Job Description

Job Header

Pharmacovigilance Representative - Manufacturing Site

Advertiser: CSL Limited3.1 out of 53.1 overall rating (30 employee reviews) More jobs from this company

Job Information

Job Listing Date
28 Nov 2019
Location
Melbourne, Northern Suburbs
Work Type
Full Time
Classification
Science & Technology, Quality Assurance & Control

Pharmacovigilance Representative - Manufacturing Site


The Opportunity:

In this newly created role you will report to the Global Manufacturing Site Pharmacovigilance Representative and you will collaborate closely with the Global Team to ensure cooperation with Global Quality and the manufacturing sites QA. You will help create and further develop the interface to the manufacturers QA. You will prepare assessments on a high scientific level and in close cooperation with relevant stakeholders.

In this role you will be highly visible on multiple management levels. You will communicate actively and initiatively on a high scientific as well on a cultivated interpersonal level. The role will require travelling in coordination with the Global MSPR.

 

To be successful in this position you will possess:

  • University graduate in life-sciences (pharmacy or pharmacology or biology or human / veterinary medicine)
  • Technical knowledge of the PV and quality relevant regulatory framework and good knowledge of international regulations and standards (such as GVP, GMP)
  • Excellent written and verbal communication skills in English.
  • Strong relationship builder and communicator at various levels of the business.
  • Sound and balanced judgment; able to assess and handle risks; self-confident, proactive and decisive.
  • Able to work effectively and collaboratively across site functions and the GCSP organization.
  • High ethical standards as well as personal credibility, the ability to gain trust at the senior executive level.
  • Willing to learn the principles of internal audits and authority inspections.
  • Good team player and networker with excellent interpersonal and communication skills.
  • Fluency in Mandarin highly desirable

 

The Company:

CSL Limited is a company that fosters a work culture emphasising Superior Performance, Innovation, Integrity, Collaboration and Customer Focus with a commitment to support, train and grow its people. As a genuine leader in the biopharmaceutical industry, CSL is a multinational ASX Listed Company that is actively growing its Australian based manufacturing operations to support global growth. CSL develops, manufactures and markets products to treat and prevent serious human medical conditions and is globally one of the largest manufacturers of plasma-derived therapies.

 

To Apply:

Applications must address the selection criteria above and include a current CV and covering letter.

Applications close Sunday, 9th of December, 2019

Employment screening, including criminal history, medical assessment, confirmation of experience and stated qualifications, Australian working rights and other relevant checks form part of the candidate suitability

The Opportunity:

In this newly created role you will report to the Global Manufacturing Site Pharmacovigilance Representative and you will collaborate closely with the Global Team to ensure cooperation with Global Quality and the manufacturing sites QA. You will help create and further develop the interface to the manufacturers QA. You will prepare assessments on a high scientific level and in close cooperation with relevant stakeholders.

In this role you will be highly visible on multiple management levels. You will communicate actively and initiatively on a high scientific as well on a cultivated interpersonal level. The role will require travelling in coordination with the Global MSPR.

 

To be successful in this position you will possess:

  • University graduate in life-sciences (pharmacy or pharmacology or biology or human / veterinary medicine)
  • Technical knowledge of the PV and quality relevant regulatory framework and good knowledge of international regulations and standards (such as GVP, GMP)
  • Excellent written and verbal communication skills in English.
  • Strong relationship builder and communicator at various levels of the business.
  • Sound and balanced judgment; able to assess and handle risks; self-confident, proactive and decisive.
  • Able to work effectively and collaboratively across site functions and the GCSP organization.
  • High ethical standards as well as personal credibility, the ability to gain trust at the senior executive level.
  • Willing to learn the principles of internal audits and authority inspections.
  • Good team player and networker with excellent interpersonal and communication skills.
  • Fluency in Mandarin highly desirable

 

The Company:

CSL Limited is a company that fosters a work culture emphasising Superior Performance, Innovation, Integrity, Collaboration and Customer Focus with a commitment to support, train and grow its people. As a genuine leader in the biopharmaceutical industry, CSL is a multinational ASX Listed Company that is actively growing its Australian based manufacturing operations to support global growth. CSL develops, manufactures and markets products to treat and prevent serious human medical conditions and is globally one of the largest manufacturers of plasma-derived therapies.

 

To Apply:

Applications must address the selection criteria above and include a current CV and covering letter.

Applications close Sunday, 9th of December, 2019

Employment screening, including criminal history, medical assessment, confirmation of experience and stated qualifications, Australian working rights and other relevant checks form part of the candidate suitability

Report this job advert

Be careful- Don’t provide your bank or credit card details when applying for jobs. If you see something suspicious .

Share this role

Applications will open the advertiser’s site.