AAV Scientist I

Job Description

The AAV Scientist I is responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing Facility (CMF). Collaborating with the Manager of GMP Operations and staff, the Scientist I will provide hands-on assistance for all day-to-day GMP/AAV production operations, including the execution of production processes, documentation, as well as facility and equipment maintenance. The Scientist I will support production efforts to deliver all products in a timely, compliant, and fiscally responsible manner by following appropriate practices, batch records, and Standard Operating Procedures (SOPs) for manufacturing biological products.

The shift is Monday to Friday from 8:00 AM to 4:30 PM, with some flexibility to start between 7:30 AM and 8:30 AM if needed.

ResponsibilitiesWork in collaboration with AAV management and staff to cultivate and enact the strategic direction of the GMP area, including determination of schedule and project timelines/capabilities.Support PD resources and supply chain, including maintaining materials inventory control to meet production goals.Work in Biosafety Cabinets.Operate and perform calibration, validation, and cleaning of all facility equipment and systems as specified in SOPs.Assist in process documentation review, revision, remediation, and process change controls.Work closely with GMP Management to ensure continuous improvement objectives are identified and met using metrics and other statistical means.Participate in making and developing viruses, including some PD work.Handle media bags and Hyperstacks, with occasional lifting of up to 40 lbs.

QualificationsBS degree in a scientific field, ideally in Biochemistry, Microbiology, Virology, or Genetics.Minimum of 1+ years of experience in the scientific industry, preferably in a GMP setting or working with cells.Knowledge and understanding of aseptic technique, cell culture, liquid separation techniques, and fluid handling with cells, specifically with Mammalian or eukaryotic.Experience with chromatography, pipetting, and centrifugation.Experience in making solutions and buffers.Experience in aliquoting.Knowledge of GMP or bioprocessing.Experience in tissue culture, virology, microbiology, mammalian cell culture, and eukaryotic systems.Proficiency in PCR, assay development, and chromatography.Work Environment

The culture is very team-oriented, with a diverse group of individuals that is continuing to grow. The team currently consists of 4 people and is expected to expand 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 shift is Monday to Friday from 8:00 AM to 4:30 PM, with some flexibility to start between 7:30 AM and 8:30 AM if needed.

Pay and Benefits

The pay range for this position is $24.00 - $26.00

• 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 Dublin,OH.

Application Deadline

This position will be accepting applications until Dec 26, 2024.

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.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our people

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 actalentaccommodation@actalentservices.com for other accommodation options.