assist in training new staff on sterile supply procedures and protocols, ensuring adherence to GMP standards.
• Leadership: Able to identify and elevate issues, perform basic troubleshooting, and capturing learnings to improve systems and processes. Organizes and prioritizes own work to meet shop floor priorities and identifies discrepancies in advance. Also attends and actively participates in safety, quality, and process improvement initiatives to enhance flexibility, efficiency, and compliance.
• Schedule Adherence: Understands schedule adherence impact and communicates risk. Maintains a continuous improvement mindset and implements initiates to increase efficiency or reduce risk to schedule adherence.
• Compliance: Identifies and addresses compliance, environmental, safety, and process deviations as appropriate while notifying management. Able to redline SOPS for continuous improvement.
• Supports investigations and implementation of corrective/preventative actions.

Positions are based in Rahway, NJ and 100% on‑site.

Education Minimum Requirements

High School Diploma/GED, with at least 5 years in pharmaceutical manufacturing or processing OR Associates Degree in Science/Engineering rel