Senior Process Engineer (Hybrid Synthesis)
- North America, United States
- Contract
- CAPEX Projects
This is a fantastic opportunity for a Senior Process Engineer to join our major, global pharmaceutical client on their latest new-build project based in Ohio, this is a large-scale greenfield capital project and investing more than $1bn.
Responsibilities:
- Guide and mentor front-line process engineers to enhance their technical skills and problem-solving capabilities.
- Provide support in the development of process knowledge and best practices within the engineering team.
- Foster a culture of continuous learning and improvement within the department.
- Develop and sustain comprehensive process knowledge across API manufacturing unit operations.
- Identify opportunities for process optimization to improve efficiency, yield, and compliance.
- Collaborate with operations and quality teams to ensure robust manufacturing processes.
- Support troubleshooting efforts to resolve process deviations and ensure production targets are met.
- Assess and enhance equipment performance to meet operational goals and regulatory expectations.
- Lead efforts in predictive and preventive maintenance strategies to maximize asset life-cycle.
- Collaborate with maintenance and reliability teams to optimize equipment uptime and efficiency.
- Develop and maintain engineering documentation, standard operating procedures, and best practices.
- Ensure compliance with GMP, safety, and corporate standards across all process engineering activities.
- Implement process improvements and automation strategies aligned with business objectives.
- Support change control processes related to process and equipment modifications.
- Bachelor's or Master’s degree in Process Engineering, Chemical Engineering, or a related field.
- Extensive experience in API manufacturing unit operations or similar environments.
- Strong technical knowledge of API processes, equipment, and associated regulatory requirements.
- Proven track record in mentoring and developing engineering teams in a fast-paced manufacturing environment.
- Experience in process optimization, troubleshooting, and performance improvement initiatives.
- Ability to work effectively across multidisciplinary teams and stakeholders.
- Strong analytical and problem-solving skills with a proactive approach to challenges.
- Willingness to work 3 days per week on-site or 2 weeks on / 2 weeks off schedule.
- Experience in biologic or pharmaceutical manufacturing environments.
- Familiarity with lean manufacturing principles and continuous improvement methodologies.
- Proficiency with process automation systems and data analytics for performance monitoring.
- Experience with asset management systems and engineering reliability programs.
#LI-AN1
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
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