HCG Process Engineer

As a Process engineer you will mechanically troubleshoot support identification and implementation of process improvements system design capital project support and investigation support. You will also ensure all documentation deliverables are generated and develop new processes and/or optimize existing ones.

Responsibilities:

• Acts as the SME for critical process operations within filling and packaging operations.

• Must have project management skills knowledge and application experience of technical design reviews commissioning and validation for pharmaceutical processes.

• Work routinely with cross functional groups throughout the site for process improvements and implementation.

• Interface with auditors and presenting onsite processes.

• Leads FAT (factory acceptance testing) and ensures protocol execution is per plan supports installation operational and performance qualification activities.

• Direct the work of other process engineers and contract engineering resources to include performance evaluations for direct reports.

• Establish methods for ongoing monitoring/trending of process/mechanical issues and will be responsible for review and approval of site documents to include calibration reports batch records SOP s change control and design specs.

Requirements

• Bachelor of Science in Engineering or related science field or technical equivalent

• Minimum of 5 years of experience as a Process Engineer at a pharmaceutical manufacturing plant along with interdepartmental project leadership management

• Solid understanding and knowledge of pharma regulations and cGMP

• Experience with technical design reviews commissioning and validation for pharmaceutical processes.

• Mechanical aptitude to trouble shoots and identify issues; you have a proactive mindset for maintenance and

• Ability to refine and develop new processes to improve production and efficiencies

• Direct experience writing documents e.g. calibration reports batch records SOP s change control and design spec

• Proactive customer centric communication style and the ability to development and maintain interdepartmental partnerships
  

Horizon Controls Group is a company rooted in humancentric values. We are dedicated to fostering diversity equality inclusion and a deep sense of belonging within our organization. We firmly believe that by creating an environment where our diverse team members can freely exchange ideas and thrive we are better equipped to serve both our organization and our diverse global clientele. We empower our staff to feel valued connected and capable of making meaningful contributions to the communities they are part of both personally and professionally. Above all we want each employee to be proud to be a member of Horizon Controls Group.

Requirements Bachelor of Science in Engineering or related science field, or technical equivalent Minimum of 5 years of experience as a Process Engineer at a pharmaceutical manufacturing plant, along with interdepartmental project leadership management Solid understanding and knowledge of pharma regulations and cGMP Experience with technical design reviews, commissioning, and validation for pharmaceutical processes. Mechanical aptitude to trouble shoots and identify issues; you have a proactive mindset for maintenance and Ability to refine and develop new processes to improve production and efficiencies Direct experience writing documents e.g. calibration reports, batch records, SOP s, change control, and design spec Proactive customer centric communication style and the ability to development and maintain interdepartmental partnerships