Process Worker - Compounding Assistant Job at Baxter (Coorparoo, Queensland)

Process Worker - Compounding Assistant

This is a fantastic opportunity for you to join our Christchurch Compounding Tea...

Location

New Zealand , Christchurch

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Experience in Healthcare, manufacturing or warehousing would be advantageous
Demonstrate a good understanding of basic mathematics
Be able to communicate effectively both verbally and in writing
Be able to use computer systems
Collaborating effectively in a team environment to achieve common goals in a fast-paced environment
Have good attention to detail
Willingness to learn new skills
Executing repetitive results in a consistent and accurate manner
Providing assistance in environments with defined procedures and protocols
Adapting to shift work schedules as needed

Job Responsibility

Picking and preparing raw materials
Labelling, inspection and sealing of compounded products
Packing of finished units for each order including final inspection of products
Labelling and dispatching of prepared products
Maintaining and housekeeping of work area consumables
Ensuring documentation is completed in accordance with Good Manufacturing Practice (GMP)
Adhering to Baxter’s Standard Operating Procedures
Other duties as required

What we offer

Full training provided
Gender Equality recognition
Support structures for working families
Strategic recruitment and promotion practices
Inclusive culture

Fulltime

Process Worker - Compounding Assistant

This is a fantastic opportunity for you to join our Coorparoo Compounding Team o...

Location

Australia , Coorparoo, Queensland

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Experience in Healthcare, manufacturing or warehousing would be advantageous
Demonstrate a good understanding of basic mathematics
Be able to communicate effectively both verbally and in writing
Be able to use computer systems
Collaborating effectively in a team environment to achieve common goals in a fast-paced environment
Have good attention to detail
Willingness to learn new skills
Executing repetitive results in a consistent and accurate manner
Providing assistance in environments with defined procedures and protocols
Adapting to shift work schedules as needed

Job Responsibility

Picking and preparing raw materials
Labelling, inspection and sealing of compounded products
Packing of finished units for each order including final inspection of products
Labelling and dispatching of prepared products
Maintaining and housekeeping of work area consumables
Ensuring documentation is completed in accordance with Good Manufacturing Practice (GMP)
Adhering to Baxter’s Standard Operating Procedures
Other duties as required

What we offer

Full training will be provided
no prior experience is required

Fulltime

Qualified Person

This is where you make a difference in our patients’ safety. As a member of the ...

Location

Ireland , Dublin

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

QP Qualification
Pharmacy Degree (or equivalent) in science-related discipline essential
Previous QP experience in a pharmaceutical company or equivalent-type role
Ideally a minimum of two years’ experience in a GMP regulated aseptic environment
Experience/qualifications in microbiology/environmental monitoring a distinct advantage
Working in a project-based environment would be advantageous
Experience of implementing changes and process development
Previous experience in an aseptic manufacturing facility
Previous experience as a batch releaser would be advantageous
Good problem solving and investigation skills

Job Responsibility

Release of Nutrition, Chemo and Antibiotic products
Oversight and quality assurance expertise and guidance of the compounding process
Ensure all products released comply with the Manufacturing Licence, Good Manufacturing Practice (GMP), Irish and European Legislation and Baxter Healthcare Ltd Standards
Responding to pharmaceutical queries concerning compounded medicinal products
Support facility projects including process development and quality improvement initiatives
Ensure products and processes comply with procedures and the principles of GMP
Supporting / Liaising with the Batch releasers responsible for product release
Supporting / Liaising with Dispatch and customer service to manage quality issues
Supporting the preparation of Deviation and QA trend reports
Supporting the preparation of Key Performance Indicators (KPIs)

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Qualified Person

The Qualified Person (QP) is primarily responsible for release of Nutrition, Che...

Location

Ireland , Dublin

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

QP Qualification
Pharmacy Degree (or equivalent) in science-related discipline essential
Previous QP experience in a pharmaceutical company or equivalent-type role
Ideally a minimum of two years’ experience in a GMP regulated aseptic environment
Experience/qualifications in microbiology/environmental monitoring a distinct advantage
Working in a project-based environment would be advantageous
Experience of implementing changes and process development
Previous experience in an aseptic manufacturing facility
Previous experience as a batch releaser would be advantageous
Good problem solving and investigation skills

Job Responsibility

Release of Nutrition, Chemo and Antibiotic products
Oversight and quality assurance expertise and guidance of the compounding process
Ensure all products released comply with the Manufacturing Licence, Good Manufacturing Practice (GMP), Irish and European Legislation and Baxter Healthcare Ltd Standards
Responding to pharmaceutical queries concerning compounded medicinal products
Support facility projects including process development and quality improvement initiatives
Ensure products and processes comply with procedures and the principles of GMP
Supporting / Liaising with the Batch releasers responsible for product release
Supporting / Liaising with Dispatch and customer service to manage quality issues
Supporting the preparation of Deviation and QA trend reports
Supporting the preparation of Key Performance Indicators (KPIs)

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Qualified Person

This is where you make a difference in our patients’ safety. As a member of the ...

Location

Ireland , Dublin

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

QP Qualification
Pharmacy Degree (or equivalent) in science-related discipline essential
Previous QP experience in a pharmaceutical company or equivalent-type role
Ideally a minimum of two years’ experience in a GMP regulated aseptic environment
Experience/qualifications in microbiology/environmental monitoring a distinct advantage
Working in a project-based environment would be advantageous
Experience of implementing changes and process development
Previous experience in an aseptic manufacturing facility
Previous experience as a batch releaser would be advantageous
Good problem solving and investigation skills

Job Responsibility

Release of Nutrition, Chemo and Antibiotic products
Oversight and quality assurance expertise and guidance of the compounding process
Ensure all products released comply with the Manufacturing Licence, Good Manufacturing Practice (GMP), Irish and European Legislation and Baxter Healthcare Ltd Standards
Responding to pharmaceutical queries concerning compounded medicinal products from customers and Baxter’s homecare nurses
Support facility projects including process development and quality improvement initiatives
Ensure products and processes comply with procedures and the principles of GMP
Supporting / Liaising with the Batch releasers responsible for product release
Supporting / Liaising with Dispatch and customer service to manage quality issues
Supporting the preparation of Deviation and QA trend reports
Supporting the preparation of Key Performance Indicators (KPIs)

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Casual Pharmacy Assistant

The Pharmacy Department has an opening for a Pharmacy Assistant at La Verendrye ...

Location

Canada

Salary:

30.36 - 34.56 CAD / Hour

Riverside Health Care

Expiration Date

Until further notice

Requirements

Education equivalent to the former designation of Certified Pharmacy Technician, or a combination of education and pharmacy assistant experience relevant to the responsibilities and duties of this position
Possess Delegation of Dispensing and Compounding status, or successful in achieving delegation status prior to completion of probationary period
Experience in computer processing, MS Office experience an asset
Efficient keyboarding skills
General office skills, and pharmacy related procedures
Excellent written and oral communication skills, including telephone etiquette
Ability to work independently as well as in a team
Effective interpersonal skills
Responsible, co-operative, versatile and takes initiative
Dependable with an excellent attendance record

Job Responsibility

Under the general direction and guidance of the Pharmacist fills prescriptions and wards stock medications and prepares sterile and non-sterile prefabricated medications, IV additives such as oncology medications and total parenteral nutrition preparations
In the absence of the Pharmacist, have responsibility for the operation of the Pharmacy Department as outlined in the policies relating to “Delegation of Dispensing and Compounding”
Dispense individual patient prescriptions and ward stock medications
Manufacture and package antiseptic solutions and other external use preparations as required by the wards including calculation of ingredients when required
Receive and record messages when the pharmacist is out of the department and accurately relay message information to the pharmacist on his/her return
Order and receive pharmaceuticals and other supplies and maintain a computerized inventory
Preparation of IV’s such as TPN and oncology medications
Process and file all invoices and packing slips having entered all necessary data into the computer inventory
Fill pharmacy shelves, being careful to rotate stock and check expiry dates
Process expired pharmaceuticals, packaging all returnable items for shipping

Parttime

Compounding Supervisor

As the Cleanroom Supervisor you will assist pharmacists and room supervisors ove...

Location

United States , Wichita

Salary:

85000.00 USD / Year

Fagron

Expiration Date

Until further notice

Requirements

7 years of experience working in a regulated environment
Minimum of 3 to 5 years’ experience in a leadership position (i.e., Shift of Line Leader, Group Leader, etc) or demonstrated leadership abilities
Good working knowledge of all functional areas of the inspection and packaging area
Solid math and effective problem-solving skills with demonstrated use of sound judgement
Good communication and organizational skills, strong interpersonal skills
Demonstrated ability to work effectively and lead a team
Ability to work with others in a positive and professional manner and to develop and maintain strong working relationships with co-workers and management
Ability to take initiative, including asking for and offering help when needed
performs work independently without being prompted
Strong attention to detail and focus on quality, accuracy, and accountability

Job Responsibility

Successfully pass and remain qualified for entrance into the ISO 7 cleanrooms
Successfully pass media fill and remain qualified to assist with tasks within the ISO VLFH as required
Must be able to stand and maneuver around the tight spaces of a cleanroom for upwards of 7 hrs. per day
Assist in overseeing all ISO 7 cleanroom activities including but not limited to: cleaning of VLFHs, the preparation of materials required to aseptically reconstitute, pool and dilute drug product, manual aseptic filling of drug product, performing calibration checks and environmental plating of operators
Must be able to rapidly assess situations, trouble shoot production concerns, guide operators, and effectively communicate complex detailed information to management outside of the cleanrooms via electronic tools frequently and quickly
Ensuring compliance to SOPs, batch records and HR policies, assisting in disciplinary action as needed
Meet Right First Time (RFT) metrics by reducing error / deviations and completing corrections quickly
Review and maintain adherence to the manufacturing schedules
Track employee training to ensure compliance
Aid in bi-annual reviews of procedures

What we offer

Competitive salary
Comprehensive benefits
Performance package
Ability to be part of an international leader in an expanding industry

Fulltime

Compliance Pharmacist

As a Compliance Pharmacist, you will be a responsible, servant leader who is met...

Location

United States , Wichita

Salary:

Not provided

Fagron

Expiration Date

Until further notice

Requirements

Pharmacist License in good standing in the state of Kansas
2+ years of experience working in a regulated environment
Solid math and practical problem-solving skills with demonstrated use of sound judgement
Excellent attention to detail and documentation skills
Strong analytical, organizational, and communication abilities
Familiarity with quality management systems, deviation/CAPA systems, and audit processes
Ability to work cross-functionally in a fast-paced regulated environment
Ability to work with others in a positive and professional manner and to develop and maintain strong working relationships with co-workers and management
Ability to take initiative, including asking for and offering help when needed
performs work independently without being prompted

Job Responsibility

Hand hygiene/Garbing
Weighing of ingredients, pH adjustments
Proper cleaning
Formulation, filling, visual inspection, labeling process assessment
Training collaborations
Evaluate current procedures/processes to identify areas of potential risk within the production operations and help develop strategies to mitigate these risks
Conduct training sessions for employees on compliance-related issues/topics
Create and update SOPs to maintain compliance with regulatory standards
Responsible for leading initiatives and tracking scrap reduction within the facility
Monitor day-to-day compounding operations to ensure compliance with FDA 503B requirements and cGMP regulations

What we offer

Competitive salary
comprehensive benefits
performance package
ability to be part of an international leader in an expanding industry

Fulltime

Process Worker - Compounding Assistant

Baxter

Location:
Australia , Coorparoo, Queensland

Category:
Manufacturing

Contract Type:
Employment contract

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
February 07, 2026

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