Job Title: General Manager Location: Swindon, UK Position Summary: The General Manager (GM) is responsible for the site P&L, compliance, administrative, and quality of the business. The GM is responsible for fostering an environment of continuous improvement with emphasis on maintaining both a positive and energetic and safe workplace, as well as providing a high-level of customer satisfaction regarding on-time delivery, first-pass quality, and Operational Excellence. The GM demonstrates a high level of leadership, vision, and business acumen within the organization. The key to this role is being able to balance the role as leader of a scientific development site with heavy involvement and customer interaction at both the early business development phase and supporting customers in the commercial phase of the relationship. The Role: Direct the development, growth and ongoing profitability of the site, by ensuring that the site is properly staffed to meet customer demand with the appropriate capabilities to support the business strategies and P&L objectives. Work with the VP/GM and functional leaders in the development of the annual revenue plan and working budget for the site. Establish the priorities for future investments to capitalize on enhancing current and future customer service opportunities. Provide technical direction and support to marketing group by providing project work plans, timetables, and costs, and securing high quality customer-funded projects through preparation of technical presentations and participation at customer's meetings. Develop and implement an effective communication strategy to present the technologies and services of the site to customers. Develop and implement a review and reporting process for the site to evaluate progress against business and budget objectives, and to discuss and decide future priorities and resources. Ensure future growth of the site through an active involvement with Business Development in developing a R&D pipeline and executing on growth projects. Drive a culture of continuous improvement through the effective use of Operational Excellence tools and approaches. Ensure site compliance with GMP standards, with customers and external government agencies and other regulatory requirements. Ensuring that all interactions and engagements are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with Catalent values. Other duties as assigned The Candidate: BS/MS in classic sciences, pharmacy or other related disciplines. MS, MBA or PhD preferred but not required Extensive experience (10 years) in pharmaceutical manufacturing operations, with a strong track record of driving successful change utilizing advanced lean manufacturing and continuous improvement methodologies. Financial/commercial acumen and a track record of P&L management. The successful candidate will have a demonstrated track record of driving successful change utilizing advanced lean manufacturing and continuous improvement methodologies. Good technical skills to understand manufacturing processes, including basic knowledge of engineering, chemistry, and microbiology principles and practices. A good working knowledge of GMP, ISO 9000, and other applicable regulatory requirements is a must. Ability to quickly evaluate the talent and operations and lead changes required. Ability to drive results and work effectively in a lean environment & understands what is needed to be in a competitive leadership position. Excellent communication and interpersonal skills, with the ability to build relationships with diverse stakeholders at all levels of the organization Strong leadership and people management skills, with the ability to inspire and motivate teams. 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 to explore career opportunities. Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law. 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 DisabilityAccommodationscatalent.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.