Program Manager - cGMP Production

Company: Disability Solutions
Location: Baton Rouge
Posted on: September 19, 2023

Job Description:

Join a team recognized for leadership, innovation and diversityThe future is what you make it.When you join Honeywell, you become a member of our global team of thinkers, innovators, dreamers and doers who make the things that make the future.Advanced Materials is a global supplier of fluorine products, fine chemicals, additives, metals, films and fibers for products including pharmaceuticals, refrigeration, semiconductors and military protection. Advanced Materials is making the world safer, cleaner and enabling the modernization of a growing middle class by enhancing our customer offerings through a differentiated portfolio of chemistries, materials, value-added solutions and superior customer service. Our mission is to attract, retain and develop diverse and highly motivated, entrepreneurial employees striving to flawlessly deliver superior value to our customers every day.We are seeking a dedicated and accomplished Program Manager - cGMP Production to join our Advanced Materials team. In this role, you will collaborate closely with program leaders, cross-functional teams, and stakeholders to drive the development and execution of transformative initiatives. Your ability to analyze project status, manage scope changes, and foster relationships will be critical in ensuring project success. You will work with department heads and teams to identify and address risks and opportunities, all while overcoming program challenges and producing insightful program reports.This role offers a Hybrid working schedule.--KEY RESPONSIBILTIES:--- Collaborate with program leaders and cross-functional teams to define clear project scopes, deliverables, required resources, work plans, budgets, and timelines for both ongoing and new initiatives.--- Regularly assess project statuses and proactively make adjustments to scopes, schedules, or budgets as necessary, ensuring alignment with project requirements.--- Foster and maintain relationships with key stakeholders, serving as the primary point of contact for day-to-day communication regarding project progress and any changes.--- Partner with department heads and teams to identify potential risks and opportunities across multiple projects within various departments.--- Utilize your analytical skills to to evaluate and overcome program risks, subsequently generating comprehensive program reports for management's review.YOU MUST HAVE--- Bachelor's degree with 5 years of experience in a STEM field--- 3+ years of experience in program or project management--- 3+ years of experience in leading/working within diverse cross-functional teams--- 3+ years of operational knowledge in pharmaceutical excipient GMP production--- 2+ years of experience in various GMP validation requirements/processes--- Due to compliance with U.S. export control laws and regulations, candidate must be a U.S. Person, which is defined as, a U.S. citizen, a U.S. permanent resident, or have protected status in the U.S. under asylum or refugee status or have the ability to obtain an export authorizationWE VALUE:--- Holding a Master's degree or possessing experience in chemical engineering or business fields--- Demonstrating a solid comprehension of the prerequisites for establishing a GMP production facility--- Holding lean six sigma certifications--- Being well-acquainted with clinical trials, DMF, IND, and NDA submissions--- Possessing comprehensive knowledge of engineering and QA principles related to pharmaceutical excipient production--- Exhibiting a strong grasp of business acumen--- Demonstrating adeptness in leadership and project management--- Displaying effective communication skills, including adeptness in presentations and report writingAdditional Information

Keywords: Disability Solutions, Baton Rouge , Program Manager - cGMP Production, Executive , Baton Rouge, Louisiana