R&D Samples Coordinator Job at Baxter (Marsa)

Director, Privacy R&D and CPO

A Director Privacy for R&D/CPO ensures compliance with global data protection la...

Location

Belgium; United Kingdom , Wavre; London

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

Expertise in essential regulation guidelines and medical governance policies and procedures applicable to R&D
Broad scientific/ pharmaceutical industry background with more than 10 years of experience in privacy EU and ex EU
Previous experience in implementing / embedding Privacy risk controls into a worldwide organization
Proven success in developing and executing activities that improve the application of the internal control framework
Good understanding of privacy regulatory framework
Relevant experience in governance type activities with understanding of the R&D, medical, commercial and compliance functions.

Job Responsibility

Develop and implement a strategy to ensure Privacy by Design into R&D & CPO processes. This includes completing new or adjusting existing privacy inventories and/or privacy risk assessments and developing and implementing mitigating controls
Oversee the privacy strategy to ensure timely create and review existing R&D & CPO privacy inventories and privacy impact assessments to identify gaps, assign appropriate actions, and track actions to completion. Ensure new innovative areas are timely addressed and risk identified including adequate review of third-party global process relevant to the enterprise risk
Provide inventory and monitor R&D/CPO privacy gaps, risks and issues as well as developing adequate risk minimization measures, corrective and preventative actions. Provide status updates to senior governance bodies such as R&D’s Risk Management and Compliance Board (RDCB) and Data Ethic and Governance Council as well as CPO related board
Support the design of privacy-related training for R&D & CPO staff to foster a privacy by design culture
Analyze and implement process changes required to enhance R&D/CPO Privacy framework
Maintain ongoing communication with relevant LOC stakeholders, Privacy Legal, Data Privacy Officer and enterprise risk ensuring continued alignment between global and local R&D/CPO Privacy processes
Coordinate efforts with the privacy lead needed to respond to Data Privacy Regulators in the event of Data Privacy Breaches. Monitor frequency and resolution of breach as well as implement remediation strategy to avoid recurrence. Coordinate with privacy lead responses to Individual Rights Management requests, ensuring engagement of the right R&D stakeholders in the information collection
Oversee and ensure adequate privacy expertise related to the data and human biological sample reuse (including adequate support to the DSAP panel)
Create and maintain R&D/CPO’s approach to the GSK Privacy Enterprise Risk Plan and maintain ongoing communication with Privacy professionals in other GSK business areas as well as maintain the R&D/CPO privacy champion network
Provide Risk Management expertise and oversight for R&D/CPO Privacy covering all therapy areas and with global-regional-local span

Fulltime

Product Development Assistant

The Product Development Assistant supports the Product Development and Technical...

Location

United States , Brooklyn, NY

Salary:

50000.00 - 60000.00 USD / Year

New York Embroidery Studio

Expiration Date

Until further notice

Requirements

Associate degree or bachelor’s degree in fashion design, fashion technology, product development, engineering, or related field preferred
Strong attention to detail with excellent documentation and organizational skills
Understanding of garment construction or sewn-product development
PPE knowledge a plus
Experience with tech pack creation, BOMs, or product specs required
Proficiency in Adobe Illustrator, Indesign, Excel, Google Sheets, or similar tools
Illustrator or CAD experience is a plus
Comfortable working in a fast-paced production environment and learning structured quality procedures

Job Responsibility

Coordinate sampling requests with production, sewing teams, R&D, and quality
Track sample status, record measurements, and consolidate feedback for revisions
Prepare sample evaluation sheets and collect required approvals before moving to pilot or production
Ensure sample materials, trims, and cut tickets are available and correctly documented
Work closely with Quality to ensure technical documentation aligns with compliance requirements
Collaborate with Engineering and R&D to update specs following process validations or production changes
Communicate updates to manufacturing teams and ensure the latest versions of documents are distributed
Assist in preparing technical documentation packages for customers, suppliers, auditors, or regulatory partners
Draft and update manufacturing instructions, layout guides, and assembly steps based on engineering and quality input
Maintain organized digital folders and master lists for all product development files

Fulltime

Metallurgical Engineer

An exceptional role for an experienced Metallurgist or Metallurgical Engineer, b...

Location

United Kingdom , Milton Keynes

Salary:

40000.00 - 50000.00 GBP / Year

Wallace Hind

Expiration Date

Until further notice

Requirements

Materials analytical skills
Metallographic preparation and associated light microscopy
Excellent optical and scanning electron microscopy skills (SEM/EDS/EDX)
Knowledge of metal cleanliness assessment techniques including PoDFA, Prefil and LiMCA
The ability and experience to perform Root Cause Failure Analysis (RCFA)
Excellent interpersonal and communication skills with the ability to deliver technical services

Job Responsibility

Help the team and support the key objectives set by the Metallurgical Manager
Enjoy both the scale and variety of exciting projects which can change daily
Cut, mount, polish and analyse customer issued PoDFA samples, (20% of role)
Re-melt customer metal samples, process through the internal PoDFA equipment, cut, mount, polish and analyse the PoDFA samples. (40% of role)
Provide high quality metallurgical analysis and reports for our global internal and external customers (40% of role)
Design, coordinate, conduct and report on melt cleanliness trials at highly strategic customer sites to demonstrate aluminium process improvements, as appropriate
Provide metallurgical services to help support internal R&D activities

What we offer

Profit sharing scheme paid twice yearly (after qualifying period)
25 days holiday (plus 8 statutory days)
Company Pension (Company contributes 7%, Employee Can Pay Up to 10% – after qualifying period)
Life Assurance (8 x Salary)
Enhanced Benefits Package
On-site Parking
Company Social Events

Fulltime

Research Scientist I

The research we do and the products we develop improve outcomes for patients aro...

Location

United States , Round Lake

Salary:

96000.00 - 132000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Degree or equivalent experience in a relevant scientific field such as chemistry or pharmaceutical sciences (BS level with 5+ years, MS level with 3+ years, or PhD level with research experience or equivalent)
Hands-on experience with analytical instrumentation including HPLC, pH measurement, UV, and GC/LC-MS
Background in analytical method development, validation, and transfer
Understanding of ICH and USP guidelines and cGxP practices
Experience working in a regulated laboratory environment with strong technical problem-solving abilities
Ability to learn quickly and apply critical thinking to solve analytical challenges
Skill in crafting experiments and interpreting data, along with the ability to thoughtfully review peers’ work
Strong ability to express ideas clearly in writing and speaking, with careful attention to detail
Solid laboratory, technical, writing, and computer skills
Ability to coordinate and communicate complex information effectively with peers and managers

Job Responsibility

Conduct critical chemical and physical analyses on finished product R&D stability samples
May also support testing of raw materials, initial, in-process, and final product samples from manufacturing facilities or other R&D initiatives
Act as a study director for studies, independently evaluating results and their impact
Provide training and supervision to junior members within the laboratory, offering advice and assistance on outstanding problems
Review test data, including documentation practices, and perform review functions in LIMS and other computerized systems
Use sophisticated laboratory instrumentation and computer systems to collect and record data
Participate in validations and transfers
Perform chemical assays requiring detailed analytical skills and understanding of chemistry principles
Complete testing, including special project/protocol testing, to meet project schedules
Lead investigations into atypical or out-of-specification/out-of-trend results, applying analytical skills to drive sound scientific conclusions

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Research Scientist I

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

Location

United States , Round Lake

Salary:

96000.00 - 132000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Degree or equivalent experience in a relevant scientific field such as chemistry or pharmaceutical sciences (BS level with 5+ years, MS level with 3+ years, or PhD level with research experience or equivalent)
Hands-on experience with analytical instrumentation including HPLC, pH measurement, UV, and GC/LC-MS
Background in analytical method development, validation, and transfer
Understanding of ICH and USP guidelines and cGxP practices
Experience working in a regulated laboratory environment with strong technical problem-solving abilities
Ability to learn quickly and apply critical thinking to solve analytical challenges
Skill in crafting experiments and interpreting data, along with the ability to thoughtfully review peers’ work
Strong ability to express ideas clearly in writing and speaking, with careful attention to detail
Solid laboratory, technical, writing, and computer skills
Ability to coordinate and communicate complex information effectively with peers and managers

Job Responsibility

Conduct critical chemical and physical analyses on finished product R&D stability samples
May also support testing of raw materials, initial, in-process, and final product samples from manufacturing facilities or other R&D initiatives
Act as a study director for studies, independently evaluating results and their impact
Provide training and supervision to junior members within the laboratory, offering advice and assistance on outstanding problems
Review test data, including documentation practices, and perform review functions in LIMS and other computerized systems
Use sophisticated laboratory instrumentation and computer systems to collect and record data
Participate in validations and transfers
Perform chemical assays requiring detailed analytical skills and understanding of chemistry principles
Complete testing, including special project/protocol testing, to meet project schedules
Lead investigations into atypical or out-of-specification/out-of-trend results, applying analytical skills to drive sound scientific conclusions

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Research Scientist I

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

Location

United States , Round Lake

Salary:

96000.00 - 132000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Degree or equivalent experience in a relevant scientific field such as chemistry or pharmaceutical sciences (BS level with 5+ years, MS level with 3+ years, or PhD level with research experience or equivalent)
Hands-on experience with analytical instrumentation including HPLC, pH measurement, UV, and GC/LC-MS
Background in analytical method development, validation, and transfer
Understanding of ICH and USP guidelines and cGxP practices
Experience working in a regulated laboratory environment with strong technical problem-solving abilities
Ability to learn quickly and apply critical thinking to solve analytical challenges
Skill in crafting experiments and interpreting data, along with the ability to thoughtfully review peers’ work
Strong ability to express ideas clearly in writing and speaking, with careful attention to detail
Solid laboratory, technical, writing, and computer skills
Ability to coordinate and communicate complex information effectively with peers and managers

Job Responsibility

Conduct critical chemical and physical analyses on finished product R&D stability samples
May also support testing of raw materials, initial, in-process, and final product samples from manufacturing facilities or other R&D initiatives
Act as a study director for studies, independently evaluating results and their impact
Provide training and supervision to junior members within the laboratory, offering advice and assistance on outstanding problems
Review test data, including documentation practices, and perform review functions in LIMS and other computerized systems
Use sophisticated laboratory instrumentation and computer systems to collect and record data
Participate in validations and transfers
Perform chemical assays requiring detailed analytical skills and understanding of chemistry principles
Complete testing, including special project/protocol testing, to meet project schedules
Lead investigations into atypical or out-of-specification/out-of-trend results, applying analytical skills to drive sound scientific conclusions

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts

Fulltime

Associate Scientist II

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

Location

United States , Round Lake

Salary:

80000.00 - 120000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor’s degree or equivalent experience in a relevant scientific field (e.g., chemistry, pharmaceutical sciences) with at least 2+ years of proven experience
Experience working with analytical chemistry instruments such as HPLC, pH meters, UV spectroscopy, titrations, particle analysis, TOC, flame photometry, and sample extraction techniques
Proficiency in a regulated environment and strong technical problem-solving skills
Excellent oral and written communication skills, strong analytical abilities, and keen attention to detail
Experience with Electronic Lab Notebooks and pharmaceutical GMP laboratories is preferred
Experience with Empower software is advantageous
Ability to manage multiple tasks concurrently and efficiently
Strong laboratory/technical, writing, and computer skills
Ability to effectively coordinate and communicate complex information with managers and peers

Job Responsibility

Conduct critical chemical and physical analyses on finished product R&D stability samples, and support testing of raw materials and other R&D initiatives
Act as a study director for studies, independently evaluating results and determining their impact
Provide training and supervision to junior members within the laboratory
Review test data meticulously, perform documentation reviews in LIMS and other computerized systems
Apply sophisticated laboratory instrumentation and computer systems for data collection and recording
Participate in validations and transfers, ensuring compliance with regulatory standards
Perform detailed chemical assays
Complete all testing, including special project/protocol testing, in a timely manner
Maintain data integrity and ensure compliance with company SOPs, FDA regulations, and other quality standards
Collaborate with various departments to solve problems, boost efficiency, improve quality, and provide outstanding product support

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Associate Scientist II

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

Location

United States , Round Lake

Salary:

80000.00 - 120000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor’s degree or equivalent experience in a relevant scientific field (e.g., chemistry, pharmaceutical sciences) with at least 2+ years of proven experience
Experience working with analytical chemistry instruments such as HPLC, pH meters, UV spectroscopy, titrations, particle analysis, TOC, flame photometry, and sample extraction techniques
Proficiency in a regulated environment and strong technical problem-solving skills
Excellent oral and written communication skills, strong analytical abilities, and keen attention to detail
Experience with Electronic Lab Notebooks and pharmaceutical GMP laboratories is preferred
Experience with Empower software is advantageous
Ability to manage multiple tasks concurrently and efficiently
Strong laboratory/technical, writing, and computer skills
Ability to effectively coordinate and communicate complex information with managers and peers

Job Responsibility

Conduct critical chemical and physical analyses on finished product R&D stability samples, and support testing of raw materials and other R&D initiatives
Act as a study director for studies, independently evaluating results and determining their impact
Provide training and supervision to junior members within the laboratory
Review test data meticulously, perform documentation reviews in LIMS and other computerized systems
Apply sophisticated laboratory instrumentation and computer systems for data collection and recording
Participate in validations and transfers, ensuring compliance with regulatory standards
Perform detailed chemical assays
Complete all testing, including special project/protocol testing, in a timely manner
Maintain data integrity and ensure compliance with company SOPs, FDA regulations, and other quality standards
Collaborate with various departments to solve problems, boost efficiency, improve quality, and provide outstanding product support

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

R&D Samples Coordinator

Baxter

Location:
Malta , Marsa

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
February 17, 2026

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