URGENTLY HIRING: Quality Specialist II

Job Description

Job Description

Quality Specialist

INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT View phone number on ziprecruiter.com TO SET UP AN IMMEDIATE PHONE INTERVIEW!!

Job Description

The Quality Specialist will play a crucial role in the Quality Control Laboratory, supporting the testing and analysis of cGMP produced viral vectors and cells. The individual will work closely with senior staff to help shape the strategic direction of the GMP area. Regular tasks will involve performing sample assays five nights a week, as well as operating, calibrating, validating, cleaning, and maintaining laboratory equipment. Under the guidance of senior staff, the specialist will also perform methods development, analyze microbiological environmental monitoring samples, write and revise SOPs, and manage materials and equipment. Additional duties include periodic cleaning of the clean room facility and assisting with viral vector product manufacturing.

Responsibilities

• Operate within the Quality Management System for the manufacture of phase-appropriate material.
• Ensure proper labeling and documentation of product samples, including sample allocation and transition.
• Maintain accountability for products across sample requirements and storage conditions.
• Evaluate and improve sample management processes.
• Complete, review, file, and archive documentation according to SOPs.
• Ensure compliance with regulatory requirements for cellular and gene therapy products.
• Perform tasks in accordance with established policies, procedures, and training.
• Work under close supervision of sr staff in a collaborative team environment.
• Document all activities performed according to regulatory and quality control standards.

Essential Skills

• Bachelor's degree in Biology or a related science field.
• Understanding of regulatory and documentation constraints in a GMP environment.
• Experience with aseptic techniques, mammalian cell culture, PCR, and ELISA procedures.

Additional Skills & Qualifications

• Experience in GMP manufacturing is highly preferred.

Work Environment

This role is within a rapidly growing company that is expanding with new state-of-the-art clean rooms and equipment in Columbus, Ohio. The work involves cross-functional team collaboration in a high-productivity environment.

This is a Contract position based out of Columbus, OH.

The pay range for this position is $24.00 - $28.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

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)

This is a fully onsite position in Columbus,OH.

This position is anticipated to close on Sep 4, 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email View email address on ziprecruiter.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.