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Reliability Manager Jobs in Pinckney, MI (NOW HIRING)

Biovire

Manager, Validation

Brighton, MI · On-site

$100K - $120K/yr

... reliability as the organization continues to scale. The Role The Manager, Validation leads ... commissioning, qualification, validation (CQV), and computer system validation (CSV) activities ...

Biovire

Manager, Validation

Brighton, MI

... reliability as the organization continues to scale. The Role The Manager, Validation leads ... commissioning, qualification, validation (CQV), and computer system validation (CSV) activities ...

Biovire

Manager, Validation

Brighton, MI · On-site

$100K - $120K/yr

... reliability as the organization continues to scale. The RoleThe Manager, Validation leads ... commissioning, qualification, validation (CQV), and computer system validation (CSV) activities ...

Minth North America

Program Manager

Wixom, MI · On-site

$100K - $110K/yr

Minimum 3 years of risk management by assessing project risks by reviewing master program timing, control timing as well as program performance, reliability, manufacturability and market ...

URS Group

Site Manager

Plymouth, MI

... operational reliability. * Respond promptly to emergency situations. * Promote and maintain a ... Manage supervisory staff and dispatch personnel. * Balance cost considerations with service quality ...

Deepview Corp.

Be Seen First

Plant Operations Manager

Plymouth, MI · On-site

$120K - $135K/yr

PLANT OPERATIONS MANAGER - AUTOMOTIVE MANUFACTURING Location: Plymouth, MI Job Type: Full-Time, ... reliability.

New

Black & Veatch

Transactions Manager

Ann Arbor, MI · Hybrid

... project assessments, reliability/availability assessments, conducting field observations ... Implements project management capabilities on assigned engagements, including but not limited to ...

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Reliability Manager information

See Pinckney, MI salary details

$58.4K

$110.8K

$158.8K

How much do reliability manager jobs pay per year?

As of Aug 14, 2026, the average yearly pay for reliability manager in Pinckney, MI is $110,755.00, according to ZipRecruiter salary data. Most workers in this role earn between $89,100.00 and $132,000.00 per year, depending on experience, location, and employer.

What is the role of a reliability manager?

A reliability manager oversees the maintenance and reliability of equipment and systems within an organization to ensure optimal performance and minimize downtime. They analyze failure data, develop maintenance strategies, and implement continuous improvement processes, often using tools like root cause analysis and reliability-centered maintenance. Strong analytical skills, technical knowledge, and certifications such as Certified Reliability Engineer (CRE) are typically required for this role.

Is reliability engineering in demand?

Reliability engineering is in high demand across industries such as manufacturing, energy, and aerospace, as companies prioritize system uptime and maintenance efficiency. Reliability Managers with skills in data analysis, failure modes, and certifications like RCM are sought after to improve equipment performance and reduce downtime.

What are the key skills and qualifications needed to thrive as a reliability manager?

A Reliability Manager needs strong analytical skills, a solid background in engineering or maintenance, and experience with reliability-centered maintenance methodologies. Familiarity with tools like Failure Mode and Effects Analysis (FMEA), Root Cause Analysis (RCA), and certifications such as Certified Reliability Engineer (CRE) are often required. Leadership, problem-solving, and the ability to communicate complex technical information clearly are crucial soft skills for this role. These skills help ensure equipment uptime, optimize maintenance processes, and foster a culture of continuous improvement within the organization.

What does a reliability manager do?

A Reliability Manager is responsible for ensuring that equipment, processes, and systems operate efficiently and consistently to minimize downtime and maximize performance. They develop and implement reliability strategies, conduct root cause analyses, and oversee preventive and predictive maintenance programs. Their role involves working closely with maintenance teams, engineers, and production staff to improve asset reliability and extend equipment lifespan. Additionally, they analyze failure data, recommend improvements, and help optimize operational costs through reliability-centered maintenance practices.

What job categories do people searching Reliability Manager jobs in Pinckney, MI look for?

The top searched job categories for Reliability Manager jobs in Pinckney, MI are:

What cities near Pinckney, MI are hiring for Reliability Manager jobs?

Cities near Pinckney, MI with the most Reliability Manager job openings:

Reliability Manager jobs near you
Infographic showing various Reliability Manager job openings in Pinckney, MI as of June 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $110,755 per year, or $53.2 per hour.

Manager, Validation

Biovire

Brighton, MI • On-site

$100K - $120K/yr

Full-time

Medical, Dental, Vision, Life, PTO

Re-posted 28 days ago

Job description

Manager, Validation
Brighton, Michigan
Biovire is advancing toward commercialization with a focus on operational excellence, compliance, and scalable GMP manufacturing systems. We are seeking a Manager, Validation, reporting to the VP, Engineering, to lead validation programs supporting equipment, facilities, utilities, and computerized systems within our regulated pharmaceutical manufacturing environment.
This is a highly visible leadership role responsible for ensuring validation programs support operational readiness, inspection readiness, and long-term manufacturing reliability as the organization continues to scale.
The Role
The Manager, Validation leads commissioning, qualification, validation (CQV), and computer system validation (CSV) activities across the Brighton site. This role provides technical oversight for validation strategy, execution, compliance, and lifecycle management of manufacturing systems and infrastructure.
This position partners closely with Quality, Operations, Manufacturing, Engineering, Maintenance, and cross-functional operational teams to ensure all systems remain compliant, qualified, and inspection-ready.
Key Responsibilities
  • Lead enterprise validation programs supporting equipment, facilities, utilities, automation, and computerized systems across Biovire's GMP manufacturing operations.
  • Oversee commissioning, qualification, and the overall validation strategy and activities.
  • Partner with Operations and Quality to maintain the qualified state of manufacturing systems.
  • Support commercialization, technology transfer, process validation, and startup activities for new manufacturing processes and facilities.
  • Serve as Validation SME during FDA and regulatory inspections.
  • Lead lifecycle management of validation systems.
  • Manage and maintain Validation Master Plans and validation lifecycle documentation
  • Lead scheduling, planning, review, and execution of validation activities
  • Support transition of equipment and systems from Engineering to operational use
  • Partner cross-functionally with Quality, Manufacturing, Engineering, and Maintenance teams
  • Provide technical guidance for risk assessments, change controls, deviations, and investigations
  • Ensure timely completion of validation protocols, reports, traceability matrices, IQ/OQ documentation, and related deliverables
  • Support audit and inspection readiness activities
  • Lead and develop validation personnel while reinforcing a strong quality and compliance culture

What You Bring
  • Bachelor's degree in Engineering, Science, Computer Systems, or related technical field
  • 5+ years of experience in pharmaceutical, biotechnology, or regulated manufacturing environments
  • Prior leadership experience within Validation, Engineering, CQV, or Quality functions
  • Experience interacting with FDA or other regulatory agencies and supporting inspections.
  • Ability to communicate technical validation concepts during inspections.
  • Strong understanding of cGMP, validation lifecycle management, and 21 CFR Part 11 requirements
  • Hands-on experience leading validation projects and technical documentation activities
  • Experience supporting manufacturing equipment, utilities, HVAC, automation systems, and/or computerized systems
  • Strong organizational, communication, and cross-functional collaboration skills

Why Join Biovire
  • Opportunity to shape and strengthen validation systems during organizational growth
  • High visibility and cross-functional leadership exposure
  • Collaborative and mission-driven GMP manufacturing environment
  • Direct impact supporting operational readiness and future commercialization
  • Company-paid medical, dental, vision, and life insurance
  • Paid Time Off supporting work-life balance

Come join us on our mission of manufacturing safe, high-quality products that improve and save lives.

Apply