What are the responsibilities and job description for the Production Process Engineer position at Stark Pharma Solutions Inc?
Hi,
My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a Production Process Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity. The detailed job description is as follows.
Job Title: Production Process Engineer
Location: Asheville, NC
Duration: Long Term
Position Overview
We are seeking an experienced Production Process Engineer to support manufacturing operations by optimizing production processes, improving operational efficiency, and ensuring product quality within a regulated pharmaceutical or medical device manufacturing environment. The ideal candidate will have experience in process optimization, manufacturing support, GMP compliance, data analysis, and cross-functional collaboration to drive continuous process improvements.
Key Responsibilities
- Optimize production and manufacturing processes to improve efficiency, productivity, and product quality.
- Monitor manufacturing process performance and identify opportunities for process improvements.
- Analyze production data, investigate process trends, and implement corrective and preventive actions.
- Ensure compliance with GMP, FDA regulations, ISO standards, and internal quality system requirements.
- Collaborate with Production, Manufacturing, Engineering, Quality Assurance, and Validation teams to support daily manufacturing operations.
- Troubleshoot production issues, perform root cause analysis, and implement sustainable process improvements.
- Develop and update process documentation, SOPs, work instructions, and manufacturing procedures.
- Support process validation, equipment qualification, and technology transfer activities.
- Participate in Lean Manufacturing, Six Sigma, and continuous improvement initiatives to reduce waste and improve operational performance.
- Assist with deviation investigations, CAPA implementation, change control, and regulatory audit readiness.
Required Qualifications
- Bachelor's degree in Mechanical Engineering, Chemical Engineering, Industrial Engineering, Manufacturing Engineering, or a related engineering discipline.
- Experience in pharmaceutical, biotechnology, or medical device manufacturing environments.
- Strong knowledge of production process optimization, manufacturing systems, and process improvement methodologies.
- Familiarity with GMP, FDA regulations, ISO standards, and regulated manufacturing practices.
- Experience analyzing manufacturing data, identifying process improvements, and implementing corrective actions.
- Knowledge of process validation, equipment qualification, and manufacturing documentation.
- Strong analytical, troubleshooting, problem-solving, and decision-making skills.
- Excellent communication, technical documentation, and cross-functional collaboration abilities.
- Experience with Lean Manufacturing, Six Sigma, or continuous improvement methodologies is preferred.
- Familiarity with MES, ERP systems, statistical process control (SPC), and manufacturing KPIs is an added advantage.
I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.
Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/