Novarad
Production and Quality Control Manager
Novarad, Provo, Utah, us, 84605
Job Type
Full-time
Description
Novarad's Enterprise Healthcare solutions help senior executives, clinicians and IT professionals deliver clinical, operational, and fiscal excellence. With a self-sustaining business model, more than three decades of technology leadership, and an intense focus on our customers' needs, Novarad brings people and technology together in ways no one else can. We're driven by innovation that truly transforms healthcare - for the provider and their patient.
Novarad is looking for a Production and Quality Control Manager to oversee the daily operations for the production of a new product. This role will manage production schedules, ensure products meet safety and quality requirements, and collaborate with various departments to optimize manufacturing processes. The ideal candidate will have a strong background in production management, quality control protocols, and be willing to perform every aspect of production process. Initially, this role will function as a team of one.
This is an onsite opportunity in our Provo office. Local candidates only, please.
Novarad Offers:
Competitive salary with generous PTOHealth, dental, vision, life, and disability insurancesHSA option with dollar-for-dollar match401k with dollar-for-dollar matchLow Cost Onsite Medical ClinicWellness programSundance corporate passesAs the Production and Quality Control Manager, you will:
Production Management :
Perform the daily production activities related to medical supplies, ensuring on-time delivery and adherence to production schedules.Develop and implement production schedules, workflows, and procedures to meet output goals while maintaining high-quality standards.Support new product introductions and scale-up activities, collaborating with R&D and other departments to ensure seamless transitions.Monitor and control production costs, materials, and resources to stay within budget while meeting production targets.Maintain accurate production records and reports, analyzing production data to identify areas for improvement.Collaborate with suppliers, procurement, and R&D to ensure raw materials meet required quality specifications.Quality Control and Compliance :
Ensure compliance with FDA, ISO 13485, and Good Manufacturing Practices (GMP) regulations and standards by maintaining quality control systems.Perform regular audits and inspections throughout the production process to identify any deviations from standards.Investigate and address product defects or issues, working closely with the Compliance team to implement corrective actions.Drive continuous improvement initiatives by utilizing process optimization methodologies.Requirements
Qualifications :
3+ years of experience in production management or quality control within the medical industry (medical devices, pharmaceuticals, etc.)In-depth knowledge of and experience with FDA regulations, ISO 13485, and GMP standards.Strong problem-solving skills with a focus on process optimization and troubleshootingExcellent organizational and communication skills.Ability to manage multiple priorities in a fast-paced manufacturing environmentPreferred Knowledge and Experience
•
Bachelor's degree in Engineering, Manufacturing, or a related field. A degree in Supply Chain Management or Business Administration is also acceptable with relevant experience.
Working Conditions :
May require occasional evening or weekend work depending on production deadlines.Involves working in a manufacturing environment with exposure to noise, dust, and machinery.
Novarad is an equal opportunity employer. All applicants will be considered for employment without regard to r race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
Full-time
Description
Novarad's Enterprise Healthcare solutions help senior executives, clinicians and IT professionals deliver clinical, operational, and fiscal excellence. With a self-sustaining business model, more than three decades of technology leadership, and an intense focus on our customers' needs, Novarad brings people and technology together in ways no one else can. We're driven by innovation that truly transforms healthcare - for the provider and their patient.
Novarad is looking for a Production and Quality Control Manager to oversee the daily operations for the production of a new product. This role will manage production schedules, ensure products meet safety and quality requirements, and collaborate with various departments to optimize manufacturing processes. The ideal candidate will have a strong background in production management, quality control protocols, and be willing to perform every aspect of production process. Initially, this role will function as a team of one.
This is an onsite opportunity in our Provo office. Local candidates only, please.
Novarad Offers:
Competitive salary with generous PTOHealth, dental, vision, life, and disability insurancesHSA option with dollar-for-dollar match401k with dollar-for-dollar matchLow Cost Onsite Medical ClinicWellness programSundance corporate passesAs the Production and Quality Control Manager, you will:
Production Management :
Perform the daily production activities related to medical supplies, ensuring on-time delivery and adherence to production schedules.Develop and implement production schedules, workflows, and procedures to meet output goals while maintaining high-quality standards.Support new product introductions and scale-up activities, collaborating with R&D and other departments to ensure seamless transitions.Monitor and control production costs, materials, and resources to stay within budget while meeting production targets.Maintain accurate production records and reports, analyzing production data to identify areas for improvement.Collaborate with suppliers, procurement, and R&D to ensure raw materials meet required quality specifications.Quality Control and Compliance :
Ensure compliance with FDA, ISO 13485, and Good Manufacturing Practices (GMP) regulations and standards by maintaining quality control systems.Perform regular audits and inspections throughout the production process to identify any deviations from standards.Investigate and address product defects or issues, working closely with the Compliance team to implement corrective actions.Drive continuous improvement initiatives by utilizing process optimization methodologies.Requirements
Qualifications :
3+ years of experience in production management or quality control within the medical industry (medical devices, pharmaceuticals, etc.)In-depth knowledge of and experience with FDA regulations, ISO 13485, and GMP standards.Strong problem-solving skills with a focus on process optimization and troubleshootingExcellent organizational and communication skills.Ability to manage multiple priorities in a fast-paced manufacturing environmentPreferred Knowledge and Experience
•
Bachelor's degree in Engineering, Manufacturing, or a related field. A degree in Supply Chain Management or Business Administration is also acceptable with relevant experience.
Working Conditions :
May require occasional evening or weekend work depending on production deadlines.Involves working in a manufacturing environment with exposure to noise, dust, and machinery.
Novarad is an equal opportunity employer. All applicants will be considered for employment without regard to r race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.