Senior Manufacturing Engineer

Senior Manufacturing Engineer at Adecco Permanent Recruitment Senior Manufacturing Engineer at Adecco Permanent Recruitment in Monroe, North Carolina Posted in about 23 hours ago.

Type:

full-time

Job Description:

Manufacturing Engineering Manager Minimum of 3+ years of experience in a pharmaceutical manufacturing environment (required) Hands-on experience with injection molding processes in a manufacturing setting (required) Position Summary The Manufacturing Engineering Manager is responsible for leading and developing the manufacturing engineering team while driving continuous improvement across production processes within a regulated pharmaceutical manufacturing environment. This role ensures efficient, safe, and high-quality manufacturing operations through process optimization, problem-solving, and cross-functional collaboration. Key Responsibilities Lead, manage, and mentor the Manufacturing Engineering team, including performance management and annual reviews Plan, prioritize, and assign engineering activities to support production and business objectives Conduct risk and opportunity assessments and implement appropriate mitigation or improvement actions Lead complex investigations, including root cause analysis and implementation of corrective and preventive actions (CAPA) Oversee production-related investigations, including quality deviations and customer complaints, and approve associated reports Drive Operational Excellence (OpEx) initiatives to improve efficiency, reduce waste, and optimize processes Design, develop, and optimize manufacturing workflows, systems, and resource utilization, with a focus on injection molding processes Ensure creation, maintenance, and compliance of manufacturing process documentation in accordance with pharmaceutical regulatory standards (e.g., GMP) Support the implementation and startup of new production systems and equipment, including injection molding technologies Initiate and manage change control processes within the department Coordinate validation and Design of Experiments (DOE) activities in a regulated environment Resolve production issues, delays, and bottlenecks in a timely manner Ensure compliance with all safety, health, environmental, and pharmaceutical regulatory requirements Identify and implement opportunities to improve safety, quality, and cost performance Support continuous development of production processes, systems, and personnel Stay current with industry trends, emerging technologies, and supplier capabilities, particularly in injection molding and pharmaceutical manufacturing Oversee training, qualification, and development of departmental personnel Perform other duties as assigned Qualifications & Experience Bachelor's degree in Engineering or a related field Minimum of 3+ years of experience in a pharmaceutical manufacturing environment (required) Hands-on experience with injection molding processes in a manufacturing setting (required) Strong knowledge of manufacturing processes, including high-throughput automated assembly and injection molding Experience working in a regulated environment with understanding of GMP and validation requirements Ability to interpret blueprints and working knowledge of pneumatic, hydraulic, electrical, mechanical, and basic programming systems Demonstrated commitment to health, safety, environmental, and regulatory compliance standards Proven problem-solving and analytical skills with the ability to troubleshoot complex production issues Strong communication and interpersonal skills Experience in project management and leading cross-functional teams Proven leadership and team management capabilities