VetJobs
Supervisor, Production; Manufacturing - Albuquerque, NM
VetJobs, Albuquerque, New Mexico, United States, 87101
Supervisor, Production; Manufacturing - Albuquerque, NM
Build your future at Curia, where our work has the power to save lives. The Production Supervisor supports the timely manufacturing of parenteral products in an aseptic environment according to Current Good Manufacturing Practice (cGMP). The supervisor responsibilities include supervising the setup of sterile filling equipment, operating dehydrogenation equipment, managing filling and capping processes, and overseeing formulation tasks. Additionally, the supervisor ensures compliance with all relevant regulations and procedures, maintains current good documentation practices (cGDP) for all activities, and participates in training and continuous improvement initiatives to enhance production processes and efficiency. The role also requires supervising the sanitation of aseptic and controlled areas with specialized solutions and equipment, adhering to sanitization protocols for sterile equipment processing, and following Standard Operating Procedures (SOPs) for all sanitation and documentation activities. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives. We proudly offer Generous benefit options (eligible first day of employment) Paid training, vacation and holidays (vacation accrual begins on first day of employment) Career advancement opportunities Education reimbursement 401K program with matching contributions Learning platform Essential Duties and Responsibilities: Manage and coordinate personnel and room activities for assigned shifts Compile area-specific shift information and line status data on time accurately conveying information to support groups and oncoming shift management team Ensure compliance with cGMPs, corporate and site-specific policies and procedures Maintain and report metrics to evaluate the performance of the assigned production unit Mentor, develop, and guide direct reports in succession planning and cross-functional training. Schedule adherence and material consumption rates relative to specific areas Manage operational and preventive maintenance of area-specific processing equipment Report and investigate safety incidents and quality deviations Become fluent in all functional areas and provide leadership in the absence of manager(s) Share resources with other production units as needed and when available Lead and/or conduct investigations, document revisions, protocol creation, and CAPA projects Other duties as assigned Other Qualifications: Must pass a background check Must pass a drug screen (Must pass random drug screens as well) May be required to pass Occupational Health Screening Must be able to obtain and maintain gowning certification Must be able to obtain and maintain media qualification Must be able to wear a respirator Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Build your future at Curia, where our work has the power to save lives. The Production Supervisor supports the timely manufacturing of parenteral products in an aseptic environment according to Current Good Manufacturing Practice (cGMP). The supervisor responsibilities include supervising the setup of sterile filling equipment, operating dehydrogenation equipment, managing filling and capping processes, and overseeing formulation tasks. Additionally, the supervisor ensures compliance with all relevant regulations and procedures, maintains current good documentation practices (cGDP) for all activities, and participates in training and continuous improvement initiatives to enhance production processes and efficiency. The role also requires supervising the sanitation of aseptic and controlled areas with specialized solutions and equipment, adhering to sanitization protocols for sterile equipment processing, and following Standard Operating Procedures (SOPs) for all sanitation and documentation activities. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives. We proudly offer Generous benefit options (eligible first day of employment) Paid training, vacation and holidays (vacation accrual begins on first day of employment) Career advancement opportunities Education reimbursement 401K program with matching contributions Learning platform Essential Duties and Responsibilities: Manage and coordinate personnel and room activities for assigned shifts Compile area-specific shift information and line status data on time accurately conveying information to support groups and oncoming shift management team Ensure compliance with cGMPs, corporate and site-specific policies and procedures Maintain and report metrics to evaluate the performance of the assigned production unit Mentor, develop, and guide direct reports in succession planning and cross-functional training. Schedule adherence and material consumption rates relative to specific areas Manage operational and preventive maintenance of area-specific processing equipment Report and investigate safety incidents and quality deviations Become fluent in all functional areas and provide leadership in the absence of manager(s) Share resources with other production units as needed and when available Lead and/or conduct investigations, document revisions, protocol creation, and CAPA projects Other duties as assigned Other Qualifications: Must pass a background check Must pass a drug screen (Must pass random drug screens as well) May be required to pass Occupational Health Screening Must be able to obtain and maintain gowning certification Must be able to obtain and maintain media qualification Must be able to wear a respirator Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.