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Site Head of Health and Safety

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Jobs by Experience drjobs

5-10years

Job Location drjobs

Indianapolis - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Job Description

  • As the Site Head of HSE/Radiation Safety Officer, you will be responsible for all HSE compliance aspects of a 24/7 radioligand therapy drug product manufacturing plant and team.
  • This role reports directly into the Site Head and will be part of the Indianapolis Senior Leadership Team.
  • Serve as the Site Radiation Safety Officer and collaborate with operations and technical teams to safely manage radioactive materials from raw materials to finished product and waste disposal.
  • Drive the implementation and execution of the HSE roadmap defined by Novartis, working closely with all functions within the site and the broader Novartis organization.
  • Maintain knowledge of and ensure strict adherence to all regulatory compliance standards applicable to the site and Company including Radiation Safety, Governance, Business Continuity & Emergency Management and Environmental Health and Safety
  • Create and maintain an injury-free work environment that protects employees from hazards, including radiation exposure.


Requirements

  • Bachelor s Degree in industrial hygiene, health and safety, engineering, or related field or a minimum of 4 additional years of relevant experience.
  • 7 years of experience in HSE management systems, cGMP environment - radio-pharmaceuticals, sterile operations, or highly potent materials, is a plus.
  • Prior experience leading HSE department at a manufacturing site is required.
  • Significant experience building an injury and error-free culture with advanced knowledge of multiple US compliance areas (EPA, OSHA, NRC, etc.) is required.
  • Prior radiation safety experience is preferred.
  • Training and/or certification in radiation safety is also preferred.


Benefits

  • PTO 18 days (Company Policy)
  • Federal 6 days
  • Employee Healthcare we have four options; one of them we cover 100% for the employee
  • Life Insurance - Employee policy 100% covered by HCG
  • Long Term Disability Insurance - Employee policy 100% covered by HCG
  • Identity Theft Insurance - Employee policy 100% covered by HCG
  • 401K - with a company match of up to 3.5%
  • HCG also offer 401K Profit Sharing
  • HCG Technical - Company Laptop provided if needed
  • HCG brand items Clothing, Stationery, Quarterly care packs etc.


We support our diversity, equity, inclusion and belonging efforts because we believe that by cultivating an environment where our diverse employees can share their ideas and thrive, we will be able to better serve our organization and our global customers. Our commitment is that we have an inclusive culture that values each of our employees background, by empowering our staff to feel valued, have a sense of belonging, make positive contributions to the communities in which they live and work, and be proud to be part of Horizon Controls Group.



6+ years of relevant pharmaceutical/biotechnology experience. 6+ years of experience as a process engineer in the bio-pharmaceutical industry preferred. Experience working in a regulated GMP environment. Demonstrable experience working to standards required for regulatory compliance of Aseptic Processing facilities. Engineering and process knowledge associated with various sterilization technologies, utilities and associated pharmaceutical processes. Experience supporting batch and continuous industrial control systems including DeltaV, preferable. Basic understanding and knowledge of bio-pharmaceutical production equipment including but not limited to bioreactors, centrifuges, CIP skids, chromatography. Proficient maintaining system life cycle documentation (drawings, design files, FRS/SDDS, etc.). Must be able to interact well with peers and senior personnel in scientific, engineering, and operational disciplines. Understanding / ability to demonstrate use of problem solving and continuous improvement techniques. (i.e., process/equipment/yield improvement projects, safety improvement projects, etc.) Ability to work as a member on cross-functional and self-directed work teams. Proven ability to provide technical support for deviations, SOP s, batch records etc.

Employment Type

Full Time

Company Industry

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