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Site Safety, Quality and Regulatory Manager
Site Safety, Quality and Regulatory ManagerBrenntag • Indianapolis, Indiana, USA
Site Safety, Quality and Regulatory Manager

Site Safety, Quality and Regulatory Manager

Brenntag • Indianapolis, Indiana, USA
[job_card.30_days_ago]
[job_preview.job_type]
  • [job_card.full_time]
[job_card.job_description]

Your Role & Responsibilities

Lead the effort and collaborate with District management supervision and employees on maintaining a sustainable safety culture within the District in concert with Company goals and objectives.

Responsible for ensuring all Safety Regulatory & Quality training is conducted documented and effective. Such as

Process Safety Management (PSM) HM126F Respirator Electrical Confined Space Entry Lockout / Tagout Hazardous

Waste Emergency Response etc.

Review all incidents and assist the branches in investigating incidents and / or near misses and developing corrective action plans to correct.

Visit each branch in the district quarterly at a minimum or as needed.

Ensure branches are compliant with all regulatory requirements through training audits etc.

Conduct proper internal safety / regulatory audits of each branch on an annually.

Ensure branches have a functional ISO 9000 system and Job 7 / Quality Teams conduct internal audits of each branchs ISO 9000 system.

Be on-site as required to assist with third party ISO 9000 audits or customer audits.

Monitor JOB 7 performance at branches and assist in making improvements to our customer service system.

Conduct customer training as needed.

Obtain / prepare regulatory / technical information for customers.

Assist branches in completing and updating PSM manuals Lockout / Tagout information and emergency contingency plans.

Review driver logs regularly to ensure correctness.

Ensure driver qualification files are up-to-date for each branch.

Assist and monitor NACD Responsible Distribution Process within the District.

Assist with Emergency Response situations that occur within the district or as needed.

Support and participate in safety meetings and safety committee meetings at each branch.

Ensure all District facility monitoring reports required in the district are completed and forwarded to the proper agency.

Ensure regulatory programs such PSM RMP Lockout / Tagout Respiratory Protection Hot Work Permit Confined Space DHS and DOT site security plans and other programs as applicable are in place and functioning.

Ensure the corporate office is notified of all regulatory inspections and that any discrepancies noted during the inspection are corrected.

Other responsibilities as designated by management.

Initiate action to prevent the occurrence of any non-conformities relating to product process and quality system.

Identify and record any problems relating to the product process and quality system.

Initiate recommend or provide solutions through designated channels.

Verify the implementation of solutions.

Control further processing delivery or installation of non-conforming product until the deficiency or unsatisfactory condition has been corrected.

Your Profile

Education and Experience :

Bachelors degree in Safety Health Environmental or related field; or a minimum of five to ten years of management experience in a chemical or related industry that must comply with OSHA EPA and DOT regulations.

Thorough understanding of the importance of customer service and the ability to work cooperatively with other branches departments and personnel in meeting customer needs.

Ability to interface well with customers.

Ability to interface and communicate in a professional manner with diverse employee groups including sales management supervision and employees.

Ability to interface and communicate in a professional manner (oral and written).

Computer skills to efficiently perform the job requirements.

Ability to understand and comply with all company policies and procedures.

Knowledge of statistical techniques used for continual quality improvement.

Experience with ISO Standard and Internal Quality Auditing.

Strong desire to succeed and lead.

Our Offer

We aim to create an environment where the best people want to work where they can turn their passion into their job and realize their full potential.

Individual development on-the-job training and development programs designed to help our employees grow in their careers.

Paid parental leave

Education assistance program

Employee assistance program

Various healthcare plan options as well as 401(k)

Interested

We look forward receiving your application.

Brenntag and its subsidiary companies will provide equal employment opportunities to all applicants without regard to any category protected by federal state or local law including as applicable applicants actual or perceived race color religion creed sex sexual orientation gender identity or expression (including transgender status) gender (including pregnancy childbirth lactation and related medical condition) genetic information military service national origin ancestry citizenship status age veteran status physical or mental disability protected medical condition as defined by applicable federal state or local law political affiliation marital status membership in an employee organization parental status expunged juvenile record or any other status protected by federal state or local law. Brenntag will provide reasonable accommodations to allow an applicant to participate in the hiring process (e.g. accommodations for a test or job interview) if so requested. When completing this application you may exclude information that would disclose or otherwise reference your race religion age sex genetic veteran status disability or any other status protected by federal state or local law. This application is considered current for sixty (60) days only. At the end of this period if you are still interested in employment it will be necessary for you to reapply by completing a new application.

If you are a qualified individual with a disability or a disabled veteran you may request a reasonable accommodation if you are unable or limited in your ability to access job openings or apply for a job on this site as a result of your disability. You can request reasonable accommodations by contacting Human Resources at (phone tty fax email etc.).

Brenntag North America Inc. and its subsidiaries use E-Verify a government-run web-based system that allows employers to confirm the eligibility of their employees to work in the United States. For more information please go to or view the poster at TA Team

Required Experience :

Manager

Key Skills

Proofreading,Adobe Acrobat,FDA Regulations,Manufacturing & Controls,Biotechnology,Clinical Trials,Research & Development,GLP,cGMP,Product Development,Chemistry,Writing Skills

Employment Type : Full-Time

Experience : years

Vacancy : 1

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