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Subramanya Nagar

Kamakshipalya

Medinova Ind

Quality Control

Gandhi Nagar Mod

Jorawer Singh Gate

WE NEED A FEMALE STAFF WHO CAN TAKE CARE THE PRODUCTION AND FINISHING DEPRATMENT IN OUR CLOTH FACTORY.


Nitin Textiles

Production Supervisor

Banjara Colony

Waluj

Auto parts to be checked in day shift for 12 hr, Fresh or having experienced can apply 


Vardhaman Auto Components Private Limited

Quality Line Inspector

Colllege Road Andarliayan Galian

Sahnewal, Ludhiana

Required Fast learner , hard working honest and punctual person


Royal Bikes

Supervisor

Gopipura

Sachin INA

We are looking for a candidate who is interested in QA/QC work.


MC Coy Drugs

QA / QC Executive

I.I.T.Main Gate

Andheri

We are looking for quality controller , Qc in our Garments production units.
We are looking for male candidate.

Our address :

DNS DESIGN AND STYLE 
A/12 Narayan plaza chandivali rd off saki vihar rd 
sakinaka 
andheri east mumbai 400072
Ph: 9833011334





Design N Style Int Mfg.Co.

Garments Quality Controller

Jetpura

Conduct routine inspections of raw materials, in-process products, and finished goods.
Perform basic laboratory tests and record results accurately.
Assist in identifying and reporting non-conformities or deviations from specifications.
Maintain and update QC documentation, logs, and quality records.
Support calibration and maintenance of testing equipment.
Ensure compliance with company quality standards, SOPs, and regulatory requirements.
Collaborate with production and warehouse teams to address quality issues.
Prepare samples for testing and ensure proper labeling and traceability.
Assist in internal audits and continuous improvement initiatives.
Follow safety and hygiene procedures within the workplace.



Smart-Bond Chemicals Private Limited

Quality Assistant

Rashtrapati Bhavan

Noida Sector 81

-Graduation pass out in 2020 or later year


Qualitronics

Quality Inspector

Gopalpura

About Company:Axestrack is India's leading provider of Digital Logistics Solutions for Heavy Commercial Vehicles, and the only Indian company to be ever featured in Gartners Market Guide for Fleet Management. We are proud to hold a dominant position in the Indian market and are actively expanding across Africa, the Middle East, and the US. Our innovative approach and scalable platforms are transforming logistics for the modern world.Website: www.axestrack.com

Position: Data Quality Executive
Location: Jaipur, Rajasthan
Job Type: Full Time
Position Overview: As an Support Executive, you will be the first line of defense in ensuring smooth operation of IT systems and support for both internal teams and external clients. You will handle hardware/software issues, assist clients with product queries, and contribute to the efficiency of our technical infrastructure.
Key Responsibilities
Provide Level 1 support for users (internal/external) related to hardware, software, and applications.
Offer product support to clients by resolving functional or technical issues.
Troubleshoot and resolve hardware-level problems, including data-related concerns.
Respond promptly to support tickets and queries, ensuring timely resolution
Handle routine IT administrative tasks including password resets, user account updates, and access management.
Maintain documentation of all troubleshooting procedures and resolutions.


Skills & Qualifications:
Basic knowledge of computer hardware and peripherals.
Fluency in Hindi and ability to speak and write basic English.
Strong communication and interpersonal skills.
Ability to prioritize tasks and work independently.




Axestrack Software Solutions Private Limited

Data Quality Executive

Senior Quality Engineer<h4>Department</h4>Ratings<h4>Job Description</h4>The role is to support an agile team in analyzing, designing, building and testing high quality risk application suite. The SQA engineer will review functional requirements and user stories from LOB’s; design test plans, write test cases, oversee test strategies and perform testing for assigned applications. The role is to submit and verify defects, maintain documentation of test results to assist in debugging and modification of new applications, analyze test results to certify existing functionality and integrations and recommends corrective action plan failures. Testing will include functional and non-functional, integration, regression, system, smoke, SpecFlow and sanity testing.MUST HAVE <ul><li>knowledge of Capital Markets </li><li>experience/ knowledge of Python BDD testing approach and tools like “SpecFlow”, selenium based automated testing. Desirable to have React based UI testing experience.</li><li>have hands-on experience in defining overall testing approach and define the test plans, test automation</li><li>Enthusiastic strong-minded person able to work closely with the development team and help instill a testing culture. </li><li>Experience of setting up test frameworks for new projects.</li><li>Knowledge of  capital markets and regulatory programs is highly desirable</li><li>Practical experience of QA testing within investment banking.</li><li>Experience with UNIX, PERL and shell scripting.</li><li>The ideal candidate will also have experience with Jira and Confluence</li></ul>Competencies:Strategic Thinking: Business knowledge, Innovation &amp; CreativityBusiness Results: Client relationships, Analytical ability, Execution.Personal Effectiveness: Communication, decisiveness, Energy &amp; drive, courage, character. <h4>Open Positions</h4>2<h4>Mandatory Skills</h4>QA Automation, automation testing, selenium, bdd, Spec Flow, SpecFlow, Agile, Unix, Shell<h4>Education Qualification</h4>Bachelor's degree in STEM / Master's degree in STEM<h4>Experience</h4>6 to 15 years

CRISIL Ltd

Senior Quality Engineer

Quality Compliance Manager<h4>Career Category</h4>Quality<h4>Job Description</h4>HOW MIGHT YOU DEFY IMAGINATION?You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.What you will doThe Quality Compliance Manager is a global role and part of the Safety &amp; Medical Quality (SMQ) team for the R&amp;D Quality Organization.SMQ Team at Amgen implements the global R&amp;D Quality strategy across R&amp;D and other functional areas requiring pharmacovigilance (PV) oversight. The team monitors the audit universe to identify compliance risks, which inform PV audit program development. They lead or support inspection readiness and management, communicate audit and inspection outcomes to stakeholders, and advise on remediation. Additionally, the SMQ Team partners with stakeholders to provide compliance guidance, highlight trends and risks from various data sources to drive process improvement, and participates in service provider governance and due diligence activities.In this vital role, the Quality Compliance Manager will ensure excellence in R&amp;D Quality processes is maintained through oversight and improvements when compliance issues are identified. They will be an integral team member working globally with Business Process Owners to ensure compliance with GPvP regulations and other business requirements including the Global Safety database and associated systems. Additionally, the Quality Compliance Manager will provide proactive end to end quality support for the management of Quality Incidents/Quality Events, working closely with Quality Leads in approving investigations, including root cause analysis (RCA) and Corrective &amp; Preventive Action (CAPA) plans.Roles &amp; Responsibilities:The Quality Compliance Manager will work both independently and in a team environment to foster collaborative relationships within R&amp;D Quality. In this dynamic role, they will be responsible for supporting processes and operational activities related to overseeing Good Pharmacovigilance Practice (GPvP) deviations, preparation of audits and inspections across R&amp;D Quality. As part of strengthening and advancing Amgen’s R&amp;D QMS, this role provides end-to-end quality support to deviation owners, RCA owners, and CAPA owners within Global Patient Safety and other parts of the organization.<ul><li>Supports the intake, triage, and categorization of deviations, ensuring appropriate classification and documentation.</li><li>Facilitates timely and thorough deviation investigations in collaboration with functional area representatives and Quality Leads</li><li>Ensures consistent and compliant documentation of deviation records within the electronic quality management system (DQMS).</li><li>Monitors and ensures adherence to timelines, escalating delays and risks as needed.</li></ul><ul><li>Supports Global Patient Safety and Global Development teams in GxP inspection management activities and GxP audits from business partners</li><li>Identifies, leads, or contributes to continuous improvement initiatives to enhance CAPA management practices.</li><li>Collaborates with cross-functional partners to ensure processes remain effective, efficient, and aligned with industry best practices and evolving regulations.</li><li>Ensures the integrity, traceability, and quality of deviation and CAPA records in compliance with ALCOA+ principles.</li><li>Monitors quality metrics and key performance indicators (KPIs) related to deviation and CAPA management.</li><li>Analyses trends and perform root cause trending to identify systemic issues and opportunities for process improvement.</li><li>Manages, organizes and analyses data through different systems, tools, or platforms, including Excel and Smartsheet</li><li>Maintains knowledge of current regulatory and quality practices/issues</li><li>Maintains the Global R&amp;D CRQ and SMQ SharePoint sites</li><li>Manages the appropriate archival and retention of audit documentation.</li></ul>What we expect of youBasic Qualifications and Experience:<ul><li>Master’s degree and 8-13 years in Pharma and Biotechnology R&amp;D Quality</li></ul>Additional Competencies/Skills:<ul><li>Comprehensive expertise in Good Pharmacovigilance Practices (GPvP), with a strong command of operational standards and the quality frameworks governing drug safety.</li><li>Understand of regulatory requirements: Knowledge of global PV regulations (e.g., EMA GVP Modules, ICH E2E/E2F, FDA safety guidelines, MHRA expectations).</li><li>Solid understanding of end-to-end case management workflows, including upstream and downstream activities, and the related systems such as global safety databases (e.g., Argus, ArisG).</li><li>Demonstrated ability to leverage artificial intelligence (AI) tools and technologies to streamline workflows, drive process automation, and support data-driven decision-making. Must be adept at identifying opportunities to apply AI for operational efficiency and continuous improvement initiatives.</li><li>Proficiency in operating Quality Management Systems (QMS), particularly TrackWise and Veeva QMS, to manage quality events, documentation, and compliance workflows.</li><li>Exceptional attention to detail and accuracy in all deliverables.</li><li>Ability to work independently and proactively in a fast-paced environment.</li><li>Proficiency in Smartsheet, Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and virtual collaboration tools (e.g., Teams, WebEx)</li><li>Good team building skills and the ability to on-board new employees and develop them over time</li></ul><ul><li>Familiarity with project management tools and methodologies.</li><li>Experience working in a multinational environment with global teams.</li></ul><ul><li>Excellent verbal and written communication skills.</li><li>High degree of professionalism and interpersonal skills.</li><li>Strong problem-solving abilities and adaptability to changing priorities.</li><li>Collaborative attitude and ability to build positive relationships across diverse teams.</li><li>Resilience, discretion, and the ability to thrive under pressure</li></ul>.<h4>Experience Level</h4>Mid Level

Amgen Technology Private Limited

Quality Control Manager

QA Team Lead<h4>ABOUT TIDE</h4>At Tide, we are building a business management  platform designed to save small businesses time and money. We provide our members with business accounts and related banking services, but also a comprehensive set of connected administrative solutions from invoicing to accounting. Launched in 2017, Tide is now used by over 1 million small businesses across the world and is available to UK, Indian and German SMEs. Headquartered in central London, with offices in Sofia, Hyderabad, Delhi, Berlin and Belgrade, Tide employs over 2,000 employees. Tide is rapidly growing, expanding into new products and markets and always looking for passionate and driven people. Join us in our mission to empower small businesses and help them save time and money.<h4>ABOUT THE ROLE</h4>The Quality Assurance Team Lead –  is responsible for leading a team of QA Analysts within Member Operations, ensuring delivery of accurate, compliant, and high-quality audits of frontline teams. The Team Lead sets performance standards, provides coaching and development, and drives quality improvement initiatives while fostering a strong compliance culture. This role serves as the key link between QA Analysts and QA Management, helping ensure the QA function operates efficiently, transparently, and in alignment with the QA Policy, business goals and regulatory expectations.<h4>Key Responsibilities:</h4><ul><li>Lead and support a team of QA Analysts, ensuring consistent delivery against KPIs, quality standards, and monthly targets.</li><li>Set up and onboard new QA Analysts; delegate, mentor, and support Senior QAs to deliver their responsibilities effectively.</li><li>Maintain QA scheduling and capacity planning to align with team availability, shrinkage trends, and departmental needs.</li><li>Organize regular 1:1s, performance reviews, calibration sessions, and weekly team meetings to drive alignment and accountability.</li><li>Coach and develop team members through structured feedback, learning plans, and career development pathways; manage RISE and PIP processes.</li><li>Ensure up-to-date QA documentation, Confluence articles, and reporting; proactively identify process gaps and recommend improvements.</li><li>Monitor dispute handling, calibration deviation, and AOA scores; resolve QA escalations professionally and fairly.</li><li>Partner with cross-functional stakeholders including Training, People, and Operations to support smooth onboarding, product/process launches, and change management.</li><li>Ensure compliance with regulatory and internal standards (GDPR, data privacy, LMS training completion) and report any breaches or disciplinary concerns.</li><li>Act as a role model for Tide’s values, tone of voice, and “Members First” approach in all QA practices and leadership behavior.</li></ul><h4>WHAT WE ARE LOOKING FOR</h4><ul><li>Experience in quality assurance, compliance, or operational leadership, preferably in a regulated industry such as fintech or financial services.</li><li>In-depth knowledge of banking operating processes, QA audit practices, and compliance risk management in customer service environments.</li><li>Strong people leadership, coaching, and mentoring capabilities with a hands-on approach to performance improvement.</li><li>Effective communication and problem-solving skills, with the ability to mediate disputes and drive alignment in cross-functional settings.</li><li>Organized, data-driven, and proactive; comfortable using QA tools and systems such as Confluence, Looker, Scorebuddy, Google Workspace, and Lattice.</li></ul><h4>WHAT YOU’LL GET IN RETURN</h4><ul><li>Competitive salary</li><li>Self &amp; Family Health Insurance</li><li>Term &amp; Life Insurance</li><li>OPD Benefits</li><li>Mental wellbeing through Plumm</li><li>Learning &amp; Development Budget</li><li>WFH Setup allowance</li><li>15 days of Privilege leaves</li><li>12 days of Casual leaves</li><li>12 days of Sick leaves</li><li>3 paid days off for volunteering or L&amp;D activities</li></ul><h4>TIDE IS A PLACE FOR EVERYONE</h4>At Tide, we believe that we can only succeed if we let our differences enrich our culture. Our Tideans come from a variety of backgrounds and experience levels. We consider everyone irrespective of their ethnicity, religion, sexual orientation, gender identity, family or parental status, national origin, veteran, neurodiversity or differently-abled status. We celebrate diversity in our workforce as a cornerstone of our success. Our commitment to a broad spectrum of ideas and backgrounds is what enables us to build products that resonate with our members’ diverse needs and lives. We are One Team and foster a transparent and inclusive environment, where everyone’s voice is heard. At Tide, we thrive on diversity, embracing various backgrounds and experiences. We welcome all individuals regardless of ethnicity, religion, sexual orientation, gender identity, or disability. Our inclusive culture is key to our success, helping us build products that meet our members' diverse needs. We are One Team, committed to transparency and ensuring everyone’s voice is heard.
 
Disclaimer
 
It has come to our attention that individuals or agencies are falsely claiming to represent Tide and are reaching out to candidates regarding job opportunities. Please be aware that:<ul><li>Tide does not charge any fees at any stage of the recruitment process.</li><li>All official Tide job opportunities are listed exclusively on our <a href="https://www.tide.co/careers/" target="_blank">Careers Page</a> and applications should be submitted through this channel.</li><li>Communication from Tide will only come from an official @tide.co email address.</li><li>Tide does not work with agencies or recruiters without prior formal engagement, and we do not authorize third parties to make job offers on our behalf.</li></ul>If you are contacted by anyone misrepresenting Tide or requesting payment, please treat it as fraudulent and report it to us immediately at <a href="mailto:talent@tide.co" target="_blank">talent@tide.co</a> Your safety and trust are important to us, and we are committed to ensuring a fair and transparent recruitment process. You personal data will be processed by Tide for recruitment purposes and in accordance with <a href="https://assets.ctfassets.net/3h69mkdgxn20/4TE0uAE3SXomATDVneocNA/aa31893960b4064dd406ad15d029dcd3/Recruitment_Privacy_Notice.pdf" target="_blank">Tide's Recruitment Privacy Notice</a>.<h4>Experience Level</h4>Senior Level

Tide Platform Private Limited

Quality Assurance Associate

Lead Operational Excellence (Commercial Excellence)<h4>Company Description</h4>Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable.  Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparencyDr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.<h4>Job Description</h4>We are looking for seasoned Marketing professionals looking to pivot their career into Operational Excellence while leveraging their rich marketing and branding experience. Job Summary We are seeking a dynamic and experienced Leader in Operational Excellence for overseeing the implementation of an operational framework, optimizing organizational processes through data analysis, and fostering continuous improvement. The role involves identifying and resolving operational issues, implementing knowledge management strategies, and enhancing employee proficiency in operational methodologies. The primary goal is to drive efficiency, resilience, and cost-effectiveness while ensuring adherence to performance metrics and targets. Roles &amp; Responsibilities <ul><li>You will be responsible to strategize and deploy the Process Excellence framework, Lean Management System, benchmarking and continuous improvement to enhance productivity across functions and teams in the business unit.</li><li>KAIKAKU (Radical change) across functions and team in the business unit.</li><li>You will be responsible to drive the process simplification and process improvement through leading a structured ideation process to drive innovation, eliminating non-value-adding activities, removing redundancies, digitizing tasks, outsourcing non-core activities and create more time for scientific endeavors.</li><li>You will be responsible to drive and implement a Cost Optimization program via Product and Cycle-time Excellence (PACE) methodology, identifying cost-saving ideas with functional leads, setting baselines and targets, and reviewing progress regularly.</li><li>You will be responsible for Business Process Redesign (BPR) and Metric Improvement through Strategic Initiatives. Also, evaluate and optimize business processes for scalability and future needs, conducting thorough analysis and workshops with stakeholders. Implement standardized work instructions and modifications to enhance efficiency and effectiveness.</li><li>You will be responsible to establish and manage knowledge sharing practices, overseeing implementation and application of knowledge, and maintaining a comprehensive repository for future reference.</li><li>You will be responsible to build leadership skills and motivate team members for improved Operational Excellence (OE) skills, enhancing their potential and resolving organizational challenges.</li></ul><h4>Qualifications</h4>Educational qualification: B.E/B.Tech preferably with an MBA Minimum work experience: 12 -15 years of experience in Pharma/ FMCG with core experience in Sales/ Marketing/ Commercial Excellence roles.  Skills &amp; attributes: Technical Skills<ul><li>Master Black Belt/ Black Belt Certifications in Lean Six Sigma, Certification in Project Management and other improvement methodology.</li><li>Prior experiences in internal/external process consulting, Process Excellence Framework</li><li>Good knowledge of Lean Six Sigma Methodology &amp; Tools</li><li>Understanding of Strategic Planning and business processes</li><li>Good in Data Analytics, visualization, deriving insights and providing recommendations</li></ul>Behavioral Skills<ul><li>Excellent communication and interpersonal skills</li><li>Business Acumen &amp; Decision Making</li><li>Strong analytical and problem-solving abilities</li><li>Ability to work collaboratively with own team and cross-functional teams</li></ul><h4>Additional Information</h4>About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com <h4>Experience Level</h4>Senior Level

Dr Reddys Laboratories

Team Leader - Operations

Manager – Quality SolutionsRole Responsibilities:<ul><li>Develop and manage project plans, including spend, resourcing and deliverables to design, configure, and develop Quality solutions using technologies such as SAP standard configuration, SAP QM, PP ,WM and FIORI</li><li>Able to Configure, design, development and implementation of Digital projects leveraging enterprise core solutions including but not limited to SAP ECC (modules – MM, PP, QM, WM), SAP S/4.</li><li>Learn and gain expertise in Pfizer’s Plant network global model template focusing on product quality and batch management.  Also learn Pfizer’s Business Processes relevant to these solution areas.</li><li>Design solutions for Continuous Improvement Enhancement Requests (ERs) that are high quality, reflect the most optimal use of available funding, and are implemented in a way that does not adversely impact Pfizer’s global SAP footprint.</li><li>Communicate effectively with stakeholders at various locations globally to ensure that they are adequately informed about the status of requests submitted by them and are kept abreast on progress made and issues encountered.</li><li>Serve as a Project Manager for bigger projects and serve as a coach to the contractors on smaller projects. Take responsibility for the deliverables and ensure cost and timeline commitments made to the business are adhere.</li><li>Conduct business requirements gathering meetings and workshops in an efficient and productive manner and documents minutes, notes and requirements concisely.</li><li>Translate business requirements into technical specifications and liaise with technical development teams to develop and implement system solutions to satisfy business needs.</li><li>Develop cost estimates for projects, create spend forecast and maintain project financial details in Pfizer internal tools and project portfolio systems.</li><li>Stay abreast of new technology trends and look for ways to apply new technologies where it makes sense.</li><li>Learn and adopt internal working procedures and foster conformance and standardization. Also suggest way to improve procedures and practices.</li><li>Partner closely with other Solutions Teams for cross-functional projects, and with other work streams within the Supply Chain Solutions Team such as TechDev, Integration, Data, Business Adoption, Compliance, BI, Serialization, and Security.</li><li>Engage with in cross functional teams including key business stakeholders within Pfizer Global Supply (PGS) and Digital colleagues to contribute to the business process and system development life cycle.</li><li>Provide technical and functional guidance to key stakeholder within PGS</li><li>Assist in unit, cycle, and integration testing of developed programs including but not limited to SAP PP, QM, WM and SAP Fiori.</li><li>Ensure compliance to GMP, deployment standards and quality guidelines with regulatory related obligations are executed with the highest standards of compliance</li><li>Support testing and other activities necessary for SAP IDOC/File interfaces.</li><li>Develop ideas and lead complex projects within and across multiple business units / Digital delivery centers</li></ul><h4>Basic Qualifications:</h4><ul><li>Bachelor’s degree in computer science or Engineering degree and 5 years of relevant experience</li><li>8 years' experience in IT system design and/or delivery, 5+ years in Pharma or business process experience</li><li>At least 5 years of experience working on SAP Quality Management Module, plus very good knowledge in LIMS interface, IDOCS and integration points with Materials Management, Process Order Execution and Warehouse Management. Experience in S4 Hana will be preferable.</li><li>Demonstrable experience in software development lifecycles using agile principles and DevOps practices</li><li>A thorough understanding of system GMP /GDP requirements in detailed knowledge of IT system design and the maintenance lifecycle in GMP environments.  </li><li>Knowledge or familiarity with the production support process, including tasks, escalation routes, communications, and other related activities</li><li>Proven track record of a successful team lead and solution design.</li><li>Excellent written and verbal communication skills, with the ability to communicate with business and technical people alike</li><li>Excellent presentation and facilitation skills, with the ability to interact with various levels of management</li><li>Excellent organization and problem-solving skills</li><li>Excellent leadership and project management skills</li><li>Quick learner. Demonstrate initiative and ownership.</li><li>Ability to operate in a global multi-cultural environment of time zones and requirements </li><li>High degree of business process acumen understanding the life cycle of product creation (Plan, Source, Make, Deliver, Return).</li></ul>PREFERRED QUALIFICATIONS<ul><li>SAP Quality Management and industry experience</li></ul> Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact. PHYSICAL/MENTAL REQUIREMENTS<ul><li>Able to manage contract resources if needed. Mentally strong, able to communicate well and work with Teams.</li></ul>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS <ul><li>Travel as needed</li></ul>  Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Information &amp; Business Tech<h4>Experience Level</h4>Mid Level

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Quality Assurance Jobs In Yelahanka - 346 Verified Vacancies