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)
Job Summary
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).
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.
Positions are based in Rahway, NJ and 100% on-site.
Matching Summary
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).
Salary
Base: $51,500 - $81,100; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Comprehensive package including medical, dental, vision, retirement, paid holidays, vacation, and sick days
Skills & Requirements
Must-have
Sterile processing and formulation
Aseptic formulation in isolator
Manual visual inspection of filled units
GMP documentation and compliance
Cleanroom gowning and behavior
Nice-to-have
Continuous improvement projects
Collaboration with cross-functional teams
Troubleshooting and problem-solving skills
PAS-X proficiency
Key Requirements
Minimum of 2 years of relevant GMP Pharmaceutical experience