R&D Samples Coordinator Job at Baxter (Marsa)

R&d Samples Coordinator

This is where new knowledge is discovered. Baxter's Research and Development tea...

Location

Malta , Marsa

Salary:

19200.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

O' Level Standard of education
ECDL Certification or proficient in using MS Office and Outlook
Fluent in English language: both written and spoken
Previous working experience in a warehouse environment and lifter user certification are preferred

Job Responsibility

Effectively manage logistical operations within the R&D function to support the Malta R&D group testing requirements
Manage samples related to R&D testing activities from sample reception to sample discard: carry boxes or pallets to the designated location (with forklift when needed) and keep the traceability of these items
Manage samples, climatic chambers and areas dedicated to real time and accelerated ageing processes
Ensure that work area is well maintained also in accordance to EHS regulations related to area of responsibility
Support in the shipment of samples to other Baxter facilities or to external companies (e.g. for sterilization)
Carry out most of the activities in the warehouse area

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

R&D Samples Coordinator

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

Location

Malta , Marsa

Salary:

19200.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

O' Level Standard of education
ECDL Certification or proficient in using MS Office and Outlook
Fluent in English language: both written and spoken

Job Responsibility

Effectively manage logistical operations within the R&D function to support the Malta R&D group testing requirements
Manage samples related to R&D testing activities from sample reception to sample discard: carry boxes or pallets to the designated location (with forklift when needed) and keep the traceability of these items
Manage samples, climatic chambers and areas dedicated to real time and accelerated ageing processes
Ensure that work area is well maintained also in accordance to EHS regulations related to area of responsibility
Support in the shipment of samples to other Baxter facilities or to external companies (e.g. for sterilization)
Carry out most of the activities in the warehouse area

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

R&D Samples Coordinator

We are looking for an R&D Samples Coordinator to join our Malta R&D team. What ...

Location

Malta , Marsa

Salary:

19200.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

O' Level Standard of education
ECDL Certification or proficient in using MS Office and Outlook
Fluent in English language: both written and spoken

Job Responsibility

Effectively manage logistical operations within the R&D function to support the Malta R&D group testing requirements
Manage samples related to R&D testing activities from sample reception to sample discard: carry boxes or pallets to the designated location (with forklift when needed) and keep the traceability of these items
Manage samples, climatic chambers and areas dedicated to real time and accelerated ageing processes
Ensure that work area is well maintained also in accordance to EHS regulations related to area of responsibility
Support in the shipment of samples to other Baxter facilities or to external companies (e.g. for sterilization)
Carry out most of the activities in the warehouse area

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

R&D Samples Coordinator

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

Malta , Marsa

Salary:

19200.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

O’ Level Standard of education
ECDL Certification or proficient in using MS Office and Outlook
Fluent in English language: both written and spoken.
Previous working experience in a warehouse environment and lifter user certification are preferred

Job Responsibility

Effectively manage logistical operations within the R&D function to support the Malta R&D group testing requirements
Manage samples related to R&D testing activities from sample reception to sample discard: carry boxes or pallets to the designated location (with forklift when needed) and keep the traceability of these items
Manage samples, climatic chambers and areas dedicated to real time and accelerated ageing processes
Ensure that work area is well maintained also in accordance to EHS regulations related to area of responsibility
Support in the shipment of samples to other Baxter facilities or to external companies (e.g. for sterilization)
Carry out most of the activities in the warehouse area

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Competitive benefits
Discretionary bonuses
Long-term incentive

Fulltime

R&D Samples Coordinator

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

Malta , Marsa

Salary:

19200.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

O’ Level Standard of education
ECDL Certification or proficient in using MS Office and Outlook
Fluent in English language: both written and spoken.
Previous working experience in a warehouse environment and lifter user certification are preferred

Job Responsibility

Effectively manage logistical operations within the R&D function to support the Malta R&D group testing requirements
Manage samples related to R&D testing activities from sample reception to sample discard: carry boxes or pallets to the designated location (with forklift when needed) and keep the traceability of these items
Manage samples, climatic chambers and areas dedicated to real time and accelerated ageing processes
Ensure that work area is well maintained also in accordance to EHS regulations related to area of responsibility
Support in the shipment of samples to other Baxter facilities or to external companies (e.g. for sterilization)
Carry out most of the activities in the warehouse area

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Competitive benefits
Discretionary bonuses
Long-term incentive

Fulltime

Associate Scientist II, R&D, Complex Product Development

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Master's in science with 8 to 12 years of Experience
Good experience in the execution of analytical method development, validation and technology transfer and routine analysis for peptides and iron colloidal drug products for regulatory submission
Competency with method relevant to iron DS/DP analysis, including particle size distribution by gel filtration chromatography, light scattering/diffraction/obscuration methods, assay of various iron forms, e.g. ferrous, ferric, labile iron, chelation assays, reduction potential and kinetics, etc, is strongly desired
Basic Knowledge and execution of Chemical Analysis using techniques relevant to complex injectables
Knowledge of pharmacopoeia, ICH Guidelines
Execution of Operational and Calibration of Instrument on periodic basis
Trouble shooting of various problems obtain during the during analysis
Knowledge of Transfer of Technology
Knowledge of Good Laboratory Practice and Good Documentation Practices
Communication skills

Job Responsibility

To plan and perform sample analysis (analytical method development, validation, technology transfer, etc) activity following GxP & GDP practices for regulatory submissions for complex injectables like peptides, iron formulations, etc
Assist in regulatory query responses for Complex Products
To perform testing of Complex Injectable samples, including, API, development, validation, stability, bulk hold, RLD, PDR and any other samples as required, according to appropriate method of analysis
To be competent in analytical problem-solving, focus on innovation, process improvement and operational excellence
To keep track of all activities related to product analysis, ensure completion in the stipulated time, and inform the Sub-department manager if any deviation or issues observed
Preparation and review of analytical reports, SOPs and MOAs by referring to GQP & current pharmacopoeia as per requirement
To carry out all testing and data recording according to the approved SOPs following GDP & ALCOA++ principles and current pharmacopoeia
To use appropriate reference and working standards for analysis and maintain their records
To complete all training as per the quality matrix targets
To perform or review the calibration records of instruments as per approved SOPs

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

Associate Scientist II, R&D, Complex Product Development

This is where new knowledge is discovered. Baxter's Research and Development tea...

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Master's in science with 8 to 12 years of Experience
Good experience in the execution of analytical method development, validation and technology transfer and routine analysis for peptides and iron colloidal drug products for regulatory submission
Competency with method relevant to iron DS/DP analysis, including particle size distribution by gel filtration chromatography, light scattering/diffraction/obscuration methods, assay of various iron forms, e.g. ferrous, ferric, labile iron, chelation assays, reduction potential and kinetics, etc, is strongly desired
Basic Knowledge and execution of Chemical Analysis using techniques relevant to complex injectables
Knowledge of pharmacopoeia, ICH Guidelines
Execution of Operational and Calibration of Instrument on periodic basis
Trouble shooting of various problems obtain during the during analysis
Knowledge of Transfer of Technology
Knowledge of Good Laboratory Practice and Good Documentation Practices
Communication skills

Job Responsibility

To plan and perform sample analysis (analytical method development, validation, technology transfer, etc) activity following GxP & GDP practices for regulatory submissions for complex injectables like peptides, iron formulations, etc
Assist in regulatory query responses for Complex Products
To perform testing of Complex Injectable samples, including, API, development, validation, stability, bulk hold, RLD, PDR and any other samples as required, according to appropriate method of analysis
To be competent in analytical problem-solving, focus on innovation, process improvement and operational excellence
To keep track of all activities related to product analysis, ensure completion in the stipulated time, and inform the Sub-department manager if any deviation or issues observed
Preparation and review of analytical reports, SOPs and MOAs by referring to GQP & current pharmacopoeia as per requirement
To carry out all testing and data recording according to the approved SOPs following GDP & ALCOA++ principles and current pharmacopoeia
To use appropriate reference and working standards for analysis and maintain their records
To complete all training as per the quality matrix targets
To perform or review the calibration records of instruments as per approved SOPs

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

Wastewater Treatment Specialist Manager

Location

United Kingdom , Eye

Salary:

Not provided

Crown Chicken LTD, Division of Cranswick PLC

Expiration Date

December 28, 2026

Requirements

Previous experience as a Wastewater Treatment Specialist Manager or good understanding of how an effluent plant operates
Level 3 H&S awareness
Sampling, testing and analysis of effluent plant
Excellent communication and interpersonal skills
Proven ability to direct and coordinate operations
Strong organisational and time management skills

Job Responsibility

Safely carry out all tasks set by the engineering management
Ensure PPM’s, maintenance, breakdowns and all work is carried out in a timely safe manner
Make sure all relevant tests on the water system are completed accurately and on time
Make sure all PPM’s relating to the odour abatement system are undertaken and documented
Oversee the daily and weekly effluent sampling and tests in accordance with ENV.810
You must make sure we remain in compliance with our environmental permit
Oversee/undertake any testing required for R and D purposes and report back results/findings
Monitor all tank levels, flow rates and trends and report and concerns to the engineering management
Maintain good manufacturing practice, investigate and record hazards, risks and near misses

What we offer

Auto enrolment into our company pension scheme
Access to our ‘Feed your Wellbeing’ hub, offering a range of retail, restaurant and entertainment discounts and wellbeing support
Cycle to work scheme
Discounted local gym membership
Death in service insurance
Free Parking and Canteen facilities

Fulltime

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R&D Samples Coordinator

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R&D Samples Coordinator

R&d Samples Coordinator

R&D Samples Coordinator

R&D Samples Coordinator

R&D Samples Coordinator

R&D Samples Coordinator

Associate Scientist II, R&D, Complex Product Development

Associate Scientist II, R&D, Complex Product Development

Wastewater Treatment Specialist Manager

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