Job Description
This role involves collaborating with management and staff to develop and implement the strategic direction of the GMP area. You will be responsible for scheduling lab testing once samples are received by the Quality department and arranging analytical test methods required by the team. Additionally, you will provide general support for document review and engage in minor technical writing over time. You will play a crucial role in supporting GMP resources and the supply chain, ensuring materials inventory control aligns with production goals. Operating and performing calibration, validation, and cleaning of all facility equipment and systems as specified in SOPs is also part of this role. You will assist in process documentation review, revision, remediation, and process change controls, while working closely with GMP Management to identify and meet continuous improvement objectives using metrics and statistical analysis.
Responsibilities
Collaborate with management and staff to determine schedule and project timelines.Help with scheduling all lab testing needed once samples are sent to the Quality department.Schedule analytical test methods required by the team.Provide general support for document review and minor technical writing.Support GMP resources and supply chain, maintaining materials inventory control.Operate and perform calibration, validation, and cleaning of all facility equipment and systems.Assist in process documentation review, revision, remediation, and process change controls.Work with GMP Management to ensure continuous improvement objectives are met using metrics and statistical means.Essential Skills
Experience in schedule planning and coordination.Proficiency with laboratory information management systems (LIMS).Lab scheduling and coordination skills.Ability to manage lab samples.Additional Skills & Qualifications
Bachelor's degree in a science field preferred.Minimum 1+ years of experience in laboratory scheduling.Prior document review experience.Strong writing, communication, and attention to detail skills.Experience in Quality preferred.Knowledge of GMP or bioprocessing.Experience in GMP and technical writing is a plus.Work Environment
The work environment is team-oriented and diverse, with a growing group of individuals. The current team consists of five people and is expected to expand by the end of the year. Collaboration and the ability to work well with others are essentia
Pay and Benefits
The pay range for this position is $24.00 - $24.00/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 Columbus,OH.
Application Deadline
This position is anticipated to close on Jul 15, 2025.
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.