Associate Lead I - Biomanufacturing, Compliance
Company: Disability Solutions
Location: Madison
Posted on: October 19, 2024
Job Description:
Associate Lead I, Biomanufacturing ComplianceCatalent 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, and our market leading
biologics analytical services 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.The Associate Lead I, Biomanufacturing
Compliance--is responsible for providing support to cGMP
manufacturing operations, and ensuring compliance for Standard
Operating Procedures, and both regulatory and client
requirements.This is a full-time on-site hourly position, Sunday -
Wednesday, 7:00am - 5:00pmCatalent 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:----
- Facilitate Rapid Response Team as deviations occur, documenting
critical information to determine true root cause
- Provide timely review of logbooks as needed to ensure data
complies with cGMP expectations; Assist to track/monitor and
provide timely, accurate information regarding status of open
investigations
- Participate in initiatives to improve process compliance
culture, including on-going cGMP understanding and application,
including self-audit and CAPA programs
- Participate in internal audits and assist in closure of
applicable findings
- Actively engage in Inspection Readiness activities and teams;
Assists in identifying improvements for safety and provides on the
floor manufacturing support
- Identify and assist with training issues, instruction problems,
or new educational needs regarding specific employees or groups or
equipment
- Assist to write and revise SOPs (Standard Operating Procedures)
when gaps are identified
- Ability to work scheduled shift and other off-shift coverage as
required.
- Other duties as assignedThe Candidate:----
- Requires Bachelor's Degree in technical discipline (e.g.,
biology, biotechnology, engineering) or related life science field,
OR
- Associate's Degree in technical discipline (e.g., biology,
biotechnology, engineering) or related life science field with a
minimum of 1 years' related experience, OR
- High School Diploma with a minimum of 4 years' related
experience.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 paid time off annually +--8--paid holidays--
- Competitive salary with yearly bonus potential--
- Community engagement and green initiatives--
- Generous 401K match and Paid Time Off accrual--
- Medical, dental and vision benefits effective day one of
employment--
- 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.--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, Dubuque , Associate Lead I - Biomanufacturing, Compliance, Other , Madison, Iowa
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