8,814 Global Quality jobs in India
Manager, Global Quality Operations
Posted today
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Our vision is to transform how the world uses information to enrich life for all.
Micron Technology is a world leader in innovating memory and storage solutions that accelerate the transformation of information into intelligence, inspiring the world to learn, communicate and advance faster than ever.
As a Global Quality (GQ) Operations Manager at Micron Technology Inc., your role involves managing Package and Device Reliability lab operations. In this capacity, you ensure optimal lab performance to support Product and Package Reliability Qualification. You will also interface with internal and external stakeholders to identify the necessary resources to support the qualification plan.
Your job is to work together with other functional groups both locally and globally to achieve organizational and business objectives. Additionally, you will lead the operation metrics for tactical and strategic qualification readiness.
You will be expected to provide regular updates and highlight critical issues to the management team. Furthermore, you will provide regular performance feedback to team members, establish goals and development plans, and provide opportunities to expand skills and career growth.
Key Responsibilities and Tasks:
Manage Team Member Performance:
Build an Effective Team:
Lab Operation :
Manage New Product Qualification Activities
Objective and Goals Setting :
Minimum Qualification:
Specialist - Global Quality & Regulatory Customer Support
Posted today
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JD: Specialist – Global Quality & Regulatory Customer Support
Are you the kind of person that is always thinking, sketching, seeking, and adjusting? Who needs to understand how things work and then figure out how they can work better? Are you a passionate, tenacious, solver who loves to work with others who share your drive? Are you positive, constructive, and ingenious?
Are you always solving?
Then we’d like to meet you and bet you’d like to meet us.
Ashland has an exciting opportunity for a Specialist – Global Quality & Regulatory Customer Support team to join our Ashland India business at our Mumbai, MH office. This is a very visible, significant role within the Company and the Quality & Regulatory function. This position will report to Manager - Quality & Regulatory.
The responsibilities of the position include, but are not limited to, the following:
This position is responsible for supporting the product regulatory affairs customer programs supporting LATAM region for excipients, APIs, nutrition products commercial activities and their related operations. The position requires collaboration with regional product regulatory staff, business partners and internal stakeholders from various functional groups. In addition to providing governance and interpretation for regulatory requirements internally.
- 5 - 7 years of Product Regulatory relevant experience.
- Bachelor's or Master's Degree, in chemistry, toxicology, biology or other science discipline.
- Sound technical knowledge of the Pharma regulatory requirements
- Pharmaceutical industry Knowledge & Background
- Background with analytical testing is an added advantage but not a necessity.
- Excellent verbal/written communication skills and ability to effectively present scientific data to management/customers.
Technical Skills, Knowledge and Abilities:
- Computer & Analytical skills (Knowledge of SAP & Salesforce an added advantage)
- Good at Time management & delivering on agreed commitments
- Customer oriented & Problem-solving approach
- Good Listener & convincing Presenter
- Interpersonal savvy & effective Communicator
- Fast learner with a flexible style and the ability to adjust to changing business
- priorities and changing regulatory landscapes
- Responsive and highly accountable: solution-, results- and action-oriented
- Excellent verbal / written communication and interpersonal skills
- Ability to interface with internal and external contacts at all levels
- Excellent organizational and prioritization skills
- Ability to handle multiple tasks / projects simultaneously.
- Actively contribute to the organizational goals by taking initiative, executing on goals and focusing on performance and safety.
- Improve the organization capacity and capabilities through building collaborative.
- relationships, optimizing diverse talent and utilizing positive communications and influence with others
Responsibilities & Customer Requests:
- Support quality/regulatory queries including quality agreements and any other quality/regulatory requests.
- Collect, evaluate, and collate information from the customer for the standard and non-standard queries and work with internal teams for preparing response to the customer within the set timeframe.
- Proactively work with internal teams to create new statements as per current regulatory guidelines. (i.e. NDMA, TGA compliance, CHP compliance)
- Responsible for preparation and finalization of regulatory standard documents based on the business/ market requirements.
- Drive continuous improvement efforts to satisfy increasing customer expectations.
- Support Ashland’s word class customer experience initiatives in LATAM.
Quality/Regulatory Support for Business Unit:
- Support on quality/regulatory related matters for better understanding regulatory trends and its impact on the business to ensure that strategic business goals are met through the sharing of knowledge and expertise.
- Develop or optimize regulatory technical packages to proactively help the Business Development and Sales teams.
- Liaison between the QA/RA team to support the LATAM region
- Participate in applicable regulatory team initiatives, meeting and projects
- Handling Food and pharma excipients and Active pharmaceutical Ingredients
- Preparation, collection, reviewing, and compilation of the technical and non-technical data for applying as per the guidelines.
- Develop standard regulatory procedures, publication of best practice guidelines.
Senior Associate Quality Assurance - Global Supply Quality
Posted 2 days ago
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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.
Senior Associate Quality Assurance - Global Supply Quality
**What you will do**
Let's do this. Let's change the world. In this vital role you will The Sr. Associate QA position is responsible for the Quality and Compliance Oversight of Raw material suppliers. This position is responsible for being an integral quality member of the Amgen cross-functional raw materials suppliers' team that includes but is not limited to business operations, analytical science, process development, and supply chain.
**Responsibilities** **:**
Working independently, the individual will be responsible for, but not limited to the following:
+ Perform QA Contact role on the Quality Events, Change Control records, Corrective and Preventive Actions, effectiveness verification and documentation
+ Work closely with all relevant stakeholders for the end-to-end process and ensure compliance to GMP/GDP.
+ Prepare, review and approve SOPs and other GMP/GDP documentation in compliance with corporate and regulatory requirements, to ensure alignment with procedures, current Good Manufacturing Practices (cGMP), Good Distribution Practices (GDP) and other applicable regulations
+ Collaborate with raw material suppliers to ensure adherence to quality agreements, identifying performance improvement opportunities
+ Understand and incorporate risk management strategy into the overall raw material lifecycle
+ Provide support to the supplier periodic monitoring oversight activities
+ Support in tactical activities related to internal/external audits and inspections
+ Perform routine quality assessments and provide approval of changes to raw material inspection profiles
+ Take part in operational improvement initiatives, programs, and projects
+ Develop solutions that are thorough, practical, and consistent with functional objectives
+ Ownership of supplier metrics, performance assessments, and other key documents to inform the health of supplier relationships.
+ Work under minimal supervision in line with Amgen Values and Leadership Attributes.
+ This role may require working in shifts or extended hours within the same shift to support global timezones.
**What we expect of you**
We are all different, yet we all use our unique contributions to serve patients. The (vital attribute) professional we seek is a (type of person) with these qualifications.
**Basic Qualifications:**
+ Master's degree and 1 to 3 years of professional experience in related fields OR
+ Bachelor's degree and 3 to 5 years of professional experience in related fields OR
+ Diploma and 7 to 9 years of professional experience in related fields
+ Understanding of GMP/GDP requirements.
+ Familiarity with raw material compendial testing
+ Experience overseeing quality of suppliers or external parties
+ Strong technical writing skills
**Preferred Qualifications:**
+ Experience and strong familiarity with digital tools and computerized systems.
+ Strong continuous improvement approach and lean practices experience.
+ Understanding of end-to-end supply chain business processes.
+ Experience in project management across multiple departments and geographies.
+ Quick process understanding, insight and visualizing.
+ Strong analytical and problem-solving skills.
+ Independent self-starter, able to work autonomously, under pressure and in teams.
+ GMP/GDP knowledge and understanding of pharmaceutical regulations.
+ Energetic, detail oriented, highly motivated with a "can do" outlook.
+ Change management skills.
+ Ability to communicate across all levels of the organization.
+ Effective written and verbal communication skills.
+ Experience with Microsoft Office Tools including Excel, Word, and PowerPoint.
+ Ability to multi-task and prioritize
**What you can expect of us**
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.
In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.
**Apply now**
**for a career that defies imagination**
Objects in your future are closer than they appear. Join us.
**careers.amgen.com**
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Transformers Global Engineering Quality Manager
Posted today
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Job Description
Description
:Job Title: Transformers Global Engineering Quality Manager
The Opportunity
Step into a pivotal role with Hitachi Energy and lead the charge in revolutionizing engineering quality strategies. As the Global Engineering Quality Manager - Transformers, you will be at the forefront of shaping quality benchmarks across global teams, driving transformative initiatives, and optimizing processes that have a lasting impact. This is an opportunity to collaborate with forward-thinking experts, tackle challenges head-on, and contribute to innovation in a meaningful way. Join a team that values inclusivity, continuous improvement, and sustainable practices, all while empowering you to grow and thrive in a diverse and dynamic environment.
How You'll Make an Impact
Your Background
Responsible to ensure compliance with applicable external and internal regulations, procedures, and guidelines.
More About Us
At Hitachi Energy, we champion innovation, inclusivity, and sustainability, offering employees the platform to create solutions that shape the future. With access to development programs and global opportunities, your growth is a shared priority. Join us to make a difference today and every day!
Qualified individuals with a disability may request a reasonable accommodation if you are unable or limited in your ability to use or access the Hitachi Energy career site as a result of your disability. You may request reasonable accommodations by completing a on our website. Please include your contact information and specific details about your required accommodation to support you during the job application process.
This is solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes will not receive a response.
Quality Management Representative
Posted 4 days ago
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Job Description
Job Description – QMS Manager
Experience Required: Minimum 10 Years
Job Summary
The QMS Manager will be responsible for establishing, implementing, and maintaining Quality Management Systems in line with IATF & ISO standards. The role involves handling third-party audits, export audits, and direct customer interactions with OEM and international clients. The incumbent will drive continuous improvement in processes, compliance, and overall quality culture within the organization.
Key Roles & Responsibilities
- Lead and manage QMS Audits (Internal & External) as per IATF 16949 & ISO standards .
- Ensure compliance with OEM-specific quality requirements and act as the primary point of contact for OEM clients.
- Manage Export & Third-Party Audits including Sedex, BSCI, Walmart, etc.
- Establish, review, and update QMS documentation, SOPs, and process controls.
- Handle customer complaints, corrective actions, and preventive actions (CAPA) effectively.
- Work closely with cross-functional teams to ensure alignment with quality standards.
- Drive continuous improvement initiatives to enhance product and process quality.
- Provide training and awareness sessions to employees on QMS, compliance, and audit readiness.
- Represent the company in front of external auditors, regulatory authorities, and global customers.
- Monitor and ensure adherence to quality metrics and report to management.
Skills & Competencies
- Strong knowledge of QMS, IATF 16949, ISO 9001 standards.
- Proven experience in Automotive OEM industry .
- Hands-on experience in handling international audits and compliance requirements.
- Excellent communication, presentation, and stakeholder management skills.
- Ability to work independently and manage cross-functional teams.
- Problem-solving, analytical thinking, and attention to detail.
Ideal Candidate Profile
- Minimum 10 years of relevant experience in Quality Management Systems .
- B.Tech (Mechanical – Regular) is mandatory.
- Prior exposure to OEM & Export customer handling .
- Successful track record in managing third-party audits (Sedex, BSCI, Walmart, etc.).
- Leadership qualities with the ability to drive quality culture across the organization.
Budget up to 8 lacs p.a.
Quality Management Representative
Posted 4 days ago
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Job Description
Experience Required: Minimum 10 Years
Job Summary
The QMS Manager will be responsible for establishing, implementing, and maintaining Quality Management Systems in line with IATF & ISO standards. The role involves handling third-party audits, export audits, and direct customer interactions with OEM and international clients. The incumbent will drive continuous improvement in processes, compliance, and overall quality culture within the organization.
Key Roles & Responsibilities
Lead and manage QMS Audits (Internal & External) as per IATF 16949 & ISO standards .
Ensure compliance with OEM-specific quality requirements and act as the primary point of contact for OEM clients.
Manage Export & Third-Party Audits including Sedex, BSCI, Walmart, etc.
Establish, review, and update QMS documentation, SOPs, and process controls.
Handle customer complaints, corrective actions, and preventive actions (CAPA) effectively.
Work closely with cross-functional teams to ensure alignment with quality standards.
Drive continuous improvement initiatives to enhance product and process quality.
Provide training and awareness sessions to employees on QMS, compliance, and audit readiness.
Represent the company in front of external auditors, regulatory authorities, and global customers.
Monitor and ensure adherence to quality metrics and report to management.
Skills & Competencies
Strong knowledge of QMS, IATF 16949, ISO 9001 standards.
Proven experience in Automotive OEM industry .
Hands-on experience in handling international audits and compliance requirements.
Excellent communication, presentation, and stakeholder management skills.
Ability to work independently and manage cross-functional teams.
Problem-solving, analytical thinking, and attention to detail.
Ideal Candidate Profile
Minimum 10 years of relevant experience in Quality Management Systems .
B.Tech (Mechanical – Regular) is mandatory.
Prior exposure to OEM & Export customer handling .
Successful track record in managing third-party audits (Sedex, BSCI, Walmart, etc.).
Leadership qualities with the ability to drive quality culture across the organization.
Budget up to 8 lacs p.a.
Quality Management Officer
Posted today
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Job Description
Interface with external parties, including vendors and regulatory bodies, to manage quality expectations.
Provide detailed reports and recommendations to senior management regarding quality improvement initiatives.
Company Overview
Sri Sai Overseas Recruitment is a leading Manpower Recruitment & Consultancy Service provider founded in 2019. Headquartered in Vadodara, the company specializes in delivering exceptional recruitment services in India, the Middle East, Europe, and beyond. With expertise gained from professionals experienced in the Gulf countries' Oil & Gas sectors, Sri Sai Overseas Recruitment is committed to understanding and fulfilling client needs across diverse industries globally. For more details, visit our website at Sri Sai Overseas Recruitment .
Job Overview
We are seeking a qualified Junior-level Quality Management Officer to join our team at our Vadodara headquarters. This full-time role involves ensuring compliance across various projects and maintaining high-quality standards. The position is ideal for professionals keen to ensure quality assurance practices and operations. With a dedicated team, Sri Sai Overseas Recruitment is committed to aligning with client needs and ensuring successful global placements.
Qualifications and Skills
- Proficiency in performing root cause analysis to identify problems and recommend effective solutions.
- Experience with statistical process control to monitor and control quality assurance processes.
- Familiarity with total quality management principles aimed at enhancing quality standards and performance.
- Capability to conduct quality audits and ensure processes comply with regulations.
- Understanding of microbiology principles relevant to quality control and assurance.
- Ability to develop and maintain standard operating procedures to enhance operational efficiency.
- Experience in total quality management for consistency and quality in processes.
- Proficiency in FDA regulations (Mandatory skill for ensuring product safety and compliance).
Roles and Responsibilities
- Indent and receipt media, chemicals, reagents for microbiology lab and maintain receipt records.
- Maintain daily usage logbooks of Balance, water bath, PH Meter, Laminar Airflow, Incubator, Fogger, and Antibiotic zone reader & colony counter.
- Maintain daily monitoring records of Refrigerators temperature, incubator temperature, relative humidity (RH), temperature & differential pressure.
- Keep calibration records of PH Meter and analytical balance, as well as all instruments in the Microbiology department.
- Maintain disinfectant preparation & microbiology area and instruments cleaning records.
- Maintain environment monitoring records of settle plate & air sampler methods.
- Prepare MLT reports of raw materials, bulk & finished products.
- Indent media and chemicals required in the microbiology lab.
- Carry out Growth promotion tests (GPT) as per SOP.
- Document daily media preparation & its record as per SOP.
- Maintain autoclave sterilization record of slow exhaust cycle & HPHV cycle.
- Conduct water sampling, analysis & record as per SOP.
- Perform microbial limit test (MLT) of stability products, bulk, raw material & its record as per SOP.
- Conduct bioassay of B12 for bulk.
- Document culture dilution & its records.
- Maintain subculturing and its records.
- Perform swab, rinse, and drains analysis.
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Engineer - Quality Management
Posted today
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External Job Description
- Quality Culture:
- Ensure awareness for quality focus to increase customer satisfaction, particularly in the development process
- Plan, implement and live Quality culture within Product Line and organization level (Implement the defined processes, improve product quality, initiate process improvements, and drive continuous improvements (CI) in projects)
- Ensuring compliance (of products) with legal and normative requirements (including tailoring of processes as appropriate)
- Effectively review product risk management activities (including Risk Analysis, Risk Management Report)
- Collaborate with onsite teams to keep project teams aligned with headquarters' expectations
- Drive best practices within the organization
- Quality Management:
- Define quality strategy in Quality Management Plan
- Drive process compliance in the complete lifecycle process of the medical device - starting with product definition till End of Support
- Act as independent reviewer for design reviews acc to QSR 820.30 (e) with the responsibility of defining and documenting the overall result of the design review.
- Work with internal delivery team and other functions in order to meet the specified Quality Goals of the project
- Supporting and consulting of employees in implementing and realizing the processes as well as decision about tailoring of defined processes - both according to the needs of the business and in compliance with statutory requirements
- Identify opportunities to improve productivity and efficiency with lower costs, reduce non-conformance costs
- Initiate and moderate the root cause analysis and monitor effective and timely implementation of CAPA
- Reporting and Coordination:
- Prepare and provide input to the periodic reports as needed by headquarter team
- Audits and Assessments:
- Conduct / Participate in Internal Audit and External Audits using MDSAP methodology.
- Coordinate and ensure timely closure of audit findings
- Qualification Requirements
- Bachelors or Masters in Engineering / MCA having an excellent academic track record.
- Proficient in managing Quality of complete Software Medical Device Development lifecycle in distributed international environment.
- Experienced in latest trends of Software Product Development (e.g. Trunk Based Development, Continuous Delivery (DevOps) etc)
- Advanced knowledge of quality tools for Metrics data analysis and decision making
- Advanced computer skills (MS Office tools like Word, Access, Excel, PowerPoint and Outlook)
- Highly energetic and "Go-getter"
- Proven ability to independently plan and successfully execute multiple projects based on business priorities.
- Display of a high level of critical thinking in bringing successful resolution to high-impact, complex and cross-functional problems is expected.
- Advanced knowledge of organization&aposs business practices and issues faced and contributions to problem resolution of those issues.
- Excellent organizational and communication skills (e.g. Moderation, presentation to all levels).
- Auditor experience in Medical Device area is preferred.
- 4 - 8 years of successful experience in Quality Management and demonstration of Key Responsibilities and Knowledge as mentioned above. Advanced degree MAY be substituted for experience, where applicable.
Skills Required
Devops, Continuous Delivery, Quality Management
Quality Management Representative
Posted today
Job Viewed
Job Description
Job Description – QMS Manager
Experience Required: Minimum 10 Years
Job Summary
The QMS Manager will be responsible for establishing, implementing, and maintaining Quality Management Systems in line with IATF & ISO standards. The role involves handling third-party audits, export audits, and direct customer interactions with OEM and international clients. The incumbent will drive continuous improvement in processes, compliance, and overall quality culture within the organization.
Key Roles & Responsibilities
- Lead and manage QMS Audits (Internal & External) as per IATF 16949 & ISO standards .
- Ensure compliance with OEM-specific quality requirements and act as the primary point of contact for OEM clients.
- Manage Export & Third-Party Audits including Sedex, BSCI, Walmart, etc.
- Establish, review, and update QMS documentation, SOPs, and process controls.
- Handle customer complaints, corrective actions, and preventive actions (CAPA) effectively.
- Work closely with cross-functional teams to ensure alignment with quality standards.
- Drive continuous improvement initiatives to enhance product and process quality.
- Provide training and awareness sessions to employees on QMS, compliance, and audit readiness.
- Represent the company in front of external auditors, regulatory authorities, and global customers.
- Monitor and ensure adherence to quality metrics and report to management.
Skills & Competencies
- Strong knowledge of QMS, IATF 16949, ISO 9001 standards.
- Proven experience in Automotive OEM industry .
- Hands-on experience in handling international audits and compliance requirements.
- Excellent communication, presentation, and stakeholder management skills.
- Ability to work independently and manage cross-functional teams.
- Problem-solving, analytical thinking, and attention to detail.
Ideal Candidate Profile
- Minimum 10 years of relevant experience in Quality Management Systems .
- B.Tech (Mechanical – Regular) is mandatory.
- Prior exposure to OEM & Export customer handling .
- Successful track record in managing third-party audits (Sedex, BSCI, Walmart, etc.).
- Leadership qualities with the ability to drive quality culture across the organization.
Budget up to 8 lacs p.a.