Label Control Manager
Company: Disability Solutions
Location: Philadelphia
Posted on: October 15, 2024
Job Description:
Label Control ManagerPosition Summary: Catalent is a global,
high-growth, private 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.----This 206,878 square-foot facility, located in the
Philadelphia area is Catalent's global Center of Excellence for
Clinical Supply Packaging.-- Catalent offers GMP secondary
packaging and clinical labeling services throughout our global
network. Packaging can be configured to hold a single product, or
multiple products as determined by study requirements. We offer
manual patient kit assembly along with semi-automated and automated
wallet sealing and high-speed automated carding to meet the needs
of studies of all sizes. For temperature sensitive products and
those with minimal to zero allowable time out of environment, we
can perform secondary packaging in refrigerated and frozen
packaging rooms or over dry ice depending upon your project
needs.-- Using our Clinicopia global labeling system with its
multi-lingual label phrase library we can design single panel,
booklet labels or our unique Peel-ID--- safe storage labels for
your studies. Single panel and Peel-ID--- safe storage labels can
be conveniently reviewed and approved online via our Fusion portal
before being printed and inspected at our facilities.Catalent
Pharma Solutions in Philadelphia, PA is hiring a Label Control
Manager.-- -- The Label Control Manager is responsible for leading
a team tasked with the design, creation, printing, receipt/control
and destruction of primary and secondary packaging labels utilized
in packaging and distribution of stability, analytical, commercial,
and clinical trial material. The responsibilities include the
creation of and control of randomization for clinical trial
studies.This is a full-time, salaried role. ----This role is
onsite, on 1st shift. The core hours are Monday - Friday,
8am-5pm.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:
- Ensure compliance with all FDA (GMP / GCP) regulations.
Implement standard operating procedures (SOPs) and training
documentation
- Manage the overall function of label receipt, creation/design,
inspection, receipt/control, storage, destruction, and release
- Ensure Label Control efficiency and cost effectiveness through
optimum utilization of resources and ongoing evaluation and
improvement of methods and systems; Develop procedures and
techniques to optimize operations and effectively service internal
and external clients
- Negotiate the terms, conditions, performance requirements and
legal obligations of vendor contracts so as to derive maximum
benefit and protection of corporate interests while minimizing risk
and cost
- Maintain and motivate a team capable of achieving all
documentation and technical targets and training requirements to
service customers on time and right first time
- Monitor investigations for timely submissions and ensure
appropriate corrective action and close out
- Analyze staffing requirements and responsibilities related to
business needs and forecasts
- All other duties as assignedThe Candidate:
- High School Diploma or GED is required
- Bachelor's Degree is preferred
- Two + years relevant experience in the pharmaceutical industry
is preferred
- Experience managing projects and people is preferred
- Knowledge of FDA, MHRA, EU and other applicable regulatory
guidelines that apply to the clinical packaging environment are
preferred
- GMP and FDA regulated industry experience is required
- Demonstrable leadership experience at Catalent (including but
not limited to participation in Catalent-sponsored leadership
programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may
be considered in place of external experience
- Individual may be required to sit, stand, walk regularly and
occasionally lift 0-15 poundsWhy You Should Join Catalent:
- Defined career path and annual performance review and feedback
process--
- Diverse, inclusive culture--
- Positive working environment focusing on continually improving
processes to remain innovative
- Potential for career growth on an expanding team within an
organization dedicated to preserving and bettering lives--
- 152 hours of PTO + 8 paid holidays
- Several Employee Resource Groups focusing on D&I
- Dynamic, fast-paced work environment
- Community engagement and green initiatives--
- Generous 401K match--
- Company match on donations to organizations
- Medical, dental and vision benefits effective day one of
employment--
- Tuition Reimbursement--- Let us help you finish your degree or
start a new degree!
- WellHub program to promote overall physical wellness--
- Perkspot - offers exclusive or private discounts from
approximately 900+ merchants in a wide array of categoriesCatalent
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, Vineland , Label Control Manager, Executive , Philadelphia, New Jersey
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