Director Continuous Improvement - Biologics
Company: Disability Solutions
Location: Madison
Posted on: November 15, 2024
Job Description:
Director, Continuous Improvement - BiologicsPosition SummaryThe
Director, Continuous Improvement - Biologics is responsible for the
maturity and execution of the CI/TCW (The Catalent Way) vision for
the Biologics network guided by the Bio Operating norms. This
includes building the CI/TCW roadmap, identifying, and monitoring
Key Performance Indicators and metrics, deploying new tools,
systems and processes that improve operations, delivering
CI-specific training, and supporting culture change initiatives.
The role will have no direct reports and will work very closely
with the Site General Managers and Site CI Directors in the
Biologics network.The primary focus of the Director, Continuous
Improvement - Biologics will be identifying and implementing
solutions that improve our ability to plan and execute the
production of commercial and late-stage clinical products
efficiently, timely, and with high quality. This position will be
the Biologics capability-building leader for Lean and Six Sigma
skills, and will build a culture of CI being leader-led across the
Biologics network by enabling first-line leaders to effectively
manage the shop floor through strong performance management,
problem solving, and being at the Gemba. The role will provide CI
subject matter expertise, leadership, and support to CI colleagues
in the areas of: Lean deployment, Benchmarking, Maturity
Assessments, Lean & Six Sigma training, Project Definition and
selection, DMAIC, Change Management, and all activities related to
sustained cultural change. The Director will do assessments of the
maturity of sites in TCW/Lean and Six Sigma. The position is
responsible for fast-tracking the deployment of TCW vision of the
Bio Executive leadership team of Lean implementation and maturity
while also developing an army of problem solvers by ensuring
EVERYONE, EVERYWHERE , EVERYDAY solves problems. This role is
highly collaborative and will require extensive leadership and
influencing skills along with extensive change management
expertise.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.--50% travel will be
required to sitesThe Role
- Development and management of the execution of the CI/TCW
Excellence roadmap. Fastrack the lean maturity at sites and make CI
leader-led
- Conduct maturity assessments on TCW and create improvement
plans. Ensure all sites are at basic level of maturity on Strategy
Deployment, Performance management (Tiered accountability), Problem
solving, 5S, Leader standard work, Operator standard work and
Gemba.
- Embed structured problem-solving into daily behaviors and ways
of working thereby creating an army of problem-solvers
- Coach and train the Biologics Executive Leadership Team on Lean
to create common language and goal alignment on CI maturity. Use
the Bio Operating norms to guide lean maturity
- Conduct Lean and Six Sigma Belt programs across sites, ensure
all sites have a strong program of yellow belt LSS, and developed
CI master trainers at each site
- Ensure a strong process in place to identify projects for GB/BB
program and provide coaching to deliver the same (min 90% success
rate in project and benefit delivery)
- Help sites deliver on the WARP metrics (Waste, Absorption,
Recover inflation, Productivity)
- Identify partnerships with external organizations to support
Catalent's goals of benchmarking and reaching industry best
standards through TCW
- Utilize, teach and enforce use of process improvement and
change management tools. Lead teams to deliver specific business
process improvement initiatives with a complex or multi-site
scopeThe Candidate
- Minimum 12 years' experience in Operations and Continuous
Improvement roles in complex manufacturing environments.--CDMO
expertise a plus
- Operational excellence certification required - minimum of
Black Belt, Master Black Belt highly preferred
- Minimally 8 years' experience in leading a team of
cross-functional professionals in a portfolio of projects
- Demonstrated mastery of quality improvement methods such as
LEAN, Six Sigma, Value stream mapping, etc
- Experience working to regulatory standards:-- FDA, Good
Engineering Practice (GEP), Good Manufacturing Procedures (GMP) and
Good Documentation Procedures (GDP).
- Extensive influential leadership experience; demonstrated
change agent with substantial hands-on experience in technical and
process problem solving
- 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 experiencePayThe anticipated
salary range for this position in Maryland is $188,320 - $258,940
plus variable incentive compensation. The final salary offered to a
successful candidate may vary, and will be dependent on several
factors that may include but are not limited to: the type and
length of experience within the job, type and length of experience
within the industry, skillset, education, business needs, etc.
Catalent is a multi-state employer, and this salary range may not
reflect positions that work in other states.--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
- Dynamic, fast-paced work environment
- 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, Racine , Director Continuous Improvement - Biologics, Executive , Madison, Wisconsin
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