Process Engineer

Kindeva • St. Louis, MO

51d • Onsite

About The Position

Kindeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our customers to improve patient outcomes around the world. Together, as One Team, we will manufacture many more tomorrows. Ready to work with purpose? Look no further, we are hiring for a motivated, talented, and passionate Aseptic Process Engineer to join our St. Louis Missouri team! ROLE SUMMARY The Process Engineer is a key technical role responsible for ensuring consistent high performance of manufacturing processing areas. The incumbent will provide focused technical ownership over manufacturing processes while driving quality, the implementation of best practices, and continuous improvement. As the technical lead on aseptic operations, the Aseptic Manufacturing Engineer partners with production, quality, and compliance colleagues to identify and implement innovative solutions. Additional duties include project management, six sigma methods, and training coordination.

Requirements

• Bachelor's degree in science (Microbiology, Biology, Biochemistry, Chemistry, Pharmacy, or related science)
• 2+ years of experience in manufacturing or quality.

Nice To Haves

• Previous aseptic manufacturing experience preferred.
• Six-Sigma training and project management experience is preferred.

Responsibilities

• Observe, analyze, and identify process improvement opportunities on the manufacturing floor.
• Effectively manage and coordinate aseptic manufacturing projects and other functions at the site in support of technical projects.
• Partner with Sterile Product Manufacturing (SPM) principals, Quality Assurance (QA), and other internal experts to develop quality investigations, assign root cause, and identify/implement CAPA solutions.
• Work with Quality Operations and Regulatory Affairs to ensure regulatory filings are completed on time and to the appropriate standard.
• Champion Process Change Proposals/Requests as relates to technical support operations.
• Act as internal technical and compliance training resource for both SPM Management and SPM production floor team.
• Ensure work activities are conducted in strict accordance with safety guidelines and processing standards, such as FDA's current Good Manufacturing Practices (cGMPs) and Standard Operating Procedures (SOPs).

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level