Principal Representative, QA
Company: Disability Solutions
Location: Bloomington
Posted on: November 11, 2024
Job Description:
We're hiring for a Principal Representative, QA in Bloomington,
IN to support aseptic and sterility assurance programs. 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.--A Principal Representative, QA's primary role is
to support serve as a Subject Matter Expert and program implementor
of the facility's aseptic program and policies. This role will
support a team that is responsible for the development and
implementation of all sterility assurance and microbiology
strategies, policies, and procedures for the company's
manufacturing facility. This is a full-time, salaried position and
is 100% site based. The schedule is Monday - Friday, 2nd
shift.Catalent Biologics in Bloomington, Indiana--is
a--state-of-the art,--GMP--manufacturing--facility,--providing--one
million--sq/ft of drug substance manufacturing, drug product
manufacturing, and related pharmaceutical services. This
award-winning facility helps customers accelerate biologic drug
development programs and bring better treatments to help patients
live better, healthier lives.The Role
- Work with a cross-functional team to develop and implement
sterility assurance and microbiology strategies, policies, and
procedures.
- Assist leadership in the implementation of quality systems and
compliance procedures, across the department.
- Service as a Subject Matter Experience in sterility assurance
and aseptic operations.
- Participate in regulatory inspections and assist in leading the
quality assessment of internal operations for any risks.
- Responsible for the Contamination Control Strategy to ensure
and improve clean room controls within the facility, to minimize
risk and cross-contamination.
- Other duties as assigned.The Candidate
- Bachelor's Degree with a minimum of 8 years relatable
experience.
- Degree in microbiology or biology, highly preferred.
- Minimum of 12 years relatable experience, or demonstrated
excellence in role, with justification.
- Minimum of 4 years GxP experience, or other regulated
industry.
- Prior experience with sterility assurance and aseptic
processing within a pharmaceutical or biotechnology manufacturing
environment, highly preferred.
- Prior experience with regulatory inspections and audits, highly
preferred.
- Must be able to read and understand English-written job
instructions and safety requirements.Why you should join Catalent
- Medical, dental, vision, and wellness benefits are effective on
the first day of employment.
- Potential for career growth on an expanding team and
organization.
- 152 hours of paid time off annually plus 8 paid holidays.
- Community engagement and green initiatives.
- Engaging D&I Employee Resource Groups.
- Tuition reimbursement program.
- Generous 401K match.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, Greenwood , Principal Representative, QA, Other , Bloomington, Indiana
Didn't find what you're looking for? Search again!
Loading more jobs...