Technician - Biomanufacturing, Upstream

Catalent Pharma Solutions; Madison (WI); On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

PTO + holidays

401K match

Medical, dental and vision benefits

Tuition reimbursement

Job summary

Catalent, Inc. in Madison, WI is seeking an entry-level Technician for Upstream Biomanufacturing. You will perform aseptic cell culture in a Grade A environment, manage large-scale cultures in single-use bioreactors, and ensure batch records and SOPs are followed with GDP-compliant documentation.

The role emphasizes safety, quality, and continuous improvement, with potential mentorship of new team members and involvement in CI projects. This is a 100% on-site, 2pm-12am shift opportunity.

Qualifications

• Must have a HS diploma or higher; two years of relevant experience or a degree without experience.
• GMP manufacturing experience preferred.
• Proficiency with Word/Excel and basic Office tools.
• Experience with TrackWise, ComplianceWire, JD Edwards, DeltaV or chromatography software is a plus.

Responsibilities

• Perform basic upstream cell culture activities in a Grade A environment.
• Operate large-scale cell culture in single-use bioreactors and clarify bulk harvest.
• Follow BPRs and SOPs, aiming for right first time execution.
• Document activities per GDPs in quality records and forms.
• Identify deviations and raise awareness via Rapid Response.
• Support CI initiatives and may coach junior teammates.

Skills

Aseptic technique

Cell culture

cGMP awareness

Documentation

MS Word

MS Excel

Education

High School Diploma

Bachelor's / Associate degree

Tools

TrackWise

ComplianceWire

JD Edwards

DeltaV

Chromatography software

Job description

Technician - Biomanufacturing, Upstream

Position Summary:

• Work Schedule: 2pm-12am (Sunday-Wednesday or Wednesday – Saturday shift availability)
• 100% on-site

Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Located in Madison, WI, this facility features advanced mammalian cell line engineering and biomanufacturing capabilities using single-use systems to support scalable production. This 263,000 sq. ft. Good Manufacturing Practice (GMP) facility offers integrated formulation and analytical services to address complex development challenges in Biologics.

This is an entry level position in the Manufacturing team and is the starting point to acquiring skills and training required for a cGMP biomanufacturing environment. The Technician is responsible for the manufacture of biopharmaceutical products within a clean room environment. The position is expected to follow detailed instructions and established procedures with frequent supervision.

The Role:

• Perform basic Upstream cell culture activities, such as aseptic manipulation of cell culture within a Grade A environment, large-scale cell culture within single-use bioreactors (SUBs), and clarification of bulk harvest product
• Accurately follows manufacturing Batch Production Records (BPRs) and Standard Operating Procedures (SOPs) in accordance with current Good Manufacturing Practices (cGMPs) and with a focus on “right first time” execution
• Documents all activities in accordance with Good Documentation Practices (GDPs) in BPRs, Forms, and other quality documentation
• Recognizes deviations from the intended procedure and raises awareness through the Rapid Response process
• Proactively identifies safety, quality, and efficiency improvements; Actively participates in the Catalent Way (Continuous Improvement Culture)
• May lead “Just Do It” (JDI) Continuous Improvement (CI) activities and engage in implementation of CI projects
• May coach more junior team members on basic execution activities and act as an “onboarding buddy” to facilitate bringing new team members quickly up to speed on culture and basic workplace expectations
• Performs general cleanroom housekeeping, including room and equipment cleaning, disposal of waste, and maintenance of 5S standards
• Other duties as assigned

The Candidate:

• Must have High School Diploma or equivalent plus at least two (2) years of relevant experience. We will also accept a Bachelors or Associates Degree in a scientific, engineering, or biomanufacturing discipline without any formal experience
• GMP manufacturing experience preferred
• Ability to use Microsoft Word and Excel, and other Office systems
• GMP manufacturing experience preferred
• Preferred experience with TrackWise, ComplianceWire, JD Edwards, DeltaV, Chromatography software
• Physical requirements: This position requires frequent sitting, standing, walking, reading of written documents and use of computer monitor screen, reaching with hands and arms, talking, writing, listening. Occasional stooping, kneeling, crouching, bending, carrying, grasping. Frequent lifting and/or moving up to 10 pounds and occasional lifting and/or moving up to 50 pounds. Must comply with EHS responsibilities for the position. Working conditions will be Heating Ventilation and Air Conditioned controlled. Ability to operate within a clean room environment as needed.

Why you should join Catalent:

• Defined career path and annual performance review and feedback process
• Diverse, inclusive culture
• Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
• 152 hours of PTO + 8 paid holidays
• Generous 401K match
• Medical, dental and vision benefits
• Tuition Reimbursement- Let us help you finish your degree or start a new degree!

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [e-mail].

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

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