Infotree Global Solutions
Process Engineer / Manufacturing Scientist
Infotree Global Solutions, Middletown, Virginia, United States, 22645
Process Engineer / Manufacturing Scientist
Job Summary: We are seeking a skilled Process Engineer / Manufacturing Scientist to lead optimization and oversight of solution manufacturing processes within a regulated pharmaceutical or medical device environment. This role will focus on enhancing process efficiency, improving product quality, ensuring regulatory compliance, and resolving documentation issues. The ideal candidate will bring hands‑on experience in chemical or pharmaceutical manufacturing and a deep understanding of formulation science, chemical processes, and process engineering. Key Responsibilities
Analyze and optimize existing solution manufacturing processes to improve yield, reduce production costs, and enhance quality and compliance. Lead and support process improvement initiatives using scientific and engineering principles. Review and maintain production documentation, including batch records, manufacturing instructions, and deviations to ensure accuracy and compliance with regulatory standards. Collaborate cross‑functionally with Quality, R&D, Production, and Facilities teams to streamline workflows and address process bottlenecks. Oversee day‑to‑day production activities, ensuring smooth and compliant manufacturing operations. Support troubleshooting activities for manufacturing issues related to formulation, process control, and equipment. Maintain and update Bill of Materials (BOMs) in collaboration with supply chain and production planning teams. Ensure all processes and documentation align with GMP, FDA, and ISO standards. Required Qualifications
Bachelor’s or Master’s degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field. Minimum 3 years of experience in pharmaceutical or medical device manufacturing. Proficiency with manufacturing documentation, including Bill of Materials (BOMs) and batch records. Experience working in GMP‑regulated environments. Understanding of regulatory compliance related to FDA, ISO 13485, or ICH Q8/Q9/Q10. Seniority level
Associate Employment type
Contract Job function
Manufacturing and Quality Assurance Industries
Medical Equipment Manufacturing and Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Infotree Global Solutions by 2x Get notified about new Process Engineer jobs in
Middletown, VA .
#J-18808-Ljbffr
Job Summary: We are seeking a skilled Process Engineer / Manufacturing Scientist to lead optimization and oversight of solution manufacturing processes within a regulated pharmaceutical or medical device environment. This role will focus on enhancing process efficiency, improving product quality, ensuring regulatory compliance, and resolving documentation issues. The ideal candidate will bring hands‑on experience in chemical or pharmaceutical manufacturing and a deep understanding of formulation science, chemical processes, and process engineering. Key Responsibilities
Analyze and optimize existing solution manufacturing processes to improve yield, reduce production costs, and enhance quality and compliance. Lead and support process improvement initiatives using scientific and engineering principles. Review and maintain production documentation, including batch records, manufacturing instructions, and deviations to ensure accuracy and compliance with regulatory standards. Collaborate cross‑functionally with Quality, R&D, Production, and Facilities teams to streamline workflows and address process bottlenecks. Oversee day‑to‑day production activities, ensuring smooth and compliant manufacturing operations. Support troubleshooting activities for manufacturing issues related to formulation, process control, and equipment. Maintain and update Bill of Materials (BOMs) in collaboration with supply chain and production planning teams. Ensure all processes and documentation align with GMP, FDA, and ISO standards. Required Qualifications
Bachelor’s or Master’s degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field. Minimum 3 years of experience in pharmaceutical or medical device manufacturing. Proficiency with manufacturing documentation, including Bill of Materials (BOMs) and batch records. Experience working in GMP‑regulated environments. Understanding of regulatory compliance related to FDA, ISO 13485, or ICH Q8/Q9/Q10. Seniority level
Associate Employment type
Contract Job function
Manufacturing and Quality Assurance Industries
Medical Equipment Manufacturing and Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Infotree Global Solutions by 2x Get notified about new Process Engineer jobs in
Middletown, VA .
#J-18808-Ljbffr