Biomanufacturing Technician

Position: Technician - Biomanufacturing, Upstream

Catalent is a prominent, rapidly expanding public organization and a key collaborator for the pharmaceutical sector in the creation and production of innovative therapies for patients globally. Your skills, insights, and enthusiasm are vital to our mission: to enhance the quality of life for individuals.

Catalent Biologics represents a dynamic segment within Catalent Pharma Solutions, dedicated to delivering cutting-edge technologies and solutions that facilitate the development of superior biologic therapies for patients. This division encompasses our proprietary GPEx cell line engineering platform, our advanced biomanufacturing facility, and our leading analytical services for biologics, alongside SMARTag Antibody Drug Conjugate technology. By leveraging our diverse technology portfolio and world-class manufacturing capabilities, Catalent Biologics is strategically positioned for substantial growth.

The Manufacturing department is tasked with executing clinical and commercial production in compliance with regulatory standards, site protocols, and client specifications. The scope of manufacturing cGMP production includes solution preparation, master and working cell bank production, upstream cell culture, downstream protein purification, mRNA and molecular therapeutics production, as well as small-scale fill and finish operations. Furthermore, the manufacturing team is committed to employing continuous improvement strategies to enhance process efficiency, optimize outputs, and minimize waste.

This role serves as an entry-level opportunity within the Manufacturing team, providing a foundation for acquiring essential skills and training pertinent to a cGMP biomanufacturing setting. The Technician will be responsible for the production of biopharmaceutical products within a controlled cleanroom environment, adhering to detailed instructions and established protocols under regular supervision.

Employment Type: Full-time, On-site, Wednesday - Saturday, 2:00 PM - 12:00 AM

Key Responsibilities:

• Conduct basic upstream cell culture tasks, including aseptic manipulation of cell cultures in a Grade A environment, large-scale cell culture in single-use bioreactors, and clarification of bulk harvest products.
• Rigorously adhere to manufacturing Batch Production Records (BPRs) and Standard Operating Procedures (SOPs) in line with current Good Manufacturing Practices (cGMPs), emphasizing accuracy and efficiency.
• Document all processes in accordance with Good Documentation Practices (GDPs) within BPRs, forms, and other quality documentation.
• Identify and report deviations from established procedures through the Rapid Response process.
• Actively seek opportunities for safety, quality, and efficiency enhancements; engage in the Catalent Way (Continuous Improvement Culture).
• Potentially lead "Just Do It" (JDI) Continuous Improvement initiatives and contribute to the implementation of CI projects.
• May mentor junior team members on fundamental execution tasks and serve as an onboarding resource to expedite the acclimatization of new team members to the workplace culture and expectations.
• Participate in daily shift meetings and may facilitate shift transition activities.
• Maintain cleanliness in the cleanroom, including equipment cleaning, waste disposal, and adherence to 5S standards.
• Perform additional duties as assigned.

Candidate Qualifications:

• Bachelor’s or Associate’s Degree in a scientific, engineering, or biomanufacturing field with no prior experience required OR
• High School Diploma with a minimum of 2 years of relevant experience.
• Experience in GMP environments is preferred.
• Ability to lift and/or move 0-10 pounds frequently, with occasional lifting/moving of up to 50 pounds.

Why Join Catalent?

• Clearly defined career progression and annual performance evaluations.
• A diverse and inclusive workplace culture.
• Opportunities for career advancement within a team dedicated to improving lives.
• 152 hours of paid time off annually plus 8 paid holidays.
• Competitive salary with potential for annual bonuses.
• Engagement in community and sustainability initiatives.
• Generous 401K matching and Paid Time Off accrual.
• Comprehensive medical, dental, and vision benefits effective from the first day of employment.
• Tuition reimbursement options.

Catalent offers rewarding career opportunities. Join a global leader in drug development and delivery and contribute to the advancement of over 7,000 life-saving and life-enhancing products for patients worldwide. Catalent is an exciting and growing international organization where employees collaborate directly with pharmaceutical, biopharmaceutical, and consumer health companies of all sizes to progress new therapies from early development through clinical trials to market. Catalent produces over 70 billion doses annually, each one relied upon by someone in need. Join us in making a significant impact.

Catalent is dedicated to the health and safety of its employees, visitors, and the clients and patients we serve. In response to the global pandemic, we have adapted many of our recruitment and onboarding processes to ensure everyone's safety. The Human Resources team will communicate all necessary safety protocols throughout each stage of the hiring process.

Catalent is an Equal Opportunity Employer, including individuals with disabilities and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, please submit your request accordingly. This option is reserved for individuals needing accommodation due to a disability.