Particle Dynamics is a global supplier of ingredients and finished dosage forms for the pharmaceutical, consumer health, over the counter, and nutraceutical products industries. The business provides a unique combination of enabling technologies, products, services, and a dynamic culture that emphasizes speed, flexibility, and customer satisfaction. The primary operations are located in St. Louis, Missouri and Seymour, Indiana. Particle Dynamics is a portfolio company of BroadOak Capital Partners.

Primary Responsibilities:

• Execute capital projects at the Seymour, Indiana site. May also be assigned to selected capital projects companywide.
• Participate in process improvement activities and the implementation of lean manufacturing/operation excellence for the Seymour, Indiana site. May also be assigned to selected process improvements companywide.
• Troubleshoot and implement corrective actions at site related to production process or equipment.
• Support operational team to improve efficiency and enable cost reduction activities through project or process changes
• Member of product development and launch teams with Product and Process Innovation Center (PPIC), Quality, Production, and Supply Chain
• Develop business case, project cost and ROI for capital investments
• Communicate and train users on new processes
• Participate in, monitor, and report progress toward completion of the capital budget for the site.
• Manage creation of annual capital budget for the site in coordination with the Executive Team and plant leadership
• Report capital metrics to the VP of Technical Operations for the site
• Keep updated with industry trends, best practices, and regulatory requirements
• Train employees on technical and optimization topics - including operational instruction for new or modified equipment.
• Participate in the purchase of new equipment for operations and assist in the installation and qualification of new equipment and/or facilities.

Job Qualifications:

• Strong computer skills MS Office, Visio, MS Project, Autocad, etc.
• Has in depth knowledge of pharmaceutical and safety compliance regulations
• Expertise in collaboration with external suppliers and contractors
• Extensive experience writing procedures and policies
• Excellent analytical and problem-solving skills
• Strong communication skills (oral and written)
• Ability to collaborate with operations, quality, regulatory, etc.
• Project management skills

Education/Experience

• Bachelor's Degree or higher in an engineering discipline (5 yrs of field experience in chemical or mechanical preferred)
• 5 years of field experience in engineering or technical role in a manufacturing environment
• 5 years' experience within GMP facilities preferred
• Professional project management certifications preferred
• Prior experience writing SOPs, and work instruction
• Prior experience with qualifications and validation strongly preferred

Benefits:

• Health, dental, vision, life insurance, STD and LTD effective the 1st day of the month following a new employees hire date
• 401k match - 4% of 5% the employee contributes (100% on first 3%, 50% on next 2%) - immediate vesting!
• This position is eligible for the following time off yearly - 120 hours of vacation, 40 hours of sick, 16 hours of personal time - vacation and personal time are available upon hire!