What Senior Workforce Planner Jobs are in Australia?

Encore are a global event technologies company that specialises in hybrid and in-person events that connect and inspire.
At Encore we believe in creating memorable event experiences that engage and transform organisations by serving as an invaluable partner on our customers' journey to success.
With our "Great Place To Work "certification, we offer a supportive and inclusive environment where your unique skills and perspectives are celebrated. If you're ready to be part of a team that's shaping the future of events and make a meaningful impact, apply now and let's transform events together.
**The Opportunity**
The role of the Workforce Coordinator is to assist with the efficient delivery of events. The primary focus is on the accurate scheduling of crew to achieve labour efficiency and successful event outcomes.
**Core Responsibilities**
+ Roster casual and full-time crew to ensure show delivery needs are met
+ Manage the rostering and payroll system (Timetarget / HumanForce) for casual and base staff to ensure all data is accurately captured and properly authorised
+ Plan the rostering of full time and casual crew to ensure payroll costs are minimised and that the skills mix on each job is accurate and appropriate
+ Liaise with venues to arrange utilisation of all crew as required
+ Respond to general phone inquiries to confirm staff shifts, troubleshoot where required
**Your Background**
+ Experience in a similar role
+ Respond to general phone inquiries to confirm staff shifts, troubleshoot where required
+ Excellent oral and written communication skills
+ Highly developed communication skills
+ Time management skills; the ability to manage multiple and competing deadlines
+ Excellent decision making skills
**Why Join Us?**
Be a part of our mission to bring people together, facilitate ideas and build relationships for our customers' and enjoy all the perks that we offer:
+ "Great Place To Work" certification, ensuring a supportive and engaging work environment
+ Diversity, equity, and inclusion programs that foster a welcoming and inclusive workplace for all
+ Wellness initiatives to prioritise your physical and mental well-being
+ Ample opportunities for career progression and professional growth
+ Commitment to sustainability initiatives, contributing to a greener future
_At Encore, we value our people as our most valuable asset. We prioritise equal opportunities and embrace diversity in all its forms. As a Circle Back Initiative Employer, we are committed to responding to each and every applicant. If you fit some of the requirements but not all, we encourage you to apply and have a chat with our team to learn more about this opportunity._
This is an onsite position.
All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status.

Product Line Planner
Job Description
Are you passionate about orchestrating production plans that deliver the right products to customers on time, every time? Then join us in our mission to pioneer smarter solutions for moving and transforming water, reducing energy consumption, and enhancing quality of life for people.
As our new Product Line Planner, you will be driving the end-to-end planning of pump and systems assembly across our Australian and New Zealand operations, managing everything from high-volume production to custom-engineered solutions and integrated projects.
This role will be directly reporting to the Supply Chain Manager and will be based in Regency Park, South Australia.
**What you will be doing**
As a key part of the Supply Chain Planning team, you'll create impact by Ensuring exceptional delivery performance by bridging supply chain and production teams to meet customer commitments across diverse and complex product lines.
Your main responsibilities include:
+ Schedule production orders using MRP and just-in-time principles, ensuring material availability and on-time delivery across multiple assembly areas
+ Input and maintain customer orders in SAP with accuracy across part numbers, pricing, technical specifications and contractual requirements
+ Monitor missing parts, investigate supply alternatives and expedite components to minimise delays and improve lead times
+ Release production orders with required assembly information and raise purchase orders for local contractor services
+ Provide status reporting to stakeholders on project sales orders and proactively resolve SAP discrepancies from planning processes
+ Drive continuous improvement initiatives to enhance efficiency, quality and delivery performance within the planning function
**What makes you a great fit**
Above all, you are a proactive and detail-oriented planning professional with strong SAP skills, manufacturing environment experience, and the ability to juggle multiple priorities while maintaining excellent stakeholder communication. We would also imagine that you have:
+ Qualification in Supply Chain, Production, Operations or Project Management, or equivalent trade qualification
+ Experience in production demand planning and scheduling within a manufacturing or engineered-product environment
+ Proficiency in SAP, particularly within production and supply chain modules, along with Microsoft Office Suite
+ Strong time management skills with demonstrated ability to manage multiple tasks and meet deadlines
It is a plus if you also have:
+ Knowledge and experience in Lean Manufacturing processes
+ Working knowledge of ISO 9001 quality management systems
+ Experience coordinating planning for custom-designed or project-based products
**Why you will love working here**
We care! Day to day, you can look forward to:
+ Annual performance bonus and a strong focus on well-being activities.
+ Three days' additional paid leave for volunteering in your community.
+ Access to on-demand training and learning sessions and carefully structured programmes to pursue personal and professional development opportunities.
Are you ready to unlock possibilities at Grundfos? Apply today!
To get to know us better, follow us on LinkedIn or visit grundfos.com
Information at a Glance
**Job details**
Workplace: Onsite Position
Job Location: Adelaide, South Australia, Australia
Contract Type: Full-Time
Employment Type: Regular

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
**We are PCI.**
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
Position Overview
The Production Associate facilitates all steps involved in label text approval and printing, and packaging and labelling activities including;
+ obtaining approvals and ensuring that the label text meets TGA and/or applicable country regulatory requirements
+ ensuring that the printing of labels is in accord with applicable GMP requirements and as per PCI SOPs
+ completing campaigns in accordance with Batch Records, PCI SOPs, Work Instructions etc. and maintains EHS requirements, and
+ cleaning and maintenance verification for facility and equipment.
Position Specifics
+ ensuring all required information for label drafting and label printing received from Project Manager are complied with and executed accordingly
+ ensuring label text for each project is compliant and ready to be approved by the client/sponsor.
+ performing day-to-day packaging and labelling activities in the production facility as scheduled by the Production Associate Manager.
+ completing batch records accurately and concurrent with packaging and labelling activities and ensuring all steps listed are completed.
+ preparing for line clearance, and removal of any production waste/rubbish once production is completed. Production Associates may be requested to perform line clearance sign off.
+ assisting in maintaining of the cGMP facility licence and may be required to assist in facility audits (e.g. PCI internal audits and audits conducted by Clients/Sponsors and Regulatory Authorities).
+ Undergoing practical training and be involved in procedural updates and provide input for process designs.
Other Position Activities
+ Completing company training requirements in accordance with curricula and other training as may be required (e.g. completion of training when SOPs, Work Instructions etc. are updated or new SOPs, Work Instructions etc. are issued that are applicable to production)
+ Facilitate all steps leading to label text approval, including preparing the draft label text for review/approval by PCI and Client
+ Liaise with all appropriate PCI employees to facilitate the preparation of draft/final label text, including label design decisions
+ Ensure that the label text meets PIC/s (Annex-13) and TGA regulatory requirements and in collaboration with the client the applicable country regulatory requirement
+ Incorporating variable text information e.g. Batch number, Product Code, Kit Number (as applicable), Retest Date etc as per client requirement
+ Manage kit lists in accordance with applicable procedures or work instructions
+ Liaise with company (or client) approved third party translators as may be required
+ Ensure that the printing of labels is conducted in a GMP compliant manner, using the correct base label and ribbon combination, that printing is in accordance with applicable PCI SOP(s) and that the appropriate PCI Forms/Records are completed and retained in the designated locations
+ Confirm that the combination of base label and ribbon will deliver a printed label that is fit for purpose for the intended substrate (packaging material) and storage conditions, and for conducting the appropriate rub/smudge/scratch adherence test on labels prior to issuance
+ Ensure that the quality of the printed labels obtain Quality approval prior to the labels being issued to production
+ Provide printed labels to be ready for production in a timely manner, supported by the applicable records/forms
+ Ensure that label printing is undertaken in such a way that there is no risk of mix-up, ensuring line clearance is undertaken prior to commencing each printing episode
+ Deface any printed labels that are damaged/not required during the printing process
+ Reconcile unprinted labels (blank labels) and printed labels that are to be used or rejected at the end of the print run.
+ Evaluate options for additional/replacement hardware as applicable
+ Liaise with external printers to coordinate printing of labels (as may be applicable)
+ Ensuring the required Batch Record has been approved and QA issued prior to use
+ Ensuring the required packaging room is ready for use and that appropriate Room logs and registers are completed
+ Following the company gowning and hygiene requirements
+ Verifying the picked released stock and equipment for labelling of clinical supplies and packaging and assembling kits of finished products in accordance with the Batch Records.
+ Ensuring that samples are taken in accordance with the batch record instructions (e.g. retention samples).
+ Reviewing production batch records and ensuring that these are completed and signed prior to Production Senior Associate review.
+ Ensuring that all deviations are reported to the Production Senior Associate or Production Associate Manager.
+ Making sure that production facilities are clean and when appropriate, disinfected.
+ Cleaning of equipment in accordance with SOPs.
+ Removing waste materials and rubbish from the packaging facilities and placing in the correct bins.
+ Verify calibrations of equipment prior to use and records kept/registers completed.
+ Ensuring that the premises and equipment are maintained and relevant records kept.
+ Reviewing labels and randomisation lists against label approval forms and master randomisation lists prior to commencing batch manufacture.
+ Preparing, reviewing and maintaining SOPs relevant to the Production facility.
+ Participating in PCI internal audits and third-party audits and assist in responding to audit findings and product complaints/recalls as may be required.
+ Follow company EHS requirements
+ Implement continuous improvement actions as may be appropriate (e.g. updating SOP(s), Work Instructions and Form(s) applicable to label generation activities and processes)
+ Completion additional tasks as allocated by the Senior Production Associates or Production Associate Manager
+ Assisting other departments as required.
The role works closely with other Production, Warehouse, Project Management and Quality employees to complete the activities in a cGMP compliant manner
Qualifications, Experience & Behavioral Requirements:
+ Previous industry experience in Pharmaceuticals and/or GMP environment
+ Bachelor of Science, Pharmacy or related Discipline
+ Excellent English written and verbal skills with good attention to detail
+ Scientific experience
+ Previous industry manufacturing/labelling experience
+ High level of professionalism, ethics, quality of work, communication and responsiveness at all times
+ Positive, 'can-do' attitude, embraces and 'lives' PCI's Vision and Values
+ Analytical thinker and solution finder/problem solver
+ Attention to detail
+ Collaborative, team player
+ Objective and robust decision maker
+ Trusting and trustworthy
+ Conscientious and diligent
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future ( Employment Opportunity (EEO) Statement:**
_PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status._
_At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture._
Why work for PCI Pharma Services?
At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how.
PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled

**About Us**
At Cargill our team of 160,000 professionals in 70 countries draws together the worlds of food, agriculture, nutrition and risk management. For more than 150 years, we have helped farmers grow more, connecting them to broader markets. We are continuously developing products that give consumers just what they're seeking, advancing nutrition, food safety and sustainability. And we help our partners innovate and manage risk, so they can nourish the world again tomorrow.
We combine 156 years of experience with new technologies and insights to serve as a trusted partner for food, agriculture, financial and industrial customers in more than 125 countries. Side-by-side, we build a stronger, sustainable future for agriculture and help the world thrive.
**Job Purpose and Impact**
To perform the tasks of Production Relief Operator, to operate and maintain the seed processing facility in a safe, efficient and result oriented manner.
**Key Accountabilities**
+ **Site Operations and Relief** Operate and maintain the preparation, extraction and weighbridge facility in a safe, efficient and result oriented manner.
+ **Housekeeping** Adhere to all necessary housekeeping practices required to maintain the facilities hygienic condition
+ **Maintenance** Perform minor maintenance repair and/or project based work whilst on site in order to ensure peak operational performance of the production facility.
+ **Safety Management** Adheres to work and safety instruction by taking an active role in contributing to building a safety culture and clearly demonstrates the ability to find and implement solutions that reduce the footprint of self and the workgroup on the environment.
+ **Team** A genuine effort to work co-operatively within the company, taking personal accountability for creating and supporting a team environment and showing a genuine respect for individuals within the team in order to encourage an environment of mutual trust.
+ **Food Safety & Quality Management** Contribute to the development of a food safety culture and adheres to processes and procedures, and directions in relation to food safety and quality management.
+ **Administration & Reporting** Reporting information regarding subsequent work required, preventative maintenance issues and completion of Work Order documentation.
**Qualifications**
**To be successful you will require:**
+ At minimum should have completed Year 11 High school
+ Fluency in English language
+ Hold forklift and elevated work platform Operator certificate of competency or obtain one within 3 months of the appointment
+ Experience in industrial chemical handling and manufacturing process experience would be highly desired
+ Basic computer literacy
+ Possession of a recognized metal trade will be a distinct advantage
+ Excellent interpersonal, communication and organisational skills
+ Ability to work independently, be self-motivated and proactive
+ Ability to work rotating day and night shift roster
+ This role is primarily worked on day shift. Where operationally required, employees may be rostered to work 12‑hour continuous shifts.
+ Contribute in a team environment through developing positive working relationships that are based on trust and integrity
**_** All candidates will undergo medical, police and drivers license checks_** **.**
In return to your experience, **we offer:**
+ Offered under enterprise agreement
+ A supportive working culture and an inclusive team environment
If you are ready to take on a rare, career defining opportunity, are self-motivated and team spirited, then we would love to hear from you.

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
**We are PCI.**
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
**_Position Overview:_**
The purpose of the Senior Production Associate - Packaging and Labelling is to provide support to Packaging and Labelling operations at PCI.
This incorporates proactively ensuring readiness to commence Packaging and Labelling activities; production facility/rooms, equipment and resources are available and ready, checking production materials availability and have been staged, and batch records are available for Packaging and Labelling activity to start.
The role works with and alongside Production Associates, Project Managers and Warehouse Associates to ensure appropriate materials, consumables, rooms, equipment and labels are available for production activities and ensures resources are allocated according to the Production Schedule.
The Senior Production Associate - Packaging and Labelling also:
+ participates in document reviews, including Master Batch Records, Logbooks and SOPs and training required upfront, or as a result of CAPA completion;
+ assists in the introduction of new equipment into the facility including ensuring SOPs are prepared, qualification/validation is complete, equipment logbooks are prepared and available, equipment and rooms are appropriately cleaned and maintained;
+ highlights and actions opportunities for efficiency, organisation and good housekeeping within the department;
+ champions safety adherence within the department and assists with closing out safety actions;
+ ensures that PPEs, gowning etc. are available and received in the production facility accordingly; and
+ assists in the maintenance of the cGMP facility licence and may assist in facility audits (e.g. PCI internal audits, and audits conducted by Clients/Sponsors, and Regulatory Authority Inspections).
**_Primary Responsibilities of this Position are:_**
This position's primary responsibility is to support the operational activities of the Packaging and Labelling facility specifically involving:
+ Completing company training requirements in accordance with curricula and other training as may be required (e.g. completion of training when SOPs are updated or new SOPs issued that are applicable to production).
+ Ensure that the Master Batch Record is reviewed, the required batch record has been approved, and Quality issued prior to use and verify that the data, and information are correct, unambiguous, and clear for Production to run the batch.
+ Ensuring that released or stock is in "I" status and correct equipment is picked for production in accordance with the batch record prior to the commencement of production activity.
+ Organise workflow by ensuring required consumables, materials and equipment have been staged in time and staff assigned.
+ Maintains a clean and safe environment.
+ Enforce strict safety guidelines and company standards.
+ Assist with the on the job / competency training of new and existing Production Associates.
+ Reviewing executed production batch records and ensuring that these are completed and signed prior to forwarding to Quality for review and release.
+ Ensure all relevant transactions have been updated in the ERP system
+ Preparation and review of documentation as required including MBRs, SOPs, qualification/validation protocols, URS etc.
+ Participating in PCI internal audits and third-party audits and assist in responding to audit findings and product complaints/recalls as may be required
+ Assisting Clinical Projects and Customer Experience Team as required in preparing and reviewing MBRs, BRs, etc. prior to approval.
+ Assisting Storage and Distribution, Projects and Quality departments as required.
+ Assist in the capture of data and metrics of production processes and report them as required.
+ Raise EVENTS in MasterControl when issues are identified during Packaging & Labelling activity affecting product quality and patient safety.
+ Assist Production Associate Manager for investigation arising due to EVENT/DEV/NONC/COMP that occurs during production activity.
+ Review/perform checks as required during production activity and provides assistance and support to Production Associates to ensure right first time on batches and product quality.
+ Other duties as required by Manager/Head of Production.
**_Mandatory Qualifications & Experience:_**
+ Previous industry experience and/or Bachelor of Science, Pharmacy or related Discipline
+ Excellent written and verbal skills with good attention to detail
+ Documented cGMP training
+ Previous industry manufacturing and/or science experience
**_Behavioural Competencies required for this Position:_**
+ High level of professionalism, ethics, quality of work, communication and responsiveness at all times
+ Positive, 'can-do' attitude, embraces and 'lives' PCI's Vision and Values
+ Analytical thinker and solution finder/problem solver
+ Collaborative Leader and team player
+ Objective and robust decision maker
+ Self-confident and self-respectful
+ Excellent interpersonal, written and verbal communication
+ Self-motivated, achievement and outcomes orientated
+ Trusting and trustworthy
+ Conscientious and diligent
+ Other duties as required by Manager/Head of Production.
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future ( Employment Opportunity (EEO) Statement:**
_PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status._
_At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture._
Why work for PCI Pharma Services?
At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how.
PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled

We are seeking a highly organised and proactive **Admin Leader - Production Upfit** to support our **Scoresby operations** .
This role is a key position within the Upfit function, acting as an extension of senior leadership to coordinate administrative, customer, supplier, and team support activities. You will play a critical role in ensuring **efficient operations, strong customer outcomes, and effective team support** , while maintaining compliance with Cummins policies and standards.
As a senior support role, you will also act as a **2IC (second in charge)** as delegated by leadership, helping drive consistency, communication, and performance across the Upfit area.
**Key Responsibilities**
**Customer & Stakeholder Support**
+ Act as a key point of contact for **internal and external customers** , supporting communication and engagement
+ Coordinate **site visits, plant tours, and customer events**
+ Ensure customer orders are completed **accurately and in a timely manner** , with full ERP system tracking
**Supplier & Commercial Support**
+ Support **supplier onboarding and management** in line with Cummins standards
+ Raise and manage **purchase orders** , ensuring correct coding and traceability
+ Maintain accurate records of supplier activity and delivery
+ Provide **analysis and reporting on supplier performance and spend trends**
**Upfit Team Support**
+ Maintain accurate **timekeeping and attendance records** (e.g. timesheets, Kronos, ADP)
+ Support team leaders with **work allocation and coordination** when required
+ Escalate team issues to leadership where necessary
+ Prepare and present **monthly reports** based on production outputs and customer demand
**Health, Safety & Environmental (HSE)**
+ Support compliance with **Cummins HSE policies and ISO standards**
+ Conduct and support **JSOs and safety activities** across the Upfit team
+ Maintain records relating to **equipment, chemicals, tooling, and contractor compliance (SDS, inductions, etc.)**
+ Champion **5S, CI, and EHS improvement initiatives** across the area
**General Administration & Leadership Support**
+ Provide high-level administrative support including **scheduling, reporting, correspondence, and coordination**
+ Act as a **central liaison between leadership, teams, and stakeholders**
+ Use judgement and initiative to manage competing priorities and improve workflow efficiency
**About You**
You are a **highly organised and detail-oriented professional** with strong communication skills and the ability to manage multiple priorities within a dynamic environment.
**You will bring:**
+ Prior experience in a **Production or Logistics** environment would be desired
+ Strong administration and coordination experience, ideally in manufacturing or operations
+ Ability to multi-task and manage competing priorities effectively
+ Experience improving and **streamlining workflows and processes**
+ Strong **customer-facing and stakeholder engagement capability**
+ Experience working with **ERP systems (e.g. SAP, Movex)** advantageous
+ Advanced proficiency in Microsoft Office (Excel, Word, PowerPoint)
+ Experience using digital tools and automation (e.g. M365 Copilot) would be preferred
+ Previous exposure to team support or informal leadership responsibilities
**_At Cummins, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, colour, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law._**
+ **Communicates Effectively** - Delivers clear communication across a variety of audiences
+ **Customer Focus** - Builds strong relationships and ensures customer needs are met
+ **Action Oriented** - Takes initiative and responds proactively to challenges
+ **Ensures Accountability** - Holds self and others accountable to deliver outcomes
+ **Plans and Aligns** - Organises and prioritises work effectively
+ **Data Analytics** - Interprets and communicates data to support decision-making
+ **Data Communication & Visualisation** - Presents insights clearly through reports and dashboards
+ **Values Differences** - Embraces diverse perspectives to improve outcomes
**Job** Manufacturing
**Organization** Cummins Inc.
**Role Category** On-site with Flexibility
**Job Type** Office
**ReqID**
**Relocation Package** No
**100% On-Site** No

**Date Posted:**

**Country:**
Australia
**Location:**
AU-WA-HENDERSON-103-CUST ~ 103 Quill Way ~ QUILL (External Site)
**Position Role Type:**
Hybrid
+ Grow your career with global expertise and local impact
+ Flexible work opportunities and a supportive culture
+ Join a team with great benefits and professional development
Your mission starts here at Raytheon Australia! Right now, we are seeking a bright and energised **Inventory Procurement Officer.** Join our team of outstanding people with expertise across a wide variety of disciplines and position yourself at the forefront of tomorrow's capabilities.
In return, we will support you with access to best practice tools, systems and processes while continually investing in your growth by providing tailored learning and development opportunities.
Working within the Minor Vessel Capability Lifecycle Manager (MV CLCM) program, the Inventory Procurement Officer is accountable to the Inventory Procurement Lead. You will support development and proactive management of the inventory procurement requirements across the vessel's lifecycle - underpinning the availability of the ships to Navy.
Key Responsibilities
+ Independently plan, coordinate and execute procurement activities of moderate complexity in accordance with mandated customer / third‑party policies, processes and delegations.
+ Initiate and support sourcing and procurement due‑diligence activities, integrating mandatory policy requirements including (but not limited to) Indigenous and local industry participation (Australian Industry Capability), Sustainability and Modern Slavery.
+ Work with internal stakeholders and subject matter experts to clarify, define and refine scope, supply requirements and statements of work.
+ Identify candidate suppliers and recommend the appropriate approach‑to‑market, including use of approved agreements and exemptions where applicable.
+ Prepare, issue and manage Requests for Quote and/or Tender in accordance with customer / third‑party requirements.
+ Evaluate supplier responses, undertake cost, schedule and risk analysis, and prepare value‑for‑money recommendations supported by judgement and experience.
+ Prepare purchase orders ensuring accuracy, completeness, appropriate approvals and compliance with financial delegations.
+ Manage procurement activities through to delivery, monitoring supplier performance to ensure scope, schedule, cost and quality requirements are met.
+ Support confirmation of goods receipt and supplier payment activities in accordance with customer / third‑party processes.
+ Make minor improvements or enhancements to procurement processes, tools or systems to improve efficiency, compliance or effectiveness of the work area.
+ Act as a point of contact for suppliers and stakeholders for assigned procurements
**Skills, Experience & Qualifications**
+ Minimum of 3-4 years prior relevant experience required.
+ Requires theoretical to advanced knowledge of supply chain (procurement, material logistics), contracting, business, commerce, law or finance work area.
+ Requires practical knowledge of projects, programs, or systems relevant to the business with the ability to make enhancements and leverage knowledge in daily work.
+ Successful candidates must be eligible to obtain and maintain a NV1 Security clearance as needed. Eligibility can be found at ( is your opportunity to join the brightest minds in the nation working for the mission on leading-edge technology to deliver Australia's most significant defence capabilities.
If you are looking to contribute to the mission that matters, click apply now or contact us at .
_RTX adheres to the principles of equal employment. All qualified applications will be given careful consideration without regard to ethnicity, color, religion, gender, sexual orientation or identity, national origin, age, disability, protected veteran status or any other characteristic protected by law._
**Privacy Policy and Terms:**
Click on this link ( to read the Policy and Terms
Raytheon Technologies is An Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age or any other federally protected class.

About The Role
To assist the Gluing operator to achieve high quality results in the conversion of printed and cut finished cartons. The role will support the day-to-day delivery of production on the line in either feeding, packing or palletizing.
Key Responsibilities
* Assist Operator with the setup of the machine to the standard required in preparation for the conversion or embellishment (make ready)
* Assess product for meeting quality standards, undertake quality checks
* Assist the Operator with the gluing machine to ensure quality and productivity requirements are met
* Conduct routine maintenance with the operator in accordance with the Daily Equipment Care checklist
* Review workload with the operator to ensure all preparation work is managed in a timely manner to ensure continuous running of the machine
* Responsible for housekeeping within department in accordance with GMP Policy and Audits.
* Assist in cross training other staff where applicable
* Coordinate and liaise with operator to ensure jobs are prepped
Qualification
* 1+ years\u2019 experience in a manufacturing or warehousing environment.
* Ability to read technical drawings (Knife/Glue Line)
* Understand basic machine function
* Understand \u2018pre make ready\u2019 process
* Knowledge of standards and process
* Ability to communicate effectively
Smurfit Westrock (NYSE:SW) is the go-to leader and partner of choice in sustainable packaging. We are dedicated to creating efficient and scalable paper and packaging solutions to help solve complex packaging challenges. Guided by our values of safety, loyalty, integrity and respect, we are committed to delivering meaningful value for shareholders, customers, employees and the communities where we operate.
Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law.

**_What Production Operation contributes to Cardinal Health_**
Manufacturing is responsible for cost of production and maintenance activities including process improvement, supply chain management, quality assurance, employee safety and engagement, and environmental commitment.
Production Operation operates light-duty bench- or floor-type machine tools and automation equipment. May set up machining machines and make adjustments, and perform maintenance on machines. Checks work using prescribed gauges, jigs and fixtures to measure close tolerances. Some machines may be numerically controlled. May monitor and verify quality in accordance with statistical process or other control procedures.
**_Job Summary_**
The Operator II, Production Operations is an entry level position at the facility responsible for the manual operational tasks within the production facility. The job is responsible for escalating major production issues and resolving minor issues as applicable. This job performs work under close supervision by the Supervisor, Manufacturing Management.
**_Responsibilities_**
+ Participates in packaging for finished products prior to shipment.
+ Loads machines with raw materials prior to production along with transporting materials from machine to machine as needed.
+ Troubleshoot basic issues on machines, to stay on production schedule.
+ Creates and modifies labels or stickers applied to products or packaging.
**_Qualifications_**
+ 1-2 years of experience, preferred
+ High School diploma, GED or equivalent, or equivalent work experience, preferred
**_What is expected of you and others at this level_**
+ Applies acquired knowledge and skills to complete standard tasks
+ Readily learns and applies new information and methods to work in assigned area
+ Maintains appropriate licenses, training and certifications
+ Works on routine assignments that require some problem resolution
+ Works within clearly defined standard operating procedures and/or scientific methods
+ Adheres to all quality guidelines
+ Works under moderate degree of supervision
+ Work typically involves regular review of output by work lead or supervisor
+ Refers complex unusual problems to supervisor
_Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._
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