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

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, and/or 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

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

New

R&D Deployment Scientist

Randstad Inhouse, Specialty Pharma, for a multinational company in consumer heal...

Location

Italy , Pomezia

Salary:

28000.00 - 34000.00 EUR / Year

Randstad

Expiration Date

September 08, 2026

Requirements

Degree in Chemistry, Industrial chemistry, Pharmaceutical Chemistry, Chemical/materials engineering, Biotechnology or similar
Demonstrated learning agility and quick-thinking skills
Proactivity and problem-solving attitude
Analytical skills in data interpretation
Excellent communication skills
Fluent written and oral English communication skills are required

Job Responsibility

Execute PD activities in Innovation/Renovation/Compliance projects
Build babies and kids cosmetic formulation and chemical science knowledge
Develop technical expertise in product design/formulation and processing awareness
Participate in technical projects work, including scale-up activities and analysis with hands-on involvement
Participate in cross-functional project team discussions defining and coordinating deliverables (e.g.:R&D, Business and Supply Chain) and to define project timing and risk management
Optimize formulated ingredients to meet business objectives
Accurately document experimental procedures, data, results, and case report forms to maintain comprehensive records and ensure data integrity
Develop, update, and apply scientific protocols, test methods, and standard operating procedures to optimize experimental and deployment approaches
Prepare scientific illustrations, diagrams, presentations to effectively communicate findings and data analysis at internal meetings to facilitate knowledge sharing and collaborative troubleshooting
Support the execution of Raw Material and Product testing, Formulations batches, samples making, once required by the projects activities

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

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R&D Samples Coordinator

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