Job Information
Catalent Pharma Solutions Senior Associate Scientist in Madison, Wisconsin
The Senior Associate Scientist will accurately, timely, and safely perform a variety of laboratory procedures in Upstream Process Development that support external client projects and internal technology development work by primarily focusing on the preparation of general lab solutions including cell culture media according to Batch Production Record (BPR) specifications. This person will also be performing routine, essential lab support assignments including equipment maintenance and cleaning, lab material stocking, general lab cleaning, and 5S organization. This work will involve applying technical knowledge in the use of standard upstream laboratory equipment and procedures such as incubators, biosafety cabinets, and culture sample analytics.
Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee.
The role:
Execute laboratory work plan according to the schedule developed by the supervisor or senior team member.
Prepare general lab solutions including cell culture media according to Batch Production Record (BPR) specifications.
Maintain and clean lab equipment including water baths, incubators, and biosafety cabinets; also wash bioreactors, glassware, plasticware, and carboys including autoclaving.
Assist with the ordering of consumables and restock general lab areas and satellite areas; work with the materials management team on stock room utilization.
Maintain lab organization and 5S standards in the development lab; execute and document 5S audits of laboratory space and update areas as needed or requested. Also, file paperwork and work orders.
Author technical documents such as protocols, test methods, development reports, certificates of testing, and operating procedures.
Review technical documents for accuracy, thoroughness, and regulatory compliance.
The candidate:
Bachelor's degree in Biotechnology or STEM discipline and 3-6 years related experience
Master’s degree in Biotechnology or STEM discipline and 0-3 years related experience
Ability to maintain high quality batch records and/or laboratory documentation in clear and accurate language in accordance with applicable regulatory guidance and site SOPs.
Ability to follow and interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
Proactively seek information to fill gaps in knowledge base.
Why you should join Catalent:
Competitive medical benefits and 401K
152 hours PTO + 8 Paid Holidays
Dynamic, fast-paced work environment
Opportunity to work on Continuous Improvement Processes
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.
Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone’s safety. The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers (https://careers.catalent.com/us/en) to explore career opportunities.
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 DisabilityAccommodations@catalent.com . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
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.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE (https://cdn.catalent.com/files/legal/CCPA-Privacy-Notice-at-Collection-for-California-Employees-and-Applicants-English.pdf) .
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