URGENTLY HIRING: Upstream GMP Scientist II @ Actalent

GMP Scientist II (Upstream)INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT 330. 397. 1302 TO SET UP AN IMMEDIATE PHONE INTERVIEW!Job DescriptionThe GMP Operations Scientist plays a pivotal role in guiding all aspects of Good Manufacturing Practices (GMP) and production within the Clinical Manufacturing Facility (CMF). Collaborating closely with GMP Operations management, the Scientist provides hands-on support and leadership for daily GMP production operations, ensuring timely, compliant, and fiscally responsible delivery of products.

Responsibilities

• Solve, correct, and prevent problems while performing tasks assigned by leadership, and assign tasks to junior staff.
• Work towards specific measurable objectives that require operational planning skills with minimal supervision.
• Lead and support a diverse and collaborative team environment through clear and concise communication.
• Provide leadership in daily operational activities related to GMP manufacturing of biological products.
• Lead and execute production processes, ensuring materials availability and proper documentation for GMP activities and product quality.
• Set and maintain professional standards within the GMP area.
• Collaborate with GMP Management to enact strategic direction and support GMP resources and supply chain.
• Maintain accurate documentation for all GMP operations.
• Train and supervise junior staff to ensure proper operation of facility equipment and adherence to documentation standards.
• Guide Operations Staff in deviation investigations, OOS results, and process troubleshooting.
• Collaborate with GMP Management to meet continuous improvement objectives using metrics and statistical means.
• Incorporate new projects and technologies into the GMP area.
• Respond to alarm notifications from monitoring systems for temperature-controlled storage units during assigned periods.
• Exercise discretion, judgment, and personal responsibility while demonstrating integrity and maintaining a positive attitude.
• Operate within the Quality Management System for manufacturing phase-appropriate material in the CMF.
• Maintain compliance with regulatory requirements for cellular and gene therapy products.
• Pay attention to detail in all job functions and operate in alignment with established policies, procedures, and techniques.

Essential Skills

• Relevant four-year Life Science degree OR Master's degree.
• 3 years of relevant experience with a four-year degree OR 1 year with a Master's degree.
• BG in life sciences, biotechnology, or gene therapy industries preferred.
• Prior experience in a GMP or GLP setting strongly preferred.
• Excellent communication, organization, and project management skills.
• Proficiency in Microsoft Office (PowerPoint, Excel, Word) including data interpretation and reporting.
• Technical writing/SOP writing experience preferred.
• Ability to work independently and collaboratively in a diverse and inclusive work environment.
• Knowledge of GMP or bioprocessing.

Additional Skills & Qualifications

• Prior experience in Suspension or Bioreactor's is a big plus.
• Experience in downstream, TFF, clarification, or large-scale cell culture is strongly preferred.

Work EnvironmentThe work culture is team-oriented and diverse, with a growing group of individuals. Collaboration is key, as no work or testing is done alone. Business casual attire is required, along with appropriate lab attire. The work schedule is flexible, generally from 7-8 AM to 5:30-6:30 PM, with adjustments as needed to balance hours.

Job Type & LocationThis is a Contract to Hire position based out of Columbus, OH.

Pay and BenefitsThe pay range for this position is $28.00 - $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)

Application DeadlineThis position is anticipated to close on Nov 28, 2026.

Workplace TypeThis is a fully onsite position in Columbus,OH.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 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 process due to a disability, please email [email protected] for other accommodation options.

San Francisco Fair Chance Ordinance

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

Massachusetts Lie Detector

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall 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 applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.