...Responsibilities:
Develop, implement, and maintain compliance programs and initiatives to ensure adherence to security requirements for ISO 27001:2022, SOC 2 Type II, HIPAA, PCI DSS, GDPR, etc.
Create and maintain policies, procedures, standards, and documentation related...
Rs 3 - 13 lakhs p.a.
...We are seeking a qualified and motivated individual to join our team as an ISO 27001:2013 Management
Representative. The ISO 27001 Management Representative will be responsible for overseeing the
implementation and maintenance of the information security management system...
Rs 6 - 8 lakhs p.a.
...ISO full form is International Organization for Standardization. It is considered as an Independent, non- governmental, non-profitable, the worldwide federation of national standards bodies that can develop and publishes international standards.
ISO full form is International...
Rs 2.16 - 3.36 lakhs p.a.
...Qualification:
Bachelor's degree in a relevant field (Quality Management, Business Administration,
etc.).
Certification in ISO standards (e.g., ISO 9001, ISO 14001) is highly desirable.
Job Location: Vadodara
Experience:
Proven experience in implementing...
Rs 2.75 - 3 lakhs p.a.
...Position: Jr. Executive - ISO
Location: Sachin near by Surat
Experience: 0- 1 Years
Industries: Chemical
Responsibilities:
The candidate should be well versed with documentation and Quality Management System
The candidate have knowledge of ISO 140001, ISO...
...Scope of Work: Consulting organizations on Technical and Management Compliances such as:
ISO 27001:2022 Information Security Risk Management, FMEA Framework, Quality Management (ISO 9001), Occupational Health & Safety Management (ISO 45001), and Environmental Management...
...discuss with the team and concerned stakeholders for the corrective actions.
Requirements
~3 to 5 years’ experience in various ISO, data protection and other compliance tools.
~ Knowledge of various security standards – ISO 27001 (ISMS), NIST, MPAA etc. would be...
Rs 2 - 6 lakhs p.a.
...and opportunities for product quality could be one of the tasks of the quality manager, and is further elaborated in clause 6.1 of the ISO 9001:2015 standard.
Responsibility and authority for the QMS: In Clause 5.3 there is a need for top management to assign responsibility...
...as DOORS, Polarion, or similar.
Experience in conducting risk assessments and applying risk management techniques in accordance with ISO 14971 and other relevant standards.
Familiarity with regulatory requirements and standards for medical devices, including FDA...
...with organizational risk assessments and relevant standards. - Conduct audits of Information Security Management System (ISMS) based on ISO 27001:2022, NIST, GDPR, ITGC & IEC62443 standards to assess compliance and identify areas for improvement.- Conduct independent and...
...Job:Product Owner/Product Manager-Cards, ISO 8583
Location:Bangalore
Experience:8-14 Years
Roles & Responsibilities (MUST HAVE)
· Consult with product stakeholders to understand business drivers and translate them into functional and non-functional requirements...
...JOB TITLE: TESTING ENGINEER (ISO-17025) Location: Peenya, Bangalore
Position Type: Full-Time
Reporting To: Managing Director
Company Overview
Ducom ( is a world leader in material characterisation. We are a fully integrated core engineering company with Application...
...exciting opportunity to manage Quality Assurance and Control for an Aerospace & Defense Company which is seeking people from Aerospace ISO 6500 and ISO 9100 Implementation Experience. Position will work closely with IITians
Client Details :
Our client is a specialist...
...Senior Manager - Product Owner Cash ISO - BFS035395
Genpact (NYSE: G) is a global professional services and solutions firm delivering outcomes that shape the future. Our 125,000+ people across 30+ countries are driven by our innate curiosity, entrepreneurial agility, and...
...This is a remote position.
Experienced implementation consultant for ISO 27001
Atleast 510yrs of experience
Requirements
Must be able to perform preparatory work and gap analysis OR renewal OR surveillance audit
Must prepare for assessment...
Rs 2.4 - 3 lakhs p.a.
...2.07.23
The candidate should be well versed with documentation and Quality Management System
The candidate have knowledge of ISO 140001, ISO 9001
ISO 14001 Experience is mandatory
Knowledge of Documentation, Retrieval, destruction and archival of QA Records,...
...dedicated level of integrity (ASIL).
2 Allocation of safetyrelevant requirements (TSR) to development domains e.g. hardware software calibration.
3 Development of Functional (FSC) and Technical Safety Concepts (TSC)
4 FMEA FTA
EIS : Functional Safety ISO 26262...
..., and review of SOC1 or SOC2 reports
Knowledge of IT risk, information security or cyber security frameworks such as COSO, COBIT, ISO, NIST etc.
IT Compliance and regulatory assessments – IT Risk and Controls assessment with exposure of any of the technologies such...
...design and development.
Has experience in automotive software development with functional safety development process. (familiarity with ISO 26262, PART6 is desirable)
Has experience in AUTOSAR architecture and development workflow
Has experience in leading and managing...
...manufacturing activities such as Intermediate buffers, Formulation, labeling & dispensing and packaging. The company is compliant with ISO 9001: 2015, ISO 13485: 2016 & EN ISO 13485: 2016, MDSAP and Beckman Coulter corporate Quality system requirements.
In this role, you will be...
...safety certifications (e.g., CDRH, IEC 60825).
Familiarity with medical device regulations and standards, such as FDA 21 CFR Part 820, ISO 13485, and IEC 60601.
Excellent problem-solving skills and the ability to work effectively in a multidisciplinary team environment....
...or Certified Quality Engineer (CQE) are advantageous.
Technical Competencies :
Proficiency in quality management systems (ISO 9001, ISO 13485, etc.).
Familiarity with quality tools (FMEA, Control Charts, Pareto Analysis, etc.).
Knowledge of statistical analysis...
...Demonstrate a thorough understanding of and adherence to FDA, ISO, and IEC design control procedures, regulations, and standards. Ensure... ...Regulatory Standards Knowledge:
Possess expertise in ISO 13485, IEC 62304, ISO 14971, and IEC 62366 standards. Stay abreast of changes...
...Mechanical) with 4-7 years of experience in Quality / Engineering / Manufacturing environment, preferably from medical industry with ISO 13485 auditor certification is a must.
Intermediate level ability to use most MS tools (Word, Excel, PowerPoint, etc.)
Technical Competencies...
...Qualification of plant equipment’s, devices and systems in several steps like IQ/OQ/PQ as per medical device Design control Process ISO-13485
~ Monitoring and coordinating local validation activities, creating reports to the local validation activities.
~Monitoring and conducting...
...maintain and further develop the ZEISS India Management System, aligned with the Corporate ZEISS Management System, maintain the ISO 9001 and ISO 13485 certification requirements for entire Delhi Location including all SSC functions.
Requirements
Education
Master /...
...experience in within medical device industry is mandatory
• Good understanding of the QSR / QMS requirements as per 21 CFR Part 820 & ISO 13485:2016
• Thorough understanding of requirements management; from user needs through verification and validation; experience with...
...improvements within the V&V function.
Play a front ending role in ISO audits and quality reviews.
Establish traceability of... ...preferred including knowledge of standards such as IEC 62304, ISO 13485.
~ Experience working with globally distributed teams and demonstrated...
..., Hazard Analysis, DFMEA, and risk management report, adhering to ISO 14971 standards .
· Serving as a mentor to junior engineers, providing... ...compliance with FDA Quality System Regulations, EU MDR, ISO 13485, ISO 14971, IEC 60601, and other relevant industry standards...
...are compliant to local requirements as and international standard ISO 14971
Participates in regulatory inspection and notified body audits... ...experience in medical device risk management
Knowledge in ISO 13485, ISO 14971, FDA CFR 820, EU 2017/745, IEC 62304, IEC 82304 and...