Global QHSE Analyst

. Crane Worldwide Logistics . • Houston, TX

4d • Onsite

About The Position

This role supports the business in quality management and serves as a subject matter expert in ISO standards and certification processes. The analyst will aid the Global Quality Manager in developing, deploying, and maintaining the global quality management system, including manuals, policies, procedures, processes, and documents. They will also assist with the global quality management strategy and objectives, pharmaceutical license support, and the development and maintenance of global quality management software. The position involves actively maintaining QMS documents in the company repository and supporting field operators in integrating existing documents into the QMS. The analyst is expected to stay updated on emerging technology changes and innovations and perform other duties as assigned.

Requirements

• Effective use of quality tools such as root cause analysis, corrective action/preventative action, QMS software & concepts and document control.
• Excellent verbal and written communication skills – ability to draft & edit policies, procedures, work instructions and forms.
• Demonstrated initiative and the ability to clearly communicate to others in a customer service oriented manner.
• Strong working knowledge of MS Office applications – Word, Excel, PPT, Outlook
• Ability to work independently and proactively.
• Ability to compile, analyze and draft summary report of large data sets.
• Ability to support in audit or compliance review processes – confident & subjective personality.
• Minimum 3 years of experience in Quality Management or general Business Administration.

Nice To Haves

• Bachelor's Degree in Business Administration or similar field preferred.

Responsibilities

• Support the business in quality management & be a reliable subject matter expert in ISO standards and certification processes.
• Aide the Global Quality Manager in developing, deploying and maintaining the global quality management system – manuals, policies, procedures, processes and forms/documents.
• Assist the Global Quality Manager in organizing the global quality management strategy and objectives.
• Pharmaceutical License support.
• Assist the Global Quality Manager with the development, deployment and maintenance of global quality management software.
• Actively maintain QMS documents in the company document repository; support field operators with integrating existing documents into the QMS where appropriate.
• Keep abreast of emerging technology changes and innovations through formal or informal study, reading business and professional publications, networking, and participation in professional organizations.
• Perform other duties as assigned.

Benefits

• Quarterly Incentive Plan
• 136 hours of Paid Time Off which equals 17 days for the year, that can be used for Sick Time or for Personal Use
• Excellent Medical, Dental and Vision benefits
• Tuition Reimbursement for education related to your job
• Employee Referral Bonuses
• Employee Recognition and Rewards Program
• Paid Volunteer Time to support a cause that is close to your heart and contributes to our communities
• Employee Discounts
• Wellness Incentives that can go up to $100 per year for completing challenges, in addition to a discount on contribution rates

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level