SHE Advisor

SHE Advisor
Centrient Pharmaceuticals Netherlands, Netherlands

Experience
1 Year
Salary
0 - 0
Job Type
Job Shift
Job Category
Traveling
No
Career Level
Telecommute
No
Qualification
Bachelor's Degree
Total Vacancies
1 Job
Posted on
Oct 25, 2022
Last Date
Nov 25, 2022
Location(s)

Job Description

Centrient Pharmaceuticals is the leading manufacturer of beta-lactam antibiotics, and a provider of next generation statins and anti-fungals. We produce and sell intermediates, active pharmaceutical ingredients and finished dosage forms.

We are a pharmaceutical company with a clear Purpose: to improve lives throughinnovative and sustainable manufacturing of medicines.

With our commitment to Quality, Reliability and Sustainability at the heart of everything we do, our over 2200 employees work continuously to meet our customers’ needs. We work towards a sustainable future by actively participating in the fight against antimicrobial resistance.

Founded 150 years ago as the ‘Nederlandse Gist- en Spiritusfabriek’, our company was known as Gist Brocades. Headquartered in Rijswijk (Netherlands), we have production facilities and sales offices in China, India, the Netherlands, Spain, the United States and Mexico. Centrient Pharmaceuticals is wholly owned by Bain Capital Private Equity, a leading global private investment firm.

The SHE department of the business Unit Production has a vacancy in its Delft offices, for the following position:

SHE Advisor

The Position

Contribute to full SHE compliance within Centrient operations by the implementation of an effective management system and the execution of policies and programs. Ensure compliance with legal- (License to Operate) and Centrient requirements.

Improve the SHE performance and minimize the risks of accidents and incidents.

Site management and shift operators are supported and advised with respect to implementing SHE requirements and improving the management system.

The main activities and responsibilities

  • Set SHE standards, authorize SHE studies, plans, procedures (SOP), processes, products and training.
  • Ensure quality and execution of Process Safety studies.
  • Act as back-up and temporary replacement for the SHE Manager.
  • Contribute to monitoring and reporting the level of SHE performance.
  • Facilitate learnings from incidents, based on adequate incident reporting and investigation.
  • Provide guidance in relevant SHE issues, advise on work permits and sign off Task Risk Assessments.
  • Deliver SHE input projects.
  • Coordinate the environmental measuring and recording program (meet- en registratieprogramma).
  • Prepare, monitor and partly execute SHE programs for Delft.
  • Secure License to Operate.
  • Comply to legal requirements and company rules.
  • Continuously improve SHE performance.
  • Implement safety culture and behavior change management plans.

The Ideal Candidate

  • HBO level or academic level, e.g. Chemical Engineering or (Bio)Chemistry.
  • 3-5 years of experience in a production or project environment, preferably in the (bio-)chemical or pharmaceutical industry.
  • Good personal interaction and communication skills.
  • Higher Safety Level (HVK) and/or Environmental Management.
  • Knowledge of authority's requirements regarding SHE.
  • Knowledge of SHE Management Systems, ISO 14001.
  • Auditing skills.
  • Professional knowledge and experience with SHE studies (e.g., RIamp;E, HAZOP, PHR, SIL) and incident analysis (e.g. TRIPOD).
  • Project management skills.

Terms and reward

We offer a local contract in a challenging, comprehensive, operational environment, with many opportunities for personal input and growth and plenty of discussions with other professionals. The organization is very flat. You have a lot of freedom and responsibility in an open, direct and informal atmosphere.

The Procedure

Please submit your application before November 7, 2022 via the 'apply' button and upload your CV amp; cover letter in English. We also ask you to include information on your current remuneration. Only applications with CV and Cover Letter will be considered.

For more detailed information about the role and about the Recruitment amp; Selection process you can contact us via . We invite you to visit our website www.centrient.com for information about our company.

Reference check procedures are part of the Centrient Recruitment amp; Selection Process. You will be contacted when a reference check is required.

Acquisition in regard to this vacancy is not appreciated

Job Specification

Job Rewards and Benefits

Centrient Pharmaceuticals Netherlands

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