Job Description

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QC Officer (Analyst)

Advertiser: Lipa Pharmaceuticals LtdMore jobs from this company

Job Information

Job Listing Date
28 Sep 2018
Location
Sydney, South West & M5 Corridor
Work Type
Full Time
Classification
Manufacturing, Transport & Logistics, Quality Assurance & Control

QC Officer (Analyst)

Lipa Pharmaceuticals is a thriving, innovative and market leading contract manufacturer of complementary health care products based at Minto (close to Campbelltown) in South West Sydney.  We currently service the bulk of Australia's leading brands and various overseas customers across North and South America, Europe, Asia and the Pacific region. 

We are seeking an accomplished and experienced Laboratory Analyst with relevant tertiary qualifications in Chemistry or a similar tertiary physical sciences technical course, to join the Quality Control (QC) team in our high throughput, analytical laboratory.

Most of your time will be spent testing a diverse range of active raw materials and finished goods that the facility processes.  In addition, depending on your level of experience and skill, you will take part in: method development and validation; instrument calibration; investigative activities for Out-Of-Specification (OOS) results; stability profiling and reporting; as well as associated administrative activities pertinent to the role of a QC Analyst.

As a member of the QC laboratory team, you will need to demonstrate ‘hands on’, operational experience and capacity to:

  • Be an efficient and effective multitask oriented analyst
  • Confidently and effectively operate various instruments inclusive of UPLC/HPLC's, ICP's, IR's, UV's and GC's,
  • Be able to maintain routine calibration and basic performance maintenance processes of those instruments,
  • Be fully conversant and familiar with GLP as regulated/administered by the TGA and or NATA,
  • Have experience and knowledge of various traditional wet chemistry analytical techniques and practices,
  • Be able to carry out analytical method development,
  • Be able to document and have input in generating revised SOPs,
  • Be a disciplined, efficient and effective analytical professional
  • Efficiently collate and document through written reports, relevant investigative activities as required.

Our QC Laboratory is a customer driven, dynamic and critical area of our business that services a number of internal and external related entities.  Working under tight deadlines and shifting priorities, you will need to demonstrate the ability to be self-driven and professional at all times, whilst functioning as an integral part of the QC team.

Please Note:  All prospective employees will be required to undergo medicals and police checks. Only those applicants deemed suitable by Lipa Pharmaceuticals and who possess full working rights for Australia will be contacted for interview.

www.lipa.com.au

Lipa Pharmaceuticals is a thriving, innovative and market leading contract manufacturer of complementary health care products based at Minto (close to Campbelltown) in South West Sydney.  We currently service the bulk of Australia's leading brands and various overseas customers across North and South America, Europe, Asia and the Pacific region. 

We are seeking an accomplished and experienced Laboratory Analyst with relevant tertiary qualifications in Chemistry or a similar tertiary physical sciences technical course, to join the Quality Control (QC) team in our high throughput, analytical laboratory.

Most of your time will be spent testing a diverse range of active raw materials and finished goods that the facility processes.  In addition, depending on your level of experience and skill, you will take part in: method development and validation; instrument calibration; investigative activities for Out-Of-Specification (OOS) results; stability profiling and reporting; as well as associated administrative activities pertinent to the role of a QC Analyst.

As a member of the QC laboratory team, you will need to demonstrate ‘hands on’, operational experience and capacity to:

  • Be an efficient and effective multitask oriented analyst
  • Confidently and effectively operate various instruments inclusive of UPLC/HPLC's, ICP's, IR's, UV's and GC's,
  • Be able to maintain routine calibration and basic performance maintenance processes of those instruments,
  • Be fully conversant and familiar with GLP as regulated/administered by the TGA and or NATA,
  • Have experience and knowledge of various traditional wet chemistry analytical techniques and practices,
  • Be able to carry out analytical method development,
  • Be able to document and have input in generating revised SOPs,
  • Be a disciplined, efficient and effective analytical professional
  • Efficiently collate and document through written reports, relevant investigative activities as required.

Our QC Laboratory is a customer driven, dynamic and critical area of our business that services a number of internal and external related entities.  Working under tight deadlines and shifting priorities, you will need to demonstrate the ability to be self-driven and professional at all times, whilst functioning as an integral part of the QC team.

Please Note:  All prospective employees will be required to undergo medicals and police checks. Only those applicants deemed suitable by Lipa Pharmaceuticals and who possess full working rights for Australia will be contacted for interview.

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