Development Engineer

Evonik; Birmingham (AL); On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

Performance-based remuneration

Occupational health benefits

Flexible working environments

Job summary

A global innovation leader in Birmingham, AL seeks a Development Engineer to oversee engineering solutions for complex parenteral formulation projects. Candidates should possess an MS in a relevant engineering field and five years of process development experience in the pharmaceutical industry. The role demands strong technical expertise, project management skills, and the ability to lead teams effectively, ensuring project goals are met within timelines and budgets. Hybrid work environment and competitive benefits are provided.

Qualifications

• Minimum five years of experience in process development in pharmaceuticals.
• Demonstrated ability to conduct tasks independently with minimal oversight.
• Experience with technical reports and presentations is required.

Responsibilities

• Oversee multiple internal and customer projects focusing on engineering solutions.
• Lead technical teams to execute complex parenteral formulation projects.
• Evaluate causes of adverse outcomes and propose resolutions.

Skills

Process development

Project management

Aseptic pharmaceutical manufacturing

Engineering principles

Education

MS in relevant engineering field

BS in relevant technical field

Tools

Laboratory and analytical equipment

Statistical Design of Experiments

Job description

Development Engineer page is loaded## Development Engineerlocations: Birmingham, ALtime type: Full timeposted on: Posted Yesterdayjob requisition id: R45668**What we offer**Explore a world of opportunities with us. Look ahead with us and help shape innovative solutions to make our world more sustainable and life healthier, more vibrant and more comfortable. At Evonik, you have the chance to explore, thrive, and grow alongside 33,000 colleagues. Among attractive career paths and high-quality development programs, we not only offer performance-based remuneration and occupational health benefits but also hybrid and flexible working environments with #SmartWork. Bring your fresh perspective, develop your strengths, break out your mold, and find a career that fits your dreams with us.**Click on the link below to learn what our employees have to say about Evonik:**Execution and / or coordination of (specialized) process development tasks for complex parenteral formulations**RESPONSIBILITIES*** Oversee and support multiple internal and customer projects and sub-projects with the focus on engineering solutions, project planning, resourcing, and execution with respect to timelines and budgets* Own complex parenteral formulation projects in the role of the technical lead of a larger cross-departmental team in regard to onboarding, engineering design, process development, GMP readiness and execution in non-GMP and GMP environment.* Drive department knowledge and capability by regularly reviewing state-of-the-art information, detecting opportunities for future business and aligning with all relevant stakeholders* Drive change by detecting, defining and owning improvement ideas in technical areas, as well as business process related areas. Lead or support the teams that drive change, uphold transparent communication towards department and site leadership.* Build high performance teams by supporting personnel development for peers and leaders inside and outside of the department e.g., through authoring and scheduling training, giving feedback, providing input for the Performance Dialog, sharing best practices, continuous exchange across boundaries, supporting mitigation option definition, stakeholder management, and people empowerment.* Support the department head or the site in organizational development e.g., task efficiency, resource allocation, business development definition, cross-departmental development.**REQUIREMENTS*** Five (5) or more years of directly related experience in process development in the pharmaceutical industry is required, experience in aseptic pharmaceutical manufacturing or development is a plus.* A minimum MS in a relevant engineering field (e.g. pharmaceutical engineering, chemical engineering); or a BS in a relevant technical field with a sufficiently demonstrated level of performance and capability, as determined by management.* Knowledge of the scientific and engineering principles pertaining to and capable in the operation of standard laboratory, analytical, and/or processing and manufacturing equipment; examples include reactor handling, extruder design, pumps, agitator design, process instrumentation, data collection, pilot plant operations, scale-up, etc.* A thorough understanding and application of relevant scientific and engineering theories, principles, and methods; familiarity or general working knowledge of other related technical fields and applications as well as the capability to use and apply standard scientific and engineering procedures and techniques.* A demonstrated ability to conduct assigned tasks independently with minimal oversight from management; utilize experience, knowledge, and technical creativity to independently determine and develop processes to meet project goals and objectives and resolve technical challenges; work on multiple activities in parallel and multi-faceted research studies or programs;; supervise other technical personnel in the execution of the above activities.* Capable of conducting engineering studies, data analysis, and creating technical reports and presentations.* Recognize unanticipated or adverse outcomes or deviations; able to use technical expertise, experience, and creativity to evaluate and identify causes of unanticipated or adverse outcomes or deviations and to propose corrective action or resolutions for problems of increasing complexity; able to take corrective action to resolve technical problems of suitable complexity* Experience contributing to department and site continuous improvement initiatives regarding policies, procedures, workflows, process standardization, etc.* Knowledge of cGMPs, phase appropriate regulatory requirements, and the ability to appropriately scope complex parenteral formulation development projects with respect to technical scope, time, and budget.* General knowledge of several fields across the pharmaceutical product development process, multiple drug delivery technologies, or multiple analytical technologies.* Experience designing and conducting studies based on statistical Design of Experiments principles.The Evonik Group adopts an Equal Employment Opportunity (EEO) approach. Candidates are assessed based on their educational qualifications, experience, job competencies and potential and shall not be discriminated against on the basis of race, ethnicity, age, gender, religion, nationality, disability or sexual orientation or other classifications protected by local, state, or provincial regulations.**Your Application**To ensure that your application is proceeded as quickly as possible and to protect the environment, please apply online via our . Further information about Evonik as Employer can be found at . Please address your application to the Talent Acquisition Manager, stating your earliest possible starting date and your salary expectations.**Your Talent Acquisition Manager:**Kelvin Seals [C]Company isEvonik Corporation