Associate Technician, Filling Operations

MSD Malaysia; Rahway (NJ); On-site; USD 46,000 - 72,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive

Job summary

MSD Malaysia seeks motivated individuals for R&D Operations roles in Rahway, NJ, to support drug product development and GMP clinical supply of sterile dosage forms. The team focuses on hands-on processing, equipment prep, and collaboration with formulation and quality groups in a dynamic FLEx environment.

Responsibilities include operating and cleaning equipment, maintaining GMP records, and contributing to safety and continuous improvement initiatives, with potential for bonus and

Qualifications

• High School Diploma/GED or higher.
• BioWork Certificate (preferred for FDA-regulated environments).
• Demonstrated troubleshooting / problem-solving skills.
• Experience with machine operations or electronics is a plus.

Responsibilities

• Prepares, operates, and cleans equipment and facilities used in clinical development and manufacturing processes.
• Maintains, inventories, and transports required processing equipment, materials, supplies, and products.
• Executes all documentation and clerical functions necessary to maintain GMP operations, using paper-based and electronic systems.
• Maintains detailed knowledge of process equipment and operations.
• Troubleshoots equipment/systems to resolve issues and aid in technology and process development.
• Attends and actively participates in safety, quality, and process improvement initiatives.
• Supports investigations and implementation of corrective/preventive actions.

Skills

Cleaning Equipment

Cleanroom Gowning

Conventional Machining

Drilling Machines

Equipment Operations

Equipment Reliability Improvement

Process Equipment

Production Scheduling

Safety Procedures

Shift Work

BioWork Certificate

Education

High School Diploma/GED or higher

BioWork Certificate

Job description

Associate 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. This position will be responsible for hands‑on processing activities that include room setup, equipment and material preparation, equipment assembly and disassembly, cleaning, and processing of raw materials into finished drug product. 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:

• Prepares, operates, and cleans equipment and facilities used in clinical development and manufacturing processes.
• Maintains, inventories, and transports required processing equipment, materials, supplies, and products.
• Executes all documentation and clerical functions necessary to maintain good manufacturing practice (GMP) operations, using paper-based and electronic systems.
• Maintains detailed knowledge of process equipment and operations.
• Troubleshoots equipment/systems to resolve issues and aid in technology and process development, and provides feedback to improve systems and processes.
• Attends and actively participates in safety, quality, and process improvement initiatives to enhance flexibility, efficiency, and compliance.
• Supports investigations and implementation of corrective/preventative actions.

Education Minimum Requirements:

High School Diploma/GED or higher

Preferred Experience and Skills:

Experience with machine operations, electronics, or similar technology. BioWork Certificate (for working in an FDA or similar regulated industry). Demonstrated troubleshooting / problem-solving skills.

Required Skills:

• Cleaning Equipment
• Cleanroom Gowning
• Conventional Machining
• Drilling Machines
• Equipment Operations
• Equipment Reliability Improvement
• Process Equipment
• Production Scheduling
• Safety Procedures
• Shift Work

Preferred Skills:

• Equipment Maintenance
• Equipment Testing
• Plant Operations

The salary range for this role is: $45,900 - $72,200

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days.

Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: No Travel Required Flexible Work Arrangements: Not Applicable Shift: 1st - Day Valid Driving License: No Hazardous Material(s): n/a

Job Posting End Date: 09/15/2026

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.