Reliability Consultant

Kansas City, Missouri

Posted in Building and Construction

This job has expired.

Job Info

Reliability Consultant - Kansas City Area

(Pharmaceutical/Biotech)-Competitive Salary, Work/Life Balance!

We offer W-2, 1099, Agency Opportunities

Previous Pharmaceutical/Biotech/Medical Device Sr.PM experience is mandatory

Compli LLC is a full-service regulatory compliance consulting services company specializing in pharma and biotech as well as food and beverage, chemical, and discrete manufacturing industries. We are seeking an experienced Reliability Consultant to join our growing Asset Management and Reliability (AMR) Services team. The successful candidate will assist our clients across the United States in providing innovative solutions. This position will be responsible for delivering technical Maintenance, Engineering and Reliability expertise across multiple projects in a professional and timely manner.


  • Support and work alongside Senior Consultants through all phases of delivery including discovery, information and data gathering and analysis, best practices gap identification, findings, recommendations and project improvement plan development
  • Provide the technical assistance needed to support all on-site maintenance activities
  • Adhere to delivering technically sound and fundamentally consistent work with established company intellectual property, processes, forms and templates
  • Develop and maintain trusted and relationships with client and industry partners at all levels of the organization
  • Leverage professional network to generate new opportunities through quality delivery and technical excellence
  • Establish credibility through thought leadership (technical papers, industry publications, digital media, etc.) and participation in industry associations, conferences, etc.
  • Support efforts to increase the firm's market share for consulting services in the chosen area(s) of focus by identifying additional projects and clients
  • Periodically develop and deliver training courses to our clients in the fields of your areas of expertise
  • All other duties as assigned

Required Qualifications:
  • Possess an in-depth understanding of industry best practices in a minimum of five of the following disciplines:
  • M&R Best Practices Gap Assessment and Improvement Plan Development
  • Computerized Maintenance Management Systems (CMMS) review
  • Asset Criticality Ranking (ACR) education and facilitation
  • Work Management/Process Workflow review and development
  • Preventive Maintenance (PM) program review and optimization
  • Job Plan and Work Instruction writing
  • Predictive Maintenance (PdM)/Condition Monitoring program implementation
  • Failure Modes and Effects Analysis (FMEA) development
  • Reliability Centered Maintenance (RCM) education and facilitation
  • Materials Management (MRO) program review and optimization
  • Maintenance Training program review and optimization/implementation
  • Maintenance Metrics and Scorecards
  • Total Productive Maintenance (TPM)/Operator Care review and enhancement
  • Shutdown Management program review and improvement
  • Change Management practices
  • Ability to play a key role in the architecture and delivery of a M&R solution utilizing our tools, systems and methodologies
  • Ability to communicate with client leadership and stakeholders ensuring they understand and recognize the value being created by the M&R project
  • Possess a minimum of five years related-work experience
  • Demonstrate strong communication skills - written, verbal and presentation skills
  • Utilize good analytical and critical thinking skills
  • Must be thorough and detail-oriented
  • Is a good team-player with strong facilitation skills
  • Possesses excellent organizational and time management skills
  • Has a good work ethic and treats documents with confidentiality
  • Proficiency in all MS Office software and spreadsheet applications
  • Ability to learn quickly and work under pressure in a fast-paced environment
  • All candidates must be legally eligible to work in the United States
  • Must be willing to travel up to 90% of their worktime regionally in the Midwest

Preferred Qualifications:
  • Bachelor's degree in architecture, engineering, computer science, business, or related field from an accredited curriculum
  • Industry certifications such as those listed next would be considered a plus: CMRP, CMRT, CMS, CRL, LM1, LM2, LME, PMP, RCM or TPMC
  • M&R Consulting experience preferred
  • Minimum of three years of Pharmaceutical/ Bio-Tech or Food and Beverage, Chemical or discrete Manufacturing industry experience
  • Proficient in the use of planning/scheduling software such as Maximo, Upkeep, etc.
  • Two years of Project Management experience
  • Past and current participation in industry associations or technical groups
  • Demonstrated network of industry partnerships in various areas of expertise

Compli, LLC was founded in 2001 to provide commissioning, validation, and regulatory support services to the life sciences industry. We serve pharmaceutical companies across the U.S. Regarding regulations and compliance, it has never been more important to understand the documentation and quality assurance activities as they relate to vendors, engineering, construction, and contractors, which is why clients trust the Compli team.

Perks of the Job:
  • Competitive Pay commensurate with experience
  • Work / Life Balance
  • Working with a small, close-knit team where you are valued as an individual
  • A learning environment and continuous advancement opportunities

Feel overqualified? Feel underqualified? Apply anyway if this sounds like the fit you are looking for! We have flexibility in how we hire the role.

To learn more and APPLY NOW:

Agencies, Compli welcomes your qualified candidates. Please email: to establish a relationship with our firm.

We are an equal opportunity employer M/F/D/V

Job Keywords: Unites States, Kansas City, KS, Kansas City, MO., Missouri, Kansas, Overland Park, KS, Olathe, KS, commission, qualification, validation, CQV, Pharmaceutical, GMP Pharma, Biotech Industry.

This job has expired.

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