Quality Assurance Associate

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A permanent full time role working as a Quality Assurance Associate is available at a manufacturer of topical skin care and pharmaceutical products.

Summary about this job

Quality Assurance & Control

Company: Baxter Laboratories

Location: Melbourne

Work type: Full Time

Salary: n\a

Phone: +61-8-2741-3619

Fax: +61-8-7006-9381

E-mail: n\a

Site:

Detail information about job Quality Assurance Associate. Terms and conditions vacancy

  • Pharmaceutical Manufacturing Company
  • Eastern Suburbs
  • Be an integral part of the Quality Assurance Team

The business

Baxter Laboratories is a manufacturer of topical skin care and pharmaceutical products.  We are looking for an experienced Quality Assurance Associate to join our team.

The role

A permanent full time role working as a Quality Assurance Associate is available with an immediate start for the right candidate, within a friendly work environment.  This is a position for someone with an exceptional understanding of cGMP and with experience in quality assurance, having worked within the pharmaceutical or similar industry.   The position offers the opportunity to work in a small cross-functional team whilst reporting to the Quality Manager.  The incumbent will have the opportunity to operate with a high degree of independence and to exercise independent judgment in the performance of duties.  The successful candidate will participate in the following:

  • Manage and provide support on, Change controls, Deviations, CAPA
  • Manage and lead in customer complaint investigations
  • Support the Vendor Assurance programme
  • Manage the document control management system
  • Assist with  Product Quality Review program
  • Participate in and provide support on all Regulatory & Customer Audits
  • Conduct and participate in Internal Audits
  • Assist with GMP Training of staff
  • Provide support in other Quality Assurance related areas

Ideal Skills and experience

Desirable applicants will possess:

  • A tertiary qualification in a relevant scientific/ engineering discipline or equivalent.
  • Preferably minimum 2 years experience in the Pharmaceutical industry.
  • Working Knowledge of cGMP
  • Ability to manage a high throughput of work while meeting quality and business requirements and deadlines by having excellent organizational skills.
  • Strong analytical, investigation, problem solving and decision making skills, conceptual skills and demonstrated high level of proficiency and accuracy.
  • A high level of initiative and ability to formulate and develop new approaches to the management and use of data to support and improve quality compliance and work flow within Baxter Laboratories.
  • The ability to train and mentor colleagues and delegate specific tasks where appropriate.
  • The ability to work well with other staff members at all levels.
  • Excellent teamwork skills and excellent written and verbal communication skills.

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