Plasmids Scientist I

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Job Description

The Plasmids R&D Scientist I is responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing Facility (CMF). The role involves collaborating with the Manager of GMP and Plasmids Operations and staff to provide hands-on assistance for day-to-day Plasmids Core production operations, including execution of production processes, documentation, as well as facility and equipment maintenance.

ResponsibilitiesConduct testing including cell growth, chromatography, microbiological testing, and assay development.Identify and coordinate the development of experiments to fill knowledge gaps.Research and develop processes for the production and purification of plasmids.Anticipate and troubleshoot issues with operations to avoid interruptions in production.Work with management to answer client questions regarding their product.Ensure the availability of materials and proper documentation surrounding GMP activities and product quality.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.Perform tasks in accordance with established policies, procedures, and techniques, requiring training, common experience, or working knowledge.Solve, correct, and prevent problems, perform tasks assigned by leadership, and assign tasks to junior staff.Work to specific measurable objectives requiring operational planning skills with little direct supervision.Document all activities performed according to Standard Operating Procedures (SOPs).Support GMP resources and supply chain by ordering and maintaining materials inventory to meet production goals.Support daily operational activities related to the manufacturing of biological products by ensuring the availability of materials with the proper documentation surrounding GMP activities.Assist in process documentation review, revision, remediation, and process change controls.Essential SkillsGood Manufacturing Practices (GMP)Tissue cultureBiologyCell cultureMolecular biologyAssay developmentMicrobiologyMammalian cell cultureEukaryotic cell cultureLaboratory skillsCell biologyQualificationsBachelor's degree in a Biological Field (Biology, Biochemistry, Microbiology, Molecular Biology, or Genetics)Industry experience in Aseptic Processing or GMPExperience in Drug Compounding, Drug Manufacturing, or Food Manufacturing/FDAPrior experience with mammalian or eukaryotic cellsKnowledge and understanding of aseptic technique, cell culture, and liquid separation techniquesComfortable with occasionally lifting/pushing/pulling 30-45 lbsWork Environment

The culture is very team-oriented, with a diverse group of individuals that is continuing to grow. You will be on your feet most of the day and will need to gown up to go into the clean rooms. The dress code includes casual lab attire (closed-toed shoes, socks covering ankles, khaki pants or jeans with no holes, and shirts with no large graphics). You will spend 50-75% of your time working in the lab and about 25% at a desk doing documentation and report writing. The shift is Monday through Friday, 8 AM to 5 PM.

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 Mar 17, 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.

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.