Associate Quality Control - Night Shift

Associate Quality Control - Night Shift

Location: West Greenwich, RI

Onsite Flexibility

Onsite

Contract Details

• Position Type: Contract
• Contract Duration: 12 months
• Pay Rate: $30.00 $38.00 / Hour (USD)
• Shift / Schedule: Tuesday Friday, 10:00 PM 8:00 AM (4 10-hour shifts)
• Work Authorization: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Job Summary

Under general supervision, this position will perform routine procedures and testing in support of the HPLC and CE (Capillary Electrophoresis) group. Quality Control is searching for an analyst (Associate QC) to support routine testing for the QC Night Shift Team D (Tuesday Friday from 10 PM 8 AM) in West Greenwich, RI. This person will be responsible for working in the Quality analytical laboratory, using GMPs and GDPs to execute analytical testing.

Key Responsibilities

• Performing analytical testing including time-sensitive samples from Manufacturing (Titer / MMV / Mycoplasma / Endotoxin / Bioburden / TOC / Conductivity), Centralized Raw Material testing (compendial testing & microbiology), Protein Concentration via UV/VIS and HPLC, Environmental Monitoring and Critical Utilities, Sample Receipt and Aliquot
• Ensures that facilities, equipment, materials, organization, processes, procedures and products comply with safety guidelines, cGMP (Good Manufacturing Practices) practices and other applicable regulations
• Generates complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks
• Operates laboratory equipment and instrumentation
• Performs review and approval of assays, documents and records
• Supports troubleshooting and problem solving
• Alerts management of quality, compliance, supply and safety risks
• Supports TRAs and deviations, as applicable
• Completes required assigned training to permit execution of required tasks
• Performs additional duties as specified by management
• Performing routine laboratory procedures
• Routine analytical testing
• Documenting, computing, compiling, interpreting, and entering data
• Maintaining and operating specialized equipment
• Initiating and/or implementing changes in controlled documents
• Must learn and comply with safety guidelines and cGMPs/CFRs, which include, but are not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems, and laboratory logbooks

Required Skills

• Ability to work in a fast-paced, GMP environment
• Familiarity with Quality ideology (GDP, GMP, etc.)
• Technical skill in wet chemistry, HPLC, microbiology, USP/EP testing
• Experience with analytical laboratory testing with the ability to plan and perform routine tasks with efficiency and accuracy
• Demonstrated ability to work independently and deliver right-first-time results
• Excellent communication skills (written and verbal)
• Must have focus on data integrity
• Commitment of a 40-hour work week (4 10-hour shifts) in West Greenwich, RI

Preferred Skills

• 1 3 years of experience in GMP analytical laboratory
• Experience executing analytical/biological testing per Methods and/or Compendia
• Experience with QC analytical systems and/or Quality systems
• Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories
• Understanding of biopharmaceuticals process and related unit operations
• Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy
• Independent, self-motivated, organized, able to multi-task in time-sensitive environments
• Demonstrated experience in investigations and QC processes
• Some lab experience is preferred

Education Requirements

• High school diploma / GED and 3 years of Quality or Analytical Laboratory experience
• OR Associate's degree and 1 2 years of Quality or Analytical Laboratory experience
• OR Bachelor's degree

Required Experience

• Experience with analytical laboratory testing with the ability to plan and perform routine tasks with efficiency and accuracy
• Qualified to work in the U.S. without employer sponsorship

Nice-to-Have Experience

• 1 3 years of experience in a GMP analytical laboratory
• Demonstrated experience in investigations and QC processes

Benefits

• Medical, Vision, and Dental Insurance Plans
• 401k Retirement Fund

About GTT

GTT is an NMSDC-certified Minority Business Enterprise (MBE) headquartered in Portsmouth, New Hampshire. GTT is a subsidiary of Chenega Corporation, an Alaska-based company and one of the largest Alaska Native-owned corporations. An Inc. 5000 honoree and one of SIA's Best Staffing Firms to Work For, GTT connects professionals with Fortune 500 organizations across IT, engineering, construction, utilities, life sciences, financial services, and healthcare throughout the U.S. and Canada. We're committed to diverse, inclusive workplaces and to placing people in roles where they can do their best work.

Job Number: 26-18355 Industry: Manufacturing & Operations

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