Associate Scientist I Job at Baxter (Marsa)

Associate Scientist I

Support the execution of product changes in compliance with international regula...

Location

Malta , Marsa

Salary:

27200.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

Qualifications in a Scientific discipline (Eg. Chemistry/Biology/Pharmaceutics/Chemical Engineering etc.): Higher Diploma (EQF Level 5) with minimum 5 years experience or Bachelor's Degree (EQF Level 6) with minimum 2 years experience or Master’s Degree (EQF Level 7) with no minimum experience
Relevant Experience - Pharmaceutical Industry or other regulated industry
Self-motivated, resourceful, and flexible
A self-starter is imperative
Strong interpersonal communication skills and ability to communicate effectively with internal and external customers
Skilled at presentations within the technical community
Technical writing proficiency to author internal reports and scientific papers
Strong human relation skills for individual leadership and project management
Ability to lead, manage and facilitate cross-function/division teams
Strong quantitative and qualitative assessment skills and critical thinking skills in support of analyzing and solving complex problems through innovative thought and experience

Job Responsibility

Manage routine and support complex supplier notice of changes (SNCs) and change control records
Support/Independently plan, execute, and manage project(s) that span multiple disciplines with team, cross functions and regions
Applying a solid understanding of theories/practices including those from other disciplines outside the primary area of expertise
Support market enhancements and operational improvements
Participate in development and improvement activities associated with the design, manufacturing and control of Nutrition products
Prepare technical protocols and reports
Adhere to the Quality Systems, understand and apply applicable corporate, divisional and departmental procedures as required

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

Associate Scientist I

Support the execution of product changes in compliance with international regula...

Location

Malta , Marsa

Salary:

27200.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

Qualifications in a Scientific discipline (Eg. Chemistry/Biology/Pharmaceutics/Chemical Engineering etc.): Higher Diploma (EQF Level 5) with minimum 5 years experience or Bachelor's Degree (EQF Level 6) with minimum 2 years experience or Master’s Degree (EQF Level 7) with no minimum experience
Relevant Experience - Pharmaceutical Industry or other regulated industry
Self-motivated, resourceful, and flexible
A self-starter is imperative
Strong interpersonal communication skills and ability to communicate effectively with internal and external customers
Skilled at presentations within the technical community
Technical writing proficiency to author internal reports and scientific papers
Strong human relation skills for individual leadership and project management
Ability to lead, manage and facilitate cross-function/division teams
Strong quantitative and qualitative assessment skills and critical thinking skills in support of analyzing and solving complex problems through innovative thought and experience

Job Responsibility

Manage routine and support complex supplier notice of changes (SNCs) and change control records
Support/Independently plan, execute, and manage project(s) that span multiple disciplines with team, cross functions and regions
Applying a solid understanding of theories/practices including those from other disciplines outside the primary area of expertise
Support market enhancements and operational improvements
Participate in development and improvement activities associated with the design, manufacturing and control of Nutrition products
Prepare technical protocols and reports
Adhere to the Quality Systems, understand and apply applicable corporate, divisional and departmental procedures as required

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

Qc Associate Scientist I

We are seeking a proactive and detail-oriented QC Associate Scientist to join ou...

Location

United Kingdom , Basingstoke

Salary:

14.00 - 14.14 GBP / Hour

Randstad

Expiration Date

August 24, 2026

Requirements

Qualified to a Level 6 equivalent (Degree) in Microbiology or a related biological science subject
Practical experience working within a microbiology laboratory environment
Proficiency in basic laboratory techniques (streaking, pouring plates, pipetting) and good numerical skills
Ability to follow strict SOPs and methods precisely, strong organization skills, a proactive attitude, and a commitment to health and safety standards

Job Responsibility

Carry out microbiological Quality Control testing in accordance with standard test specifications and methods
Perform core laboratory tasks including media preparation, plating out, streaking, swabbing, pipetting, and utilizing autoclaves
Record test results accurately within company management software (SAP) and maintain precise training records
Complete Out of Specification (OOS) reports and assist with laboratory investigations
Maintain laboratory standards through equipment checks, cleaning, waste management, and restocking consumables
Participate in daily team meetings and contribute to continuous improvement and lean processes

Fulltime

New

Clinical Scientist Associate Director – Late Development, Oncology

Join Amgen's Mission of Serving Patients. At Amgen, if you feel like you're part...

Location

Portugal , Lisbon

Salary:

79656.90 - 107771.10 EUR / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 3 years of life sciences/healthcare experience
Master's degree and 5 years of life sciences/healthcare experience
Bachelor's degree and 7 years of life sciences/healthcare experience

Job Responsibility

Support set up and execution of late phase clinical trials with a focus on data quality
Assist in authoring clinical protocols, Investigators Brochures and other regulatory documents ensuring consistency and clarity
Provide input into and implementation of data management plan, CRF design, and data review oversight
Support review, analysis, and presentation preparation of clinical trial data for internal decision making, external interactions, and regulatory submission
Assists the management of collaborators, consultants, and/or Clinical Research Organizations in completion of key projects
Anticipate and actively manage problems across a broad spectrum of cross-functional teams
Work cross-functionally within teams to ensure clinical strategy is translated into the development of the study concept document, study protocol and related documents
Support appropriate training, recruitment, and development requirements for matrix team resources

What we offer

Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
Discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models, including remote and hybrid work arrangements, where possible

Fulltime

New

Associate Scientist - II, R&D - SPO

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 Pharmaceutics or equivalent
Postgraduate with minimum 07 years of experience in pharmaceutical industry preferably in formulation development
Hands on experience in laboratory batch execution and drive the towards the expected result
Good communication skills for effective liaison and teamwork
Problem-solving skills, analytical skills and attention to detail
Excellent organizational skills and the ability to work on several tasks or projects concurrently
Presentation skills - for presenting ideas and findings to colleagues and customers
Ability to work well independently, with minimum supervision
Drive, enthusiasm and self-motivation
An aptitude for mathematics and statistics and highly developed IT and technical skill

Job Responsibility

Actively Support launch and sustenance of Baxter commercial products globally by following the Baxter Quality Management Systems
Assist in the management of the Baxter product design throughout the product lifecycle and maintenance of the product DHF, or similar product design governance documents for a particular product family
Identify and analyze design problems to achieve optimal solutions that satisfy cost and technical requirements
Formulate new, innovative approaches to solve technical problems on a consistent basis
Actively involve in commercialized product investigation, execute batches in laboratory, prepare report to support the investigation
Involve in compendial product change/proposal discussion, assess the proposed change impact on the product quality & patient safety
Provide support to analytical team by providing the required product solution/placebo solution samples
Execute batches in laboratory, assess the study outcome to support the compendial product change requirement
Ensure response to customer queries, agencies query, market compliance
Design and execute batches/experiments in laboratory, prepare report to support queries/market compliance

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

New

Associate Scientist - Oncology

Amgen Oncology Research is seeking an Associate Scientist who supports our T cel...

Location

United States , South San Francisco

Salary:

98299.10 - 132992.90 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Master's Degree
Bachelor's Degree and 2+ years of relevant experience
Associate's degree and 4 years of relevant experience
High school diploma / GED and 6 years of relevant experience

Job Responsibility

Support preclinical pipeline programs by performing assays and delivering scientific evidence of drug candidates in a timely manner
Operate and maintain standard lab equipment
Maintain organized laboratory notebooks and repositories
Interact closely with cross-functional team
Support publication and presentation at scientific conferences

What we offer

Comprehensive employee benefits package including Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
Discretionary annual bonus program
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Associate Scientist – In Vivo Pharmacology, Oncology

At Amgen, if you feel like you’re part of something bigger, it’s because you are...

Location

United States , South San Francisco

Salary:

98299.10 - 132992.90 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree and 2+ years of experience in in-vivo work with rodents
OR Bachelor’s degree and 4+ years of experience in in-vivo work with rodents
OR High school diploma / GED and 6 years of experience in in-vivo work with rodents

Job Responsibility

Carry out hands-on in vivo work in mice, including handling, tumor inoculation and measurement, dosing (oral, SC, IP, and IV), blood and tissue collection, and health monitoring
Perform necropsies and support ex vivo tissue activities, including dissection, processing, sample preparation, and experimental readouts
Perform in vitro work including multiparametric flow cytometry and molecular biology techniques associated with in vivo studies
Strong communication to support study execution, maintain accurate study records, and present results
Active participation and presentation at cross-departmental teams and meetings
Participate in dosing rotations, including occasional evening or weekend work

What we offer

health and welfare plans for staff and eligible dependents
financial plans with opportunities to save towards retirement or other goals
work/life balance
career development opportunities
Retirement and Savings Plan with generous company contributions
group medical, dental and vision coverage
life and disability insurance
flexible spending accounts
discretionary annual bonus program
stock-based long-term incentives

Fulltime

New

Associate Scientist - II, R&D - SPO

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Master's in Pharmaceutics or equivalent
Hands on experience in laboratory batch execution and drive the towards the expected result
Good communication skills for effective liaison and teamwork
Problem-solving skills, analytical skills and attention to detail
Excellent organizational skills and the ability to work on several tasks or projects concurrently
Presentation skills - for presenting ideas and findings to colleagues and customers
Ability to work well independently, with minimum supervision
Drive, enthusiasm and self-motivation
An aptitude for mathematics and statistics and highly developed IT and technical skill
Postgraduate with minimum 07 years of experience in pharmaceutical industry preferably in formulation development

Job Responsibility

Actively Support launch and sustenance of Baxter commercial products globally by following the Baxter Quality Management Systems
Assist in the management of the Baxter product design throughout the product lifecycle and maintenance of the product DHF, or similar product design governance documents for a particular product family
Identify and analyze design problems to achieve optimal solutions that satisfy cost and technical requirements
Formulate new, innovative approaches to solve technical problems on a consistent basis
Actively involve in commercialized product investigation, execute batches in laboratory, prepare report to support the investigation
Involve in compendial product change/proposal discussion, assess the proposed change impact on the product quality & patient safety
Provide support to analytical team by providing the required product solution/placebo solution samples
Execute batches in laboratory, assess the study outcome to support the compendial product change requirement
Ensure response to customer queries, agencies query, market compliance
Design and execute batches/experiments in laboratory, prepare report to support queries/market compliance

What we offer

Apoyo a las padres
Educación continua/ Desarrollo profesional
Salud de los empleados y Beneficios de bienestar
Tiempo libre pagado
2 días al año para ser voluntario

Fulltime

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Associate Scientist I

Job Description

Job Responsibility

Requirements

What we offer

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