Description

Quality Control is searching for an analyst Associate QC to support routine testing for the QC Night Shift Team

This person will be responsible for working in the Quality analytical laboratory using GMPs and GDPs to execute analytical testing.

The ideal candidate enjoys tackling challenges and excels at time management with attention to detail.

Responsibilities will include but are not limited to:

- Performing analytical testing including time sensitive samples from Manufacturing Titer/ MMV/ Mycoplasma/ Endotoxin/ Bioburden/ TOC/ Conductivity Centralized Raw Material testing compendial testing microbiology 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

What we are looking for:

- 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

- Qualified to work in the U.S. without employer sponsorship

- Commitment of a 40-hour work week 4 x 10hr shifts in West Greenwich RI

Additional Skills & Qualifications

Experience:

o Bachelors degree

OR

o Associate's degree and 1-2 years of Quality or Analytical Laboratory experience

OR

o High school diploma/GED and 3 years of Quality or Analytical Laboratory experience

Preferred Qualifications

- 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

- Self-motivated strong organizational skills and ability to manage multiple tasks at one time with minimal supervision

- Strong communication skills both written and verbal

- 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

Schedule::

9:45pm - 8:15am either Tuesday-Fri or Saturday-Tuesday

Job Type & Location

This is a Contract position based out of West Greenwich, RI.

Pay and Benefits

The pay range for this position is $25.00 - $30.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in West Greenwich,RI.

Application Deadline

This position is anticipated to close on Feb 10, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.