1,337 Quality Assurance Measures jobs in India
QA Specialist
Bangalore, Karnataka
Danaher Corporation
Posted 1 day ago
Job Viewed
Job Description
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Beckman Coulter Diagnostics, one of Danaher's ( 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory's role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making-we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence.
Learn about the Danaher Business System ( which makes everything possible.
The Senior Manufacturing Quality Engineer for Beckman Coulter Diagnostics is responsible for:
+ Provide Quality and Compliance expertise for system compliance, authoring, and reviewing end to end Design deliverables.
+ Prepare documentation adhering to product development, Software Development Life Cycle processes, and regulatory requirements.
+ Collaborate with teams guidance to project teams on implementing and adhering to quality standards.
+ Maintain and develop IDC quality systems and infrastructure, and to monitor QMS performance and drive its fulfillment.
+ Ensure compliance with organizational policies and regulatory requirements, including FDA, ISO 13485, and ISO 14971, with knowledge of IVDR.
+ Send daily status reports to management, highlighting any risks.
+ Support audits by liaising with management and qualify software for validation labs in conjunction with FSCs.
This position is part of the International Quality Operations located at Bengaluru, India and will be on-site. At Beckman Coulter, our mission is to Relentlessly Reimagine Healthcare, One Diagnosis at a Time.
You will be a part of the Quality, Regulatory and Clinical Affairs and report to the Senior Manager Quality and Regulatory Affairs. If you thrive in a multifunctional role and want to work to build a world-class Quality organization-read on.
In this role, you will have the opportunity to:
+ Define programs for software design quality improvement
+ Execute and participate in audits(supplier audits, external audits etc)
+ Liaise with Tech-ops and R&D departments on validation requirements for new and current products and processes as well as with the regional and global Q&RA organization to support the growth of and ensure alignment with BEC global policies and procedures
The essential requirements of the job include:
+ Minimum of 10 years' experience in software quality in either medical devices or pharma industry or with background in a highly regulated environment with Bachelors in life sciences, engineering or quality management or equivalent
+ Excellent organizational and communication skills and fluent in English language is required
+ Solid working knowledge of EU, FDA and related regulations including QSR's, (FDA 21 CFR 820), ISO 13485 or ISO 9001, IVD's, IEC62304
It would be a plus if you also possess previous experience in:
+ Experienced in quality management methods (8D, Six Sigma, Statistical Tools, FMEA)
+ Experienced in working within multi-functional, multi-regional teams
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Beckman Coulter Diagnostics, one of Danaher's ( 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory's role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making-we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence.
Learn about the Danaher Business System ( which makes everything possible.
The Senior Manufacturing Quality Engineer for Beckman Coulter Diagnostics is responsible for:
+ Provide Quality and Compliance expertise for system compliance, authoring, and reviewing end to end Design deliverables.
+ Prepare documentation adhering to product development, Software Development Life Cycle processes, and regulatory requirements.
+ Collaborate with teams guidance to project teams on implementing and adhering to quality standards.
+ Maintain and develop IDC quality systems and infrastructure, and to monitor QMS performance and drive its fulfillment.
+ Ensure compliance with organizational policies and regulatory requirements, including FDA, ISO 13485, and ISO 14971, with knowledge of IVDR.
+ Send daily status reports to management, highlighting any risks.
+ Support audits by liaising with management and qualify software for validation labs in conjunction with FSCs.
This position is part of the International Quality Operations located at Bengaluru, India and will be on-site. At Beckman Coulter, our mission is to Relentlessly Reimagine Healthcare, One Diagnosis at a Time.
You will be a part of the Quality, Regulatory and Clinical Affairs and report to the Senior Manager Quality and Regulatory Affairs. If you thrive in a multifunctional role and want to work to build a world-class Quality organization-read on.
In this role, you will have the opportunity to:
+ Define programs for software design quality improvement
+ Execute and participate in audits(supplier audits, external audits etc)
+ Liaise with Tech-ops and R&D departments on validation requirements for new and current products and processes as well as with the regional and global Q&RA organization to support the growth of and ensure alignment with BEC global policies and procedures
The essential requirements of the job include:
+ Minimum of 10 years' experience in software quality in either medical devices or pharma industry or with background in a highly regulated environment with Bachelors in life sciences, engineering or quality management or equivalent
+ Excellent organizational and communication skills and fluent in English language is required
+ Solid working knowledge of EU, FDA and related regulations including QSR's, (FDA 21 CFR 820), ISO 13485 or ISO 9001, IVD's, IEC62304
It would be a plus if you also possess previous experience in:
+ Experienced in quality management methods (8D, Six Sigma, Statistical Tools, FMEA)
+ Experienced in working within multi-functional, multi-regional teams
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
This advertiser has chosen not to accept applicants from your region.
0
Chat and Voice Bot QA Specialist
Karnataka, Karnataka
Yubi
Posted 3 days ago
Job Viewed
Job Description
We are looking for a detail-oriented and analytical Chat and Voice Bot QA Specialist to join our Conversational AI team. In this role, you'll be responsible for evaluating the performance and quality of AI-driven chat and voice assistants. The ideal candidate brings a high level of first-principles thinking to assess bot responses, understands the fundamentals of generative AI, and is passionate about delivering seamless user experiences.
This is a non-technical role that doesn't require coding, but does require a foundational understanding of how conversational bots work, how workflows are structured, and how to methodically test and evaluate them.
Key Responsibilities
- Evaluate AI Responses: Systematically test chat and voice bot outputs for coherence, relevance, tone, factual accuracy, and alignment with business objectives.
- Test Workflows: Assess conversation flows and user journeys for edge cases, logical consistency, and usability across different platforms (web, mobile, IVR).
- First-Principles Problem Solving: Analyze and break down complex issues using first-principles thinking; question assumptions and propose better alternatives.
- Scenario Creation: Develop diverse test scenarios and real-world prompts to validate AI performance across varied contexts and user intents.
- Feedback & Reporting: Document bugs, inconsistencies, and improvement opportunities; work closely with product, design, and engineering teams.
- AI Alignment Audits: Ensure the AI responses align with user intent, brand tone, and ethical guidelines.
- Collaborate on Evaluation Frameworks: Help define or refine qualitative and quantitative criteria for bot performance and user experience.
Requirements
Qualifications
- 2-4 years of experience working in chatbot/voice testing, or a related field.
- Strong analytical skills and a problem-solving mindset grounded in first-principles thinking.
- Prior experience in QA, user research, product evaluation, or content moderation is a plus.
- Familiarity with generative AI technologies (like ChatGPT, Bard, or Claude) and LLMs.
- Basic understanding of conversation design, chat/voice interfaces, and user journey mapping.
- Ability to write clear, concise test documentation and reports.
- Excellent communication skills and attention to detail.
- Curious, user-centric mindset with a drive for continuous improvement.
This advertiser has chosen not to accept applicants from your region.
1
QA Design Specialist
Pune, Maharashtra
Cybage Software
Posted 3 days ago
Job Viewed
Job Description
Cybage has a mature testing practice with a strong team working on verification and validation of some of the most complex products. We are looking for sharp engineers with an aptitude for learning new domains and testing methodologies to join our team.
Experience: 3+ Years
Location: Pune
Description:
- Candidate should work in US Business hours - (9.30pm to 5.30am IST)
- Excellent communication skills and proficiency over English Language
- To be able to spot grammatical errors and suggest changes.
- To be able to sift through client input and be able to write a creative Brief for the designer.
- Experience having worked as a QA specialist with a Digital Marketing Agency/ Advertising Agency / Media house.
- Should be able to evaluate the creatives against the Brand Guidelines and spot design inconsistencies and suggest changes in the layout.
- Should be able to check technical specifications of the creative (File format / Resolution / File size / File naming etc.)
- Candidate should have experience working with a digital Media agency. Be familiar with doing QC for digital campaigns.
- Although he need not be a designer, he should have a keen eye for spotting inconsistencies in design along with technical knowledge of the production process and various file formats etc.
This advertiser has chosen not to accept applicants from your region.
2
Specialist QA
Hyderabad, Andhra Pradesh
Amgen
Posted 1 day ago
Job Viewed
Job Description
**AIN Specialist QA - Job Description**
**Join Amgen's Mission of Serving Patients**
At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
**Position Summary:**
The AIN Specialist QA plays a critical role in supporting product disposition related tasks across the Amgen Quality Operations Network. The Specialist QA will leverage industry, technical, and quality systems knowledge to provide support of product expiry management processes, product complaints processes, disposition manager training, and fulfillment of disposition related data requests across the network. The position will be responsible for tasks including the key responsibilities documented below and other disposition related job functions.
This candidate will primarily work during regular working hours (9 am - 6 PM local time) to enable the business in delivering Amgen's mission to serve patients and may lead a shift-based team that provides coverage in support of the Amgen network across multiple time zones. The candidate may need to work outside of his/her routine workday to support business needs and will be responsible for determining the same for their staff. The individual will be required to work from our office located in Hyderabad India (Amgen India-AIN). The candidate will also lead the remote support from AIN to Amgen sites across multiple time zones globally.
**Key Responsibilities**
**DSI/DS/DP material shelf-life extension**
- Executing the GMP process to extend expiration dates for clinical and commercial products produced at Amgen.
- Updating batch product expiration dates in the Amgen SAP inventory management system.
- Evaluating (approve or reject) expiry-SAF forms (expiry stability assessment forms).
**Disposition Support of Partner Requests**
- Support requests made by Amgen partners for data and information related to their partnered product batches manufactured at Amgen sites.
- Data recovery from systems including, but not limited to, manufacturing execution system electronic batch records, the quality control laboratory information system, the regulatory information management system, and the Amgen enterprise resource management system (SAP).
- Uploading and communication of collected data to Amgen partners.
**COA Generation, special requests after disposition**
- Generation and provision of Certificate of Analysis (CofA) records for Amgen drug substance, drug product, or final drug product batches.
- Uploading and communication of collected documentation to requestor (i.e. Amgen partners, regulatory compliance to support RTQs, process development).
**Disposition Manager Training**
- Execution and delivery of quality systems training to new disposition managers across the Amgen network via virtual meetings.
- Training subject matter to include use of quality systems applied to execute the disposition process (i.e. ERP/SAP, MES/EBR, ARRS, LIMS, TW, CDOCS, DQMS, Kneat, etc.)
- Maintenance and revision of training document materials in the controlled documents management system (CDOCs).
**Product Complaints**
- Execution of the drug substance, drug product, and final drug product complaint full batch record review process.
- Assessing electronic batch record (EBRs) documentation in the manufacturing execution system (MES) to identify any potential issues relevant to the complaint.
- Recording the results of the complaints batch record assessment in the Bioconnect quality system.
**Preferred Qualifications**
- Experience in project management and related systems
- Proficiency in technical writing and data visualization tools; experience with Smartsheet, Tableau, or equivalent platforms preferred.
- Excellent verbal and written communication skills
- Proven ability to lead and collaborate within cross-functional teams in a dynamic, fast-paced setting.
- Experience in manufacturing environments
**Core Competencies**
- Experience working in a regulated environment with knowledge of Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) requirements.
- Experience working with Quality Systems that may include enterprise resource planning (ERP/SAP), regulatory information management (RIM), controlled document management (CDOCS), change control (QMTS), deviation (DQMS), and quality control laboratory information management systems (LIMS).
-Experienced in staff training and development.
- Technical Document Drafting and Workflow Ownership
Basic Qualifications and Experience:
- Master's degree with 8-12 years of Pharma and Biotech commercial or clinical manufacturing Quality experience.
**Join Amgen's Mission of Serving Patients**
At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
**Position Summary:**
The AIN Specialist QA plays a critical role in supporting product disposition related tasks across the Amgen Quality Operations Network. The Specialist QA will leverage industry, technical, and quality systems knowledge to provide support of product expiry management processes, product complaints processes, disposition manager training, and fulfillment of disposition related data requests across the network. The position will be responsible for tasks including the key responsibilities documented below and other disposition related job functions.
This candidate will primarily work during regular working hours (9 am - 6 PM local time) to enable the business in delivering Amgen's mission to serve patients and may lead a shift-based team that provides coverage in support of the Amgen network across multiple time zones. The candidate may need to work outside of his/her routine workday to support business needs and will be responsible for determining the same for their staff. The individual will be required to work from our office located in Hyderabad India (Amgen India-AIN). The candidate will also lead the remote support from AIN to Amgen sites across multiple time zones globally.
**Key Responsibilities**
**DSI/DS/DP material shelf-life extension**
- Executing the GMP process to extend expiration dates for clinical and commercial products produced at Amgen.
- Updating batch product expiration dates in the Amgen SAP inventory management system.
- Evaluating (approve or reject) expiry-SAF forms (expiry stability assessment forms).
**Disposition Support of Partner Requests**
- Support requests made by Amgen partners for data and information related to their partnered product batches manufactured at Amgen sites.
- Data recovery from systems including, but not limited to, manufacturing execution system electronic batch records, the quality control laboratory information system, the regulatory information management system, and the Amgen enterprise resource management system (SAP).
- Uploading and communication of collected data to Amgen partners.
**COA Generation, special requests after disposition**
- Generation and provision of Certificate of Analysis (CofA) records for Amgen drug substance, drug product, or final drug product batches.
- Uploading and communication of collected documentation to requestor (i.e. Amgen partners, regulatory compliance to support RTQs, process development).
**Disposition Manager Training**
- Execution and delivery of quality systems training to new disposition managers across the Amgen network via virtual meetings.
- Training subject matter to include use of quality systems applied to execute the disposition process (i.e. ERP/SAP, MES/EBR, ARRS, LIMS, TW, CDOCS, DQMS, Kneat, etc.)
- Maintenance and revision of training document materials in the controlled documents management system (CDOCs).
**Product Complaints**
- Execution of the drug substance, drug product, and final drug product complaint full batch record review process.
- Assessing electronic batch record (EBRs) documentation in the manufacturing execution system (MES) to identify any potential issues relevant to the complaint.
- Recording the results of the complaints batch record assessment in the Bioconnect quality system.
**Preferred Qualifications**
- Experience in project management and related systems
- Proficiency in technical writing and data visualization tools; experience with Smartsheet, Tableau, or equivalent platforms preferred.
- Excellent verbal and written communication skills
- Proven ability to lead and collaborate within cross-functional teams in a dynamic, fast-paced setting.
- Experience in manufacturing environments
**Core Competencies**
- Experience working in a regulated environment with knowledge of Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) requirements.
- Experience working with Quality Systems that may include enterprise resource planning (ERP/SAP), regulatory information management (RIM), controlled document management (CDOCS), change control (QMTS), deviation (DQMS), and quality control laboratory information management systems (LIMS).
-Experienced in staff training and development.
- Technical Document Drafting and Workflow Ownership
Basic Qualifications and Experience:
- Master's degree with 8-12 years of Pharma and Biotech commercial or clinical manufacturing Quality experience.
This advertiser has chosen not to accept applicants from your region.
3
Quality Control
Ernakulam, Kerala
JobStars HR Solutions Pvt Ltd
Posted 21 days ago
Job Viewed
Job Description
Qualifications and Skills
- Familiarity with statistical process control to foster continuous improvement in manufacturing processes and product quality.
- Understanding of quality management systems to maintain excellence in organizational processes and customer satisfaction.
- Knowledge of lean manufacturing concepts to enhance process efficiency and minimize waste effectively in the production environment.
- Ability to perform non-destructive testing techniques for ensuring product quality and reliability in compliance with industry standards.
- Experience or foundational knowledge in testing and evaluating rubber for distinct industry applications and product development.
- Proficiency in sample collection from factory environments to ensure quality compliance and adherence to predefined standards.
- Capable of conducting thorough quality control activities to verify product conformity and maintain high-quality benchmarks.
- Effective communication and problem-solving skills to address quality concerns with relevant stakeholders and facilitate improvements.
Roles and Responsibilities
- Conduct routine quality checks on raw materials and finished products to maintain standards and ensure customer satisfaction.
- Implement quality control procedures and processes aligned with QMS to uphold product quality and safety requirements.
- Collaborate with production teams to address quality issues and introduce corrective actions for continuous process improvements.
- Prepare detailed reports on quality findings and recommend strategic adjustments for superior production outcomes.
- Perform audits on production processes and quality management practices to identify areas for enhancement and operational efficiency.
- Monitor production environments to prevent defects and ensure adherence to established quality parameters.
- Identify root causes of quality deviations and work collaboratively with cross-functional teams to develop effective solutions.
- Keep abreast of industry best practices and technological advancements in quality control to drive innovation across operational functions.
This advertiser has chosen not to accept applicants from your region.
4
Quality Control
Samba, Jammu and Kashmir
Kaiser Industries Limited
Posted 21 days ago
Job Viewed
Job Description
Company Overview
Kaiser Industries Limited is a prominent manufacturer of surfactants and specialty chemicals, serving the agro-chemical industry for over 30 years. With state-of-the-art plants in Haryana, J&K, and Gujarat, the company boasts a cutting-edge R&D facility and industry's best quality assurance systems. Besides agrochemical surfactants, it operates in paints, synthetic lubricants, cosmetics, oil field chemicals, textiles, and leather chemicals sectors. The company headquarters is located in Bahadurgarh, Haryana.
Job Overview
Kaiser Industries Limited is seeking a Mid-Level Quality Control professional, specializing in chemical quality control, to join our team in Samba (J&K). This full-time position requires a maximum of 3-6 years of work experience. The ideal candidate will ensure that our chemical manufacturing processes meet the highest quality standards. As a pivotal part of our operations, you will be responsible for maintaining the reliability and efficiency of our products.
Qualifications and Skills
- Proficient with Statistical Process Control (SPC) including data analysis and interpretation to maintain chemical processes (Mandatory skill).
- Thorough understanding and implementation of ISO 9001 Standards to enhance quality assurance (Mandatory skill).
- Strong experience with Quality Management Systems (QMS) to oversee quality throughout the production (Mandatory skill).
- Ability to use calipers and micrometers for precise measurements in quality assessments of manufactured chemicals.
- Knowledge of Non-Destructive Testing (NDT) methods to inspect materials without causing damage.
- Expertise in Root Cause Analysis to effectively identify and rectify issues impacting product quality.
- Familiarity with Lean Manufacturing Techniques for process optimization and waste reduction in the production line.
- Experience in Automated Inspection Systems to foster efficiency and accuracy in quality checks.
Roles and Responsibilities
- Conduct regular quality inspections and tests on raw materials and finished products to maintain high standards.
- Implement and monitor Statistical Process Control (SPC) methods to improve production efficiency.
- Ensure compliance with ISO 9001 and other quality management standards in all areas of manufacturing.
- Analyze quality test results and provide technical expertise for quality system improvements.
- Coordinate with production and R&D teams to ensure process and materials meet predefined specifications and standards.
- Investigate and document any product or process non-conformance, recommending corrective actions.
- Drive continuous improvement initiatives through effective root cause analysis and solution implementation.
- Maintain up-to-date documentation of quality control processes and improvement actions.
This advertiser has chosen not to accept applicants from your region.
5
QA/ Process Specialist - RCM
Bangalore, Karnataka
Huron Consulting Group
Posted 1 day ago
Job Viewed
Job Description
Huron helps its clients drive growth, enhance performance and sustain leadership in the markets they serve. We help healthcare organizations build innovation capabilities and accelerate key growth initiatives, enabling organizations to own the future, instead of being disrupted by it. Together, we empower clients to create sustainable growth, optimize internal processes and deliver better consumer outcomes.
Health systems, hospitals and medical clinics are under immense pressure to improve clinical outcomes and reduce the cost of providing patient care. Investing in new partnerships, clinical services and technology is not enough to create meaningful and substantive change. To succeed long-term, healthcare organizations must empower leaders, clinicians, employees, affiliates and communities to build cultures that foster innovation to achieve the best outcomes for patients.
Joining the Huron team means you'll help our clients evolve and adapt to the rapidly changing healthcare environment and optimize existing business operations, improve clinical outcomes, create a more consumer-centric healthcare experience, and drive physician, patient and employee engagement across the enterprise.
Join our team as the expert you are now and create your future.
Postion Summary:
As a QA/ Process Specialist, you will be responsible for team handling, work allocation, client interactions and generate, distribute RCM metrics reports to the leadership team.
Excellent communication skills, attention to detail, and strong technical and problem solving skills are essential aspects of this role.
JOB DETAILS:
- Experience in handling a team / group of 15 to 20 FTEs
- Thorough understanding of RCM processes like Billing, Cash Posting, Credit Balance, Accounts Receivables, Denial Management & Correspondence review
- Very good understanding of RCM metrics like Days in AR, Ageing above 90 days, Collections and bad debt
- Periodically review teams performance and recommend performance improvement plan wherever required
- Hands on in preparing daily, weekly & monthly operational metrics reports from the Practice Management/Billing System and workflow tool using MS-Excel
- Identify trends and patterns from the generated reports and initiate action plan to resolve the AR issues
- Responsible for work allocation / distribution to the team and monitor the team work
- Create and maintain daily operational scorecards to track and report KPI's; assist in volume forecast and capacity planning as required
- Generate and distribute management reports in accurate and timely manner
- Perform data analysis for generating reports on periodic basis including adhocs
- Establish a strong relationship with Team Managers by demonstrating the gaps, trends & patterns identified during the data/report compilation
- Suggest ways of improving the process using Lean Six Sigma methodology and suggesting automation of repetitive processes
- Able to interact with the client effectively
- Willing to work in night shift / US timings
QUALIFICATIONS:
- 5+ years of industry experience
- 3+ year Experience in relevant billing functions is a must
- Proficient in MS Excel and creating Excel macros
- Strong ability to analyze raw data, draw conclusions and develop actionable recommendations
- Ability to handle multiple tasks of reporting simultaneously
- Ability to adapt quickly to new and changing technical environments as well as strong analytical, problem solving and quantitative abilities.
Solid verbal and written communication skills are required.
Education/Certifications:
- Graduate in any disclipline.
**Position Level**
Associate
**Country**
India
At Huron, we're redefining what a consulting organization can be. We go beyond advice to deliver results that last. We inherit our client's challenges as if they were our own. We help them transform for the future. We advocate. We make a difference. And we intelligently, passionately, relentlessly do great work.together.
Are you the kind of person who stands ready to jump in, roll up your sleeves and transform ideas into action? Then come discover Huron.
Whether you have years of experience or come right out of college, we invite you to explore our many opportunities. Find out how you can use your talents and develop your skills to make an impact immediately. Learn about how our culture and values provide you with the kind of environment that invites new ideas and innovation. Come see how we collaborate with each other in a culture of learning, coaching, diversity and inclusion. And hear about our unwavering commitment to make a difference in partnership with our clients, shareholders, communities and colleagues.
Huron Consulting Group offers a competitive compensation and benefits package including medical, dental, and vision coverage to employees and dependents; a 401(k) plan with a generous employer match; an employee stock purchase plan; a generous Paid Time Off policy; and paid parental leave and adoption assistance. Our Wellness Program supports employee total well-being by providing free annual health screenings and coaching, bank at work, and on-site workshops, as well as ongoing programs recognizing major events in the lives of our employees throughout the year. All benefits and programs are subject to applicable eligibility requirements.
Huron is fully committed to providing equal employment opportunity to job applicants and employees in recruitment, hiring, employment, compensation, benefits, promotions, transfers, training, and all other terms and conditions of employment. Huron will not discriminate on the basis of age, race, color, gender, marital status, sexual orientation, gender identity, pregnancy, national origin, religion, veteran status, physical or mental disability, genetic information, creed, citizenship or any other status protected by laws or regulations in the locations where we do business. We endeavor to maintain a drug-free workplace.
Health systems, hospitals and medical clinics are under immense pressure to improve clinical outcomes and reduce the cost of providing patient care. Investing in new partnerships, clinical services and technology is not enough to create meaningful and substantive change. To succeed long-term, healthcare organizations must empower leaders, clinicians, employees, affiliates and communities to build cultures that foster innovation to achieve the best outcomes for patients.
Joining the Huron team means you'll help our clients evolve and adapt to the rapidly changing healthcare environment and optimize existing business operations, improve clinical outcomes, create a more consumer-centric healthcare experience, and drive physician, patient and employee engagement across the enterprise.
Join our team as the expert you are now and create your future.
Postion Summary:
As a QA/ Process Specialist, you will be responsible for team handling, work allocation, client interactions and generate, distribute RCM metrics reports to the leadership team.
Excellent communication skills, attention to detail, and strong technical and problem solving skills are essential aspects of this role.
JOB DETAILS:
- Experience in handling a team / group of 15 to 20 FTEs
- Thorough understanding of RCM processes like Billing, Cash Posting, Credit Balance, Accounts Receivables, Denial Management & Correspondence review
- Very good understanding of RCM metrics like Days in AR, Ageing above 90 days, Collections and bad debt
- Periodically review teams performance and recommend performance improvement plan wherever required
- Hands on in preparing daily, weekly & monthly operational metrics reports from the Practice Management/Billing System and workflow tool using MS-Excel
- Identify trends and patterns from the generated reports and initiate action plan to resolve the AR issues
- Responsible for work allocation / distribution to the team and monitor the team work
- Create and maintain daily operational scorecards to track and report KPI's; assist in volume forecast and capacity planning as required
- Generate and distribute management reports in accurate and timely manner
- Perform data analysis for generating reports on periodic basis including adhocs
- Establish a strong relationship with Team Managers by demonstrating the gaps, trends & patterns identified during the data/report compilation
- Suggest ways of improving the process using Lean Six Sigma methodology and suggesting automation of repetitive processes
- Able to interact with the client effectively
- Willing to work in night shift / US timings
QUALIFICATIONS:
- 5+ years of industry experience
- 3+ year Experience in relevant billing functions is a must
- Proficient in MS Excel and creating Excel macros
- Strong ability to analyze raw data, draw conclusions and develop actionable recommendations
- Ability to handle multiple tasks of reporting simultaneously
- Ability to adapt quickly to new and changing technical environments as well as strong analytical, problem solving and quantitative abilities.
Solid verbal and written communication skills are required.
Education/Certifications:
- Graduate in any disclipline.
**Position Level**
Associate
**Country**
India
At Huron, we're redefining what a consulting organization can be. We go beyond advice to deliver results that last. We inherit our client's challenges as if they were our own. We help them transform for the future. We advocate. We make a difference. And we intelligently, passionately, relentlessly do great work.together.
Are you the kind of person who stands ready to jump in, roll up your sleeves and transform ideas into action? Then come discover Huron.
Whether you have years of experience or come right out of college, we invite you to explore our many opportunities. Find out how you can use your talents and develop your skills to make an impact immediately. Learn about how our culture and values provide you with the kind of environment that invites new ideas and innovation. Come see how we collaborate with each other in a culture of learning, coaching, diversity and inclusion. And hear about our unwavering commitment to make a difference in partnership with our clients, shareholders, communities and colleagues.
Huron Consulting Group offers a competitive compensation and benefits package including medical, dental, and vision coverage to employees and dependents; a 401(k) plan with a generous employer match; an employee stock purchase plan; a generous Paid Time Off policy; and paid parental leave and adoption assistance. Our Wellness Program supports employee total well-being by providing free annual health screenings and coaching, bank at work, and on-site workshops, as well as ongoing programs recognizing major events in the lives of our employees throughout the year. All benefits and programs are subject to applicable eligibility requirements.
Huron is fully committed to providing equal employment opportunity to job applicants and employees in recruitment, hiring, employment, compensation, benefits, promotions, transfers, training, and all other terms and conditions of employment. Huron will not discriminate on the basis of age, race, color, gender, marital status, sexual orientation, gender identity, pregnancy, national origin, religion, veteran status, physical or mental disability, genetic information, creed, citizenship or any other status protected by laws or regulations in the locations where we do business. We endeavor to maintain a drug-free workplace.
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Head of Quality Control / Assurance
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Quality Control Chemist
Bathinda, Punjab
Cargill
Posted 1 day ago
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Job Description
**Job Purpose and Impact**
The Assistant Manager - QC will provide expertise with all daily operations in quality control laboratories. In this role, you will support the buildup and maintenance of the rapid technology platform by providing reliable accurate analytical figures as well as perform validation and troubleshooting of new analytical methods to ensure they meet the requirements and deadlines.
**Key Accountabilities**
+ Provide analytical support to Rapid Technology Application platform by releasing precise and accurate results and ensure scope of testing parameter is sufficient to build MPA module.
+ Provide ongoing technical support to stakeholders, investigate quality problems and deliver improvement actions with follow up.
+ Perform method validation and verification to roll out new testing method in the lab.
+ Document standard operating procedures, identify possible trends in testing results with data analysis software and provide input to team members to improve quality control system.
+ Organize and maintain accurate and pertinent data, including spreadsheets, graphs and reports.
+ Maintain systems and techniques for reporting data across functional areas.
+ Organize and participate ring tests with the goal to check and control methods and equipment.
+ Handle basic issues and problems under direct supervision, while escalating more complex issues to appropriate staff.
+ Other duties as assigned
**Qualifications**
**Minimum Qualifications**
+ Bachelor's degree in a related field or equivalent experience
**Preferred Qualifications**
+ "Able to work independently, possess positive working attitude with high initiative level, and communicate effectively"
+ Necessary English reading capacity
+ Experience with chemical analysis (preferable)- oils and fats, starch, sweeteners, etc.
+ Knowledge in calibrate, maintain and troubleshoot various analytical instruments such as GC, HPLC, AAS, ICP, NIR etc
+ Able to demonstrate sound understanding of Statistical Process Control (SPC), method validation and report writing
+ Minimum of Three years of working experience in the Food industry Lab
The Assistant Manager - QC will provide expertise with all daily operations in quality control laboratories. In this role, you will support the buildup and maintenance of the rapid technology platform by providing reliable accurate analytical figures as well as perform validation and troubleshooting of new analytical methods to ensure they meet the requirements and deadlines.
**Key Accountabilities**
+ Provide analytical support to Rapid Technology Application platform by releasing precise and accurate results and ensure scope of testing parameter is sufficient to build MPA module.
+ Provide ongoing technical support to stakeholders, investigate quality problems and deliver improvement actions with follow up.
+ Perform method validation and verification to roll out new testing method in the lab.
+ Document standard operating procedures, identify possible trends in testing results with data analysis software and provide input to team members to improve quality control system.
+ Organize and maintain accurate and pertinent data, including spreadsheets, graphs and reports.
+ Maintain systems and techniques for reporting data across functional areas.
+ Organize and participate ring tests with the goal to check and control methods and equipment.
+ Handle basic issues and problems under direct supervision, while escalating more complex issues to appropriate staff.
+ Other duties as assigned
**Qualifications**
**Minimum Qualifications**
+ Bachelor's degree in a related field or equivalent experience
**Preferred Qualifications**
+ "Able to work independently, possess positive working attitude with high initiative level, and communicate effectively"
+ Necessary English reading capacity
+ Experience with chemical analysis (preferable)- oils and fats, starch, sweeteners, etc.
+ Knowledge in calibrate, maintain and troubleshoot various analytical instruments such as GC, HPLC, AAS, ICP, NIR etc
+ Able to demonstrate sound understanding of Statistical Process Control (SPC), method validation and report writing
+ Minimum of Three years of working experience in the Food industry Lab
This advertiser has chosen not to accept applicants from your region.
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