Sr. GMP Technician
Job in
Rahway, Union County, New Jersey, 07065, USA
Listed on 2026-06-18
Listing for:
Vita Global Sciences, a Kelly Company
Full Time
position Listed on 2026-06-18
Job specializations:
-
Manufacturing / Production
Pharmaceutical Manufacturing, Manufacturing & Industrial Operations
Job Description & How to Apply Below
Kelly Science and Clinical FSP is currently seeking a Sr. GMP Technician for a long-term engagement in Rahway, NJ with one of our Global Pharmaceutical clients. This position is onsite. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options.
As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.
- Following local procedures
- Completing required training
- Adhering to GMP requirements for documentation of activities
- Cleaning, sanitizing, and breaking down equipment
- Operating GMP manufacturing/cleaning equipment
- High School Diploma
- Certifications:
Not required, but a certification in pharm processing would be beneficial
- 2-4 years’ experience in a GMP facility
- Prepare the appropriate disinfectants as per SOP.
- Understand the dwell time for all cleaning agents/chemicals.
- Cleaning of the processing rooms following manufacturing processes and as required per procedure. Remove all trash/biohazard waste bags from the MFG area.
- Stocks all gowning materials in all air locks and locker rooms.
- Execute cleaning of major and minor pieces of equipment and ancillary equipment
- Disassembly and reassembly of equipment per procedure (as required)
- Perform cleaning activities on the isolators and filling line
- Perform cleaning verification activities to support cleaning validation
- Accurately documenting activities in the appropriate logbooks.
- Able to work with a respirator during special assignments, if required.
- Maintain materials inventory.
- Report any unexpected observations to area management.
- Perform tasks under minimal supervision, and within tight timelines to meet production schedule.
- Coordinate with engineers & maintenance personnel in facility upkeep
- Author and revise SOPs and logbooks.
- Reviews logbooks at the end of the shift to ensure proper GDP.
- Good interpersonal skills and attention to detail.
- Previous experience in cleaning the GMP area is required.
- Must be able to follow GMP regulations during operations, including adherence to written procedure and contemporaneous documentation.
- Must be able to record data accurately and legibly.
- Ability to perform in a team setting in a controlled environment for long periods of time.
- Physically capable of donning and wearing cleanroom/protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves. PPE is essential for the health and safety of employees
- Perform operations within ISO Class clean rooms
- Employees must be able to lift and/or move up to 40 pounds
- Must be able to squat, bend, kneel, and or reach for 40% of a shift
- Must be able to stand, walk, and/or move about for 40% of a shift
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