Require Senior Specialist at Baxter @ Apply Now

Post : Sr. Specialist, Total Rewards, APAC

Job Description 
Compensation & Benefits Specialist APAC will provide support for the assessment, design and implementation of compensation and incentive programs and policies. Will be responsible for providing analytical support required for the administration of compensation plans and programs and day to day support to the Total Rewards CoE.

Depending on focus of role (CoE), incumbent may have the following responsibilities:
• Responsible for the execution of the global compensation & benefits strategy in the APAC region by supporting the Sr Mgr, Total Rewards in the design of regional/local solutions adapted to the business needs and local legal requirements, and consistent with our strategy
• Responsible for developing local benefits policies. Adequate understanding on general benefit programs is expected in order to support countries in design, development and implementation of benefits and ensure competitiveness through the on-going assessment of benefit programs
• Work with the APAC countries to implement consistent job evaluation framework. Prior knowledge of Mercer’s IPE methodology is a plus
• Provides day to day operational support to existing processes at the direction of Sr Manager, Total Rewards, APAC
• Implement use of process analysis and documentation methodologies, tools and standards
• Analyze compensation and incentive programs and policies. Participate in implementation activities.  Includes base pay programs, incentives, etc.
• Determine level, grades, market ranges, bonus and equity targets
• Ensure that processes exist to support the integrity of compensation-related data in Workday and other HRIT portfolio applications.
• Maintain documentation of global compensation plan information.
• Develop and maintain strong working partnerships with key stakeholders
• Leverage technology appropriately to improve service levels and efficiency
• Research and resolve issues/inquiries related to the plans, processes and tools involved in compensation.
• Support Annual Compensation Review (ACR), pay and step structure, location differentials (City Clusters), and other processes as necessary.
• Proactively monitor and make recommendations based on knowledge of industry standards, competitive landscape, benchmarking data, and service methodologies and mode

Candidate Profile
• 5+ years of C&B specialization 
• MBA degree in HR (Tier 1/2 only)
• Exposure to global HR operating environment a plus
• Prior experience with Workday is a plus
• Excellent Microsoft office – Excel and PPT skills desired
• Technology acumen
• Excellent English communication skills
• Analytical skills - Strong analytical skills using both qualitative and quantitative data.
• Experience with relevant analytical tools (strong focus on spreadsheet applications).
• Critical HR Competencies, including process management, analytical skills & decision-making, and cultural awareness & global application.
• Understanding of HR operating environment, including policies and procedures
• Technology orientation

Additional Information
Qualification : MBA degree
Experience : 5+
Location : Gurgaon
Industry Type : Pharma
Job Category : Human Resources
End Date : 20th May, 2019

Walk in Interview at Baxter @31.03.2019

Require Quality Surviellance at Baxter @ Apply Now

Post : Sr Exec, Quality Surviellance

Job Description
• Working on complaints in Baxter complaint management systems
• Preparation of APAC monthly metrics ( presentations)
• Working on preparation of Management review data for APAC
• Working with global team and APAC Mfg sites for top complaints reductions
• Working with APAC countries/ mfg sites  for NCR/ CAPA management
• Working in  Product Hold Management system and knowledge of JDE ( electronic system for inventory management and other transactions)
• Providing trainees to new hire on complaint management systems.

Requisites
• Project management skills
• Hands on experience on MS word( especially excel and power points)
• Knowledge of Quality Systems ( Holds, NCR, CAPA etc…)
• Good communication skills

Additional Information
Qualification : B.Pharm/M.Pharm
Location : Gurgaon, HR
Industry Type : Pharma
Functional Area : Quality
End Date : 10th April, 2019

Walk in Interview at Baxter : 24 Feb 2019

Regulatory Affairs Associate at Baxter@ Apply Now

Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-centre dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. Baxter’s employees worldwide are building upon the company’s rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care.

Post : Associate, RA Variations Support

Job Purpose
This role is responsible for providing regulatory support for on-market products.  Activities include change assessment, variation planning, creation of submission documentation, identification of local submission requirements, product/facility change management, process support, and participation in project sub-teams.

Key Responsibilities
• Review and provide regulatory impact assessments for changes
• Manage global submission deliverables for product variation submissions
• Responsible for working with other parts of the regulatory organization to achieve desired results.
• Execute global plans and regulatory submission deliverables for sustaining variations
• Utilize regulatory knowledge to prepare submission deliverables that will achieve desired results
• Ensure identified standards and content requirements are met for regulatory submissions
• Timely, actively support query responses
• Engage with Global Business Unit Regulatory teams and Regional Regulatory teams to ensure regulatory activities are in alignment with business requirements
• Interface and align with other regulatory affairs sub-functions to provide seamless regulatory support to the project sub-team(s).
• Maintain regulatory files in a format consistent with requirements
• Track of status and progress of regulatory documentation
• Review, edit and proofread regulatory documentation

Key skills and competencies
• Experience operating in a regulated environment
• Ability to operate in a matrixed environment and manage multiple activities, priorities and deadlines
• Exercise independent judgement
• Scientific knowledge and ability to discuss technical matters with cross-functional team members
• Knowledge of regulations and ability to communicate and apply
• Ability to identify compliance risks and escalate when necessary

Candidate Profile
• Bachelor’s Degree or country equivalent in related scientific discipline
• Higher degree/PhD will be an advantage
• RA experience
• Manager - Minimum of 7 years’ regulatory experience in RA or related fields
• Specialist - Minimum of 5 years’ regulatory experience in RA or related fields
• Sr. Associate - Minimum of 2 years’ regulatory experience in RA or related fields
• Associate – No regulatory experience required.
• Higher degree/PhD will be an advantage.
• Experience in an healthcare environment required

Additional Information
Experience : 2 - 7 years
Qualification : B.Sc, Ph.D
Location : Bangalore, KA
Industry Type : Pharma
Functional Area : Regulatory Affairs
End Date : 10th January, 2019

Require Research Associate at Baxter @ Apply Now Online

Post : Research Associate II

Job Description
• Plan and execute experimental designs following a forensic approach with limited guidance.
• Communicate experimental plans with alignment to strategic objectives, follow up with execution and summary to management and internal partners.
• Partner with colleagues in matters of subject expertise including microscopy, characterization and particulate matter.
• Devise new approaches to solve routine and non-routine problems using basic analytical chemistry and microscopy techniques.
• Operate, own, and maintain laboratory equipment and procedures.
• Maintain knowledge of relevant Quality System Regulations and safety requirements while building knowledge of other regulatory requirements related to R&D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities.

Candidate Profile
• Bachelor of Science degree with 2-4 years of GxP laboratory experience or advanced degree. Degree in physical science required.
• Writing and computer skills relevant to recording original data as well as creating protocols, reports, and presentations to communicate with partners and team members. The ability to energetically attack a problem and synthesize the results into a clear and logical summary in a timely manner is critical.
• Ability to learn and master new techniques and develop new methods where appropriate.
• Communication skills to build relationships across functional and geographical boundaries and present technical concepts to technical and non-technical teams.
• Personal responsibility and ownership of analysis and results.

Additional Information
Experience : 2-4 years
Qualification : B.Sc
Location : Bangalore, KA
Industry Type : Pharma
Functional Area : R&D
End Date : 30th December, 2018

Apply for Research Associate at Baxter @ Click here for more info

Baxter International Inc. develops, manufactures and markets products that save and sustain the lives of people with hemophilia, immune disorders, infectious diseases, kidney disease, trauma, and other chronic and acute medical conditions. As a global, diversified healthcare company, Baxter applies a unique combination of expertise in medical devices, pharmaceuticals and biotechnology to create products that advance patient care worldwide. Baxter had 2012 sales of $14.2 billion and has approximately 50,800 employees.

Post : Research Associate

Job Summary
Scientist with expertise in toxicology and product safety evaluation including development of nonclinical plans for drug development, toxicology and impurity study design development and monitoring, and development of toxicology risk assessments. Hazard evaluation of chemicals used in manufacturing. In-depth knowledge in Toxicology or a related field required.

Essential Duties and Responsibilities
• Generation of toxicology risk assessment in accordance with ICH and ISO10993-17.
• Hazard evaluation of chemical and pesticide used in manufacturing
• Maintain current knowledge of relevant regulatory requirements related to toxicology, product development, design and safety.
• Perform as preclinical/toxicology representative on project teams
• Utilize Lhasa Derek and Sarah Nexus software to assess toxicological endpoints.
• Independently plan and execute a series of design and/or technical tasks that may not be well-defined, have multiple variables, and require advanced techniques within negotiated deadlines.
• Devise new approaches to complex problems through adaptations and modifications of standard technical principles. Incorporate new methods and technologies for improving existing or new products/processes

Candidate Profile
• Bachelor’s degree with 5-7 years’ experience or 3-5 years’ experience with Masters and 0-3 years’ experience with PhD
• The position requires relevant technical knowledge in toxicology and safety evaluation. General understanding of pharmacology highly desired.
• Ability to understand and apply global regulatory guidelines including OECD and FDA GLP, ICH guidance, ISO10993.
• Good oral and written communication in English language.
• Utilize a logical, methodical approach when problem solving, developing solutions and making recommendations.
• Ability to work independently and prioritize assignments to meet project schedules.
• Ability to make routine decisions independently
• Ability to design experiments, monitor toxicology studies, interpret the results and draw meaningful conclusions from the data.

Additional Information:
Location: Bengaluru
Experience : 0-7 years
Education: B.Pharm, B.Sc, M.Sc,M.Pharma, Ph.D
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Toxicology
End Date: 25th December, 2018

Senior Research Scientist require at Baxter

Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-centre dialysis;sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy, automation, software and services. Baxter GDC a global IT shared services center, in Bangalore to deliver Baxter’s global enterprise IT needs. We develop and deploy enterprise wide IT solutions that support critical operations from HR to Manufacturing, Finance, Quality Compliance, Legal and other functions within the organization.

Post : Senior Research Scientist

Job Description
• Understand Baxter technology landscape and look for external opportunities to build new innovation technology and platform
• Drive innovation culture and establish multi-lateral collaboration mechanism for local R&D team

Walk in Interview at Baxter @28 July 2018

Baxter require Validation Specialist

Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-centre dialysis;sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy, automation, software and services. Baxter GDC a global IT shared services center, in Bangalore to deliver Baxter’s global enterprise IT needs. We develop and deploy enterprise wide IT solutions that support critical operations from HR to Manufacturing, Finance, Quality Compliance, Legal and other functions within the organization.

Post : Validation Specialist

Job Description
This position will be focused on ERP upgrade assignment
• Responsible for assuring a system/application meets its requirements and is compliant with applicable Baxter QMS documents, and the documentation set outlined in the Validation Plan for the project.
• Responsible for creating  the documents required for the development and validation of the computerized system.

Research Associate at Baxter

Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-centre dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. Baxter’s employees worldwide are building upon the company’s rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care.

Post : Research Associate

Vacancy for Manager in Research and Development ( Baxter International )

Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-center dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. Baxter’s employees worldwide are building upon the company’s rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care.

Post : Mgr II-Research and Development

Job Description
Manage a diverse preclinical team to support global drug and device safety evaluation.  Utilizes solid understanding of theories and practices of a variety of preclinical disciplines to manage complex projects or programs within boundaries of quality, time and budget.  Based on significant toxicology expertise, design, review and/or approve complex study design concepts or toxicology assessments and provides general direction to staff.

Walk in Interview at Baxter