Associate Scientist I - Quality Control
Company: Disability Solutions
Location: Madison
Posted on: November 15, 2024
Job Description:
Associate Scientist I - Quality ControlPosition SummaryCatalent
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 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.--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.The Associate Scientist I - Quality Control is
an entry level laboratory role with the expectation that the
candidate is able to be trained on technical procedures and once
trained, execute them consistently and reliably. The Associate
Scientist I - Quality Control may support preventative maintenance
and basic laboratory maintenance activities while maintaining a GMP
quality system.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
- Executes and properly documents cGMP Quality Control testing
with supervision.
- Operates basic cGMP Quality Control equipment. Accurately
completes routine and preventive maintenance on basic
equipment.
- Performs self-review of analytical data for accuracy and
consistency with SOP.
- Enters data into Laboratory Information Management System
(LIMS) or laboratory reports.
- Performs solution preparations. Perform facility monitoring of
gas and water sampling.
- Perform routine Environmental Monitoring in manufacturing
environment: active air sampling, non-viable particulate
monitoring, surface and personnel sampling.
- Log in samples into laboratory tracking software.
- Performs general lab housekeeping in adherence to 5S
standards.
- Stages materials/components for use within cGMP Quality Control
Lab.
- Other duties as assigned.The Candidate
- Bachelor's Degree in Biology, Biotechnology, Chemistry, or
related life sciences field, OR Associate Degree in Biology,
Biotechnology, Chemistry, or related life sciences field with a
minimum of 1 year of industry experience, OR High School Diploma or
equivalent with a minimum of 4 years of industry experience.
- Basic understanding of analytical chemistry and simple lab
equipment preferred.
- Familiarity with clean room procedure, aseptic technique, and
general lab equipment experience.
- cGMP, Good Documentation Practices (GDP), Good Laboratory
Practices (GLP) knowledge, and experience following standard
operating procedures (SOP) preferred.
- General laboratory equipment experience, including
micropipettes.
- 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 in a lab environment will require working with
skin irritants, lung irritants, electrical equipment, sharp
instruments, toxic materials, and hazardous waste. Safety
procedures will be followed to minimize exposure, including clean
room gowning. Working conditions will be Heating Ventilation and
Air Conditioned controlled.Why You Should Join Catalent
- Several Employee Resource Groups focusing on D&I--
- Tuition Reimbursement---- Let us help you finish your degree or
earn a new one!--
- Generous 401K match--
- 152 hours accrued PTO + 8 paid holidays--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.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, Oshkosh , Associate Scientist I - Quality Control, Other , Madison, Wisconsin
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