1,299 Medical Quality Assurance jobs in India
Medical Copy Quality Assurance Specialist
Hyderabad, Andhra Pradesh
Roche
Posted 2 days ago
Job Viewed
Job Description
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
**The Position**
**Medical Copy Quality Assurance Specialist**
**Roche India - Roche Services & Solutions**
**Hyderabad**
Roche is a stable and innovative biotechnological company offering exceptional career paths and great benefits for fresh graduates and outstanding professionals. We are continuously expanding, looking for new talents to join our transforming Roche Services & Solutions Center. We offer a flexible working framework (2 office days/week on average).
The Global Digital Hub growing business line within Roche Services & Solutions Center. Our main purpose is to strengthen the digital capabilities of Roche globally by supporting central initiatives with Social Media Management, Brand Support, Digital Publishing Services, Marketing Automation, Content Creation, and Creative Design.
**Position Summary**
As a Medical Copy Quality Assurance Specialist in the growing medical copy and content team within Roche Services & Solutions, you will play a crucial role in reviewing and editing various forms of content, such as articles, blog posts, social media posts, website content, and promotional materials related to medical and healthcare topics. This specialized team focuses on generating commercial content intended for various digital formats (emails, videos, banners, infographics, websites, etc.). Their work plays a crucial role in supporting the communication strategies developed by Roche's global and local business teams.
**Your Opportunity:**
We are seeking a meticulous and detail-oriented Medical Copy Quality Assurance (QA) Specialist to ensure the accuracy, consistency, and compliance of digital medical / scientific materials designed for the US market. The primary responsibility of this role is to conduct comprehensive quality checks (QC) for various digital materials such as emails, banners, and advertisements, with a focus on medical and scientific accuracy. This position demands a keen eye for detail and the ability to collaborate with cross-functional teams to maintain the highest standard of quality.
Day-to-Day Role Description:
+ Review and QC of Medical/Scientific Digital Materials:
+ Examine emails, banners, ads, and other digital assets, checking:
+ Foundational quality and fit to brief
+ Language use, style, spelling, grammar, formatting, etc.
+ Scientific and medical accuracy
+ Consistency with brand guidelines and technical specifications
+ Collaborate with Teams:
+ Work closely with writers, designers, and project managers to address feedback and implement revisions.
+ Provide constructive feedback to enhance the accuracy and quality of deliverables.
+ Maintain Documentation:
+ Keep thorough records of QC findings and suggestions.
+ Track revisions and document outcomes for continuous improvement.
Step-by-Step Checklist for Medical/Scientific QC of Digital Materials:
+ Check the Accuracy of Content:
+ Verify that all scientific and medical claims are evidence-based and supported by reliable sources.
+ Confirm that the content aligns with current medical guidelines and applicable regulatory standards.
+ Conduct a Thorough Language Check:
+ Review for grammar, punctuation, and spelling errors.
+ Ensure clarity, conciseness, and readability, tailoring the language to the target audience.
+ Verify Consistency:
+ Confirm that terminology, branding, and tone are consistent throughout the material.
+ Ensure completeness of all text elements, e.g., footnotes, references, abbreviations, special formatting, etc.
+ Cross-check for any conflicting information.
+ Check for copy formatting/layout issues.
+ Validate Visual Elements:
+ Review images, charts, or graphics for scientific accuracy and appropriate usage.
+ Ensure visual elements enhance the overall message without introducing errors.
+ Check Compliance:
+ Ensure compliance with US regulations, industry standards, and client-specific guidelines.
+ Flag any material that requires further legal or medical review.
+ Perform Final Review:
+ Reassess the material after all changes have been implemented.
+ Give final approval, ensuring it is error-free and ready for distribution.
**Who You Are**
We are looking for knowledgeable individuals who are highly involved and passionate about writing and language!
+ 2-3 years of experience in similar position
+ Strong medical or science background
+ A higher degree in life sciences is highly preferred, but candidates with other relevant experience will also be considered
+ Minimum C2 level proficiency in English, with excellent written and verbal communication skills
+ Proven experience in quality control processes, particularly in reviewing medical or scientific content
+ Collaborative attitude - working effectively across our diverse resources and business stakeholders
+ Ability to work within a team and in different time zones
+ Excellent attention to detail, consistency, clarity, and scientific rigor
+ Customer-service mentality & can-do attitude
+ Experience with the standard IT applications, preferably including Google suite
+ Continuous improvement and growth mindset
+ Ability to work in a fast-paced and changing environment, ability to prioritize tasks
**Who we are**
A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
**Roche is an Equal Opportunity Employer.**
**The Position**
**Medical Copy Quality Assurance Specialist**
**Roche India - Roche Services & Solutions**
**Hyderabad**
Roche is a stable and innovative biotechnological company offering exceptional career paths and great benefits for fresh graduates and outstanding professionals. We are continuously expanding, looking for new talents to join our transforming Roche Services & Solutions Center. We offer a flexible working framework (2 office days/week on average).
The Global Digital Hub growing business line within Roche Services & Solutions Center. Our main purpose is to strengthen the digital capabilities of Roche globally by supporting central initiatives with Social Media Management, Brand Support, Digital Publishing Services, Marketing Automation, Content Creation, and Creative Design.
**Position Summary**
As a Medical Copy Quality Assurance Specialist in the growing medical copy and content team within Roche Services & Solutions, you will play a crucial role in reviewing and editing various forms of content, such as articles, blog posts, social media posts, website content, and promotional materials related to medical and healthcare topics. This specialized team focuses on generating commercial content intended for various digital formats (emails, videos, banners, infographics, websites, etc.). Their work plays a crucial role in supporting the communication strategies developed by Roche's global and local business teams.
**Your Opportunity:**
We are seeking a meticulous and detail-oriented Medical Copy Quality Assurance (QA) Specialist to ensure the accuracy, consistency, and compliance of digital medical / scientific materials designed for the US market. The primary responsibility of this role is to conduct comprehensive quality checks (QC) for various digital materials such as emails, banners, and advertisements, with a focus on medical and scientific accuracy. This position demands a keen eye for detail and the ability to collaborate with cross-functional teams to maintain the highest standard of quality.
Day-to-Day Role Description:
+ Review and QC of Medical/Scientific Digital Materials:
+ Examine emails, banners, ads, and other digital assets, checking:
+ Foundational quality and fit to brief
+ Language use, style, spelling, grammar, formatting, etc.
+ Scientific and medical accuracy
+ Consistency with brand guidelines and technical specifications
+ Collaborate with Teams:
+ Work closely with writers, designers, and project managers to address feedback and implement revisions.
+ Provide constructive feedback to enhance the accuracy and quality of deliverables.
+ Maintain Documentation:
+ Keep thorough records of QC findings and suggestions.
+ Track revisions and document outcomes for continuous improvement.
Step-by-Step Checklist for Medical/Scientific QC of Digital Materials:
+ Check the Accuracy of Content:
+ Verify that all scientific and medical claims are evidence-based and supported by reliable sources.
+ Confirm that the content aligns with current medical guidelines and applicable regulatory standards.
+ Conduct a Thorough Language Check:
+ Review for grammar, punctuation, and spelling errors.
+ Ensure clarity, conciseness, and readability, tailoring the language to the target audience.
+ Verify Consistency:
+ Confirm that terminology, branding, and tone are consistent throughout the material.
+ Ensure completeness of all text elements, e.g., footnotes, references, abbreviations, special formatting, etc.
+ Cross-check for any conflicting information.
+ Check for copy formatting/layout issues.
+ Validate Visual Elements:
+ Review images, charts, or graphics for scientific accuracy and appropriate usage.
+ Ensure visual elements enhance the overall message without introducing errors.
+ Check Compliance:
+ Ensure compliance with US regulations, industry standards, and client-specific guidelines.
+ Flag any material that requires further legal or medical review.
+ Perform Final Review:
+ Reassess the material after all changes have been implemented.
+ Give final approval, ensuring it is error-free and ready for distribution.
**Who You Are**
We are looking for knowledgeable individuals who are highly involved and passionate about writing and language!
+ 2-3 years of experience in similar position
+ Strong medical or science background
+ A higher degree in life sciences is highly preferred, but candidates with other relevant experience will also be considered
+ Minimum C2 level proficiency in English, with excellent written and verbal communication skills
+ Proven experience in quality control processes, particularly in reviewing medical or scientific content
+ Collaborative attitude - working effectively across our diverse resources and business stakeholders
+ Ability to work within a team and in different time zones
+ Excellent attention to detail, consistency, clarity, and scientific rigor
+ Customer-service mentality & can-do attitude
+ Experience with the standard IT applications, preferably including Google suite
+ Continuous improvement and growth mindset
+ Ability to work in a fast-paced and changing environment, ability to prioritize tasks
**Who we are**
A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
**Roche is an Equal Opportunity Employer.**
This advertiser has chosen not to accept applicants from your region.
0
Quality Control
Ernakulam, Kerala
JobStars HR Solutions Pvt Ltd
Posted 23 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.
1
Quality Control
Samba, Jammu and Kashmir
Kaiser Industries Limited
Posted 23 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.
2
Senior Quality Assurance Engineer - Medical Devices
682001 Kochi, Kerala
₹80000 Annually
WhatJobs
Posted 10 days ago
Job Viewed
Job Description
Our client is seeking a highly meticulous and experienced Senior Quality Assurance Engineer specializing in medical devices. This remote role is crucial for ensuring that our client's innovative medical products meet the highest standards of safety, efficacy, and regulatory compliance. You will be responsible for developing, implementing, and maintaining comprehensive quality management systems (QMS) that align with global regulatory requirements such as FDA, ISO 13485, and CE marking. The ideal candidate possesses a deep understanding of the medical device product lifecycle, risk management principles (ISO 14971), and validation processes. You will lead quality assurance activities, including design controls, CAPA management, complaint handling, and internal audits. Your expertise will be instrumental in driving product quality throughout the development and manufacturing stages. As a remote Senior QA Engineer, you will collaborate closely with cross-functional teams, including R&D, manufacturing, regulatory affairs, and clinical affairs, utilizing digital collaboration tools to ensure seamless communication and project execution.
Responsibilities:
Responsibilities:
- Develop, implement, and manage the Quality Management System (QMS) for medical devices.
- Ensure compliance with relevant regulatory standards, including FDA 21 CFR Part 820, ISO 13485, and other international regulations.
- Lead and participate in design control activities throughout the product development lifecycle.
- Establish and manage processes for Corrective and Preventive Actions (CAPA).
- Oversee the complaint handling process and ensure timely investigation and resolution.
- Conduct internal audits of QMS processes and manufacturing operations.
- Develop and implement risk management strategies in accordance with ISO 14971.
- Write, review, and approve quality-related documents, such as SOPs, work instructions, and validation protocols.
- Collaborate with cross-functional teams to ensure product quality and compliance.
- Provide training on quality system requirements and best practices.
- Support external regulatory inspections and audits.
- Contribute to the continuous improvement of quality processes and systems.
- Stay current with evolving regulatory requirements and industry trends in the medical device sector.
- Bachelor's degree in Engineering (Biomedical, Electrical, Mechanical) or a related scientific field.
- Minimum of 7 years of experience in Quality Assurance within the medical device industry.
- In-depth knowledge of QMS requirements for medical devices (ISO 13485, FDA 21 CFR Part 820).
- Proven experience with design controls, risk management (ISO 14971), and CAPA processes.
- Familiarity with validation and verification methodologies.
- Excellent analytical, problem-solving, and decision-making skills.
- Strong written and verbal communication skills.
- Ability to work independently and manage multiple priorities effectively in a remote environment.
- Experience with audit preparation and hosting regulatory inspections.
- Relevant certifications (e.g., ASQ Certified Quality Engineer) are a plus.
- Must be comfortable and productive working remotely, utilizing all necessary digital collaboration tools.
This advertiser has chosen not to accept applicants from your region.
3
Senior Quality Assurance Engineer (Medical Devices)
682001 Kochi, Kerala
₹1300000 Annually
WhatJobs
Posted 17 days ago
Job Viewed
Job Description
Our client, a leader in medical device manufacturing, is seeking a meticulous and experienced Senior Quality Assurance Engineer to join their dedicated team in **Kochi, Kerala, IN**. This role is integral to ensuring that our products meet the highest standards of quality, safety, and regulatory compliance. You will be responsible for developing, implementing, and maintaining quality assurance systems and processes throughout the product lifecycle, from design and development to manufacturing and post-market surveillance. Key responsibilities include conducting internal audits, managing non-conformances, performing root cause analysis, and implementing corrective and preventive actions (CAPA). You will also play a vital role in ensuring compliance with international standards such as ISO 13485, FDA regulations, and other relevant quality management system requirements. The Senior QA Engineer will collaborate closely with R&D, manufacturing, and regulatory affairs teams to integrate quality considerations into all aspects of product development. The ideal candidate will have a strong background in quality assurance, preferably within the medical device or pharmaceutical industry. A thorough understanding of quality management systems, regulatory requirements, and statistical process control is essential. Experience with risk management methodologies (e.g., FMEA) and validation processes is highly desirable. Excellent analytical, problem-solving, and documentation skills are required. A Bachelor's or Master's degree in Engineering (Biomedical, Mechanical, Electrical) or a related scientific field is preferred. This role offers a hybrid work arrangement, allowing for flexibility while ensuring essential on-site presence in **Kochi, Kerala, IN**, for critical quality assurance activities.
This advertiser has chosen not to accept applicants from your region.
4
Head of Quality Control / Assurance
Vadodara, Gujarat
GB Solar
Posted 4 days ago
Job Viewed
Job Description
This advertiser has chosen not to accept applicants from your region.
5
Quality Control Chemist
Bathinda, Punjab
Cargill
Posted 2 days ago
Job Viewed
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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6
Quality Control Executive
Mumbai, Maharashtra
ThermoFisher Scientific
Posted 2 days ago
Job Viewed
Job Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials
**Job Description**
**About the Company**
Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. Our Innovative Laboratory technologies & Services makes it easier for customers.
**Responsibilities:**
+ Responsible to carry out analysis on analytical instruments like HPLC, GC, ICP, GCMS etc.
+ Responsible to analyse and interpretate the analytical data basis customer requirement on Window based tools
+ Process knowledge of chemical testing, Analytical work, basic trouble shooting, method preparation/validation, handling and calibration of instrument like HPLC, GC, ICP, GCMS etc.
+ Responsible to maintain and carry out chemical analysis basis ISO/NABL standards 17025 and 17034.
+ Responsible for good laboratory practice in Quality control lab.
+ Perform analysis and reporting of raw materials, packing materials, Finished products, in-process and routine analysis.
+ Preparation of volumetric solutions, reagents, buffer solutions, indicator and maintain its records.
+ Perform standardization of volumetric solutions.
+ Preparation of Quality control SOP's.
+ Responsible to be self aware of Safety and Quality compliance and adhere to set compliance norms.
**Experience and Skill Sets:**
+ B.Sc. Chemistry with five years experience
+ M.Sc in Analytical / Inorganic chemistry with three years experience
+ The role needs good communication, presentation skill & solution-oriented approach.
**Benefits:**
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
At Thermo Fisher Scientific, each one of our 100,000 extraordinary minds have a unique story to tell.
ThermoFisher is committed to crafting a diverse work environment that values and respects individuals.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials
**Job Description**
**About the Company**
Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. Our Innovative Laboratory technologies & Services makes it easier for customers.
**Responsibilities:**
+ Responsible to carry out analysis on analytical instruments like HPLC, GC, ICP, GCMS etc.
+ Responsible to analyse and interpretate the analytical data basis customer requirement on Window based tools
+ Process knowledge of chemical testing, Analytical work, basic trouble shooting, method preparation/validation, handling and calibration of instrument like HPLC, GC, ICP, GCMS etc.
+ Responsible to maintain and carry out chemical analysis basis ISO/NABL standards 17025 and 17034.
+ Responsible for good laboratory practice in Quality control lab.
+ Perform analysis and reporting of raw materials, packing materials, Finished products, in-process and routine analysis.
+ Preparation of volumetric solutions, reagents, buffer solutions, indicator and maintain its records.
+ Perform standardization of volumetric solutions.
+ Preparation of Quality control SOP's.
+ Responsible to be self aware of Safety and Quality compliance and adhere to set compliance norms.
**Experience and Skill Sets:**
+ B.Sc. Chemistry with five years experience
+ M.Sc in Analytical / Inorganic chemistry with three years experience
+ The role needs good communication, presentation skill & solution-oriented approach.
**Benefits:**
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
At Thermo Fisher Scientific, each one of our 100,000 extraordinary minds have a unique story to tell.
ThermoFisher is committed to crafting a diverse work environment that values and respects individuals.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
This advertiser has chosen not to accept applicants from your region.
7
Mgr, Quality Control
Pudupakkam, Tamil Nadu
Endo International
Posted 2 days ago
Job Viewed
Job Description
**Job Description Summary**
To manage 12-member team of analysts, senior analysts in QC - microbiology laboratory.
To prepare plans, protocols, reports and to execute day to day operations in microbiology laboratory.
**Job Description**
To manage a team of analysts, senior analysts, trainees in QC - microbiology laboratory.
To prepare plans, protocols, reports and to execute day to day operations in microbiology laboratory.
**Commitment to Diversity, Equity, and Inclusion:**
At Endo, our diversity unites and empowers us as One Team, and we are committed to cultivating, and valuing, each person's unique perspective. We actively promote a culture of inclusion that draws strength from our broad spectrums of diversity, including race, ethnicity, religion, gender identity or expression, national origin, color, sexual orientation, disability status, age, and all our other unique characteristics, qualifications, demonstrated skills, achievements, and contributions, backgrounds, experiences, cultures, styles, and talents.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
To manage 12-member team of analysts, senior analysts in QC - microbiology laboratory.
To prepare plans, protocols, reports and to execute day to day operations in microbiology laboratory.
**Job Description**
To manage a team of analysts, senior analysts, trainees in QC - microbiology laboratory.
To prepare plans, protocols, reports and to execute day to day operations in microbiology laboratory.
**Commitment to Diversity, Equity, and Inclusion:**
At Endo, our diversity unites and empowers us as One Team, and we are committed to cultivating, and valuing, each person's unique perspective. We actively promote a culture of inclusion that draws strength from our broad spectrums of diversity, including race, ethnicity, religion, gender identity or expression, national origin, color, sexual orientation, disability status, age, and all our other unique characteristics, qualifications, demonstrated skills, achievements, and contributions, backgrounds, experiences, cultures, styles, and talents.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
This advertiser has chosen not to accept applicants from your region.
8
Quality Control Engineer
Jak Industries
Posted today
Job Viewed
Job Description
Company Description
JAK Industries, based in Chennai, specializes in Heavy Fabrication with over 20+ years of experience. Led by a team of professionals with nearly 40 years of expertise in Heavy Structural Fabrication, the company works with materials such as Carbon Steel, Stainless Steel, and Aluminium.
Job Role
This is a full-time on-site role for a Quality Control professional at JAK Industries in Chennai. The role involves tasks related to quality assurance, quality management, and utilizing analytical skills to ensure high standards of fabrication.
Requirements:
- Qualified Mechanical Diploma/ Engineering degree holders Required for Quality Department at Ambattur.
- Knowledge in welding will be an added advantage.
- Immediate joiners are most preferred.
- Should follow the standard requirements of ISO 9001:2015, ISO 14001:2015 & ISO 45001:2018.
- Job Types: Full-time, Permanent
Qualifications
- Minimum 2 yrs of Experience in Quality Control
- Quality Control and Quality Assurance skills
- Strong Analytical Skills
- Effective Communication abilities
- Experience in Quality Management
- Attention to detail and problem-solving skills
- Qualifications in Engineering or related field
This advertiser has chosen not to accept applicants from your region.
9