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Sr. GMP Technician

Job in Rahway, Union County, New Jersey, 07065, USA
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
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
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.

Senior GMP Technician General Requirements
  • 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
Education
  • High School Diploma
  • Certifications:

    Not required, but a certification in pharm processing would be beneficial
Experience
  • 2-4 years’ experience in a GMP facility
Responsibilities
  • 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.
Requirements
  • 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.
Physical Requirements
  • 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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