Technician, Shared Services Operations (Onsite)
Merck
2 hours ago
On-site
Rahway, NJ
Operations
Technician, Operations (FLEx Sterile Supply Technician) — Rahway, NJ (100% on-site). Supports GMP sterile dosage form development and clinical manufacturing/supply.
Responsibilities:
- Assemble sterile equipment using drawings; sterilize/clean equipment (parts washers, dry heat ovens, autoclaves).
- Receive, inspect, and store sterile supplies; maintain proper inventory/organization.
- Perform sterile formulation per protocols/batch records (closed formulation; open aseptic inside a Grade A isolator).
- Conduct manual visual inspection of filled vials/syringes and identify nonconformities.
- Maintain accurate GMP documentation and electronic records; follow GMP/SOPs and report/address deviations.
- Adapt to batch/procedure/schedule changes; gown/work in Grade C cleanroom; support training, investigations, CAPA, and continuous improvement.
Qualifications (Required):
- High School Diploma/GED+.
- 2+ years relevant GMP pharmaceutical experience.
- Good written/verbal communication.
- Computer proficiency (MS Office, Equipment HMI, SAP, calibration/maintenance databases).
- Good eyesight; lift 50 lbs; bend/stoop/squat/crawl/twist/climb; cleanroom gowning incl. respirators; overtime flexibility.
Preferred:
- 2+ years GMP manufacturing/processing; GDP familiarity.
- Experience with isolators/containment, automated aseptic filling, visual inspection in glass vials, SAP/ERP, automated systems (MES/SAP), troubleshooting; Associate degree; BioWork certificate.
Benefits/Comp:
- Salary range: $51,500–$81,100; annual bonus and long-term incentive (if applicable); medical/dental/vision, 401(k), paid holidays/vacation, compassionate and sick days.
Responsibilities:
- Assemble sterile equipment using drawings; sterilize/clean equipment (parts washers, dry heat ovens, autoclaves).
- Receive, inspect, and store sterile supplies; maintain proper inventory/organization.
- Perform sterile formulation per protocols/batch records (closed formulation; open aseptic inside a Grade A isolator).
- Conduct manual visual inspection of filled vials/syringes and identify nonconformities.
- Maintain accurate GMP documentation and electronic records; follow GMP/SOPs and report/address deviations.
- Adapt to batch/procedure/schedule changes; gown/work in Grade C cleanroom; support training, investigations, CAPA, and continuous improvement.
Qualifications (Required):
- High School Diploma/GED+.
- 2+ years relevant GMP pharmaceutical experience.
- Good written/verbal communication.
- Computer proficiency (MS Office, Equipment HMI, SAP, calibration/maintenance databases).
- Good eyesight; lift 50 lbs; bend/stoop/squat/crawl/twist/climb; cleanroom gowning incl. respirators; overtime flexibility.
Preferred:
- 2+ years GMP manufacturing/processing; GDP familiarity.
- Experience with isolators/containment, automated aseptic filling, visual inspection in glass vials, SAP/ERP, automated systems (MES/SAP), troubleshooting; Associate degree; BioWork certificate.
Benefits/Comp:
- Salary range: $51,500–$81,100; annual bonus and long-term incentive (if applicable); medical/dental/vision, 401(k), paid holidays/vacation, compassionate and sick days.