Senior Specialist, Engineering

Senior Specialist, Engineering – GES Tech Center

Global Engineering Solutions (GES) is responsible for the design, construction, and delivery of advanced manufacturing facilities and laboratories worldwide. We provide premier engineering solutions in the pharmaceutical industry through technical innovation and project management to deliver important life-saving medicines and vaccines to patients. With our extensive range of facilities and environments, our Engineers have opportunities to impact Large and Small Molecule areas within our company's Manufacturing Division and Animal Health division lines of business, including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation. Our Engineers provide solutions for internal and external manufacturing needs in support of operational efficiencies, continuous improvement, and innovations.

Our Animal Health Division is investing $895 million in expanding our manufacturing and research & development facilities in De Soto, Kansas — the state's largest economic development project to date. The Senior Specialist operates under the guidance of the GES Process Lead and is part of a high performing team accountable for implementation of this major project within our Company's growing portfolio of Animal Health work. The individual collaborates with other Integrated Project Team (IPT) members (e.g., Project Management, Technology, Maintenance, Automation, Plant Operations and Safety), Engineering Firms and Vendors to progress deliverables. The Senior Specialist would be responsible for leading the planning, design, and implementation of engineering solutions on a suite team. Core work includes equip/scope generation, process & facility design, equipment selection, vendor interaction, factory acceptance testing, technology transfer, construction support, equipment qualification, facility start-up and process demonstrations.

Preferred candidates will possess experience with engineering design, equipment operation, startup, and troubleshooting, and C&Q activities. They should demonstrate a proven aptitude for leading project design endeavors and offering creative solutions that align with business objectives. Additionally, the role may involve supervising junior engineers and collaboration with resources from an engineering firm. Previous managerial experience in a similar position is desirable.

The Senior Specialist primary responsibility entails:

• Exhibiting strong technical/engineering leadership, interpersonal, collaboration and communication skills for both decision making and guiding team members.
• Leading a cross functional suite team of 5-10 members through the stage gates of a project and setting them up for success with knowledge transfer.
• Ensuring deliverables conform to our standards and practices; and are technically sound.
• Providing technical guidance during project implementation, assures viability of technology to meet design intent.
• Collaborating with other technical functions to ensure successful technology transfers of new and in-line products.
• Flexibility with travel up to 50%.

Job Description in Primary Posting Language

• This position will function as the technical/engineering process engineer with prior experience supporting Biologics, Vaccine and/or Sterile Projects.

Education Minimum Requirement:

• B.S. degree in Engineering (Chemical or Mechanical) or Science is required. An advanced degree in Engineering, Science, or Business is preferred.

Required Experience and Skills:

• Minimum five (5) years of experience in Pharmaceutical/Biotech industry such as Process-Equipment Engineering Design, Capital Project implementation, Technical Operations, or Operations/EMU.
• 3+ years experience leading cross functional teams in the startup and C&Q execution of capital projects.
• Experience with an equipment life cycle approach including specification, selection, testing & commissioning, troubleshooting and qualification.
• Understanding of unit operations specific to vaccine/biologic manufacturing, including hygienic design and aseptic requirements for Buffer Prep, Formulation, and CIP/SIP and experience with primary and secondary packaging operations.
• Experience with capital projects that followed a stage gate capital management process.
• Excellent collaboration and engagement as a team player with dependable interpersonal and communication skills.
• Analytical and problem-solving skills.
• Multitasking/time management skills which deliver on time and quality work.
• Core knowledge should include specification of unit operations, P&ID reviews, Hazard Analysis, equipment operation, commissioning & qualification execution.
• Work independently and meet timelines in a fast-paced team-based environment.
• Strong self-motivation; proactive, high-energy, "can do" work ethic; ability to handle potentially stressful situations with a positive attitude.

Required Skills:

Adaptability, Capital Projects, Change Control Processes, Collaborative Communications, Construction, Customer-Oriented, Engineering Standards, Equipment Commissioning, Equipment Specifications, Global Engineering, Good Manufacturing Practices (GMP), Knowledge Transfer, Maintenance Engineering, Manufacturing Process Validation, Multitasking, Process Optimization, Project Implementations, Project Management, Self Motivation, Strategic Thinking, Teamwork, Technical Support, Technical Transfer, Working Independently

The salary range for this role is $117,000.00 - $184,200.00