Validation & Engineering Group, Inc.

Preventive Maintenance Engineer

Validation & Engineering Group, Inc.  •  Carolina, PR (Onsite)  •  17 hours ago
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Job Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Preventive Maintenance Engineer

We are seeking an experienced Preventive Maintenance Engineer to support a pharmaceutical manufacturing facility in Greenville, SC. This is a hands-on, on-site assignment focused on evaluating and optimizing preventive maintenance (PM) programs for manufacturing and packaging equipment.

The engineer will assess preventive maintenance strategies by combining OEM recommendations, equipment failure history, maintenance records, and feedback from maintenance and production personnel to optimize maintenance tasks, maintenance frequencies, and overall equipment reliability.

The successful candidate must be capable of working independently, quickly understanding the equipment and maintenance program, and delivering improvements with minimal ramp-up time.

Responsibilities

  • Review and evaluate existing preventive maintenance programs for manufacturing and packaging equipment.
  • Review OEM manuals, maintenance recommendations, and equipment documentation.
  • Analyze maintenance work orders and equipment failure history to identify trends and opportunities for improvement.
  • Interview maintenance technicians and production personnel to better understand equipment performance, recurring issues, and current maintenance practices.
  • Evaluate preventive maintenance frequencies, inspection intervals, spare parts replacement schedules, and maintenance tasks based on engineering judgment, equipment history, and operating conditions.
  • Recommend improvements to preventive maintenance strategies to improve equipment reliability and reduce unplanned downtime.
  • Update preventive maintenance job plans and related documentation.
  • Prepare periodic reports documenting completed assessments, recommended improvements, and quantified benefits, including expected improvements in equipment reliability, preventive maintenance effectiveness, reduction of unplanned downtime, and overall maintenance performance.
  • Work closely with Engineering, Maintenance, and Production personnel throughout the assessment and implementation process.
  • Utilize the site's computerized maintenance management system (CMMS) to review maintenance history and support PM optimization activities.

Qualifications

  • Bachelor's degree in Mechanical Engineering or another Engineering discipline, preferred.
  • Minimum of 5 years of engineering experience in maintenance, reliability, manufacturing, mechanical, or equipment engineering within an industrial manufacturing environment.
  • Experience developing, reviewing, or optimizing preventive maintenance programs.
  • Strong mechanical aptitude and the ability to interpret OEM manuals, equipment documentation, and engineering drawings.
  • Experience analyzing equipment failures and applying engineering judgment to improve equipment reliability.
  • Ability to work independently with minimal supervision and begin producing results quickly.
  • Excellent communication skills and the ability to collaborate effectively with maintenance, production, and engineering personnel.
  • Experience in pharmaceutical, biotechnology, medical device, or other FDA-regulated manufacturing environments.
  • Familiarity with manufacturing systems used for sterile liquid pharmaceutical products, including:
    • Mixing and formulation vessels
    • Product transfer and distribution piping
    • Pumps, valves, and associated process equipment
    • Aseptic filling equipment
    • Bottle handling, labeling, packaging, and secondary packaging systems
  • Familiarity with plant utility systems supporting pharmaceutical manufacturing, including compressed air, purified water, steam, and related utilities.
  • Experience with CMMS software such as MP2, Maximo, SAP PM, or similar maintenance management systems.
  • Experience applying reliability engineering principles to optimize preventive maintenance strategies and improve equipment performance.

Work Environment

  • Full-time, on-site assignment in Greenville, SC.
  • Must be comfortable working directly in manufacturing and packaging areas while interacting closely with maintenance, engineering, and production personnel.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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Validation & Engineering Group, Inc.

About Validation & Engineering Group, Inc.

Validation & Engineering Group, Proudly serving our clients since 1997.

Our Mission states in part: "provide our clients with the best resources to meet their needs". In our search for the best talent, we are inclusive and do not discriminate. V&EG is proud to be an equal opportunity workplace and is an affirmative action employer.

Validation & Engineering Group provides world-class service and expertise to the pharmaceutical, medical device and biotechnology industries. We offer our clients: Validation, Control System Solutions, Instrumentation, Training, Equipment Rentals, and Regulatory Compliance Services to ensure adherence to Federal and European regulatory agencies. Our group had serve in solid dosages, liquids, creams, lyophilizers, and parenteral dosage.

Our agility in responding to our clients’ needs, access to the best pool of talent, and the combined experience and technical expertise of our resources make Validation & Engineering Group a leader in the pharmaceutical, medical devices, and biotechnology industries.

At Validation & Engineering Group we provide professional expertise in the areas of:

•Audit and Assessment

•Automated Process Control System Qualification

•Equipment and Facilities Qualification

•Facilities Start-Up and Commissioning

•GAP Analysis

•Information Systems Computer Validation

•Packaging and Process Analysis

•Process & Cleaning Validation

•Project Management

•Quality Systems

•Risk Based Approach

•Regulatory Compliance

•Standard Operating and Maintenance Procedures

•Training

•Utilities Support and Qualification

In addition we offer Equipment Rentals and training to your workforce such as: Temperature & Relative Humidity, Electrical, Process, Environmental, and. Analytical.

Our Offices:

Puerto Rico:

Centro Internacional de Mercadeo I 100 Carr. 165 Ste 703, Guaynabo, 00968 Puerto Rico

Phone: (787) 622-0996

United States:

2180 Satellite Blvd, Suite 400Duluth, Georgia 30097 United States

Phone: (770) 403-5802

Industry
Architecture & Engineering
Company Size
51-200 employees
Headquarters
Guaynabo, PR
Year Founded
1997
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