Sr. Solution Architect- Java Microservice – USA

The position is for Sr. Solution Architect- Java Microservice. 

Location: Brentwood TN, USA

Experience: 12 – 15 Years

Salary: 
As per Industry Standards.

Key Skill: Java 8, Microservices.

Mandatory Skills: Java 8, Spring boot, Spring core, Hibernate, Microservices, Google Cloud Platform.

Desired Skills: Docker, Google Kubernetes Engine, Cloud DataFlow, Cloud Spanner, Kafka, Elastic search, Jenkins, GIT, JIRA.

Job Description:

  • 12+ years of professional experience in Java technology based application/product development with good solid understanding of Application Migration to Google Cloud platform.
  • Solid hands-on experience using Spring Boot, Spring Core, Spring Boot, Spring Cloud, Spring Integration, Hibernate, and Microservices.
  • Should have experience in writing & consuming REST API.
  • Good understanding with NoSQL such as Cassandra, Couchbase, Realm.
  • Experience in Design patterns, microservices.
  • Experience with Kafka, streaming.
  • Experience in multithreading and data structures.
  • Experience working on Docker containers.
  • Should be able to provide technical solutions to problems raised / arised in a product development.
  • Should be able to probe the technical solutions suggested and vet the aptness of the solution from a holistic perspective.
  • Play a senior role on the team to facilitate code reviews, interact effectively with senior Java team mates at Client slide.
  • A combination of Google certifications desired – Google Associate Cloud Engineer; Google Professional Cloud Architect.
  • Hands-on experience in Application Migration to Google Cloud Platform is preferred.
  • Need to have excellent communication skills (including English conversation skills), demonstrate excellent problem solving and critical thinking skills.
  • Agile product development experience is required.
  • Excellent team player with strong communication, interpersonal, presentation skills.
  • Experience in working with multi-location and offshore teams.
  • Good understanding of US HC, especially on RCM (revenue cycle management), clinicals (medications, orders, labs, etc) will be an added advantage.

About the Client:

The client has played a deep and meaningful role in accelerating technology innovation and shaping the way healthcare is delivered to patients. They are a specialist provider of healthcare technology services and solutions, with a strong presence across the globe. The client focuses on multiple areas of digital technology, such as Business Intelligence, mobility & IoT, Big Data, cloud computing, predictive analytics & data science. They have won several awards such as the 2019 Innovators Award for the Best Value-Based Care Solution.

 

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Lead Java Developer – USA

The position is for Lead Java Developer – US.

Location: Brentwood, TN, USA.

Experience: 7 – 10 Years

Salary: As per Industry Standards.

Key Skill: Java Mandatory Skills Java 8, Spring boot, Microservices,SQL,Hibernate.
Desired Skills: Jenkins, GIT,JIRA. 

Job Description:
Hands on experience on developing unit tests with JUnit or a comparable framework.
Solid experience using Spring Boot, Spring Core, Spring Boot, Spring Cloud, Spring Integration ,Hibernate, and Microservices
Should have experience in writing & consuming REST API
Good understanding with NoSQL such as Cassandra, Couchbase, Realm
Experience in Design patterns, microservices
Experience with Kafka, streaming.
Experience in multithreading and data structures.
Experience working on Docker containers.
Experience using GIT, Junit, Maven, Jenkins, Sonar.
Agile product development experience is required.
Excellent team player with strong communication, interpersonal, presentation skills.
Good understanding of US HC, especially on RCM (revenue cycle management), clinicals (medications, orders, labs, etc) will be an added advantage.

 

About the Client:

The client has played a deep and meaningful role in accelerating technology innovation and shaping the way healthcare is delivered to patients. They are a specialist provider of healthcare technology services and solutions, with a strong presence across the globe. The client focuses on multiple areas of digital technology, such as Business Intelligence, mobility & IoT, Big Data, cloud computing, predictive analytics & data science. They have won several awards such as 2019 Innovators Award for the Best Value-Based Care Solution.

 

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Senior Scientist – Analytical Chemistry – USA

The position is for Senior Scientist – Analytical Chemistry.

Location:  Central Islip, New York, USA.

Experience: 1-3 Years

Salary: 
As per Industry Standards.

Job Description
SCOPE

The content and statements documented in this job description are designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job.  This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications.  The intent of this job description is to be representative of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position satisfactorily and in accordance with the established performance expectations.

PURPOSE

The R&D Senior Scientist Analytical Chemistry position is an individual contributor role and reporting to a Manager of Research & Development (R&D). The job duties for this position include but are not limited to the following:

  • Operates as the subject matter expert (SME) on analytical methods for products that are under development, products that are commercialized and in support of process analytical technologies (PAT) for commercial manufacturing processes.
  • Operate as the subject matter expert (SME) on analytical methods for various internal and external projects. Independently develop, assess and/or verify and validate analytical test methods for APIs, excipients, packaging components, devices and drug products using industry standard methodologies including QbD principles for analytical methods; US FDA or EU guidance and requirements; United States Pharmacopoeia (USP) guidelines; International Council for Harmonization (ICH) guidelines. Techniques may include standard tools like HPLC, UPLC, UV, GC, LC-MS, Viscometer, Karl-Fisher, IR, Particle size analyses, XRPD, DVS, Rheometer etc. to more specialized techniques such as LS-MS/MS, NMR, SS-NMR, Synchrotron etc.
  • Lead and define strategy on all topics extractable and leachables (E&L).
  • Evaluate material from new vendors for suitability of material based on physico-chemical properties and perform studies in support of vendor qualifications.
  • Lead drafting of product specifications and analytical procedures.
  • Lead analysis of samples for various R&D and GMP stability studies.
  • Support Product Development activities by analyzing the samples at different stages of pre-formulation, formulation and process development.
  • Implement new analytical techniques that are not currently utilized at the site.
  • Conduct trend analysis of data including kinetic modeling, statistical analysis etc.
  • Draft high-quality documents in support of dossiers (protocols, reports, technical memos)
  • Lead investigation for quality events (planned and unplanned deviations) with appropriate justifications
  • Act as single-point technical contact for contract research organizations (CROs) and/or contract development and manufacturing organizations (CDMOs). Collaborate with project management (PM) function to lead execution of activities against approved plan.
  • Provide relevant subject matter expertise in collaboration with external partners in the form of participation in technical strategy discussions; consultation on technical studies; hands-on characterization and/or third-party interface (e.g., CROs, CDMOs etc.)
  • Draft high-quality industry standard technical documents (protocols, reports, technical memorandums, position papers etc.).
  • Lead and/or participate in conducting data and hypothesis driven investigations for quality events (planned and unplanned deviations) with recommendations of relevant corrective and preventative actions (CAPAs) to line functions.
  • Independently draft and/or review standard operating procedures (SOPs).
  • Maintain effective and proactive communication and coordination of activities with multi-functional stakeholders.
  • Draft and/or participate in drafting relevant sections of dossiers towards 505(b)(1), 505(b)(2) or 505(j) submissions. Lead studies in support of responses to United States Federal Drug Administration (FDA) information requests or deficiency letters for various dossiers.
  • Lead studies in support of responses to United States Federal Drug Administration (FDA) information requests or deficiency letters for various dossiers.
  • Write reports for US FDA submissions such as a Quality Overall Summary.
  • Train peers and junior staff members on new techniques.

TYPICAL DAY-TO-DAY ACTIVITIES

  • New product development
  • R&D activities such as pre-formulation, formulation, process development or analytical method development
  • Technical Troubleshooting
  • Technology Transfer
  • Process Validations
  • Method Validations
  • New Analytical Method Development
  • Leading activities at CROs and CMOs
  • Drafting dossier supportive documents
  • Drafting and responding to relevant requests from the US FDA or EU authorities
  • Working with external partners on technical activities

EDUCATION AND EXPERIENCE

  • Doctorate in Analytical Chemistry, Pharmaceutical Chemistry, Organic Chemistry or Medicinal Chemistry.
  • In-depth understanding of analytical methods, theoretical principles of laboratory analytical techniques, physical pharmacy, physical chemistry, thermodynamics, chemical reaction kinetics is a must.
  • In depth understanding of UV-Vis, Liquid Chromatography (LC), Gas Chromatography (GC) and Spectroscopy techniques such that IR is a must. Experience with analytical techniques such as Dissolution, Particle Size Analysis, dynamic vapor sorption (DVS), x-ray powder diffraction (XRPD), mass spectrometry (MS), nuclear magnetic resonance (NMR) etc. is a plus.
  • In-depth understanding of theoretical principles of laboratory analytical techniques is a must.
  • Experience with extractable and leachables (E&L) studies is a big plus.
  • Experience with process analytical technologies (PAT) is a plus.


PROFESSIONAL COMPETENCIES AND TECHNICAL SKILLS

  • Must possess strong documentation and technical writing skills, and be able to apply relevant scientific principles and practices.
  • Strong command over written and verbal English is a must. Past publication experience is a plus.
  • Must be able to work under minimal supervision and able to work independently and in a team environment.
  • Must be able to exercise appropriate professional judgment on matters of significance.
  • Must be proficient in computer skills and software applications such as Microsoft Office tools.
  • Knowledge of statistical packages is a plus.
  • Must communicate clearly and concisely across levels, both orally and in written.

About the Client:

The client is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. They are trusted by healthcare professionals and patients across geographies. Over the last eight decades, they have strengthened their leadership in India’s pharmaceutical industry and fortified their promise of strengthening their global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.  Client employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead them to prosperity and growth in the future. Driven by the vision, none shall be denied, Client’s focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.

 

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Associate Scientist – Analytical Chemistry – USA

The position is for Associate Scientist – Analytical Chemistry

Location:  Central Islip, New York, USA

Experience: 1-4 Years

Salary: 
As per Industry Standards.

Job Description
SCOPE
The content and statements documented in this job description are designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job.  This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications.  The intent of this job description is to be representative of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position satisfactorily and in accordance with the established performance expectations.

PURPOSE

The Associate Scientist position is an individual contributor role and reports to the Research & Development (R&D) Manager for the Client at  New York. The job duties for this position include but are not limited to the following:

  • Under supervision designing and conducting laboratory scale pre-formulation, formulation and process development experiments  to develop formulations and products.
  •  Under supervision developing independently or participating in the development and validation of analytical methods.
  •  Conducting characterization of samples from pre-formulation, formulation and process development studies.
  •  Conducting assessment of various unit processes during manufacturing process to recommend acceptance criteria.
  •  Conducting development and optimization of manufacturing processes at laboratory scale by optimizing various parameters under   Quality by Design paradigm.
  •  Conducting manufacture of lab-scale and pilot-scale batches.
  • Conducting statistical analysis of process development data to recommend acceptance criteria for various unit processes
  • Reviewing analytical characterization data including data from pre-formulation, formulation, process development and stability studies during the course of product development.
  • Leading scale-up and technology transfer of process from R&D to Commercial Operations.
  • Leading and conducting process development, process verifications, process validations, site and equipment qualifications in collaboration with stakeholders.
  • Drafting technical documents (protocols, reports, technical memorandums).
  •  Investigating incidents and deviations during the manufacturing process, and if required, conducts investigations, as per standard     operating procedures (SOPs).
  • Working with the change control system for the technical services department.
  •  Maintaining effective communication and coordinating activities with multi-functional stakeholders.
  • Drafting and maintaining of electronic copies of all approved mater formula cards utilized in the manufacturing of products and maintaining written record of all activity associated with approvals of electronic copies.
  • Understanding and following all policies and procedures as outlined in pertinent SOPs.

EDUCATION AND EXPERIENCE

Masters’ degree with 1-4 years of experience in relevant discipline.
In-depth understanding of physical pharmacy, physical chemistry, thermodynamics, analytical chemistry tools, chemical reaction kinetics is a must.
Must possess strong documentation and technical writing skills, and able to apply relevant scientific principles and practices.
Strong command over written and verbal English is a must.
Must be proficient in computer skills and software applications such as Microsoft Office tools.
Must communicate clearly and concisely across levels, both orally and in written.
Strong organization skills, attention to detail, and the ability to work in a team environment.

ABOUT THE CLIENT

The client is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. They are trusted by healthcare professionals and patients across geographies. Over the last eight decades, they have strengthened their leadership in India’s pharmaceutical industry and fortified their promise of strengthening their global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.  Client employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead them to prosperity and growth in the future. Driven by the vision, none shall be denied, Client’s focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.

 

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Encapsulation Operator- Capsule Filling- USA

City:  New York, USA

Location: Central Islip, NY

Experience: 2 – 10 Years 

Salary: As per Industry Standards.

Job Description

Job Summary:

This position is a Production Operator assigned to support capsule filling.  This is an hourly laborer and individual contributor role that will report to a Front-Line Supervisor.  This position may be based at the Company’s manufacturing units in Hauppauge or Central Islip, New York.

Person should be able to operate AF90T & ZRO200 from ACG PAM independently

There are 2 positions open for Encapsulation.

2 positions open for the Evening shift (3pm – 11.30pm)

Job Responsibilities:

Person should be able to operate AF90T & ZRO200 from ACG PAM independently
Execute manufacturing processes in accordance with batch manufacturing record (BMR) and Standard Operating Procedures (SOP)      requirements.
Perform machine changeovers, cleaning and set up as per SOPs. Ensure the proper area & equipment cleanliness and setup in stipulated time.
Prepare a room and equipment for line clearance, replace room filters, Ensure verification and calibration of balance/scale and check pressure differential for the rooms.
Ensure line clearance before initiating manufacturing activities in each area.
Receive/transfer material from/to dispensing/manufacturing storage and check dispensed materials/final mix blend/compressed tablets and labeling as per BMR.
Wear appropriate personal protective equipment (PPE) as stated in the SOP/BMR before initiating the process.
Able to operate applicable equipment independently as per area of operation.
Troubleshoot and make appropriate adjustments to equipment to maintain product/BMR specifications.
Ensure adherence to quality standards during all stages of the manufacturing process.
Complete manufacturing documents on time, ensuring accuracy and completeness.
Responsible for training on all relevant SOPs and always maintaining compliance with related SOPs and current Good Manufacturing Practices (cGMP) in the manufacturing process.
Perform duties through the proper, safe use of equipment, according to Health & Safety procedures and Equipment Manuals.
Flexible to work extended hours, to achieve manufacturing schedule when needed.
Should maintain discipline and comply with company policies and procedures.
Should perform entire duties as communicated from time to time by department management/designee.

Minimum Requirements:

Solid mechanical aptitude.
Minimum of 2 years of experience working in industrial environments such as pharmaceutical manufacturing and related settings.
Must have excellent communication skills.
Must be able to clearly communicate in English (verbally and in writing).
Positive, professional attitude toward work and willingness to cooperate with co-workers and supervisors.
Must be able to work different shifts as per organizational requirement and should be flexible for working additional hours such as overtime and weekends.

Physical Requirements

Should not have any restriction to work with powder containing active pharmaceutical ingredients.
This position requires the ability to do heavy lifting / bending frequently.
Long periods of standing up/walking during the working hours; ability to ascent/decent ladders; and able to lift to 35 pounds.
Must be able to move pallets/equipment weighing about 200 – 300 kgs using suitable moving equipment like pallet jacks.

 

About the client:

Client is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. Our client is trusted by healthcare professionals and patients across geographies. Over the last eight decades, they have strengthened their leadership in India’s pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.  Client employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Client’s focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.

Client is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants.

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Manufacturing Operator – Compression – USA

City:  New York, USA

Location: Central Islip, NY

Experience: 2 – 20 Years

Salary: As per Industry Standards.

Job Description

Job Summary:

This position is a Production Operator assigned to support Compression.  This is an hourly labourer and individual contributor role that will report to a Front-Line Supervisor. This position may be based at the Company’s manufacturing units in Hauppauge or Central Islip, New York.

The person should be able to operate Sejong & Cadmach compression machines independently (PREFERRED)

There are positions open for Compression, and these will be in either Morning Shifts or Evening Shift.
Morning Shift (7am – 3.30pm)
Evening shift (3pm – 11.30pm)

Job Responsibilities:

  • Persons should be able to operate Sejong & Cadmach compression machines independently (PREFERRED)
  • Execute manufacturing processes in accordance with batch manufacturing record (BMR) and Standard Operating Procedures (SOP) requirements.
  • Perform machine changeovers, cleaning and set up as per SOPs. Ensure the proper area & equipment cleanliness and setup in stipulated time.
  • Prepare a room and equipment for line clearance, replace room filters, Ensure verification and calibration of balance/scale and check pressure differential for the rooms.
  • Ensure line clearance before initiating manufacturing activities in each area.
  • Receive/transfer material from/to dispensing/manufacturing storage and check dispensed materials/final mix blend/compressed tablets and labelling as per BMR.
  • Wear appropriate personal protective equipment (PPE) as stated in the SOP/BMR before initiating the process.
  • Able to operate applicable equipment independently as per the area of operation.
  • Troubleshoot and make appropriate adjustments to equipment to maintain product/BMR specifications.
  • Ensure adherence to quality standards during all stages of the manufacturing process.
  • Complete manufacturing documents on time, ensuring accuracy and completeness.
  • Responsible for training on all relevant SOPs and always maintaining compliance with related SOPs and current Good Manufacturing Practices (cGMP) in the manufacturing process.
  • Perform duties through the proper, safe use of equipment, according to Health & Safety procedures and Equipment Manuals.
  • Flexible to work extended hours, to achieve a manufacturing schedule when needed.
  • Should maintain discipline and comply with company policies and procedures.
  • Should perform entire duties as communicated from time to time by department management/designee.


Minimum Requirements:

  • Solid mechanical aptitude.
  • Minimum of 2 years of experience working in industrial environments such as pharmaceutical manufacturing and related settings.
  • Must have excellent communication skills.
  • Must be able to clearly communicate in English (verbally and in writing).
  • Positive, professional attitude toward work and willingness to cooperate with co-workers and supervisors.
  • Must be able to work different shifts as per organizational requirement and should be flexible for working additional hours such as overtime and weekends.

Physical Requirements:

  • Should not have any restriction to work with powder containing active pharmaceutical ingredients.
  • This position requires the ability to do heavy lifting/bending frequently.
  • Long periods of standing up/walking during the working hours; ability to ascent/descent ladders; and able to lift to 35 pounds.
  • Must be able to move pallets/equipment weighing about 200 – 300 kgs using suitable moving equipment like pallet jacks.

About the client:

The client is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, client has strengthened our leadership in India’s pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.  The client employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Client’s focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.

Manufacturing Operator-Coating – USA

Location: New York, USA.

City: Central Islip, NY

Experience: 2 – 10 Years

Salary: As per Industry Standards.

Job Description:

Job Summary:

This position is a Production Operator assigned to support coating.  This is an hourly laborer and individual contributor role that will report to a Front-Line Supervisor.  This position may be based at the Company’s manufacturing units in Hauppauge or Central Islip, New York.

Person should be able to operate Neocota, Xiaolun coating pans independently.

There are 2 positions open for Evening shift (3pm – 11.30pm)

Job Responsibilities:

  • Person should be able to operate Neocota, Xiaolun coating pans independently
  • Execute manufacturing processes in accordance with batch manufacturing record (BMR) and Standard Operating Procedures (SOP)      requirements.
  • Perform machine changeovers, cleaning and set up as per SOPs. Ensure the proper area & equipment cleanliness and setup in stipulated time.
  • Prepare a room and equipment for line clearance, replace room filters, Ensure verification and calibration of balance/scale and check pressure differential for the rooms.
  • Ensure line clearance before initiating manufacturing activities in each area.
  • Receive/transfer material from/to dispensing/manufacturing storage and check dispensed materials/final mix blend/compressed tablets and labeling as per BMR.
  • Wear appropriate personal protective equipment (PPE) as stated in the SOP/BMR before initiating process.
  • Able to operate applicable equipment independently as per area of operation.
  • Troubleshoot and make appropriate adjustments to equipment to maintain product/BMR specifications.
  • Ensure adherence to quality standards during all stages of the manufacturing process.
  • Complete manufacturing documents on time, ensuring accuracy and completeness.
  • Responsible for training on all relevant SOPs and always maintain compliance with related SOPs and current Good Manufacturing Practices (cGMP) in the manufacturing process.
  • Perform duties through the proper, safe use of equipment, according to Health & Safety procedures and Equipment Manuals.
  • Flexible to work extended hours, to achieve manufacturing schedule when needed.
  • Should maintain discipline and comply with company policies and procedures.
  • Should perform entire duties as communicated time to time by department management/designee.

Minimum Requirements:

  • Solid mechanical aptitude.
  • Minimum of 2 years of experience working in industrial environments such as pharmaceutical manufacturing and related settings.
  • Must have excellent communication skills.
  • Must be able to clearly communicate in English (verbally and in writing).
  • Positive, professional attitude toward work and willingness to cooperate with co-workers and supervisors.
  • Must be able to work different shifts as per organizational requirement and should be flexible for working additional hours such as overtime and weekends.

Physical Requirements

  • Should not have any restriction to work with powder containing active pharmaceutical ingredients.
  • This position requires the ability to do heavy lifting / bending frequently.
  • Long periods of standing up/walking during the working hours; ability to ascent/decent ladders; and able to lift to 35 pounds.
  • Must be able to move pallets/equipment weighing about 200 – 300 kgs using suitable moving equipment like pallet jacks.

About the client:

The client is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, client has strengthened our leadership in India’s pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.  Client employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Client’s focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.

 

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Sr. Solution Architect- Java Microservice – USA

Location: Brentwood TN, USA

Experience: 12 – 15 Years

Salary: 
As per Industry Standards.

Key Skill: Java 8, Microservices.

Mandatory Skills: Java 8, Spring boot, Spring core, Hibernate, Microservices, Google Cloud Platform.

Desired Skills: Docker, Google Kubernetes Engine, Cloud DataFlow, Cloud Spanner, Kafka, Elastic search, Jenkins, GIT, JIRA.

Job Description:

  • 12+ years of professional experience in Java technology based application/product development with good solid understanding of Application Migration to Google Cloud platform.
  • Solid hands-on experience using Spring Boot, Spring Core, Spring Boot, Spring Cloud, Spring Integration, Hibernate, and Microservices.
  • Should have experience in writing & consuming REST API.
  • Good understanding with NoSQL such as Cassandra, Couchbase, Realm.
  • Experience in Design patterns, microservices.
  • Experience with Kafka, streaming.
  • Experience in multithreading and data structures.
  • Experience working on Docker containers.
  • Should be able to provide technical solutions to problems raised / arised in a product development.
  • Should be able to probe the technical solutions suggested and vet the aptness of the solution from a holistic perspective.
  • Play a senior role on the team to facilitate code reviews, interact effectively with senior Java team mates at Client slide.
  • A combination of Google certifications desired – Google Associate Cloud Engineer; Google Professional Cloud Architect.
  • Hands-on experience in Application Migration to Google Cloud Platform is preferred.
  • Need to have excellent communication skills (including English conversation skills), demonstrate excellent problem solving and critical thinking skills.
  • Agile product development experience is required.
  • Excellent team player with strong communication, interpersonal, presentation skills.
  • Experience in working with multi-location and offshore teams.
  • Good understanding of US HC, especially on RCM (revenue cycle management), clinicals (medications, orders, labs, etc) will be an added advantage.

About the Client:

The client has played a deep and meaningful role in accelerating technology innovation and shaping the way healthcare is delivered to patients. The Client is a specialist provider of healthcare technology services and solutions, with a strong presence across the globe. The client focuses on multiple areas of digital technology, such as Business Intelligence, mobility & IoT, Big Data, cloud computing, predictive analytics & data science. The client has won several awards such as the 2019 Innovators Award for the Best Value-Based Care Solution.

 

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RPA Developer with OpenConnect, USA

10 Openings

Information technology (IT)

Location : Atlanta, Georgia, USA
Client Details

Our client is a leading IT Staffing and Solutions Company located in New Jersey, USA. Leveraging on years of staffing and consulting experience, the company has pioneered in the field of IT and outsourcing services. With a wide range of project execution models and costing models, their solutions are very client-centric, cost-effective and process driven.Job Details

Experience: 8 – 15 Years

Annual Salary: 100000-150000 USD

Work Location: Atlanta, Georgia, USA

Domain: Information technology (IT)

Job Description

Responsible for building and implementing enterprise business solutions utilizing robotics software.Primary duties include, but are not limited to:

o Creates and maintains BOTs or macros that will interact with multiple internal and external applications.

o Works with Business Users and Business Automation Analysts for process identification and feasibility, solving issues that arise in day to day running and providing timely responses and solutions as required.

o Performs Proof of Concepts to help the business recognize the feasibility of an automated solution using Robotic Process Automation software.

o Leads structured peer reviews and walkthroughs.

o Participates in the technical design and development including creating and maintaining solution documentation.

o Engages cross-functional team members effectively to develop high quality products.

o Maintains and improves existing applications by working closely with business stakeholders to map existing work processes and identify productivity opportunities.

o Ensures best practices are being followed at each stage of development and test procedures and scenarios for the pre-UAT phases are documented.

Skills Required:

o Requires a BS/BA

o 4 years of relevant experience, with at least 2 years of experience building Robots utilizing Robotics Process Automation (RPA) software called Open Connect. Additional experience desired with development using Automation Anywhere, Visual Basic.NET, MS Visual Studio, Microsoft SQL Server, UiPath, SQL Query Building, MS Excel Macros with VBA.

o Degree in Computer Science desired.

o Experience working on multiple tasks while still being able to be organized.

o Ability to communicate well in English in both written and verbal forms.

  If interested, please send your resume to jobs@enflexis.com

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