Plant Maintenance Engineer

Grifols SA

Clayton, NC

JOB DETAILS
SKILLS
Biotech and Pharmaceutical, Change Control, Communication Skills, Conflict Resolution, Consulting, Continuous Improvement, Cross-Functional, Depth Perception, GMP (Good Manufacturing Practices), Healthcare, Identify Issues, Instrumentation, International Health, Inventory Management, Lift/Move 50 Pounds, Manufacturing, Manufacturing Operations, Material Moving, Medical Conditions, Medical Products, Medicine, Operational Improvement, Operational Strategy, Outsourcing, Plasma, Presentation/Verbal Skills, Problem Solving Skills, Process Improvement, Process Management, Project Engineering, Recruiting/Staffing Agency, Regulatory Compliance, Root Cause Analysis, Safety Compliance, Technical Writing, Writing Skills
LOCATION
Clayton, NC
POSTED
30+ days ago

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

Responsibilities:

This role provides plant maintenance engineering support for 24x7 manufacturing operations at the Grifols Clayton site, Fractionation Areas

The Maintenance/Plant engineer has the primary responsibility for:

  • Ensure reliable production area operation in compliance with safety, regulatory, and production requirements while making independent decisions and resolving conflict within defined areas of responsibility.
  • Troubleshoot and identify root-cause mechanical system issues and process related problems so they can be corrected.
  • Become the mechanical SME for the areas of responsibility within the building while serving as a consultant to management within that specified area.
  • Plans and organizes cross-functional activities. Partner with operations, maintenance and project engineering to identify and resolve issues (redesign, rebuild, repair, etc).
  • Actively pursue and manage process optimization technology, help improve operational efficiency, and implement continuous improvement projects. Advances technical project proposals through to completion.
  • Oversee outsourced vendor support.
  • Assist in training maintenance, instrumentation, and operations personnel.
  • Additional responsibilities include materials clearance, spare parts inventory, change controls, incident investigation, participating in safety reviews, specifications, leading projects during plant shutdowns and other common GMP engineering tasks.

Additional Skills Needed:

  • Self-motivated and driven to succeed
  • Hands-on and a problem solver.  Greater time in the field than at the desk.
  • Communicates effectively and promptly at all levels of the organization.
  • Strong theoretical and practical technical understanding with strong troubleshooting skills.
  • Works well with technical and non-technical personnel.
  • Solid technical writing and verbal communication skills.
  • Candidates with GMP and/or pharmaceutical industry experience are preferred

Requirements based on level:

Engineer III:

  • Bachelor's Degree in engineering or related field. Professional certifications and licenses as appropriate.
  • At least 4 years of experience.
  • Biotech, Chemical or Industrial experience preferred.

Engineer IV

  • Bachelors Degree in Engineering or related field.
  • Typically requires 5 years of related experience.
  • Biotech, Chemical or Industrial experience preferred.

Senior Engineer

  • BS degree (related engineering discipline).
  • Minimum of 6 years of applicable engineering experience.
  • Experience in Biotech, Pharmaceutical or Chemical Industry preferred.

Staff Engineer

  • Bachelors Degree in Engineering or related field.
  • Professional registration and/or certifications as appropriate.
  • Minimum 7 years of related experience.
  • Experience in Biotech, Pharmaceutical or Chemical Industry preferred.

Principal Engineer

  • Minimum Education:  Bachelors Degree in Engineering.
  • Professional registration and/or certifications as appropriate.
  • Minimum 8 years of experience.
  • Experience in Biotech, Pharmaceutical or Chemical Industry preferred.

Work is performed in an office and a laboratory/manufacturing environment. Exposure to biological fluids with potential exposure to infectious organisms.   Exposed to occasional extreme cold below 32 degrees C* in production areas. Exposure to electrical office and laboratory equipment. Personal protective equipment required such as protective eyewear, garments and gloves. Frequently sits for 4-6 hours per day. Stands for 2-4 hours per day. Frequent movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists.  Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Occasionally walks. Occasionally bends and twists neck and waist. Frequent foot movements.  Color perception/discrimination, depth perception and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Light to moderate lifting and carrying objects with a maximum lift of 50lbs. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken and written words and sentences.  Frequently performs routine tasks by following a set of written or oral instructions/procedures.

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Third Party Agency and Recruiter Notice:

Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.

Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.

Location: NORTH AMERICA : USA : NC-Clayton:USNC0002 - Clayton

Learn more about Grifols

About the Company

G

Grifols SA

At Grifols, what we do matters

Are you passionate about making a difference in the world? At Grifols, we are pioneers in the development of therapies derived from blood and plasma. We contribute to building the future of healthcare to improve people's well-being. Since 1909, we have been defined by passion, innovation, teamwork and a sense of responsibility. Our people change lives while growing and developing into a forward-looking international company.

Your future at Grifols

At Grifols, you will be part of a growing international team of more than 23,000 people in more than 30 countries and regions with a common goal: to improve people's lives. You will contribute to developing scientific advances and providing innovative solutions for healthcare professionals and essential medicines for patients. We want to count on determined professionals who, by cultivating their talent, contribute to creating a positive impact on society.

COMPANY SIZE
10,000 employees or more
INDUSTRY
Healthcare Services
FOUNDED
1909
WEBSITE
https://www.grifols.com/