Job openings

Are you experienced in Quality Assurance and thrive on achieving excellence in a dynamic environment? Do you deliver standout results first time, every time?

If so, you’ll fit right in at Mayne Pharma. What’s in it for you? You’ll help us achieve our mission of delivering better, safer and more accessible medicines.
At Mayne Pharma, the results speak for themselves

About Mayne Pharma

Mayne Pharma is a global pharmaceutical company offering end-to-end pharmaceutical development and manufacturing to customers around the world. Our heritage makes us one of the most well-known and respected pharmaceuticals companies in Australia. 

Mayne Pharma Australia are passionate about bringing globally valued pharmaceuticals to Australian patients and consumers. Our values of Passion, Integrity, Accountability, Creativity, Empowerment and Agility are the foundation for everything we do. 

Why Join Us?

• Attractive remuneration packages
• Exclusive Health Insurance Benefits
  Financial Flexibility
• Well-being Programs
• Professional Development
• Mayne Perks: Enjoy exclusive discounts and savings
• Community Service
• Recognition and Team Events
• Health and Wellness

Here’s where you come in

Are you an experienced Quality Assurance Associate that wants a new challenge in the pharma industry and are wanting to build your experience?  If so, you’ll join a fast-paced environment that pushes you to achieve your best as you partner the business to deliver its products and improve its processes. 

But you won’t do it alone. You’ll be supported – every step of the way as part of a large, high achieving Quality Assurance Team. 

Your responsibilities, at a glance, will include:

• Maintenance of procedures and processes to ensure compliance with Regulatory and Company quality standards.
• QA release of raw materials, packaging materials, intermediates and finished products.
• Delegate to the ‘Authorised Person’ who will have responsibility for ‘Release for Supply’, ensuring product compliance to Market Authorisation.
• Assist in all aspects of the QMS including Training, QE’s, CAPA’s, Change Controls, Product complaints, Risk Assessments, Specifications and SOP’s.
• Support manufacturing and laboratory investigations using Root Cause Analysis tools.
• Participation in Regulatory, Customer and Internal audits.
• Preparation and analysis of Product Quality Reviews.
• Support New Product Introductions. 
• Participate in site Quality Continuous Improvement plans.

You need to tick these boxes

We pick applicants based on capability and aptitude. But we also emphasise cultural fit.

Therefore, you’ll need to have a positive mindset and be prepared to take ownership of your performance.

To be successful in this role you will also have:

• Tertiary qualifications in a relevant scientific discipline (Pharmaceutical Science, Chemistry, Pharmacy) or related field
• 3+ years of experience in Quality Assurance, preferably in the Pharma industry
• Computer literate (MS Office Word, Excel and Outlook)
• Thorough knowledge of cGMP
• Ability to work autonomously within a highly functioning team.
• Strong organisational skills with the ability to prioritise and multi task.
• Sound technical knowledge with good communication skills, customer focus and problem solving and decision making skills
• Ability to clearly and logically present complex technical information in written and oral format
• Effective time management and organisation skills, with excellent attention to detail and high level of accuracy
• A flexible, adaptable and responsive approach to changing business needs

Ready to become part of the Mayne Pharma story?. 

How To Apply - Click the APPLY NOW button

Mayne Pharma is seeking a proactive and organised Facilities Coordinator to join our Engineering and Maintenance team at our Salisbury manufacturing site. Reporting to the Maintenance Manager, this role will coordinate external contractors and support the safe, compliant and efficient operation of site utilities and facilities.

About the role

The Facilities Coordinator will act as the first point of contact for utilities, facilities issues and external contractors attending site. The role is responsible for arranging repair and maintenance work, coordinating service contractors, maintaining contractor documentation, and ensuring work is completed in line with GMP, WHS and internal compliance requirements.

Key responsibilities

• Coordinate external contractors for building repairs, plumbing, painting, gutters and other facility maintenance work.
• Manage service providers for fire systems, building management systems, boilers, water plants, chillers, air handling, pest control, security and grounds keeping.
• Act as the key contact and subject matter expert for Building Management Systems, including Schneider and Johnson Controls systems, daily alarm review and deviation follow-up.
• Ensure contractor permits, licences, approvals, inductions, reports and records are current, authorised and stored correctly.
• Ensure all contractor work is completed safely and in accordance with WHS regulations, internal standards and GMP requirements.
• Drive services-related Change Controls and Quality Events in partnership with the Quality team.
• Support contractual service schedules, requisition replacement parts as required and contribute to engineering and maintenance team goals.
• Provide backup support to the Maintenance and Engineering leadership team when required.

About you

You will be a strong communicator who can build effective working relationships with internal teams, external contractors and site stakeholders. You will bring a safety-focused mindset, sound documentation practices and the ability to manage multiple priorities in a regulated manufacturing environment.

Essential requirements

• Mechanical/electrical trade qualification, Engineering degree or equivalent practical experience in facilities, utilities, or maintenance operations.
• Strong experience managing external contractors.
• Minimum 3 years’ experience in a chosen field of work.
• Minimum 3 years’ experience in a manufacturing plant.
• High level of documentation skills in a regulated environment.
• Ability to develop strong working relationships with internal and external stakeholders.
• Excellent communication and interpersonal skills across all levels of the organisation.
• Applications from candidates with a mechanical or electrical trade background are strongly encouraged, and equivalent practical experience will be highly regarded.

Desirable experience

• Relevant post-trade or tertiary qualifications in engineering, facilities, utilities, or maintenance management (desirable).
• Understanding of GMP requirements.
  Experience in a similar facilities, utilities or contractor coordination role.
• Understanding of CMMS systems.
• Knowledge of manufacturing processes and equipment.
• Experience with continuous improvement tools such as RCA and FMEA.

Key relationships

In this role, you will work closely with Maintenance and trade team members, Project and Manufacturing Engineers, Production supervisors and operators, the Maintenance Planner, QA, EHS, external contractors and visitors.

Why join us?

This is an opportunity to play an important role in supporting safe, reliable and compliant operations at a regulated manufacturing site. You will contribute to continuous improvement, contractor performance, site compliance and the successful delivery of facilities and utilities services.

The Role
Join a dynamic pharmaceutical manufacturing environment where you will play a key role in improving manufacturing performance, equipment reliability and operational efficiency.

As a Manufacturing Engineer, you will lead and support capital and continuous improvement projects across the manufacturing area while providing day-to-day technical support to Production and Maintenance teams. You will work closely with cross-functional stakeholders to troubleshoot equipment and process issues, optimise manufacturing performance and ensure engineering activities are delivered safely and in compliance with pharmaceutical regulatory requirements.

The role will also contribute to equipment commissioning and qualification, New Product Introductions (NPI), reliability initiatives and broader engineering projects under the direction of the Engineering Manager.

About Mayne Pharma
Mayne Pharma is a global pharmaceutical company offering end-to-end pharmaceutical development and manufacturing to customers around the world. Our heritage makes us one of the most well-known and respected pharmaceutical companies in Australia.

Mayne Pharma Australia is passionate about bringing globally valued pharmaceuticals to Australian patients and consumers. Our values of Passion, Integrity, Accountability, Creativity, Empowerment and Agility are the foundation for everything we do.

Why Join Us?

• Attractive remuneration packages
• Professional Development
• Mayne Perks: Enjoy exclusive discounts and savings
• Community Service
• Recognition and Team Events
• Exclusive Health Insurance Benefits
• Well-being Program

Here’s where you come in!
Your responsibilities, at a glance, will include:

• Lead and support capital and continuous improvement projects, including project scoping, cost estimates, timelines, execution and reporting, ensuring delivery on time and within budget.
• Provide day-to-day technical support to Production and Maintenance teams, troubleshooting equipment and process issues to minimise disruption to manufacturing operations.
• Lead the commissioning of new plant, equipment and manufacturing processes and support associated qualification and validation activities, including IQ/OQ/PQ.
• Prepare and manage GMP documentation associated with engineering projects, including change controls, risk assessments, commissioning documentation and technical records.
• Support and lead root cause investigations into equipment and process-related issues and implement appropriate corrective and preventive actions (CAPA).
• Drive continuous improvement initiatives focused on equipment reliability, operational efficiency, process robustness and manufacturing performance.
• Apply Lean Manufacturing and Six Sigma principles to identify waste, reduce variability and optimise equipment and manufacturing processes.
• Collaborate on New Product Introductions (NPI) and commercial product transfers, ensuring equipment capability and technical readiness.
• Support the development and optimisation of Preventive Maintenance programs to improve equipment uptime and reliability.
• Utilise Enterprise Asset Management (EAM)/CMMS systems and equipment data to analyse asset performance and support site reliability initiatives.
• Participate in the design and development of manufacturing processes, production flows, equipment improvements and automation opportunities.
• Ensure engineering and GMP documentation, including SOPs, maintenance procedures, P&IDs and equipment specifications, remains current, accurate and compliant.
• Support cross-functional teams during internal audits and regulatory inspections, including TGA and FDA inspections.
• Collaborate with suppliers and contractors on equipment design, specification, procurement, installation and commissioning.
• Provide technical training and support to operators and Maintenance team members on new equipment, processes and associated safety requirements.
• Support environmental sustainability initiatives, including energy reduction and waste minimisation projects.
• Ensure all engineering activities are undertaken in accordance with GMP, WHS, environmental requirements and company quality systems.
  Promote a culture of operational excellence, continuous improvement, safety and regulatory compliance.
• Perform other duties considered appropriate for the position, as required.

You need to tick these boxes

We select applicants based on capability and aptitude, while also placing a strong emphasis on cultural fit. You will need a positive mindset, a practical approach to problem solving and a willingness to take ownership of your performance.

You will also bring:

• Tertiary qualifications in an Engineering discipline.
  Relevant engineering experience within pharmaceutical, food and beverage, medical device or another highly regulated manufacturing environment.
• Experience supporting manufacturing equipment, capital projects, commissioning and/or continuous improvement activities.
• An understanding of GMP requirements and engineering activities within a regulated manufacturing environment.
• Strong analytical and problem-solving skills, with the ability to investigate equipment and process issues and develop practical solutions.
• A driven, self-motivated and independent approach, with the ability to work effectively with minimal supervision.
• Excellent communication and interpersonal skills, with the ability to work collaboratively across Production, Maintenance, Quality and other functional teams.
• Strong attention to detail, particularly in relation to engineering documentation, change control and GMP requirements.
• Experience with Lean Manufacturing, Six Sigma, EAM/CMMS systems, equipment qualification or validation would be highly regarded.

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