Manufacturing Process Technician - West Greenwich RI

VetJobs

West Greenwich (RI)

On-site

USD 54,000 - 74,000

Full time

12 hours ago
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Job summary

VetJobs is seeking a Manufacturing Process Technician for days on-site at West Greenwich, Rhode Island. You will perform bulk manufacturing tasks in aseptic and non-aseptic environments according to SOPs and batch records.

You will clean equipment, set up single-use materials, weigh raw materials, monitor processes, collect samples, and ensure proper documentation in electronic batch records. The shift is 12 hours, 7am–7pm, with a two-week rotation and weekends off.

Qualifications

  • High school/GED + 1 year of Manufacturing or Operations work or military experience.
  • Associate's degree required or preferred depending on candidate profile.
  • Experience in a GMP/regulated environment is advantageous.
  • Ability to stand or sit for extended periods and maintain focus during repetitive tasks.

Responsibilities

  • Equipment and parts cleaning using manual and automated methods.
  • Set up and breakdown of single use materials.
  • Weigh and dispense of raw materials.
  • Operation and process monitoring of clean systems, autoclaves, and processing equipment.
  • Sample collection, processing, storage and delivery.
  • Documentation of process tasks in electronic batch records.

Skills

GMP knowledge
Attention to detail
Teamwork
Communication skills

Education

High School/GED
Associate's degree

Tools

Electronic Batch Records

Job description

Job Description

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.

Manufacturing Process Technician - Days
What you will do

Let’s do this! Let’s change the world! In this vital role you will routinely perform simple to moderately complex processes according to Standard Operating Procedure and Batch Records. Generally, this will include all aspects associated with bulk manufacturing in aseptic and non-aseptic environments.

Responsibilities
  • Equipment and parts cleaning using manual and automated methods and equipment
  • Set up and breakdown of single use materials
  • Weigh and dispense of raw materials
  • Operation and process monitoring of clean systems, autoclaves, and processing equipment
  • Sample collection, processing, storage and delivery
  • Product and component reconciliation
  • Solution preparation and transfer
  • Materials handling, weighing and dispensing, power industrial vehicle operation
  • Strict adherence to current Good Manufacturing Practices (cGMP's), responsible to accurately complete process-associated documentation, make calculations and perform the physical tasks associated with bulk manufacturing and other duties as assigned.

You will be expected to join a shift team working a 12-hour shift. The shift pattern will be 7am-7pm with a two-week rotation covering 7 days per week. The rotating shift offers several benefits, with an average of 14 days on shift per month with every other weekend off. The schedule during the initial on-boarding phase for this role (2-6 weeks) will be administrative (Monday through Friday, approximately 8am to 5pm).

Auto req ID 487247BR

Minimum Education Required

High School/GED

Additional Qualifications/Responsibilities

What we expect of you We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is an excellent teammate with these qualifications.

Basic Qualifications
  • High school/GED + 1 year of Manufacturing or Operations work or military experience OR
  • Associate's degree
Preferred Qualifications
  • Experience in a GMP/ other regulated environment.
  • Demonstrated knowledge of GMP principles.
  • Drug substance manufacturing experience.
  • Ability to stand or sit for extended periods of time.
  • Ability to maintain focus during repetitious tasks over the course of a shift.
  • Ability to assemble, disassemble, operate and understand simple to moderately complex equipment per procedures.
  • Basic understanding of measurements, calculations and the metric system.
  • Ability to work effectively in an individual and team setting.
  • Ability to document process tasks in electronic batch records.
  • Coachable, ability to take coaching/critique and show learned/measurable improvement.
  • Capacity to follow written procedures, recognize and report malfunctions.
  • Strong communication skills.
  • Ability to perform assignments with a high degree of focus/attention to detail.

Salary Range 54,411.05USD -73,614.95 USD

City* West Greenwich

State* Rhode Island

Job_Category Management

Job Code Pharmaceutical Pharmaceutical

Affiliate Sponsor Amgen

Salary Range >$100,000

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