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!