Authorised Person at Viatris

, Queensland, Australia -

Full Time

Start Date

Immediate

Expiry Date

05 May, 26

Salary

0.0

Posted On

04 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, GMP, Regulatory Requirements, Communication Skills, Organization Skills, Report Writing, Data Presentation, Attention to Detail, Minimal Supervision, Continuous Improvement, Deviation Review, CAPA, Trend Assessment, Product Quality Review, Manufacturing Support, Packaging Support

Industry

Pharmaceutical Manufacturing

Description

Alphapharm Pty. Ltd. At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life. We do so via: Access – Providing high quality trusted medicines regardless of geography or circumstance; Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and Partnership – Leveraging our collective expertise to connect people to products and services. This posting supports ongoing hiring needs and may be used to consider candidates for upcoming opportunities. Currently our Quality Assurance department is seeking an Authorised Person to join the team at our Carole Park site for a fixed term contract until September 2026. Key responsibilities of the Authorised Person include: Review of deviations (incidents and investigations), CAPA’s, Effectiveness Checks and complete trending for all deviations (incidents and investigations), raise Trend Assessments and attend the Trend Review Board meetings To ensure master batch manufacturing and packaging documents as well as SAP recipes are complete and correct and to approve these for use Support and encourage continuous improvement initiatives for the benefit of the Quality department and the wider business Provide support to manufacturing, packaging and maintenance regarding any queries relating to quality matters Approve Annual Product Quality Reviews Support and encourage continuous improvement initiatives for the benefit of the Quality department and the wider business Ensure activities comply with GMP, legal and ethical standards To be considered for the Authorised Person role, candidates should have: Tertiary qualification in Science or related field Minimum 5 years’ experience in the Pharmaceutical Industry (desired but not essential) Understanding of GMP and regulatory requirements Excellent communication and organization skills Experience with writing reports and presenting data Demonstrated attention to detail Proven ability to work under minimal supervision Viatris Benefits: Employee rewards and discount platform Annual wellness allowance Recognition programs State of the art canteen onsite with a variety of subsidised food options Benefits for health and financial wellness Corporate deals with vendors including superannuation fund, health insurance and others Viatris Product loyalty program Free annual flu vaccination 2 days of paid volunteer leave per annum Additional paid parental leave Career and development planning for continuous growth and learning Retirement savings plans Annual leave loading, as well as paid additional bereavement leave Culture Viatris has been named in Forbes’ World’s Best Employers 2022 list. We have now received this recognition in each of our first two years – and for 2022, we are ranked in the top 10% of the 800 global employers who made the ranking. Viatris strives to create a positive, productive work environment where integrity, dignity and mutual respect for all is ingrained each and every one of us. Together, we are building a highly inclusive organization where employees are welcome to bring their best, authentic selves to work every day. Our goal is to provide a safe, supportive community where employees feel they belong and can use their unique experiences, perspectives and skills to make a difference in the lives of others. At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. Viatris is an Equal Opportunity Employer. Viatris is a global healthcare company formed in 2020 through the combination of Mylan and Upjohn, a legacy division of Pfizer. By integrating the strengths of these two companies, including our global workforce, we aim to deliver increased access to affordable, quality medicines for patients worldwide, regardless of geography or circumstance. We believe in healthcare as it should be – empowering people worldwide to live healthier at every stage of life. Because of our unwavering belief that better access leads to better health, we leverage our best-in-class manufacturing and scientific expertise and proven commercial capabilities to bring quality medicines to patients when and where they need them.

Responsibilities

The Authorised Person will review deviations, CAPAs, and ensure compliance with GMP and regulatory standards. They will also support continuous improvement initiatives and provide quality-related support to manufacturing and packaging.