Research Associate II Job at Baxter (Ahmedabad)

Research Associate II

The Advanced Cell Engineering (ACE) Hub in the Cell Therapy department at Genent...

Location

United States , St. Joseph

Salary:

Not provided

College of Saint Benedict and Saint Johnâ€™s University

Expiration Date

July 14, 2026

Requirements

A self-motivated candidate with MS + 3 years industry experience, or PhD in Molecular Biology, Cell Biology, Genetics, or a related discipline
Qualified candidates must have demonstrable strong mammalian cell culture techniques and ability to generate high-quality data
Candidates must have strong hands-on proficiency in molecular and cell biology methodologies including PCR, lentivirus/piggyBac, transfection, CRISPR engineering and flow cytometry (FACS)
Skilled in processing and analyzing data from molecular and cellular assays using softwares (e.g., GraphPad Prism, FlowJo)
Excellent written and verbal communication skills, and able to generate high quality data and present at team meetings
Highly organized with a proven ability to multi-task and execute deliverables across a diverse array of projects
Strong troubleshooting capabilities with a proactive mindset and a strong eagerness to learn new technical skills
Collaborative and team-oriented
Ready to start ASAP

Job Responsibility

Generate engineered cells (including cancer cell lines, iPSCs, and primary cells) using stable integration (both lentivirus and piggybac) and CRISPR gene editing
Transfection/ gene editing optimization
Troubleshoot cell engineering protocols
Characterize engineered cells using genomics and molecular assays
Follow and establish SOPs, maintain and quality check cell lines in culture

Fulltime

Research Associate II

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

Location

Malta , Marsa

Salary:

24000.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

A-Levels in Chemistry/Biology or other science-based subjects
Flexible and ability to shift gears between projects comfortably
Self-motivated, resourceful, and flexible. A self-starter is imperative
Good team player, but demonstrates autonomy and leadership
Strong interpersonal communication skills and ability to communicate effectively with internal and external customers
Fluent in English

Job Responsibility

Support/manage lifecycle and operational activities for the Clinical Nutrition Solutions On-Market team, such as routine supplier notice of changes (SNCs), change control records, product code obsolescence and product label review activities in addition to general technical administrative tasks
Support/manage market enhancements and operational improvements, in addition to improvement activities associated with the design, manufacturing and control of Nutrition products
Support the metrics system to track the progress of operational activities and critical KPIs
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

Fulltime

Research Associate II

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

Location

Malta , Marsa

Salary:

24000.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

Relevant technical discipline, preferably a degree in Chemistry/Biology/Pharmaceutics or in the absence of a degree relevant work experience will be considered
Good knowledge of the below areas will be considered an asset: Statistical Analysis and/or Lean/Six Sigma tools
International/regional/national regulations and standards
Self-motivated, resourceful, and flexible
Strong interpersonal communication skills and ability to communicate effectively with internal and external customers
Strong human relation skills for group leadership, individual leadership, and project management
Ability to manage and facilitate cross-function/division teams
Strong quantitative and qualitative assessment skills and critical thinking skills in support of analysing and solving complex problems through innovative thought and experience
Ability to design and implement projects/studies outside area of expertise
Demonstrates flexibility and ability to shift gears between projects comfortably

Job Responsibility

Support lifecycle and operational activities for the Clinical Nutrition Solutions On-Market team, such as, supplier notice of changes (SNCs), change control records, in addition to general technical administrative tasks
Support the metrics system to track the progress of operational activities and critical KPIs
Adhere to the Quality Systems, understand and apply applicable corporate, divisional and departmental procedures as required
Under minimal supervision, organize, plan and execute product changes in compliance with international regulations and quality standards
coordinate and set up cross-functional team meetings to ensure change execution, problem-solving and decision making
Under minimal supervision, plan and manage project(s) that span multiple disciplines with team, cross functions and regions

What we offer

Support for Parents
Continuing Education/Professional Development
Employee Health & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
competitive benefits
discretionary bonuses
long-term incentive

Fulltime

Research Associate II

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

Location

Malta , Marsa

Salary:

24000.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

A-Levels in Chemistry/Biology or other science-based subjects
Demonstrates flexibility and ability to shift gears between projects comfortably
Self-motivated, resourceful, and flexible
Good team player, but demonstrates autonomy and leadership
Strong interpersonal communication skills and ability to communicate effectively with internal and external customers
Fluent in English

Job Responsibility

Support/manage lifecycle and operational activities for the Clinical Nutrition Solutions On-Market team, such as routine supplier notice of changes (SNCs), change control records, product code obsolescence and product label review activities in addition to general technical administrative tasks
Support/manage market enhancements and operational improvements, in addition to improvement activities associated with the design, manufacturing and control of Nutrition products
Support the metrics system to track the progress of operational activities and critical KPIs
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

Fulltime

Research Associate II

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

Location

Malta , Marsa

Salary:

24000.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

Relevant technical discipline, preferably a degree in Chemistry/Biology/Pharmaceutics or in the absence of a degree relevant work experience will be considered
Good knowledge of the below areas will be considered an asset: Statistical Analysis and/or Lean/Six Sigma tools
International/regional/national regulations and standards
Self-motivated, resourceful, and flexible
Strong interpersonal communication skills and ability to communicate effectively with internal and external customers
Strong human relation skills for group leadership, individual leadership, and project management
Ability to manage and facilitate cross-function/division teams
Strong quantitative and qualitative assessment skills and critical thinking skills
Ability to design and implement projects/studies outside area of expertise
Demonstrates flexibility and ability to shift gears between projects comfortably

Job Responsibility

Support lifecycle and operational activities for the Clinical Nutrition Solutions On-Market team, such as supplier notice of changes (SNCs), change control records, in addition to general technical administrative tasks
Support the metrics system to track the progress of operational activities and critical KPIs
Adhere to the Quality Systems, understand and apply applicable corporate, divisional and departmental procedures as required
Under minimal supervision, organize, plan and execute product changes in compliance with international regulations and quality standards
coordinate and set up cross-functional team meetings to ensure change execution, problem-solving and decision making
Under minimal supervision, plan and manage project(s) that span multiple disciplines with team, cross functions and regions

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

Research Associate II

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

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
Responsible for ensuring the availability of required licenses and materials (raw material, packaging materials) in laboratory

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

Research Associate II / Senior Research Associate

We are seeking a proactive, enthusiastic candidate at the Research Associate 2 o...

Location

United States , Frederick

Salary:

89000.00 - 105000.00 USD / Year

Theradaptive

Expiration Date

Until further notice

Requirements

Bachelor's degree in Bioengineering, Biomedical Engineering, Chemistry, Biology, or a related field
Strong scientific fundamentals, analytical background, and mathematical reasoning capability
Experience designing, organizing, and executing multiple experiments and handling multiple testing activities simultaneously
Experience with bioassays, immunoassays, protein binding assays
Experience with Chromatography and Separation (e.g. SDS-PAGE) techniques
3-7 years of work experience in an industrial setting is preferred
Experience with operating under controlled procedures and documentation such as GLP or GMP is desirable
Experience with standard data analysis tools (Excel, GraphPad Prism)
Proficiency in MS Office (Word, PowerPoint, Excel)
Ability to work in a laboratory and office setting full time

Job Responsibility

Work closely with scientists and engineers to advance R&D and product development projects
Execute cell culture activities including aseptic technique, passaging, inoculations, cell differentiation, and data analysis
Execute biochemical analyses using separation techniques such as column chromatography, SDS-PAGE/CE-SDS, and RP-HPLC
Conduct a wide variety of assays, including bioassays, protein binding assays, and immunoassays
Participate in maintaining capabilities, laboratories, equipment, and supplies
Understand and adhere to laboratory safety precautions and proper use of personal protective equipment
Employ self-reliance in drawing experiment conclusions and interpreting results. Take initiative to verify the accuracy and validity of data
correct any errors
Communicate project status, roadblocks and results to supervisors and managers

Fulltime

Clinical Research Associate II / Senior Clinical Research Associate Large Pharma

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

Germany , Frankfurt

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Master or Bachelor's degree in a scientific or healthcare-related field
Minimum of 2 years of experience as a Clinical Research Associate
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Strong organizational and communication skills, with attention to detail
Ability to work independently and collaboratively in a fast-paced environment
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
Excellent communication skills in German and English
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

Job Responsibility

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations

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

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Research Associate II

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