Research Associate I, R&D Complex Product Development Job at Baxter (Ahmedabad)

Research Associate I, R&D Complex Product Development

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

Masters (Pharmacy, or equivalent discipline) with 6 to 10 years of experience
PhD (biophysics, biochemistry or equivalent discipline) with 0 to 5 years of experience
Competency in the acquisition, processing and data analysis by SEC-UV-MALS and light scattering/diffraction/obscuration techniques for analysis of peptides and iron colloidal products for regulatory submissions is mandatory
Basic understanding of working principles of biophysical & spectroscopic methods
Knowledge of pharmacopoeia, ICH Guidelines
Experience in the operation, calibration and preventive maintenance of NMR and other instruments
Knowledge of good laboratory practices and good documentation practices
Communication skills
Presentation skills
Analytical skills

Job Responsibility

To perform advanced characterization of complex injectable drugs
To manage outsourced studies at CROs, academic institutes & other external facilities
To demonstrate subject matter expertise and help overcome technical challenges in product development
To provide necessary assistance for various procurement activities
To complete the planned work in the stipulated time frame
To keep track of each activity related to product analysis and development activities
To carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle
To verify the shelf life of the chemical or reagent before performing analysis
To follow Good Documentation Practices & Good Laboratory Practices
To investigate if any deviation / abnormalities are observed

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Research Associate I, 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

Masters (Pharmacy, or equivalent discipline) with 6 to 10 years of experience, or, PhD (biophysics, biochemistry or equivalent discipline) with 0 to 5 years of experience in SEC-UV-MALS and related methods encompassing liquid chromatography, light scattering, diffraction and light obscuration
Competency in the acquisition, processing and data analysis by SEC-UV-MALS and light scattering/diffraction/obscuration techniques for analysis of peptides and iron colloidal products for regulatory submissions is mandatory
Basic understanding of working principles of biophysical & spectroscopic methods, like CD, FTIR, UV, EPR, Mossbauer, and fluorescence spectroscopy, particle XRD, microscopy methods (AFM & EM) & related orthogonal methods to assess structural properties of proteins and iron colloids
Proficiency in literature search through publication and patent databases, repositories (e.g. Pubmed), scientific webinars by regulatory agencies, etc, to remain updated on advanced characterization methods and recent scientific developments
Knowledge of pharmacopoeia, ICH Guidelines and means to implement them for product development
Experience in the operation, calibration and preventive maintenance of NMR and other instruments to ensure continued usage
Trouble shooting of various problems obtain during the product development
Knowledge of good laboratory practices and good documentation practices
Communication skills
Presentation skills

Job Responsibility

To perform advanced characterization of complex injectable drugs, including iron formulations, proteins & peptides, oligonucleotides, carbohydrates & other biomolecular APIs and various impurities in lyophilized, liquid, emulsions & other formulations for regulatory submission following GLP norms
To manage outsourced studies at CROs, academic institutes & other external facilities, from study design, execution, analysis and report preparation
To demonstrate subject matter expertise and help overcome technical challenges in product development, by liaising with formulation and other cross-functional teams as a Subject Matter Expertise (SME)
To understand the project with guidance of Sub-department Manager and follow their instructions
To provide necessary assistance for various procurement activities, review quotations, engage suppliers to procure required goods & services in a timebound manner
To complete the planned work in the stipulated time frame, inform the Sub-department Manager if any deviation or issues are observed
To keep track of each activity related to product analysis and development activities
To carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle and current pharmacopoeia
To verify the shelf life of the chemical or reagent before performing analysis of the material or product
To follow Good Documentation Practices & Good Laboratory Practices, maintain lab notebooks & other records appropriately

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

Research Associate I - 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

Masters (Pharmacy, or equivalent discipline) with 6 to 10 years of experience, or, PhD (biophysics, biochemistry or equivalent discipline) with 0 to 5 years of experience with spectroscopic and biophysical methods, including CD, FTIR, fluorescence spectroscopy
Competency in the acquisition, processing and data analysis by CD, FTIR, and fluorescence spectroscopy for analysis of proteins and peptides for regulatory submissions is mandatory
Expertise in computational chemistry, molecular modeling and statistical methods are beneficial attributes
Basic understanding of working principles of liquid chromatographic methods, dynamic light scattering, AF4-MALS, SV-AUC, & related orthogonal methods to assess protein higher order structures
Proficiency in literature search through publication and patent databases, repositories (e.g. Pubmed), scientific webinars by regulatory agencies, etc, to remain updated on advanced characterization methods and recent scientific developments
Knowledge of pharmacopoeia, ICH Guidelines and means to implement them for product development
Experience in the operation, calibration and preventive maintenance of NMR and other instruments to ensure continued usage
Trouble shooting of various problems obtain during the product development
Knowledge of good laboratory practices and good documentation practices
Communication skills

Job Responsibility

To perform advanced characterization of complex injectable drugs, including proteins & peptides, oligonucleotides, iron formulations, carbohydrates & other biomolecular APIs and various impurities in lyophilized, liquid, emulsions & other formulations for regulatory submission following GLP norms
To manage outsourced studies at CROs, academic institutes & other external facilities, from study design, execution, analysis and report preparation
Traveling to external facilities, as and when required, is a mandatory requirement for this position
To demonstrate subject matter expertise and help overcome technical challenges in product development, by liaising with formulation and other cross-functional teams as a Subject Matter Expertise (SME)
To understand the project with guidance of Sub-department Manager and follow their instructions
To provide necessary assistance for various procurement activities, review quotations, engage suppliers to procure required goods & services in a timebound manner
To complete the planned work in the stipulated time frame, inform the Sub-department Manager if any deviation or issues are observed
To keep track of each activity related to product analysis and development activities
To carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle and current pharmacopoeia
Data recording in ELN and sign off must be completed on time

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 I - 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

Masters (Pharmacy, or equivalent discipline) with 6 to 10 years of experience, or, PhD (biophysics, biochemistry or equivalent discipline) with 0 to 5 years of experience with spectroscopic and biophysical methods, including CD, FTIR, fluorescence spectroscopy
Competency in the acquisition, processing and data analysis by CD, FTIR, and fluorescence spectroscopy for analysis of proteins and peptides for regulatory submissions is mandatory
Expertise in computational chemistry, molecular modeling and statistical methods are beneficial attributes
Basic understanding of working principles of liquid chromatographic methods, dynamic light scattering, AF4-MALS, SV-AUC, & related orthogonal methods to assess protein higher order structures
Proficiency in literature search through publication and patent databases, repositories (e.g. Pubmed), scientific webinars by regulatory agencies, etc, to remain updated on advanced characterization methods and recent scientific developments
Knowledge of pharmacopoeia, ICH Guidelines and means to implement them for product development
Experience in the operation, calibration and preventive maintenance of NMR and other instruments to ensure continued usage
Trouble shooting of various problems obtain during the product development
Knowledge of good laboratory practices and good documentation practices

Job Responsibility

To perform advanced characterization of complex injectable drugs, including proteins & peptides, oligonucleotides, iron formulations, carbohydrates & other biomolecular APIs and various impurities in lyophilized, liquid, emulsions & other formulations for regulatory submission following GLP norms
To manage outsourced studies at CROs, academic institutes & other external facilities, from study design, execution, analysis and report preparation
To demonstrate subject matter expertise and help overcome technical challenges in product development, by liaising with formulation and other cross-functional teams as a Subject Matter Expertise (SME)
To understand the project with guidance of Sub-department Manager and follow their instructions
To provide necessary assistance for various procurement activities, review quotations, engage suppliers to procure required goods & services in a timebound manner
To complete the planned work in the stipulated time frame, inform the Sub-department Manager if any deviation or issues are observed
To keep track of each activity related to product analysis and development activities
To carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle and current pharmacopoeia
To verify the shelf life of the chemical or reagent before performing analysis of the material or product
To follow Good Documentation Practices & Good Laboratory Practices, maintain lab notebooks & other records appropriately

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 Director, R&D Product Development, Wellbeing Collective

The Americas & EU Technical Leader, Wellbeing International R&D is responsible f...

Location

United States , Trumbull

Salary:

146200.00 - 219400.00 USD / Year

Unilever

Expiration Date

Until further notice

Requirements

Strong R&D TPL experience (senior-level)
Deep expertise in gummy formulation
Based in China with Mandarin fluency to speak to the manufacturers in China
Experience working on TPL projects beyond China, ideally with a regional or global lens
Bachelor's degree required in science or engineering
BS with 12+ years, Masters with 10+ years, or PhD with 7+ years’ experience in formulation development or technology development of which at least 3 years as Technical Project Lead
Excellent understanding of Product development Principles – formulation development for consumer-friendly ingestible dosage forms such as Powders, Gummies/capsules, material understanding, product scale up, product costing, ingredient sources and GMP
Experience working with cross functional teams across geographies
Ability to lead more complex portfolio of innovation/quality & Value Improvement Project (VIP) projects including multiple brands/regions/technologies
Technical leadership by exhibiting and fostering initiative, motivation, judgment, flexibility, and breadth

Job Responsibility

Drive best-in-class product development to support growth ambitions of the Wellbeing Collective international business
Lead innovation and new market entry across Canada, Latin America, the UK, and Europe for WBC brands
Own end-to-end technical delivery for innovation and market expansion
Partner closely with cross-functional teams (Marketing, Supply Chain, Procurement, SERs, Nutrition Science, Quality, and Regulatory) to deliver projects on time and in compliance
Build and deliver a robust innovation pipeline in partnership with the global marketing team
Drive cost savings and strategic business continuity initiatives
Lead and develop a team of formulators and process engineers
Lead end-to-end product development and commercialization
Design cost-effective, sensorially superior, and scalable formulations
Own technical delivery on project teams

What we offer

Health insurance (including prescription drug, dental, and vision coverage)
Retirement savings benefits
Life insurance and disability benefits
Parental leave
Sick leave
Paid vacation and holidays
Access to numerous voluntary benefits
Bonus eligible
Long-Term Incentive (LTI) eligible

Fulltime

Senior/Principal R&D Systems Engineer - Component and Material Evaluation

We are seeking an R&D Systems Engineer for the Component and Material Evaluation...

Location

United States , Albuquerque

Salary:

117500.00 - 235700.00 USD / Year

Sandia National Laboratories

Expiration Date

Until further notice

Requirements

A bachelor's degree in a relevant discipline and five (5) years of directly relevant experience, or an equivalent combination of directly relevant education and engineering or scientific experience that demonstrates the knowledge, skills, and ability to perform independent research and development
Ability to obtain and maintain a DOE Q Clearance and Sigma 15 access, which will require random polygraphs

Job Responsibility

Plan and manage the execution of engineering programs for Sandia's customers and sponsors
Serve as the primary representative to customers and partners for ND modernization programs, negotiating, managing, and delivering all component evaluation scope for several technology families
Establish strong relationships with key influencers and collaborate with cross-functional teams, including systems and component engineering teams, our Science and Technology (S&T) community, independent technical assessment partners, and production agencies
Identify defects and aging trends, understand performance margins, and make predictive assessments of weapon components and their materials through comprehensive component evaluation activities
Chair Stockpile Finding Investigations (SFIs) as a System Evaluation Engineer (SEE) to determine the root cause of anomalies discovered during component evaluations, assess their impact on the safety, security, and reliability of the stockpile, and guide discussions to ensure thorough understanding and resolution of issues
Engage in lifecycle management of evaluated components, focusing on key phases such as design, testing, and production
Identify and manage risks associated with component evaluations, employing strategies for risk assessment and mitigation
Document findings and recommendations, preparing reports that communicate complex technical information clearly and effectively to stakeholders

What we offer

Challenging work with amazing impact that contributes to security, peace, and freedom worldwide
Extraordinary co-workers
Some of the best tools, equipment, and research facilities in the world
Career advancement and enrichment opportunities
Flexible work arrangements for many positions include 9/80 (work 80 hours every two weeks, with every other Friday off) and 4/10 (work 4 ten-hour days each week) compressed workweeks, part-time work, and telecommuting (a mix of onsite work and working from home)
Generous vacation, strong medical and other benefits, competitive 401k, learning opportunities, relocation assistance and amenities aimed at creating a solid work/life balance

Fulltime

Pentest Product Associate

We’re looking for a Application Security Product Analyst to join our Product tea...

Location

Israel , Tel Aviv

Salary:

Not provided

Wiz

Expiration Date

Until further notice

Requirements

1+ years of hands-on experience in AppSec or penetration testing, including proficiency with enterprise tools like Burp Suite, OWASP ZAP, or Acunetix
Solid knowledge of networking concepts, the OSI model, and cloud infrastructure (AWS, Azure, or GCP)
Hands-on experience with Linux, Windows, Docker, Kubernetes, and a strong command of web protocols (HTTP/S, REST, GraphQL) and auth mechanisms (OAuth, SAML)
Proficiency in scripting languages such as Python, Bash, or Go to automate security tasks and interact directly with the codebase
An analytical mindset with the ability to diagnose complex logs and scans to distinguish between tool failures, configuration issues, and valid security findings
Self-motivated with the ability to work collaboratively and communicate high-stakes security concepts effectively across teams
Applicants must have the legal right to work in the country where the position is based, without the need for visa sponsorship.

Job Responsibility

Engineer Detection & Attack Logic: Develop advanced detection algorithms to classify cloud technologies while fine-tuning the attack policies that define how our agents identify and exploit vulnerabilities
Validate Complex Findings: Analyze cloud services, APIs, and log payloads to review complex attack paths, reducing false positives and ensuring compliance with industry standards
Research Novel Threats: Stay at the forefront of novel attack vectors and emerging cloud/API threats, translating new techniques into executable behaviors for the Wiz DAST engine
Drive Product Evolution: Collaborate directly with Research, Backend, and R&D teams to turn operational insights into feature requests, positioning Wiz as the market leader in vulnerability management

Fulltime

Associate Product Engineer

Product Engineering 2 job supports the merchandising team in the development, va...

Location

Mexico , Ensenada

Salary:

Not provided

Hunter Douglas

Expiration Date

Until further notice

Requirements

Solid knowledge of mechanical, industrial, wood, and electrical engineering principles
Demonstrated experience with extrusion, metal die casting, and injection molding manufacturing processes
Proficient in standard business and engineering software, including Microsoft Word, Excel, PowerPoint, and CAD tools
Excellent written and verbal communication skills, including the ability to prepare technical documentation, business justifications, and budget proposals
Strong interpersonal skills with the ability to build effective working relationships across all levels of the organization
Ability to read and interpret mechanical drawings and electrical schematics
Proven ability to analyze and synthesize complex information from multiple sources
Bachelor’s degree in Mechanical Engineering, Electrical Engineering, or a related engineering discipline required
Prior experience in engineering project management is strongly preferred
English 80%

Job Responsibility

Work on multiple concurrent engineering projects, contributing technical expertise to support the development, validation, and launch of new product lines and line extensions, including components, hardware, and fabrication tooling
Plan and coordinate engineering activities in alignment with divisional priorities, collaborating with cross-functional product development teams to leverage organizational expertise and ensure successful project execution for component design, materials R&D, and improvements to fabrication tools, methods, and processes
Support prototype builds and trial runs to evaluate product performance, manufacturability, and cost feasibility
Coordinate product testing activities in partnership with the research and development team. Analyze, interpret, and communicate test results from internal and external laboratories, translating technical data into actionable insights for cross-functional stakeholders
Develop and maintain product SOPs, specifications, and configuration guidelines to support system readiness, order entry, and production, including charts, components, BOMs, and system prompts
Create and maintain engineering documentation, including exploded views, part drawings, specification sheets, and quick reference guides for internal teams, customer care, and installers
Configure, validate, and maintain products within e-PIC, and Polaris, including BOM setup, usage definitions, front-end configuration, and production screen validation
Develop and execute validation and testing plans for new products, components, and materials, including pre-production testing, DV1/LV1, PPAP coordination, and first article or pilot approvals
Coordinate product lifecycle activities, including phase-in/phase-out of components, forecasting support, and material planning in collaboration with cross-functional teams
Build and maintain strong working relationships across departments to promote collaboration, alignment, and effective execution of merchandising and business objectives

What we offer

competitive and robust total compensation and benefit packages

Fulltime

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Research Associate I, R&D Complex Product Development

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Research Associate I, R&D Complex Product Development

Research Associate I, R&D Complex Product Development

Research Associate I, R&D Complex Product Development

Research Associate I - R&D, Complex Product Development

Research Associate I - R&D, Complex Product Development

Associate Director, R&D Product Development, Wellbeing Collective

Senior/Principal R&D Systems Engineer - Component and Material Evaluation

Pentest Product Associate

Associate Product Engineer

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