GMP Filling Technician - Sterile & OS Dosage

Merck & Co.; Rahway (NJ); On-site; USD 56,000 - 88,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive

401(k) plan

Paid holidays

Vacation

Job summary

Merck & Co. in Rahway, NJ, is seeking hands-on GMP operations professionals for the FLEx Center to support drug product development and GMP clinical supply of oral solid dosage, sterile, and specialty dosage forms.

The roles involve equipment setup, cleaning, materials handling, and documentation, with collaboration across formulators, engineers, Quality, Safety, and Facilities to drive performance; candidates must show GMP experience and ability to work both independently and as a team.

Qualifications

• 1+ years of GMP Pharmaceutical experience or equivalent.
• Demonstrated written and verbal communication skills.
• Proficiency with Microsoft Office (Word, Excel, Outlook), Equipment HMI, SAP, Calibration/Maintenance databases.
• Ability to lift 50 lbs and wear cleanroom gowning including respirators.
• Able to work independently and in a team.

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 GMP documentation using paper and electronic systems.
• Maintains knowledge of process equipment, troubleshoots issues.
• Participates in safety, quality, and process improvement initiatives.
• Supports investigations and implementation of corrective/preventive actions.

Skills

GMP Experience

Communication Skills

Team Collaboration

Microsoft Office

Equipment Handling

Safety Compliance

Problem Solving

Education

High School Diploma/GED

Tools

SAP

Equipment HMI

Calibration/Maintenance DB

Job description

Merck & Co. in Rahway, NJ, is seeking hands-on GMP operations professionals for the FLEx Center to support drug product development and GMP clinical supply of oral solid dosage, sterile, and specialty dosage forms.

The roles involve equipment setup, cleaning, materials handling, and documentation, with collaboration across formulators, engineers, Quality, Safety, and Facilities to drive performance; candidates must show GMP experience and ability to work both independently and as a team.