Compounding Manager Job at Baxter (Old Toongabbie, New South Wales)

Compounding Manager

This is a rare and exciting opportunity to join our Compounding Operations as th...

Location

Australia , Old Toongabbie

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Pharmacy Degree, Science Degree or approved equivalent qualification
Lean Manufacturing
Leadership and Management skills
Production/Operations/Manufacturing experience
Problem Solving Skills
Sound business acumen
Sound decision making skills
Excellent communication skills
Ability to build and maintain effective relationships with internal/external customers
Negotiation skills

Job Responsibility

People leadership across the facility
Providing leadership development, coaching and motivation to all team members
Strategic workforce planning, including resourcing
Oversight of training and development plans for all team members
Oversight of implementation of EHS policies and procedures
Budget management
Driving Process and productivity improvement at the site
Ensure quality standards and procedures are being maintained
Oversight of Quality incidents and investigations
Management of customer relationships

Fulltime

Qp & Quality Manager Compounding

This is where your work makes a difference. At Baxter, we believe every person d...

Location

Ireland , Dublin

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

6-10 years’ experience of Quality implementation in Pharma industry
Proven knowledge or experience in applicable regulations and standards e.g. EU GMP Annex 1 particularly in relation to aseptic manufacturing environments
Proven aseptic manufacture experience with knowledge in Sterility assurance and risk management
Proven leadership experience with a track record of consistently meeting results
Ability to operate effectively in a fast-paced environment and prioritize multiple tasks
Proven ability to manage/supervise a large and diverse team of employees

Job Responsibility

Ensure the compounding site follows Good Manufacturing Practice for Medicinal Products for Human Use
Act as a Qualified Person (QP) responsible for implementing the quality management system
Lead all aspects of the compounded products release process
Serve as the primary contact with the regulatory agency (HPRA) regarding Manufacturing Licence, GMP inspections, and any potential compounding product quality issues
Develop and maintain an internal review process to ensure continuous compliance
Lead and manage the audit process for the facility
Measure and analyze site quality metrics and indicators
Develop and implement risk management strategies
Coordinate the management, execution, and approval of quality documents and records

What we offer

Pension
Competitive package
Health Insurance
Life Assurance and much more

Fulltime

Qp & Quality Manager Compounding

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

Location

Ireland , Sandyford Dublin 18

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

6-10 years’ experience of Quality implementation in Pharma industry
Proven knowledge or experience in applicable regulations and standards e.g. EU GMP Annex 1 particularly in relation to aseptic manufacturing environments
Proven aseptic manufacture experience with knowledge in Sterility assurance and risk management
Proven leadership experience with a track record of consistently meeting results
Ability to operate effectively in a fast-paced environment and prioritize multiple tasks
Proven ability to manage/supervise a large and diverse team of employees

Job Responsibility

Ensure the compounding site follows Good Manufacturing Practice for Medicinal Products for Human Use
Act as a Qualified Person (QP) responsible for implementing the quality management system
Serve as the primary contact with the regulatory agency (HPRA) regarding Manufacturing Licence, GMP inspections, and any potential compounding product quality issues
Develop and maintain an internal review process to ensure continuous compliance, preparing the site for audits at any time
Lead and manage the audit process for the facility, ensuring that audit findings are thoroughly investigated and addressed promptly
Measure and analyze site quality metrics and indicators, comparing performance against targets, and implement data-driven actions for continuous improvement of processes and products
Develop and implement risk management strategies to minimize product and process risks, ensuring patient safety
Coordinate the management, execution, and approval of quality documents and records for the site, including Nonconformance investigations, CAPA plans, Change Controls, SOPs, Validation Protocols, and Reports

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Pension
Competitive package
Health Insurance
Life Assurance and much more

Fulltime

Qp & Quality Manager Compounding

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

6-10 years’ experience of Quality implementation in Pharma industry
Proven knowledge or experience in applicable regulations and standards e.g. EU GMP Annex 1 particularly in relation to aseptic manufacturing environments
Proven aseptic manufacture experience with knowledge in Sterility assurance and risk management
Proven leadership experience with a track record of consistently meeting results
Ability to operate effectively in a fast-paced environment and prioritize multiple tasks
Proven ability to manage/supervise a large and diverse team of employees
Strong leadership skills to motivate teams, make decisions and guide the organization toward quality objective
Excellent organizational skills for managing tasks, coordinating resources, and ensuring prompt quality data driven decision making
Excellent communication and interpersonal skills to build relationships with collaborators and facilitate collaboration with other Compounding functions

Job Responsibility

Ensure the compounding site follows Good Manufacturing Practice for Medicinal Products for Human Use according to Eudralex Volume 4 and Commission Directive 2003/94/EEC
Act as a Qualified Person (QP) responsible for implementing the quality management system and lead all aspects of the compounded products release process
Serve as the primary contact with the regulatory agency (HPRA) regarding Manufacturing Licence, GMP inspections, and product quality issues
Develop and maintain an internal review process to ensure continuous compliance
Lead and manage the audit process for the facility
Measure and analyze site quality metrics and implement data-driven actions for continuous improvement
Develop and implement risk management strategies to minimize product and process risks
Coordinate the management, execution, and approval of quality documents and records including Nonconformance investigations, CAPA plans, Change Controls, SOPs, Validation Protocols, and Reports

What we offer

Pension
Competitive package
Health Insurance
Life Assurance and much more
Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

New

Automated Dispensing Unit, Pharmacy Technician

We're building a world of health around every individual — shaping a more connec...

Location

United States , Spartanburg

Salary:

17.00 - 28.46 USD / Hour

CVS Health

Expiration Date

July 26, 2026

Requirements

Verifiable High School Diploma or GED is required
Certification/licensed/registered pharmacy technician or as required by state law
The ability to concentrate on a task over a period without being distracted
Use and understand verbal and written communication to interact with customers and colleagues
Actively listening by giving full attention to what others are saying, taking time to understand the points being made, asking questions as appropriate, and not interrupting at inappropriate times
The ability to use math to solve a problem, such as calculating day's supply of a prescription
Is able to judge when something is wrong or is likely to go wrong
recognizing there is a problem
Choosing the best course of action when faced with a complex situation with several available options
Customer service orientation

Job Responsibility

Responsible for ADU operation, appearance/cleanliness, quick reference guide replacement
Restocking / destocking ADUs with medication located at Omnicare serviced facilities
Completing monthly medication audits of ADUs (inspect and verify med qty, expiration, damage, etc)
ADU software and user database maintenance
Review ADU reports for discrepancies, errors, and dispensing data
Train facility staff training as needed on ADU operation
Support coordination of New ADU installation
pharmacy and facility readiness including initial ADU inventory, user set-up, etc
Responsible for troubleshooting ADU issues with the facility and pharmacy
Review and complete ADU policies, training and SOPs yearly

What we offer

Medical coverage
Dental coverage
Vision coverage
Paid time off
Retirement savings options
Wellness programs

Fulltime

New

Operations Lead

The Operations Support Lead will be based at the Baghdad Embassy Compound (BEC) ...

Location

Iraq , Baghdad

Salary:

47000.00 USD / Year

Amentum

Expiration Date

Until further notice

Requirements

One (2) or more years in an overseas environment
One (2) or more years in a customer service or administrative-related position
Excellent MS Office Suite experience (Excel, Outlook, Powerpoint, PowerBI and Word)
Speak, read and write English
A high school diploma or GED
Valid drivers' license
Possess a valid passport with a minimum of 18 months remaining to expiration date with 8 blank pages
Already possess a Moderate Risk Public Trust (MRPT) or be able to obtain a favorable MRPT certification prior to being hired
Strong, professional, oral and written English communication skills
Favorable passage of a drug screen and physical examination

Job Responsibility

Responsible for maintaining a safe workplace and ensuring that safety is the highest priority in the workplace
Comply with all Environmental Health & Safety and Quality Assurance requirements and goals
Provide a full range of general support services for the BLiSS program under the direction and supervision of the PMO Operations Manager
Update the Mission Accountability System (MACS) as defined by Embassy requirements and align this data with the IEP accountability processes
Perform all administrative and clerical services necessary in support of program Operations at the Baghdad Embassy Compound (BEC)
Submit visitor access requests (VARs) and compile visa packets in coordination with Site Access
Support the program with a full working knowledge of the DOS contract and obtain data from Department Leads as needed
Coordinate visitor arrivals ensuring Housing and Travel related coordination is completed
Prepare responses to questions and data requests received from the Operations team
Responsible for the coordination of information to support the creation/update of Quarterly Performance Metrics Review (PMR) with the Department of State, Plan of Action and Milestones (POAM) for the BLiSS and OMSS contract projects, and performance analysis to be incorporated into reporting requirements

What we offer

Health, dental, and vision insurance
Paid time off and holidays
Retirement benefits (including 401(k) matching)
Educational reimbursement
Parental leave
Employee stock purchase plan
Tax-saving options
Disability and life insurance
Pet insurance

Fulltime

New

Director, Research Services, Oncology

As a Director, Research Services at ICON, you will be responsible for working wi...

Location

United States , Blue Bell

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Degree in a scientific/life sciences field
Pharm.D. or Ph.D. preferred
Minimum of 8 years of experience in oncology research or related field
Demonstrated experience leading clinical development programs in oncology (preferably late-stage)
Experience with global regulatory interactions and submissions (FDA, EMA, or other agencies)
Strong understanding of oncology clinical endpoints, trial design, and statistical considerations
Proven ability to work effectively in a cross-functional matrix environment and influence without direct authority
Track record of scientific publications and/or conference presentations
Excellent written and oral communication skills
Strong analytical and scientific writing skills

Job Responsibility

Development of protocols for clinical studies
Preparation of clinical development plans
Drafting of clinical scientific documents such as IND, IND amendments, Investigator’s Brochures, Annual Reports and other FDA submissions
Monitor, perform data review, and summarize safety and efficacy data in ongoing studies
Assist with study design for exploratory development
Lead the clinical matrix teams for assigned compounds
Represent exploratory development on project teams
Develop relationships with appropriate consultants
Write abstracts and present data at scientific meetings, both internally and externally
Serve as liaison to project teams, CROs and others

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

New

Storeperson, Compounding

A great opportunity has become available for a Storeperson to join our Compoundi...

Location

Australia , Old Toongabbie

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Ability to adhere to procedure with good attention to detail
Good communication and people skills
Ability to work autonomously and in a team
Good time management skills
Technician level (for internals)

Job Responsibility

Complies with mandatory GMP/GDP/EHS
Complies with Pharmacy Operations EHS Requirements
Maintaining inventory/stock
Purchasing Baxter lines from Distribution Centres and receiving all inventory into JDE (and Merlin where applicable)
Assisting pharmacy with daily production needs
Transferring stock to other pharmacy sites if needed
Ensuring stock counts are completed accurately and on schedule
Implementation of lean in store area
Organising credit/debit for under/over supply or damaged stock
Liaising with suppliers and Central Purchasers when necessary

Fulltime

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Compounding Manager

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