158 Quality Documentation Jobs - Page 6

Responsibilities: As a A Quality Management System (QMS) Engineer * Develop & maintain quality docs, including compliance with industry standards * Implement QMS,IATF, ISO standards, PPAP Process t audits. continuous improvement initiatives Provident fund Annual bonus Food allowance Health insurance Office cab/shuttle

Experience: 4+ years of experience Key Responsibilities Help define/improvise actionable and decision driving management information Ensure streamlining, consistency and standardization of MI within the handled domain Build and operate flexible processes/reports that meet changing business needs Would be required to prepare the detailed documentation of schemas Any other duties commensurate with position or level of responsibility Desired Profile Prior experience in insurance companies/insurance sector would be an added advantage Experience of Azure Technologies (include SSAS, SQL Server, Azure Data Lake, Synapse) Hands on experience on SQL and PowerBI. Excellent understanding in developing stored procedures, functions, views and T-SQL programs. Developed and maintained ETL (Data Extraction, Transformation and Loading) mappings using ADF to extract the data from multiple source systems. Analyze existing SQL queries for performance improvements. Excellent written and verbal communication skills Ability to create and design MI for the team Expected to handle multiple projects, with stringent timelines Good interpersonal skills Actively influences strategy by creative and unique ideas Exposure to documentation activities Key Competencies Technical Learning - Can learn new skills and knowledge, as per business requirement Action Orientated - Enjoys working; is action oriented and full of energy for the things he/she sees as challenging; not fearful of acting with a minimum of planning; seizes more opportunities than others. Decision Quality - Makes good decisions based upon a mixture of analysis, wisdom, experience, and judgment. Detail Orientation : High attention to detail, especially in data quality, documentation, and reporting Communication Collaboration : Strong interpersonal skills, effective in team discussions and stakeholder interactions Qualifications B.Com/ BE/BTech/MCA from reputed College/Institute

Dear Candidate, Hiring at Nathupur Industry area In Automobile company. salary - 40 to 45k required experience - 6 to 8yrs. qualification - B.tech or Diploma mechanical. interested candidate call /whatsapp on 8222829929

Role & responsibilities In Process Quality check and control. Knowledge of mechanical drawings. Troubleshooting and resolving process issues. Conduct regular inspections, audits to maintain quality control through out the manufacturing process. Implement preventive measures & corrective measures to avoid welding, fitting and bending mistakes during manufacturing process. To work with other teams to improve quality by various QC techniques. Responsible for quality documentations. Monitor all QMS related activities.

Role & responsibilities inspect incoming raw materials, in-process production, and finished products. Measure products using tools such as callipers, micrometres, gauges, and other inspection equipment. Read and interpret engineering drawings, blueprints, and specifications. Document inspection results and report quality issues or non-conformities. Work with the NPD/ production team to ensure quality standards are met. Maintain calibration of measuring instruments and test equipment. Perform root cause analysis and assist in corrective/preventive actions (CAPA). Ensure compliance with internal procedures and industry regulations. Assist with audits and support continuous improvement initiatives experience in sheet metal & Machining related work. Preferred candidate profile

Process and Product Quality: Ensuring that processes and products meet established quality standards and specifications. Testing and Inspection: Conducting tests and inspections of raw materials, components, and final products to verify their quality. Problem Solving: Identifying and investigating quality issues, recommending and implementing corrective actions to resolve problems. Documentation: Creating and maintaining quality documentation, including test plans, procedures, and defect reports. Data Analysis: Analyzing data to identify trends and areas for improvement in quality processes. Continuous Improvement: Working with the engineering and production teams to implement and improve quality control systems. Compliance: Ensuring that products and processes comply with industry regulations and standards. Supplier Management: Working with suppliers to ensure the quality of raw materials and components. Training: Providing training to other team members on quality standards and procedures. Auditing: Performing audits of quality processes to ensure compliance and identify areas for improvement. Role & responsibilities Preferred candidate profile Perks and benefits

Role & responsibilities 1. Prepare standard documents (SOP, batch records, specs etc) adhering to policies, procedures and regulatory requirements. 2. Responsible for sharing of periodic review reports to stake holders. 3. Responsible for carrying out all the tasks assigned by the reporting manager. 4. Expert in using Track wise digital or any Electronic Documentation Management System. 5. Responsible for carrying out admin role as per the requirement in support to stake holders. 6. Knowledge of quality systems and GMP regulations 7. Excellent verbal, organizational, written, and interpersonal skills required. 8. Sound keyboard skills and knowledge of Microsoft Office applications including Word, Outlook, Excel and PowerPoint. 9. Ability and desire to work in a team-based setting. 10. Ability to work independently and to continuously improve Quality processes. Preferred candidate profile B.Pharmacy, M.Pharmacy , M.S. degree in Chemistry, Microbiology or related field. 1 to 3 years of experience in the pharmaceutical industry (commercial manufacturing sites within API or DP), with experience in Quality Assurance. Experience of Shared Services strongly preferred (dedicated unit for the execution of specific operational tasks for the multiple business units within the organization). Strong knowledge of the pharmaceutical industry regulations applicable to API and Drug Product manufacturers. Good understanding on Good Manufacturing Practices, with practical experience on the field. Expert in using Track wise digital or any Electronic Documentation Management System

Responsibilities & Key Deliverables "?? Responsible for ensuring customer centricity by responding to next stage/line for various quality concerns and taking corrective and preventive actions, ?? Responsible for ensuring customer centricity by responding to next stage/line by supplying bodies as per TACT, ?? Responsible for ensuring manpower and allocation of work to associates as per their skills to produce first time right and every time right products from his stage/line, To resolve the next customer and TCF line complaints at minimum possible time in order to attain good customer satisfaction, To Monitor and control absenteeism on line by planning associates leave, To find cost effective solution for the FOS Items by monitoring, suggesting, Participating, implementing I4 ideas/Kaizens To monitor and reduce the number of concerns occurring at NOVA P, NOVA C, RFI by reviewing the daily concerns and implementing actions, To create a conducive environment for safe and engaged working, To monitor and improve the MQS and MAPS score of his BWT through continuous up gradation of processes, To improve the quality level and skill of associates in BWT continuous monitoring and nominating associates for re dexterity as per 3X3 Matrix " Experience 4 to 8 Years Qualifications Industry Preferred Tech/ DSCT( Surface Coating ) General Requirements

CLARWE MANUFACTURING BUSINESSES PRIVATE LIMITED is looking for Quality Engineer to join our dynamic team and embark on a rewarding career journey Develop and implement quality control procedures and processesConduct quality audits and inspections of products and processesIdentify and report quality issues and work with production and engineering teams to resolve themDevelop and analyze statistical data and product specifications to determine quality standards and to monitor process capabilitiesDevelop and maintain quality documentation and recordsEnsure compliance with relevant quality standards and regulationsParticipate in product and process design reviews to ensure quality requirements are metStrong understanding of quality control principles and practicesExperience with quality tools and methodologies such as Six Sigma and Lean ManufacturingExcellent communication and interpersonal skills

Youll support the sales team, distribute product information, and ensure our solutions are integrated into key projects Equipped with the latest Hilti technologies, youll conduct technical seminars and strive for zero errors in technical solutions, helping to shape the future of construction Key Roles & Responsibilities: Specification & Technical Consulting Ensure Hilti products are included in project specifications by engaging with structural consultants, architects, and decision-makers Provide technical expertise, design recommendations, and best practices for fastening, anchoring, and other key technologies Conduct in-depth project analysis to maximize Hilti product penetration beyond market share Track and manage specifications in the CRM, ensuring alignment with project timelines and technical requirements Visit project sites to provide on-ground technical support and identify new business opportunities Drive specification sales by positioning Hilti as the preferred solution provider Build long-term partnerships with specifiers, understanding their needs and influencing project specifications Provide training and technical seminars to clients, ensuring they are up to date with Hilti s latest innovations Develop strong business relationships with key stakeholders to drive project success Stay updated on the latest industry trends, codes, and standards to provide accurate, error-free technical solutions Share knowledge with colleagues and the sales team to strengthen overall technical expertise Maintain high-quality documentation, ensuring all specifications meet the required standards Known for our focus on providing fulfilling careers and a culture of Performance with Care, we are Ranked 19th amongst India s Best Workplaces and 4th Among Asia s Best Workplaces by Great Place to Work Institute What do we offer? Your responsibilities will be great and, with them, we ll give you the freedom and autonomy to do whatever it takes to deliver outstanding results We ll offer you opportunities to move around the business to work abroad, experience different job functions and tackle different markets It s a great way to find the right match for your ambitions and achieve the exciting career you re after We have a very thorough people review process which enables your career progression as soon as you re ready for the next challenge What you need is: Degree in Civil/Structural/mechanical/ electrical engineering or Architecture 4 to 10 years of experience Understanding of key civil/structural design/MEP construction concepts Experience of interacting with structural consultants, MEP consultants and architects Problem Solving, Drive for Results/Drive to Outperform, Collaboration/Team-Work should be able to support this with live examples Communication Skills structured & precise communication, presentation skills Understanding of technical specification concept prior experience in specifications or Business Development Why should you apply?

Freespace is looking for a Senior Technical Writer to produce high-quality documentation that contributes to the overall success of our products. We are looking for a seasoned Technical Writer who can set up the Document charter, work collaboratively with developers, quality engineers, product managers, and usability experts to make our products easier to use. You should have excellent knowledge of the B2B SaaS product documentation requirements and tools with all its artifacts and techniques. You ll also need the ability to coordinate people and projects with your mind set on deliverables. If you re a strong communicator, a capable leader and you re invested in IOT-SaaS Product documentation, we d like to meet you. Objectives of the role Work with product team to create documentation of the hardware and software for the customers. This includes both user-facing documentation, such as product overview, user manuals, customer facing troubleshooting guides, implementation guides etc AND technical specifications for hardware, such as Product Information, Specifications, Installation procedures, support documentation etc. Having a strong understanding of the products being documented to explain complex concepts in simple language. Also play a role in editing and proofreading the existing or new documentation that other members of the product teams have created. Conducting user testing, to ensure that documentation is suitable for the end-user. The goal is to produce high-quality documentation that meets the needs of its intended audience. Role & Responsibilities Develop comprehensive documentation that meets organizational standards Obtain a deep understanding of products and services to translate complex product information into simple, polished, and engaging content Writes user-friendly content that meets the needs of the target audience, turning insights language that sets our users up for success Develop and maintain detailed databases of appropriate reference materials, including research, usability tests, and design specifications Evaluate current content and develop innovative approaches for improvement Research, outline, write, and edit new and existing content, working closely with various departments to understand project requirements Independently gather information from subject matter experts to develop, organize, and write procedure manuals, technical specifications, and process documentation Work with product teams to identify all documentation repositories, revise and edit, and determine the best solution for data compilation and centralized storage Research, create, and maintain information architecture templates that uphold organizational and legal standards, and allow for easy data migration Develop content in alternative media forms for maximum usability, with a consistent and cohesive voice across all documentation Use photographs, drawings, diagrams, animation, and charts that increase users understanding Select appropriate medium for message or audience, such as manuals or online videos Standardize content across platforms and media Gather usability feedback from customers, designers, and manufacturers Revise documents as new issues arise Required skills & experience Proven working experience in technical writing of product documentation Ability to deliver high quality documentation paying attention to detail Understand and explain complex technical concepts Strong research and analytical skills Ability to undertake multiple projects and deliver on tight deadlines Excellent written skills in English Excellent verbal communication skills Strong working knowledge of Microsoft Office Solid grip on documentation publishing software such as Atlassian Confluence, SnagIt and other product documentation tools Documentation using text, pictures and videos Strong understanding of end user ease on usage of the documentation over the Web using Menu, TOC, Related Articles, Search Keywords etc. Basic familiarity with the SDLC and software development University degree in Computer Science, Engineering or equivalent preferred Behaviours and Mindset Be an advocate for high data quality standards. Ensure high standards by instilling data quality checks and documentation in work and team practices. Be a clear thinker with a systematic problem-solving approach, breaking the problem down into simple achievable and realistically estimated steps. Able to challenge processes & tools in zeal to creating the best Product Documentation practice. Create an open, trusting working environment with open communication and input from all. Be unafraid to own mistakes and push their own development as well as others in collaborating teams Always ensure customer priority and focus

Our mission: to eliminate every barrier to mental health. At Spring Health, we re on a mission to revolutionize mental healthcare by removing every barrier that prevents people from getting the help they need, when they need it. Our clinically validated technology, Precision Mental Healthcare , empowers us to deliver the right care at the right time whether it s therapy, coaching, medication, or beyond tailored to each individual s needs. We proudly partner with over 450 companies, from startups to multinational Fortune 500 corporations, as a leading provider of mental health service, providing care for 10 million people. Our clients include brands you use and know like Microsoft, Target, and Delta Airlines, all of whom trust us to deliver best-in-class outcomes for their employees globally. With our innovative platform, we ve been able to generate a net positive ROI for employers and we are the only company in our category to earn external validation of net savings for customers. We have raised capital from prominent investors including Generation Investment, Kinnevik, Tiger Global, Northzone, RRE Ventures, and many more. Thanks to their partnership and our latest Series E Funding, our current valuation has reached $3.3 billion. We re just getting started join us on our journey to make mental healthcare accessible to everyone, everywhere. As a Workplace Mental Health Consultant, you will provide individual therapy to employees, management consultations, training, critical incident response, and assessment and referral mental health support to employees at a leading Fortune 500 company in the Biopharmaceutical Industry. You may also provide consultation to HR, program managers, and supervisors on workplace and organizational issues. What you ll be doing: Provide consultation and support to managers, people teams, and members that enhances employee wellbeing and workplace effectiveness for 16 hours per week onsite at the customer location in Chennai, India on two days, ideally between Mon-Thurs Proactively develop strong and trusting relationships with leaders and HR POCs and execute against a local action plan for your site Develop expert-level understanding of the Spring Health and customer benefit ecosystems/ available support programs, and provide appropriate referrals to members. Provide individual therapy to employees on site and virtually Assess for risk and manage member and organizational crises by providing in-the-moment support, triage, safety planning, and follow up. Coordinate and deliver critical incident response Conduct company tailored trainings and Spring Health benefit promotion events Complete required internal training and assignments and attend Spring Health Clinical Team meetings Follow Spring Health policies and maintain all confidentiality, compliance, and ethical standards Identify and problem-solve issues that serve as a barrier or disruption to care, with support from leadership. Complete accurate and timely documentation of all service delivery. Track and monitor available data to identify strategic workplace wellbeing insights, recommend targeted interventions, and collaborate with customer points of contact to successfully deliver targeted interventions. Other duties as assigned What we expect from you: You have a minimum of 3 years of post-graduate experience with at least 1 year of post-licensed experience. You have training and experience in delivering management consultation, critical incident response, and training presentations. Youre comfortable with technology and are telehealth competent. You have training and experience in evidence-based modalities of care, including short-term, solution-focused therapy You have an unrestricted license to practice psychotherapy in Chennai, India (Psychologist, Clinical Psychologist,Therapist, Social Worker, Counselor, etc.). We are not able to accept applications from anyone requiring licensed supervision. You are proficient in English, Tamil and Hindi. You are comfortable with providing safety planning and intervention during situations where a client might present with higher risks. You are committed to high quality documentation of service delivery that is completed in a timely manner You like working independently, but would also enjoy having the support of a team and opportunities for connections and collaboration with other providers and our master s level clinical care navigators. You acknowledge and embrace diversity and inclusion amongst teams and clients The target hourly rate for this position is $25/hr-$35/hr USD. Individual pay may vary from the target range and is determined by a number of factors including experience, location, internal pay equity, and other relevant business considerations. We review all employee pay and compensation programs annually at minimum to ensure competitive and fair pay.

Meet quality standards and specifications. IATF Documentation and Audits (Internal/External), New Product Development, New Vendor Developments, PPAP Documents, Kaizen, 5S, 4M. Knowledge of Sheet Metal Stamping, power press Tool Making and Validation. Required Candidate profile b.tech/ diploma in production minimum 4-5 years experience should be ready to travel

Responsible for using CMM to inspect & measure manufactured parts Review drawings & specifications to define inspection criteria Knowledge of dimensional & visual inspection, Measuring instruments, Calibration & CAPA Knowledge on QMS Required Candidate profile Develop CMM programs for Aeronautical parts as per AS9100 standards Drawing interpretation & GD&T knowledge Ability to identify & resolve drawing issues Determine quality metrics for mf procedures Perks and benefits Insurance, Free Cab & Canteen, PF, Incentive,Bonus

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

Highlight the main responsibilities - Initiate the QRQC in QIM database - participate to the containment and validate the robustness of the containment - Support APU Managers / Site Manager in the analysis of issues assigned in the QRQC activities - Update the APU quality tracking charts : Customer Returns - Cost of Non Quality - Perform audits on the line to detect non-respect of the Standard and identify with the APU the actions to be completed to therefore comply with the Standard - Participate in the eradication of Customer issues and Non Quality issues - Along the APU QRQC meeting ensure that rules are respected and Stop at first disagree and Stop at first no are applied - Perform the revision of the control plan after an issue - Verify 4M matrix respect with regards product or process changes and ensure customer awareness and approval of changes in accordance with the 4M matrix - Update the quality documents following a process related change - Verify the continuous conformance of the process to generate product to specification in accordance with the control plans (machine capability - yearly product audit ) - Has authority to stop a manufacturing / assembly line in any situation where Standards are not respected or a safety or quality risk for the operator or for the customer has been detected or following a LLC Stability audit demonstrating lower than 100% - Represent Customer within Valeo on Quality matters (communication/Escalation) - In case of APU Quality Leader position, he will report to this position and will not supersede APU Quality Leader and Site Quality Manager authority. - In charge of PD , CA and closure management for Internal Suppliers incidents .

Job Title: Quality Engineer Department: Quality Department Location: Chakan, Pune Reporting To: Manager Job Description: We are seeking a motivated and detail-oriented Quality Engineer to join our Quality Department. The ideal candidate will have relevant experience in ISO standards implementation and in-process inspection. This role involves supporting the planning, execution, and follow-up of internal and external audits, maintaining compliance with ISO standards, and driving continuous improvement in quality systems. Key Responsibilities: Assist in the implementation, maintenance, and continual improvement of ISO standards: ISO 9001, ISO 45001, and ISO 14001 . Plan and coordinate internal and external audits , including third-party and surveillance audits. Conduct in-process inspections to ensure adherence to quality requirements at all stages of production. Identify process non-conformities and assist in the root cause analysis and corrective action implementation. Maintain and update documentation related to Quality Management Systems (QMS) , Environmental Management Systems (EMS) , and Occupational Health and Safety Management Systems (OHSMS) . Coordinate with various departments to ensure compliance and system effectiveness . Prepare audit reports, maintain audit records, and track closure of audit findings. Support training and awareness sessions related to quality and ISO standards. Participate in continuous improvement initiatives to enhance overall system efficiency and product quality. Candidate Requirements: Education: Diploma/Bachelors degree in Engineering, Quality Management, or a related field. Experience: 15 years in a Quality role with exposure to ISO standards and in-process inspections. Technical Skills: Working knowledge of ISO 9001, ISO 14001, and ISO 45001. Familiarity with audit processes and documentation. Hands-on experience with in-process inspection tools and techniques.

Job Description The selected candidate should be a Graduate Engineer or BSc / MSc with 10 to 15 years of experience in Quality. There are a total of 2 vacancies. 1 Vacancies are for Quality Manager ( 1 in Chakan, Pune )- 7-10 years experience 1 Vacancy is for Senior Manager QMS (Quality Management System) ( 1 in Chakan , Pune )- 11-15 years experience. The selected candidate should have work experience of Inward , in-process and outward quality. He should be experienced in developing new forms and formats and procedures for continuous improvement of the Quality system. To develop, implement and maintain the Quality Management Systems of ISO 9001, IATF 16949 , ISO 14001, ISO 45001, ISO 13486 etc. this means that the candidate has to organise internal audits, maintain quality records, and handle all certification and surveillance audits. Handling of customer complaints, training of juniors from the basic level is also the responsibility of the selected candidate. Handling customer audits, submitting corrective actions for quality issues and closing the open audit findings of the Customer audit team is also the responsibility. ONLY CANDIDATES who send an application by email to opportunities@frontlineelectronics.com will be considered by this company and will be screened for shortlisting. 100% preference to electronics engineering candidates or other engineering candidates with at least 10 years of experience in electronic manufacturing industry or to candidates from an IATF certified auto components company. Candidates with experience in automotive tier 1 or automotive auto component ancillaries are welcome.

Manage and oversee project quality to ensure compliance to codes, standards, regulations, specifications, and QMS requirements Coordinate inspections, audits, and quality documentation with subcontractors, vendors, and client representatives Required Candidate profile Drive cost savings, ensure safety adherence, and deliver quality assurance through effective site execution. Implement the QA/QC management system at site,

Our mission: to eliminate every barrier to mental health. At Spring Health, we re on a mission to revolutionize mental healthcare by removing every barrier that prevents people from getting the help they need, when they need it. Our clinically validated technology, Precision Mental Healthcare , empowers us to deliver the right care at the right time whether it s therapy, coaching, medication, or beyond tailored to each individual s needs. We proudly partner with over 450 companies, from startups to multinational Fortune 500 corporations, as a leading provider of mental health service, providing care for 10 million people. Our clients include brands you use and know like Microsoft, Target, and Delta Airlines, all of whom trust us to deliver best-in-class outcomes for their employees globally. With our innovative platform, we ve been able to generate a net positive ROI for employers and we are the only company in our category to earn external validation of net savings for customers. We have raised capital from prominent investors including Generation Investment, Kinnevik, Tiger Global, Northzone, RRE Ventures, and many more. Thanks to their partnership and our latest Series E Funding, our current valuation has reached $3.3 billion. We re just getting started join us on our journey to make mental healthcare accessible to everyone, everywhere. Onsite Employee Assistance Program (EAP) Counselor Our mission: to eliminate every barrier to mental health. Spring Health is a comprehensive mental health solution for employers and health plans. Unlike any other solution, we use clinically validated technology called Precision Mental Healthcare to pinpoint and deliver exactly what will work for each person whether that s meditation, coaching, therapy, medication, and beyond. Tday, Spring Health equips over 800 companies, from start-ups to multinational Fortune 500 corporations, as a leading and preferred mental health service. Companies like General Mills, Guardian, Bain, and Instacart use the Spring Health platform to provide mental health services to thousands of their team members globally. We have raised over $300 million from prominent investors including Kinnevik, Tiger Global, Northzone, RRE Ventures, Rethink Impact, Work-Bench, William K Warren Foundation, SemperVirens, Able Partners, True Capital Ventures, and a strategic investor, Guardian Life Insurance. Thanks to their partnership, our current valuation has reached $2 billion. The Onsite EAP Counselor role is a unique and exciting opportunity to provide EAP counseling, management consultations, program promotion, critical incident response, and training, etc. to employees. You may also provide consultation to HR, program managers, and supervisors on workplace and organizational issues. This role will report to the Spring Health Clinical Manager. What you ll be doing: Provide on-site support to managers, people teams, and members onsite at the customer location; the hours for this role will be a 32 hours total in 8 hour shifts that falls between regular business hours Monday through Thursday. Provide management consultation to leaders in order to enhance employee wellbeing and workplace effectiveness Coordination and delivery of critical incident response services Conduct trainings, coordinate training requests and facilitate Spring Health benefit promotion and Spring Health launch events Participates in Threat Management Team consultations Develop expert-level understanding of the customer benefit ecosystem and available support programs Provide solution-focused employee mental health counseling, consultation, support, and connection to appropriate resources Complete required internal training and assignments and attend Spring Health Clinical Team meetings Follow Spring Health policies and maintain all confidentiality, compliance, and ethical standards Assess for risk and manage member and organizational crises by providing in-the-moment support, triage, safety planning, and follow up Identify and problem-solve issues that create barriers or disruption to care, with support from leadership Maintain accurate and complete documentation of required information that meets risk management and regulatory requirements Other responsibilities as it applies to the success of this role What we expect from you: Masters level Psychologist with minimum of 3 years experience (independent licensure required). You have an unrestricted license to practice psychotherapy in the location (city/state/country) you are practicing in. Bilingual in English and Hindi required EAP experience Supervisory experience and/or experience working with management and human resource professionals preferred Demonstrated SUD experience Experience working with diverse populations (multilingual preferred) Knowledge of healthcare settings and community resources Tech and computer savvy: comfortable adopting new technologies and platforms and efficient in tech-related tasks. Excellent written and verbal communication skills (English) You have been trained and have experience in delivering management consultation, management referrals, critical incident response, and EAP presentations You have training and experience in evidence-based modalities of care, including short-term, solution-focused therapy We are not able to accept applications from anyone requiring licensed supervision You are comfortable with providing safety planning and intervention during situations where a client might present with higher risks You are committed to high quality documentation of service delivery that is completed in a timely manner You like working independently, but would also enjoy having the support of a team and opportunities for connections and collaboration with other providers and our master s level clinical care navigators Individual pay may vary from the target range and is determined by a number of factors including experience, location, internal pay equity, and other relevant business considerations. We review all employee pay and compensation programs annually at minimum to ensure competitive and fair pay. Not sure if you meet every requirement Research shows that women and people from historically underrepresented communities often hesitate to apply for roles unless they meet every qualification compared to other similarly-qualified candidates. At Spring Health, we are committed to fostering a workplace where everyone feels valued, empowered, and supported to Thrive . If this role excites you, we encourage you to apply. Ready to do the most impactful work of your lifeLearn more about our values, what it s like to work here, and how hypergrowth meets impact at Spring Health: Our Values

Assistant Manager (Statutory Audit) Posted On: 27 Feb 2025 Apply Now Job Summary Qualification CA Location Pune Experience 2 years+ post qualification No. of Positions 1 Job Description Responsibilities: 1. Conducting Stat Audits & Tax Audits of Listed & Pvt. Ltd. Companies 2. Timely completion of audit field work and quality documentation 3. Raising the issues identified promptly with Audit Manager(s) and Partner(s) 4. Guiding the junior team members in the team Skills Set Required: 1. Knowledge of Ind AS and IFRS. 2. Having good exposure in Ind AS, Due Diligence, review and finalization of Audits. 3. Having experience of preparation/assisting in preparation of Audit Reports 4. Must be ready to travel intercity. Apply Now Upload Resume (PDF) How did you come to know about this job Submit

Quality Management (QC/QA) Experience in the welding materials industry Major Tasks - Inspection of raw material and product quality - Process Quality Monitoring and rejection countermeasures - Establishment of quality standards and improvement activities - Customer response and quality document management - Various Certification/Standard Management (BIS, ISO, etc) Required qualification - At least 2 years of experience in quality control - Ability to use inspection equipment - Understanding the certification/Quality Standards (BIS, ISO, etc.) - English/Tamil communication skills Preferred Qualification - Experience in certification/standards (BIS, ISO) - Experience in the welding materials industry - Quality Data Analysis Capabilities (Excel, Minitab, etc.) Interested Please Call Mithra HR 9176616016

Role & responsibilities Assist QA head in the day to day QA operation Collate Documents related to Quality Assurance from various departments Prepare monthly reports for QA head Maintain documents for ISO Preferred candidate profile The candidate must meet the following requirements Must be a Graduate Decently fluent with English for written communication Know MS Office etc Experience of at least 1 year in similar area of work Female candidates will be preferred

Position Summary: We are seeking an experienced and proactive Quality Control Manager with a strong background in In Vitro Diagnostics (IVD) to lead and oversee all QC activities within our manufacturing and development operations. The QC Manager will be responsible for ensuring that IVD products meet internal quality standards and comply with international regulatory requirements. This role plays a key part in managing a QC team, improving processes, and supporting product development and commercial release. Role & responsibilities Lead and manage the Quality Control team, ensuring daily testing activities are conducted efficiently and in compliance with regulatory requirements (ISO 13485, FDA 21 CFR Part 820, and CE-IVD). Develop, implement, and maintain QC procedures for raw materials, in-process controls, and final product testing for IVD devices, including immunoassays, molecular diagnostics, and rapid tests. Oversee method validation, equipment qualification (IQ/OQ/PQ), and routine calibration and maintenance of laboratory instruments. Review and approve QC test results, reports, and batch records, ensuring timely product release. Manage investigations of non-conformances, deviations, out-of-specification (OOS) results, and implement corrective and preventive actions (CAPAs). Participate in cross-functional teams for new product development, transfer-to-manufacturing activities, and continuous improvement initiatives. Ensure compliance with GLP/GMP requirements and prepare for internal and external audits (e.g., ISO, FDA, notified bodies). Provide leadership, training, and mentorship to QC staff, fostering a culture of quality and accountability. Monitor QC metrics and KPIs, and report regularly to senior management. Maintain and improve the Quality Control Laboratory environment, including documentation, data integrity, and safety practices. Education: Bachelors or Masters degree in Biotechnology, Biochemistry, Microbiology, Life Sciences, or a related field. Experience: Minimum 610 years of experience in Quality Control, with at least 3 years in a managerial or supervisory role within the IVD or medical device industry. Skills: In-depth knowledge of IVD regulations and quality standards (ISO 13485, FDA QSR, CE-IVD). Strong leadership, team-building, and project management skills. Proven experience in implementing and improving QC systems and processes. Excellent problem-solving skills and experience with RCA and CAPA tools. Proficiency in LIMS, statistical analysis, and data management tools. Preferred candidate profile Experience with regulatory submissions, audits, and inspections (FDA, ISO, EU MDR). Familiarity with risk management (ISO 14971), design controls, and product lifecycle management. Quality certifications (e.g., ASQ CQM/OE, Six Sigma Green/Black Belt) are a plus

Responsibilities: * Develop quality procedures & documentation * Conduct internal audits as QA specialist * Ensure compliance with industry standards * Lead quality initiatives & improvements * Implement quality management systems Provident fund Annual bonus Employee state insurance