MSD Quality Assurance Associate 

Australia, New South Wales 

943900386

Job Description

QA Associate Specialist, In Market Quality

• Looking for a different challenge as a Quality Assurance Associate whereby you can still utilise your skills?

• Permanent, Full-timeposition with competitive renumeration and benefits

• Hybrid, work from home and office environment, with a dedicated and welcoming team

• Upskill and growth in an area you’re passionate about , whilst being fully supported and encouraged

• Join a trusted Global Leading Pharmaceutical organisation

Responsibilities include, however not limited to:

• Assist in the implementation and maintenance of quality assurance processes and procedures in accordance with regulatory requirements and company standards.

• Provide support to Australia and New Zealand Quality Responsible Person (QRP) Lead with any recall matters.

• Assist with the management for local vaccine release activities.

• Ensure periodic customer qualifications are performed in a timely manner.

• Support Australia and New Zealand Lead QRP with quality and compliance related activities at our company’s outsourced warehouses.

• Work closely with cross-functional teams to investigate and resolve quality issues, deviations, and non-conformances. Conduct root cause analysis and implement corrective and preventive actions.

• Support change control processes by assessing the impact of proposed changes on product quality and ensuring proper documentation and approval.

• Collaborate with internal teams to provide training and guidance on quality assurance processes, standards, and compliance requirements.

• Maintain accurate and up-to-date documentation related to quality assurance activities.

What You Must have

• Bachelor's degree in a related field, such as Pharmacology, Science, Engineering, or a relevant discipline.

• Strong attention to detail and excellent organizational skills.

• Knowledge of quality assurance principles and processes, advantageous not essential.

• Familiarity with TGA and Medsafe regulatory requirements and industry standards, advantageous not essential.

• Good problem-solving and analytical skills, with the ability to conduct root cause analysis and implement corrective actions.

• Effective communication skills, both written and verbal.

• Ability to work well within a team and collaborate with cross-functional departments.

• Proficiency in using Microsoft Office applications and other relevant software systems.

• Prior experience or internships in a quality assurance, operation or regulatory role in pharmaceutical industry, advantageous not essential.

What You Can Expect

• Work autonomously whilst being supported, encouraged and being part of a trusted Global Leading Pharmaceutical organisation

• Exposure to upskill and develop in your role

• Flexibility and opening doors to other opportunities and skillsets

• Joining acollaborativeteam oflikeminded individuals

Current Contingent Workers apply

Hazardous Material(s):

Job Posting End Date:05/27/2024

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