Job Title: Biologics Manufacturing Consultant - Gene Therapy
Job Description

We are looking for a Biologics Manufacturing Consultant with experience in gene therapy product development and manufacturing, specifically utilizing AAV viral vectors. The role involves developing biologics manufacturing purification processes and supporting GMP manufacturing for clinical trials. The consultant will work under general supervision and report to a supervisor or manager.

ResponsibilitiesSupport GMP manufacturing readiness with respect to documentation, raw materials, and equipment.Provide on-the-floor support as Person in Plant during clinical manufacturing.Review executed batch records.Provide deviation resolution support.Guide the development of manufacturing unit operations.Review development protocols and reports.Essential SkillsBachelor's Degree in a relevant field.Specific experience with AAV vector manufacturing and testing.Experience working with Contract Development and Manufacturing Organizations (CDMOs).4-6 years of relevant experience.Additional Skills & QualificationsExperience with AAV producer cell line manufacturing.Work Environment

The work environment includes both laboratory and manufacturing settings. The role requires adherence to GMP standards and involves working with advanced biologics manufacturing equipment and processes.

Pay and Benefits

The pay range for this position is $26.00 - $27.00

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 Chesterfield,MO.

Application Deadline

This position will be accepting applications until Jan 26, 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.