Manufacturing Specialist

Kelly Services; Houston (TX); On-site; USD 103,155,000 - 114,616,000; Full time

Benefits offered by this job

Benefits package

Holiday pay

Transit spending account

Paid sick leave

Job summary

Kelly Science & Clinical in Houston, TX is seeking two Manufacturing Specialists to support gene therapy product production in a GMP setting. Role includes hands-on manufacturing, cell culture, and viral vector purification for preclinical and clinical programs.

12-month contract with day shift and occasional weekends. The role requires a Bachelor’s degree in Biology/Biotechnology and experience in upstream/downstream processes, aseptic operations, and GMP documentation.

Qualifications

• Working knowledge of cGMP requirements and regulated manufacturing environments.
• Understanding of deviation investigations, root cause analysis, CAPAs, and GMP quality systems.
• Ability to follow written procedures, protocols, and manufacturing instructions.
• Experience with high-velocity documentation and change controls.

Responsibilities

• Operate manual, semi-automated, and automated equipment in production of biopharmaceuticals.
• Perform cell culture using single-use bioreactor systems.
• Conduct process-scale chromatography and viral vector purification.
• Prepare buffers and stage equipment in production areas.
• Support deviation investigations and CAPAs with cross-functional teams.
• Assist with validation, data collection, and inventory management.

Skills

GMP knowledge

Aseptic technique

Documentation accuracy

Cross-functional communication

Education

Bachelor’s degree in Biology/Biotechnology

Tools

Single-use bioreactor

Process-scale chromatography

TFF

Biosafety cabinets

Job description

Job Title: Manufacturing Specialist (contract)

Location: Houston, TX

Rate: $36-40/hr.

Schedule: Day Shift; occasional weekend work may be required

Duration : 12 months

About the Company

Kelly Scientific is partnering with a clinical-stage biotechnology company focused on developing life-changing genetic medicines for patients and families affected by rare neurological diseases.

Position Overview

We are seeking (2) Manufacturing Specialists to support the production of gene therapy products. The Manufacturing Specialist will perform hands‑on manufacturing activities supporting the production of preclinical and clinical biopharmaceutical products and help maintain a reliable supply of materials for ongoing clinical trials.

The level of the position will be determined based on the candidate’s relevant education, technical experience, and GMP manufacturing background.

Responsibilities

• Operate manual, semi-automated, and automated equipment in support of routine production of preclinical and clinical biopharmaceuticals

• Perform large-scale cell culture using single-use disposable bioreactor systems

• Perform viral vector purification using process-scale chromatography equipment

• Prepare buffer solutions

• Stage equipment and raw materials in production suites

• Support and conduct non-critical deviation investigations, including gathering relevant information, assisting with root cause analysis, documenting investigation findings, and supporting appropriate corrective and preventive actions (CAPAs) in collaboration with Quality and cross-functional teams

• Assist with other production-related activities such as validation, data collection, inventory management, and maintenance of process equipment

• Perform cleaning of facility and unit process equipment

• Write and review SOPs and change control documents for manufacturing work areas

• Ensure proper documentation is completed to meet quality system requirements

• Participate in facility safety programs

• Resolve technical problems through collaboration with internal teams and external resources, including vendor support

Additional Responsibilities for Advanced Roles

• Author technical documentation such as summary reports

• Lead project meetings

Required Qualifications

Education

• Bachelor’s degree in Biology, Biotechnology, or a related scientific field

Experience

• Biopharmaceutical manufacturing experience in a GMP-regulated environment is preferred but not required

• Experience in upstream and/or downstream manufacturing processes is strongly preferred, including experience with:

• Single-use bioreactor systems

• Cell culture

• Aseptic processing and sterile operations

• Biosafety cabinets

• Process-scale chromatography

• Tangential Flow Filtration (TFF)

• Buffer preparation

• Viral vector manufacturing or purification

Knowledge & Skills

• Working knowledge of cGMP requirements and regulated manufacturing environments

• Understanding of deviation investigations, root cause analysis, CAPAs, and other applicable GMP quality systems

• Understanding of complex manufacturing equipment and process instrumentation

• Strong aseptic technique and attention to contamination control

• Ability to accurately follow written procedures, protocols, and manufacturing instructions

• Ability to develop or revise procedures when required

• Comfortable performing repetitive laboratory/manufacturing tasks, including pipetting

• Strong attention to detail and commitment to accurate documentation

• Ability to communicate and collaborate effectively with personnel across multiple departments and levels of the organization

• Ability to troubleshoot routine technical issues and elevate appropriately

Cleanroom & Physical Requirements

• The majority of work will be performed in a GMP manufacturing cleanroom environment

• Must be comfortable working in controlled environments, including areas operating up to ISO 5 / Grade A following appropriate training

• Must be willing and able to follow gowning requirements, which may include coveralls, face masks, shoe covers, hair/beard nets, and other PPE

• Ability to lift up to 50 lbs. with assistance

• Work may involve exposure to high-pressure gases, flammable materials, cryogenic operations, and chemical hazards including strong acids and bases

• Must consistently follow all applicable safety, environmental, and GMP procedures

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Please note: The following benefits reflect Kelly's general offerings. Eligibility may vary by assignment, location, and job type. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (https://www.mykelly.com/help-support-working-with-kelly-us/#Benefits) for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.

Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice (https://www.kellyservices.com/hubfs/myKelly/Resources/Employment_Policies/Recruitment-Artificial-Intelligence-Notice.pdf?hsLang=en) .

Kelly Services is proud to be an Equal Employment Opportunity and Affir mp? Wait: The content: ... A conviction does not automatically bar individuals from employment.