Director, Continuous Improvement – Process Optimization **Position Summary** The Director, Continuous Improvement – Process Optimization is responsible for developing and delivering process optimization across the Biologics network, which includes process simplification, complexity reduction, and introducing CI in development, clinical product, and processes. The role will have no direct reports and will work closely with the Site General Managers and Site CI Directors within the Biologics network. The focus of this Director, Continuous Improvement – Process Optimization will be identifying top pain points/complexity within processes and implementing network-wide solutions to simplify and standardize processes. This will include processes across the make, test, and ship within Biologics while also developing the playbook, tools & measurement systems for process optimization. This position 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. The scope of the role covers the entire product lifecycle including M&A, technology, and NPI assessments, but the primary focus of the role will be CI of commercial or clinical products. This Director will launch the COPQ (Cost of Poor Quality) program across the network while also establishing best practices in product transfers within the Product Development (PD) and Manufacturing Science & Technology (MS&T) functions using DFSS, QBD, APQP principles. The position will be highly collaborative and will require extensive leadership and influencing skills along with extensive change management expertise. As part of CI, the Director will develop, implement, and maintain a playbook with the Catalent Way team on how to simplify/standardize processes. 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 to sites within the Biologics network **The Role** + Development, management, and execution of process optimization + Work with multiple sites and teams to roll out the simplification, and complexity reduction with the network. Implement division-wide process re-engineering projects to achieve process improvements and simplification needed to satisfy evolving customer needs + Standardize/re-engineer processes that can help build scale at a global level + Identify and implement manual process improvement opportunities that can be automated to achieve process optimization, simplification, reduction in defects, enhanced employee experience and potential cost savings + Executing process improvement analysis by conducting deep dives to identify gaps and map processes, conduct root cause analysis, formulate actionable recommendations, design soluitons and trainings to quantify operational benefits + Launch the Lean in NPI & proactive problem-solving process using APQP/QBD concepts and use tools like FMEA, DOE, SPC to help sites optimize products and processes + Support Quality & Continuous Improvement functional teams in building quality right the first time, waste elimination, and overall value creation + Lead Site project teams to deliver high-quality transformation projects. Establish and maintain relationships with key stakeholders to ensure implementation of the initiatives and ensure they are delivered on time and within budget **The Candidate** + Minimum 12 years experience in Operations and Continuous Improvement roles in complex manufacturing environments. CDMO or Automotive industry expertise a plus + Black Belt, Master Black Belt or equivalent experience highly preferred + 8 years experience in leading a team of cross-functional professionals in a portfolio of projects + 5 years experience in process simplification and standardization + Substantial hands-on experience with value stream mapping, QBD, APQP, COPQ reduction, etc. + Demonstrated mastery of quality improvement methods such as LEAN, Six Sigma, Value stream mapping, etc required + Preferred 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 + Strong knowledge of cGMP and QbD regulations/guidance pertaining to the pharmaceutical industry preferred + 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 **Pay** The 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 reimbursement **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 Catalent Careers (https://careers.catalent.com/us/en) 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 DisabilityAccommodations@catalent.com . 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. 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