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SENIOR SCIENTIST (FINISH FILL)

INTERESTED CANDIDATES MAY SEND UPDATED RESUMES TO: JGASSER @ ACTALENTSERVICES.COM

OR TEXT JENNA TO SETUP A PHONE INTERVIEW: 419. 980. 5823

Job Description

We are immediately hiring for a Senior Scientist role in a Cell and Gene Therapy manufacturing environment. An ideal candidate for this role will have either 5 years of relevant experience with a Bachelors Degree, or 2 years of relevant experience with a Masters Degree (PhD level candidates will likely not be considered for this role).

Responsibilities

+ Solve, correct, and prevent problems while performing tasks as assigned by leadership, as well as assigning tasks to junior staff.

+ Work towards specific measurable objectives requiring operational planning skills with little direct supervision.

+ Lead and support a diverse and collaborative team environment, utilizing clear and concise communication to deliver high productivity and contribute to team and organizational goals.

+ Provide leadership in daily operational activities related to the GMP manufacturing of biological products, including ensuring the availability of materials and proper documentation surrounding GMP activities and product quality.

+ Set and maintain a professional standard within the GMP area.

+ Work with GMP Management to enact the strategic direction of the GMP area.

+ Support GMP resources and the supply chain, including ordering and maintaining materials inventory to meet production goals.

+ Maintain high standards of accurate documentation on all GMP operations.

+ Train and supervise junior staff to ensure proper operation of facility equipment and adherence to accurate documentation surrounding GMP activities and product quality.

+ Guide the Operations Staff in deviation investigations, OOS results, and process troubleshooting while working with GMP management and Quality Assurance.

+ Collaborate with GMP Management to identify and meet continuous improvement objectives using metrics and other statistical means.

+ Collaborate with GMP Management to incorporate new projects and technologies into the GMP area.

+ Respond to and take action from alarm notifications from the applicable monitoring system(s) for laboratory temperature-controlled storage units during assigned periods of responsibility.

+ Exercise discretion, judgment, and personal responsibility.

+ Demonstrate a high level of integrity and maintain a positive attitude.

+ Operate within the Quality Management System applicable to the manufacture of phase-appropriate material in the CMF.

+ Maintain compliance with applicable regulatory requirements for cellular and gene therapy products.

+ Pay attention to detail in all job functions.

+ Operate in alignment with established policies, procedures, and techniques, requiring relevant training, practical experience, or a working knowledge of the tasks involved.

+ Document all activities performed according to SOPs.

Essential Skills

+ Four-year Life Science degree or Master's degree.

+ Five years of relevant experience with a four-year degree or two years with a Master's degree.

+ Background in the life sciences, biotechnology, or gene therapy industries preferred.

+ Prior experience in a GMP or GLP setting strongly preferred.

+ Knowledge of GMP or bioprocessing.

Additional Skills & Qualifications

+ Prior experience in Suspension or Bioreactor's is a big plus.

+ Experience with downstream processes, TFF, clarification, or large-scale cell culture is strongly preferred.

Work Environment

The culture is very team-oriented, with a diverse group of individuals that continues to grow. The team is currently composed of 4 people and is expected to grow significantly by the end of the year. Collaboration is essential, as no work or testing can be done alone. The dress code is business casual with appropriate lab attire. The work schedule is a 4-day week from 7-8 AM to 5:30-6:30 PM, with some flexibility required for late days, which will be balanced by starting later the next day when possible.

Pay and Benefits

The pay range for this position is $31.00 - $36.00/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 May 22, 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 [email protected] (%[email protected]) for other accommodation options.