Scientist - Process Development, Downstream
Company: Disability Solutions
Location: Madison
Posted on: May 3, 2024
Job Description:
Position Title:-- Scientist - Process Development, DownstreamM-F
1st shiftSummary:Catalent Biologics is a fast-growing business
within Catalent Pharma Solutions focused on providing innovative
technologies and solutions to help more and better biologic
treatments get to patients.-- The business includes our proprietary
GPEx cell line engineering platform, our new state-of-the-art
biomanufacturing facility in Madison, WI, and our market leading
biologics analytical services in Kansas City, MO and Research
Triangle Park, NC, as well as SMARTag Antibody Drug Conjugate
technology in Emeryville, CA.-- Leveraging our growing
differentiated technology portfolio, world class manufacturing
capability, and other integrated services across the Catalent
network, Catalent Biologics is positioned to drive significant
growth for Catalent.Working for Catalent Biologics is an
opportunity to join an entrepreneurial team.-- Catalent Biologics
is making significant investments in people and capabilities.--
This is a unique opening to join a small, fast-growing business,
backed by a global public company.-- People joining our team will
have the opportunity for career development as our business
continues to grow and expand.-- Catalent-Madison employees are
helping to improve future patient outcomes by working on products
that are designed to treat COVID-19, cancer, various autoimmune,
fibrotic and blood disorders, HIV, diabetes, heart, and lung
diseases as well as Alzheimer's.The Scientist - Process
Development, Downstream will perform a variety of laboratory
procedures in Downstream Process Development. The Scientist -
Process Development, Downstream is expected to have advanced
knowledge of principles, theories, and concepts applicable to wide
range of work in a downstream discipline and broad knowledge of
principles and concepts applicable to protein purification. This
position is expected to apply technical and functional knowledge to
assist in experiment/project design that will enable the downstream
process development team to meet goals.----The Role:--
- Execute laboratory work plan (including data entry).
- Schedule development plans with input from supervisor or senior
team member. --
- Author and may approve technical documents such as protocols,
test methods, test reports, certificates of analysis, and operating
procedures.
- Review technical documents for accuracy, thoroughness, and
regulatory compliance.
- Participate in client meetings offering technical support and
leading the project.
- Manage client projects.
- Act as the technical lead for client development projects,
communicate project status internally and externally, and
effectively provide technical explanation/rationalization.
- Critically analyze complex data, interpret and integrate
experimental results with project objectives.
- Write procedural SOPs, batch production records, and
reports.
- Accurately review batch records and other data, ensuring
consistency.
- Execute purification experiments including automated
chromatography (AKTA platform), filtration, clarification, column
packing, and tangential flow filtration independently.
- Knowledge of protein purification and analysis with an in depth
understanding of all modes of chromatography.
- Knowledge of scale up principles with respect to purification
and filtration.
- Update group members on background and status of client
projects by giving oral updates or internal presentations.
- Troubleshoot and problem solve in order to initiate and
execute/monitor corrective actions.The Candidate
- Bachelor's degree in a STEM discipline and 6-9 years related
experience, OR
- Master's degree in a STEM discipline and 3-5 years related
experience, OR
- Doctorate Degree in a STEM discipline and 0-2 years related
experience.
- Process scale chromatography and filtration (viral,
chromatography, tangential flow, normal flow) experience
- Operating, maintaining, and troubleshooting chromatography
workstations and process skids, preferably in an industrial
setting
- Viral clearance validation, process scale up, and technology
transfer
- Knowledge and experience working in a cGMP environment
- Good documentation practices (GDP)
- Aseptic technique experience
- Experience writing standard operating procedures, batch
records, and reports
- Experience mentoring junior staff regarding laboratory
procedures and scientific projectsPosition Benefits:
- 152 days PTO & 8 Holidays
- Medical, Dental & Vision Benefits and 401k
- Tuition ReimbursementCatalent 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 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
. 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 .
Keywords: Disability Solutions, Madison , Scientist - Process Development, Downstream, Other , Madison, Wisconsin
Didn't find what you're looking for? Search again!
Loading more jobs...