9 Quality Inspection jobs in Australia

Title:
Assistant Quality Assurance Manager
At KBR - We do things that matter.
We deliver science, technology and engineering solutions to governments and companies around the world. KBR employs approximately 38,000 people worldwide with customers in more than 80 countries and operations in over 29 countries.
KBR is proud to work with its customers across the globe to provide technology, value-added services, and long-term operations and maintenance services to ensure consistent delivery with predictable results. At KBR, We Deliver.
Think.KBR.com
KBR in Australia
With over 65 years working on some of Australia's largest and most complex projects, KBR has unmatched experience supporting the nation's critical infrastructure, energy transition and national security priorities. KBR has around 2,000 employees throughout Australia, who are focused on delivering innovative technology and engineering solutions for a safer, more secure and sustainable future.
Learn more about KBR in Australia
Belong, Connect and Grow at KBR
At KBR, we are passionate about our people and our Zero Harm culture. These inform all that we do and are at the heart of our commitment to, and ongoing journey toward being a People First company. That commitment is central to our team of team's philosophy and fosters an environment where everyone can Belong, Connect and Grow. We Deliver - Together.
The Opportunity:
Our client, a leading Managed Services Provider (MSP) supporting Defence capability, is seeking an Assistant Quality Manager with strong systems engineering experience to join a high-performing team on a Defence program in Brisbane. This position plays a key role in ensuring engineering processes, quality frameworks, and compliance obligations are met in line with Defence standards.
Reporting to the Quality Manager, you will support the assurance of engineering and technical deliverables, contributing to risk management, systems safety, and quality audits throughout the systems lifecycle. This role supports supply chain optimisation by conducting network studies, coordinating with stakeholders, and ensuring the timely delivery of goods and services. Through independent problem-solving and collaboration, the specialist contributes to the effective execution of logistics operations and supports continuous improvement initiatives across the organisation.
Responsibilities:
+ Support the development, implementation and continuous improvement of the Quality Management System (QMS) in accordance with ISO 9001 and AS9100 standards.
+ Ensure engineering processes align with Defence and MSP quality standards and customer requirements.
+ Conduct internal quality audits and support external audits (e.g., by CASG, primes, or other stakeholders).
+ Assist in systems safety and assurance tasks aligned with the One Defence Capability System (ODCS) and other acquisition frameworks.
+ Engage with multi-disciplinary engineering teams to embed quality into the design, development, and sustainment processes.
+ Participate in root cause analysis, risk reviews, and engineering change control procedures.
+ Maintain quality records and contribute to lessons-learned repositories.
+ Liaise with systems engineers and project managers to ensure compliance and traceability throughout the V&V lifecycle.
As the ideal candidate you will bring:
+ Engineering degree in Systems, Aerospace, Mechanical, Electrical, or related field.
+ Experience in Defence engineering environments and understanding of Defence capability lifecycle (ODCS).
+ Sound knowledge of quality management systems, assurance frameworks, and ISO/AS standards.
+ Strong background or exposure to Systems Engineering, particularly in requirements traceability, verification and validation (V&V), and interface management.
+ Exposure to systems safety and risk management principles (e.g. MIL-STD-882, T&E, hazard logs).
+ Proficiency in document control and configuration management tools (e.g. DOORS, Windchill, Teamcenter).
+ Strong communication and stakeholder engagement skills.
All candidates will be required to hold and maintain an active NV1 Defence Security Clearance. Only candidates holding a NV1 Clearance or above should apply.
What we will offer you:
· A workplace culture certified as a Great Place To Work
· Flexible working
· Competitive salary (including annual reviews)
· Paid parental leave
· Income protection
· Corporate rewards
· Salary packaging/Novated leasing
· Employee stock purchase plans
· Flu shots, skin checks and discounted private health insurance
· Career development: Online learning, mentorship and career pathways
If you're ready to shape tomorrow, let's get started. Apply Now!
As a Major Service Provider of the Australian Defence Force, an AGSVA security clearance will be required and compliance to International Traffic in Arms Regulations (ITAR). As such, our hiring decisions are based on the key requirements of each role and candidates are selected based on their unique strengths and experiences.

Director, Quality Assurance APAC
Australia
Japan
Sydney, New South Wales, Australia
Singapore
+ **Market leading developer & manufacturer of medical devices for Women's Health**
+ **Newly created role with an innovative and growing organisation**
+ **Australia or Singapore based with role scope across APAC**
Are you looking for a place where the work you do is directly connected to positively impacting lives around the world? Are you searching for an opportunity that allows you to focus on your strengths each day? Let us start a conversation.
Hologic is an innovative medical technology company primarily focused on improving Women's Health and well-being through early detection and treatment. We develop, manufacture and supply life-changing Diagnostics, GYN Surgical and Breast & Skeletal Solutions that are founded on science and driven by technology; allowing healthcare professionals to diagnose and proactively treat patients with growing certainty, precision, and greater peace of mind.
Join us as a Senior Manager, Quality Assurance where you will represent a leading brand and be responsible for managing the APAC commercial quality organization. You will ensure high quality standards and compliance with regulatory requirements and internal policies. In this role you will be responsible for assessing current systems and practices, identifying gaps and developing comprehensive solutions to harmonize and optimize quality processes across the APAC region. You will be based in either Australia or Singapore and lead a team of three (based in Australia, Singapore and Japan), supporting them with managing QA requirements for their region.
To be successful in this role, you are an authentic leader and team player who is passionate about coaching, developing and mentoring your team members. You have a Bachelor's degree in a scientific discipline and at least 8 years previous experience in quality with at least 3 years successfully leading a QA team across the APAC region. It will be essential that you have advanced knowledge of QSRs, ISO 13485, ISO 14971, MDSAP, and IVDR. Impeccable communication and presentation skills is a must as you will need to communicate and influence a variety of internal stakeholders
To be the best, we want the best.
In return, you will be joining a team that is talented, high achieving and collaborative. A team that is driven by the impact we have on our global community. We are proud of our positive team environment where work life balance, engagement and the wellbeing of our employees is a priority. We are offering a competitive salary that is based on experience as well as participation in an annual bonus structure. We offer a flexible working environment, where most of our employees work hybrid between home and our office.
As part of this role, you will be required to travel across APAC.
We make hiring decisions based on your experience, skills, and passion. Please note that interviews may be conducted virtually. When you apply, please tell us the pronouns you use and any reasonable adjustments you may need during the interview process
_If you are driven by the pursuit of a healthier & more enriched life for yourself, family & those around you, please apply._
#LI-TL1

Director, Quality Assurance APAC
Australia
Japan
Sydney, New South Wales, Australia
Singapore
+ **Market leading developer & manufacturer of medical devices for Women's Health**
+ **Newly created role with an innovative and growing organisation**
+ **Australia or Singapore based with role scope across APAC**
Are you looking for a place where the work you do is directly connected to positively impacting lives around the world? Are you searching for an opportunity that allows you to focus on your strengths each day? Let us start a conversation.
Hologic is an innovative medical technology company primarily focused on improving Women's Health and well-being through early detection and treatment. We develop, manufacture and supply life-changing Diagnostics, GYN Surgical and Breast & Skeletal Solutions that are founded on science and driven by technology; allowing healthcare professionals to diagnose and proactively treat patients with growing certainty, precision, and greater peace of mind.
Join us as a Senior Manager, Quality Assurance where you will represent a leading brand and be responsible for managing the APAC commercial quality organization. You will ensure high quality standards and compliance with regulatory requirements and internal policies. In this role you will be responsible for assessing current systems and practices, identifying gaps and developing comprehensive solutions to harmonize and optimize quality processes across the APAC region. You will be based in either Australia or Singapore and lead a team of three (based in Australia, Singapore and Japan), supporting them with managing QA requirements for their region.
To be successful in this role, you are an authentic leader and team player who is passionate about coaching, developing and mentoring your team members. You have a Bachelor's degree in a scientific discipline and at least 8 years previous experience in quality with at least 3 years successfully leading a QA team across the APAC region. It will be essential that you have advanced knowledge of QSRs, ISO 13485, ISO 14971, MDSAP, and IVDR. Impeccable communication and presentation skills is a must as you will need to communicate and influence a variety of internal stakeholders
To be the best, we want the best.
In return, you will be joining a team that is talented, high achieving and collaborative. A team that is driven by the impact we have on our global community. We are proud of our positive team environment where work life balance, engagement and the wellbeing of our employees is a priority. We are offering a competitive salary that is based on experience as well as participation in an annual bonus structure. We offer a flexible working environment, where most of our employees work hybrid between home and our office.
As part of this role, you will be required to travel across APAC.
We make hiring decisions based on your experience, skills, and passion. Please note that interviews may be conducted virtually. When you apply, please tell us the pronouns you use and any reasonable adjustments you may need during the interview process
_If you are driven by the pursuit of a healthier & more enriched life for yourself, family & those around you, please apply._
#LI-TL1

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
**Job Description**
At Gilead, we're committed to creating a healthier world for everyone - no matter the challenges ahead of us. For more than 30 years, we've pursued the impossible, chased it down, tackled it for answers and surrounded it for a way in. We have worked tirelessly to bring forward medicines for life-threatening diseases. Through bold and transformative science, we're driving innovation that has the potential to become the next generation of life-changing medicines. Our ambition is evident in our mission. Because the impossible is not impossible. It's what's next.
The Position:
We are seeking a highly experienced and motivated individual to join us as Associate Director or Senior Manager, Product and Distribution Quality in ANZ. You will work with Quality, Commercial, Regulatory, Supply Chain, and Medical Affair in supporting our efforts in this exciting area of cancer immunotherapy. This individual will work cross functionally to lead a multi-market organization focused on implementing and ensuring the qualification and monitoring program for hospital apheresis centers and treatment sites that will provide treatment to patients with our commercial products, investigations related to product complaints, the cross-functional work for global labeling capabilities, the full set of capabilities associated to Responsible Person (RP) in ANZ and other APAC region as needed, and representing QA in ANZ regional Leadership teams as well as representing Kite with external partners and others.
Key Responsibilities will include:
+ Establish, execute and manage the new and established apheresis centers and treatment centers sites (ACTS) qualification process that will use risk-based tools for qualification, training and monitoring.
+ With Global Site Qualification will determine strategy for maturing the ongoing program, sustainability and compliance to regulatory changes.
+ Collaborate with cross-functional departments to ensure timely implementation of quality processes.
+ Provide leadership and direction in the industry in the area of site qualification process and management.
+ Assess and approve any changes to the courier tracking and order intake systems to assure the validated state of the systems is maintained.
+ Lead Quality's collaboration efforts with Commercial in the start-up and routine management of the ATCS relationship and Supply Chain to ensure compliance across the Kite product Journey and best customer experience
+ Implement, assess and report on metrics monitoring per schedule and provide updates to approved ATC list.
+ Assure business systems are developed, supported and maintained validated state for patient traceability.
+ Act as Quality contact, or delegate, for ATCS issues and discrepancies, and lead/manage the investigations to resolve the issues.
+ Interacts with the Kite T cell Facilities as needed for product release, issue resolving or other as applicable
+ Support inspection readiness plans and interact with regulatory agencies during inspections on ATCS-related matters.
+ Work with Global Site Qualification, America, EME and APAC regional leads , as needed.
+ Collaborate with our Gilead affiliates in the routine management of the ACTS relationships and in other areas as needed
+ Serve as Gilead RP per the local guidelines (TGA, HSA etc.). Act as back-up for RP in other APAC region as needed. Verify lot distribution confirmation for Kite cell therapy product and related activities in compliance with local regulations and internal SOPs and supervise quality/regulatory aspects of distribution in Australia and Singapore.
+ Provide quality oversight and execute responsibilities designated for the Responsible Person in country that includes the following QMS: distribution (under GDP), product complaints, recall, returns, self-inspection.
+ Provide oversight of deviation investigations which occur during the manufacturing, packaging and shipment of products and provide QA oversight and approval of Change Control records impacting Cell Therapy products in Australia, Singapore and other APAC region.
+ Maintain local Quality System to comply with local regulation.
+ Quality lead for Material Review Board for Cell Therapy Finished Products for Australia and Singapore
+ Perform other duties as assigned. These duties can be delegated to designated deputies of a satisfactory qualification level as needed.
Knowledge, Experience and Skills Required:
+ Bachelor's degree in medical or biological sciences or related field; Master's or PhD degree preferred
+ Minimum of 7 years progressive experience in medical, pharmaceutical or biologics quality assurance' roles; preferred cell therapy.
+ Experience in areas such as Clinical Research, Medical Liaison, Cell Therapy and/or Apheresis and Cell Therapy Medical Centers preferred.
+ Experience auditing blood banks, plasma centers, apheresis centers, external suppliers and/or internal GMP systems.
+ Experience working in multi-national companies with management responsibilities of staff located in multiple regions/countries.
+ Proficiency in English is required
+ Strong working knowledge of and ability to apply GMP in conformance to ANZ.
+ Experience responding to regulatory agency audits.
+ Demonstrated ability to develop, coach, and mentor employees
+ Excellent interpersonal, verbal, and written communication skills are essential in this collaborative work environment.
+ Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities
+ Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of initial job description.
+ Ability to travel up to 40%, could include some weekend travel for arrival to/return from destinations
**Gilead Core Values**
Integrity (always doing the right thing)
Teamwork (collaborating in good faith)
Excellence (working at a high level of commitment and capability)
Accountability (taking personal responsibility)
Inclusion (encouraging diversity)
**Being Here Matters**
_At Gilead we are committed, hardworking and passionate about improving the lives of the patients who use our products. Our values - integrity, inclusion, teamwork, accountability and excellence - are evident in everything we do. We are a close-knit team where you can see the tangible results of your contributions, where every individual matters, and everyone has a chance to enhance their skills through ongoing development._
_We want all our employees to embrace and leverage each other's talents and diverse perspectives, foster a sense of belonging, achieve their full career potential and contribute to the team's success? This is demonstrated through our Silver Status in the Australian Workplace Equity Index?_
_As an equal opportunity employer, Gilead Sciences is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, colour, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws._
**For Current Gilead Employees and Contractors:**
Please apply via the Internal Career Opportunities portal in Workday.
Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.

Description
We're seeking for ICQA (Inventory Control & Quality Assurance) Process Assistants to join the team for the upcoming launch of our brand new Fulfillment Center in Cranbourne West.
The Process Assistant is assigned to the Area Manager, and will hold responsibilities specific to the different Fulfillment Center areas.
Key Job Responsibilities:
- Support and work in all departments as required,
- Helping support daily management of department duties, including allocating labor, leading meetings, assigning job duties,
- Providing coverage for Area Managers,
- Providing policy follow-up, attendance tracking (duties do not extend to discipline),
- Tracking and reporting of ATS/labor hours,
- Assisting the floor as an associate resource, training associates and verifying SOP compliance,
- Ensuring successful area performance, through tracking, reporting and feedback of associate performance,
- Participating in Operational Excellence initiatives in some capacity,
- Fully understanding workflow and daily production goals,
- Assisting in keeping work area clean and organised,
- Identifying and addressing safety hazards within the work area,
- coaching associates to work safely at all times
- Referring all job injuries immediately to area manager.
Basic Qualifications
- Previous experience leading teams,
- Availability to work 38 hours+/week, and overtime as required,
- Comfortable in lifting up to 16 kilos, stand/walk for up to 10-12 hours, and be able to frequently push, pull, squat, bend and reach, all with or without reasonable accommodation,
- Excellent written and verbal communication and interpersonal skills to coach, train and assist team members,
- Experience working with computers and Microsoft Office (Outlook, Word, Excel).
Preferred Qualifications
- Experience working within a similar field (manufacturing/distribution/warehousing/large retail),
- Experience with performance metrics and lean process improvement.
Acknowledgement of country:
In the spirit of reconciliation Amazon acknowledges the Traditional Custodians of country throughout Australia and their connections to land, sea and community. We pay our respect to their elders past and present and extend that respect to all Aboriginal and Torres Strait Islander peoples today.
IDE statement:
Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status.
Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner.

Job Description:
McDonald's Australia is the largest quick service restaurant operation in the country. Fondly known as "Macca's", we have been a household name in Australia for over 50 years, we believe that our customers are the heart and soul of everything we do and make it our mission to make every moment count! As an employer of choice winner time and time again, working with us means taking pride and having fun along the way; while growing and developing your career in a dynamic and supportive environment.
Could you be our next Quality Assurance Coordinator?
The McDonald's Quality Assurance team have an exciting opportunity for someone to join them on a 12-month initial contract. As a Quality Assurance Coordinator, you will manage and communicate market and global quality systems and policies to internal and external stakeholders. You will support food safety and quality standards across Australia and New Zealand, working closely with suppliers and Quality Assurance Managers (QAMs) to develop and execute validation programs for food products and equipment. Do you have a passion for food safety and quality standards? Apply today!
What can you expect on a day-to-day basis?
+ Maintaining and updating the McDonald's Australia and New Zealand Quality Systems Manual
+ Conducting product and equipment validations in the test kitchen
+ Supporting Quality Assurance Managers in creating and maintaining product specifications
+ Coordinating restaurant trials for quality assurance projects
+ Leading the quality assurance information for the Implementation Deployment Team
+ Serving as the Digital Champion for McDonald's reporting systems
+ Analysing complaint data and audit results to identify trends
+ Managing the Class 1 Supplier Good Manufacturing Practice Unannounced Audit Schedule
+ Participating in annual audits for the test kitchen
+ Arranging importation of product samples for sensory analysis
+ Completing food safety checks for equipment and products
Your keys to success:
+ Degree/Diploma Qualified in Food Science/Technology or nearing completion
+ Committed to principles of food safety and driven to uphold these principles
+ A proven ability to work under pressure in both acute and planned environments
+ Self-motivated and proactive, takes the initiative to pre-empt opportunities
Relish in the Macca's difference when you join the Golden Arches:
+ Macca's Staff Discount & Retail Discounts. Enjoy discounted Macca's at any restaurant across Australia and access to hundreds of retail discounts.
+ Birthday & Volunteer Leave. Enjoy a day-off during your birthday month and 3 days annually to volunteer for a registered charity you are passionate about.
+ Modern Office with Sustainable Amenities. Newly revamped office located in Thornleigh featuring the latest technology and electric car chargers to support eco-friendly commuting.
+ Ongoing Professional Development. We are committed to developing our people by investing in leadership programs and free access to LinkedIn Learning.
+ Access To Our 24/7 Wellbeing Partner (Sonder) For You & Your Immediate Family. Using the Sonder app, access free and confidential safety, medical and mental health support via chat or phone with accredited professionals.
+ A Fun & Vibrant Culture. Immerse yourself in local and Macca's only events and experiences from day one of working with us.
At Macca's, our doors are open to everyone, and we will always do our best to ensure our restaurants and workplaces are inclusive spaces where everyone is welcomed and strength in diversity is valued. No matter who you are or where you're from, everyone at Macca's contributes their talents and skills to what makes us golden and what makes us Macca's. We strive to make every moment through the recruitment process a feel-good moment that is fair, equitable and accessible. If you have disability, illness, or injury, we know that it may be helpful for us to adjust our process. Our doors are open for a conversation to discuss adjustments and answer any questions or suggestions you may have about our recruitment process.
Requsition ID: 1791

**The Position**
Product Quality is that part of Commercial Quality whose primary focus is on transactional tasks i.e., release-for-distribution, customer complaints, assessment of market returns etc. The focus of this position will initially be release-for-distribution.
**Tasks & Responsibilities**
+ Perform release-for-distribution activities, including liaising with manufacturing sites, external warehouses, supply chain, and regulatory affairs.
+ Use the GoTrack (Trackwise) system to raise quality records such as Deviations, Events, CAPAs, Change Control, Quality Risk Management, etc., as per approved procedures.
+ Report on release performance (i.e., KPIs) at the quarterly Quality Management Review.
+ Process Technical Product Complaints in the GoTrack system and in accordance with relevant standard operating procedures (SOPs) as may be required due to staff absences or workload.
+ Process market returns as per local procedures and timelines as may be required due to staff absences or workload. Liaise with Customer Service as necessary to obtain all required information.
+ Participate in the development and implementation of local quality-related processes and procedures, ensuring compliance with applicable local regulations and Corporate requirements.
+ Maintain appropriate quality records as required by applicable procedures.
+ Participate in self-inspections as may be required.
+ Undertake any other duties or tasks directed by the Head of Commercial Quality.
**Requirements**
+ Relevant scientific degree e.g. Chemistry, Pharmacy, Life Sciences etc.
+ At least 2 years' experience in the Human Pharmaceutical or Veterinary Medicine industries
+ Experience with QA IT platforms such as GoTrack (TrackWise)
+ Knowledge of the regulatory requirements for the pharmaceutical industry (human and/or veterinary medicines)
+ Intermediate to advanced level in core Microsoft packages, particularly Word, Excel, Power Point and Outlook.
+ Experience with ERP systems e.g. SAP
+ Previous experience performing Quality audits
+ Pharmaceutical/veterinary medicine manufacture
**Why Boehringer Ingelheim?**
Our workplace is a creative and dynamic place to be - with the future always on our minds. Your personal journey is one you can develop from the very start, with leadership that nurtures your ambition with you.
Boehringer Ingelheim offers a competitive remuneration, attractive bonus scheme, subsided health insurance, employee assistance program, development programs and career development opportunities.
Our people are the beating heart of Boehringer Ingelheim and we have been recognised as a global Top Employer for five years. We value diversity by embracing various perspectives, fostering an inclusive environment that benefits our people, patients, and communities.
**What's next? - How to apply**
If you would like to be part of this highly driven and successful team, please submit your CV addressing the key criteria above.
You must have the right to live and work in this location to be considered for this opportunity.
It is our policy not to accept speculative resumes from recruitment agencies.
**Position Area**
Group Functions
**Position Location**
NSW
**Organization**
Boehringer Ingelheim
**Schedule**
Full Time
**#LI-BI**
All qualified applicants will receive consideration for employment without regard to a person's actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Abcam, one of Danaher's ( 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
Progress happens together
At Abcam, we believe the scientific community goes further, faster when we go there together. That's why we work with life scientists to provide biological reagents and solutions that enable faster breakthroughs in critical areas like cancer, neurological disorders, infectious diseases and metabolic disorders. Our talented team of over 1,400 colleagues worldwide is our greatest asset. By applying our expertise and pushing boundaries, together we strive to better serve our customers, strengthen our impact across our industry, and ultimately our positive impact on society.
Learn about the Danaher Business System ( which makes everything possible.
The Research Associate is primarily responsible for the production and quality control (QC) of all kit components used in the SureFire and ELISA cell-based immunoassay kits at TGR BioSciences (an Abcam company) in accordance with GLP.
This position reports to the Quality Manager and is part of the In-House-Manufacturing (IHM) Team at TGR BioSciences located in Adelaide, South Australia and will be an on-site role.
In this role, you will have the opportunity to:
+ Prepare and QC kit components used in the SureFire and ELISA immunoassay kits; including but not limited to reagent preparations, antibody conjugations and immunoassay analytical techniques.
+ Culture a broad range of mammalian cell lines to prepare control lysates for use in kits.
+ Assist with updating of procedures (Microsoft Excel and Word-based) and training of new staff.
The essential requirements of the job include:
+ A Bachelor of Science or Biotechnology with Honours.
+ A person who is willing to work in a team environment and can work to time pressures to ensure shipping deadlines and on-time delivery demands are met.
+ A person who has a high level of attention to detail and sound analytical and problem-solving skills to ensure kit quality is maintained and in line with customer expectations.
Travel, Motor Vehicle Record & Physical/Environment Requirements:
+ Job may require some manual handling.
It would be a plus if you also possess previous experience in:
+ A biological laboratory with experience in cell culture, protein chemistry and immunoassay analytical techniques.
+ Antibody conjugation techniques.
+ Microsoft Excel
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.