The Association of Technology, Management and Applied Engineering
Director, Engineering
The Association of Technology, Management and Applied Engineering, Rahway, New Jersey, us, 07065
Job Description
We are seeking a highly skilled and strategic
Reliability Engineering Director
to lead our reliability engineering efforts within the vaccine manufacturing environment. This role is critical to ensuring the continuous, compliant, and efficient operation of manufacturing equipment and systems that support drug production.
Key Responsibilities
Lead and develop the reliability engineering team focused on vaccine manufacturing equipment and systems.
Develop and implement reliability strategies to maximize equipment uptime, reduce unplanned downtime, and extend asset life while ensuring compliance with FDA, EMA, and other regulatory requirements.
Collaborate closely with Quality Assurance, Validation, Manufacturing, Maintenance, and Engineering teams to embed reliability best practices into equipment design, maintenance, qualification, and operation.
Facilitate RBAM on key manufacturing assets and utilize/track key reliability metrics such as MTBF, MTTR, and OEE, ensuring actions are completed and driving improved performance and risk ranking of assets.
Drive root cause analysis and failure investigations for critical equipment, ensuring corrective and preventive actions (CAPA) are implemented effectively.
Oversee reliability‑centered maintenance (RCM) programs and predictive maintenance initiatives using condition monitoring and data analytics.
Ensure all reliability activities comply with Good Manufacturing Practices (GMP) and support audit readiness.
Lead risk assessments related to equipment reliability and support validation activities, including IQ/OQ/PQ protocols.
Manage budgets, resources, and timelines for reliability projects and continuous improvement initiatives.
Communicate reliability goals, progress, and outcomes to senior leadership and cross‑functional stakeholders.
Education Requirements
Bachelor's degree in engineering (Mechanical, Electrical, Chemical, or related technical field)
Master's degree preferred.
Required Experience and Skills
10+ years of experience in reliability engineering or maintenance engineering within pharmaceutical manufacturing or a highly regulated industry.
Minimum 5 years in a leadership role managing reliability or maintenance teams.
Strong knowledge of pharmaceutical manufacturing processes, equipment, and regulatory requirements (FDA, EMA, GMP).
Expertise in reliability engineering tools and methodologies such as FMEA, RCM, Weibull analysis, fault tree analysis, and root cause analysis.
Experience with Enterprise Asset Management systems (EAM) and reliability data analytics tools.
Proven ability to lead cross‑functional teams and influence at all organizational levels.
Excellent problem‑solving, communication, and project management skills.
Preferred Experience and Skills
Experience with pharmaceutical equipment qualification and validation processes.
Certifications such as Certified Reliability Engineer (CMRP), Six Sigma, or Lean Manufacturing.
Familiarity with risk management frameworks (e.g., ICH Q9).
Knowledge of automation and control systems used in pharmaceutical manufacturing.
Benefits and Salary
Competitive salary range: $169,700.00 – $267,200.00
Opportunity to lead reliability initiatives critical to patient safety and product quality.
Dynamic and collaborative work environment within a leading pharmaceutical company.
Professional development and career advancement opportunities.
Comprehensive benefits package including medical, dental, vision, retirement (401(k)), paid holidays, vacation, compassionate, and sick days.
Eligible for annual bonus and long‑term incentive, if applicable.
Hybrid work model in the U.S.: three on‑site days per week (Monday‑Thursday) with Friday remote, except for field‑based, facility‑based, or research‑based positions.
Location and Eligibility US and Puerto Rico residents only.
San Francisco residents: we will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance.
Los Angeles residents: we will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with LA's Fair Chance Initiative for Hiring Ordinance.
Equal Employment Opportunity As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit EEOC Know Your Rights, EEOC GINA Supplement. We are proud to be a company that embraces the value of bringing together talented and committed people with diverse experiences, perspectives, skills, and backgrounds. Our inclusive environment encourages respectful challenge and collective problem‑solving.
#J-18808-Ljbffr
Reliability Engineering Director
to lead our reliability engineering efforts within the vaccine manufacturing environment. This role is critical to ensuring the continuous, compliant, and efficient operation of manufacturing equipment and systems that support drug production.
Key Responsibilities
Lead and develop the reliability engineering team focused on vaccine manufacturing equipment and systems.
Develop and implement reliability strategies to maximize equipment uptime, reduce unplanned downtime, and extend asset life while ensuring compliance with FDA, EMA, and other regulatory requirements.
Collaborate closely with Quality Assurance, Validation, Manufacturing, Maintenance, and Engineering teams to embed reliability best practices into equipment design, maintenance, qualification, and operation.
Facilitate RBAM on key manufacturing assets and utilize/track key reliability metrics such as MTBF, MTTR, and OEE, ensuring actions are completed and driving improved performance and risk ranking of assets.
Drive root cause analysis and failure investigations for critical equipment, ensuring corrective and preventive actions (CAPA) are implemented effectively.
Oversee reliability‑centered maintenance (RCM) programs and predictive maintenance initiatives using condition monitoring and data analytics.
Ensure all reliability activities comply with Good Manufacturing Practices (GMP) and support audit readiness.
Lead risk assessments related to equipment reliability and support validation activities, including IQ/OQ/PQ protocols.
Manage budgets, resources, and timelines for reliability projects and continuous improvement initiatives.
Communicate reliability goals, progress, and outcomes to senior leadership and cross‑functional stakeholders.
Education Requirements
Bachelor's degree in engineering (Mechanical, Electrical, Chemical, or related technical field)
Master's degree preferred.
Required Experience and Skills
10+ years of experience in reliability engineering or maintenance engineering within pharmaceutical manufacturing or a highly regulated industry.
Minimum 5 years in a leadership role managing reliability or maintenance teams.
Strong knowledge of pharmaceutical manufacturing processes, equipment, and regulatory requirements (FDA, EMA, GMP).
Expertise in reliability engineering tools and methodologies such as FMEA, RCM, Weibull analysis, fault tree analysis, and root cause analysis.
Experience with Enterprise Asset Management systems (EAM) and reliability data analytics tools.
Proven ability to lead cross‑functional teams and influence at all organizational levels.
Excellent problem‑solving, communication, and project management skills.
Preferred Experience and Skills
Experience with pharmaceutical equipment qualification and validation processes.
Certifications such as Certified Reliability Engineer (CMRP), Six Sigma, or Lean Manufacturing.
Familiarity with risk management frameworks (e.g., ICH Q9).
Knowledge of automation and control systems used in pharmaceutical manufacturing.
Benefits and Salary
Competitive salary range: $169,700.00 – $267,200.00
Opportunity to lead reliability initiatives critical to patient safety and product quality.
Dynamic and collaborative work environment within a leading pharmaceutical company.
Professional development and career advancement opportunities.
Comprehensive benefits package including medical, dental, vision, retirement (401(k)), paid holidays, vacation, compassionate, and sick days.
Eligible for annual bonus and long‑term incentive, if applicable.
Hybrid work model in the U.S.: three on‑site days per week (Monday‑Thursday) with Friday remote, except for field‑based, facility‑based, or research‑based positions.
Location and Eligibility US and Puerto Rico residents only.
San Francisco residents: we will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance.
Los Angeles residents: we will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with LA's Fair Chance Initiative for Hiring Ordinance.
Equal Employment Opportunity As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit EEOC Know Your Rights, EEOC GINA Supplement. We are proud to be a company that embraces the value of bringing together talented and committed people with diverse experiences, perspectives, skills, and backgrounds. Our inclusive environment encourages respectful challenge and collective problem‑solving.
#J-18808-Ljbffr