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We are Hiring For "Medical Coders" Certification is Mandatory / Qualification: Any Degree CODERS : 1. IPDRG Coder : Noida / Hyd / Chennai / Mumbai || CTc upto 13 LPA || 2. Surgery Coder : Hyderabad / Chennai / bangalore || CTc upto 10 lpa || 3. Denials : Chennai / Hyderabad || CTc upto 10 lpa || 4. Radiology : Chennai / bangalore || upto 48k Take home || 5. ENM : Chennai / bangalore || upto 48k Take home || 6. Anesthesia : Hyderabad || take home upto 48k || 7. ED Profee: Chennai / Bangalore || take home upto 48k || 8. ED Blended : Chennai || CTc upto 8.5 lpa || 9. Surgery Obgyn / Cardio / neuro : Chennai /|| CTc upto 10 lpa || Experience : Minimum 1 year relevant experience is mandatory QUALITY ANALYST: 1. Surgery : Hyderabad/ Chennai / Bangalore || take home upto 60k || 2. Home Health : Chennai || CTC Upto 10 LPA || 3. IPdrg : Hyderabad || CTC upto 12lpa || 4. Denials : Hyderabad || CTc upto 9.5 lpa || 5. Radiology +IVr: Hyderabad || CTc upto 9.5 lpa || 6. Anesthesia : Hyderabad || take home upto 60k || 7. ENM : Chennai / bangalore || upto 60k Take home || Eligibility : Min 4 years as a Coder and 1 year exp as QA on (Or) off paper PROCESS COACH : 1. Surgery : Chennai / Bangalore || CTC Upto 9 LPA || 2. ENm : Chennai /Bangalore || CTC Upto 9 LPA || Eligibility : Min 4 years as a Coder and 1 year exp as QA on (Or) off paper TEAM LEAD: 1. SDS : Bangalore / chennai / hyderabad || CTC Upto 12 LPA || 2. Home Health : Bangalore || CTC Upto 12 LPA || 3. ENM : Bangalore / chennai || CTC Upto 12 LPA || Eligibility : Min 6 years exp as coder with exp 1 year (on papers) teamlead Work from office / Relieving is mandatory Interested candidates can share your updated resume to HR Mounika 9849854938 ( Via What's app ) Reference are highly appreciate

Medical coding SDS Chennai & Hyderabad Roles and Responsibilities: - Accurately code SDS and Special Procedures through review of medical record documentation and encounter forms for Outpatient facility Utilize EPIC and 3M systems for SDS/OBS/Special Procedure coding. Assign CPT procedure codes, ICD-10 diagnosis codes, and modifiers based on documentation, government teaching physician documentation requirements and LCD/NCD/ NCCI policies. Should have working experience in all Surgery procedures (10000-69990 CPT series) Should have good knowledge in Cardiac catheterization with 9xxxx series codes. Desired Candidate Profile: - Should be a Science Graduate. Minimum of 1+ years of experience in SDS. Basic knowledge of medical terminology and anatomy. Comfortable to work from office. Effective verbal and written communication skills (Should have capability to reply properly to client and stakeholders. Successful completion of CPC or CCS certification must be active during joining and verified. Able to work independently and willing to adapt and change as per business/ process requirements. For More Information: Contact : Aravind - 7013671172 or Aravind.Nirudi@Sutherlandglobal.com Note: "Sutherland never requests payment or favors in exchange for job opportunities. Please report suspicious activity immediately to TAHelpdesk@Sutherlandglobal.com "

IMCD Group, based in Rotterdam, the Netherlands, is a global market leader in the marketing, sales, and distribution of speciality chemicals and ingredients. Its result-driven professionals provide market-focused solutions to suppliers and customers across EMEA, Americas and Asia-Pacific, offering comprehensive product portfolios ranging from home, industrial and institutional care, beauty and personal care, food and nutrition and pharmaceuticals to lubricants and energy, coatings and construction, advanced materials, and synthesis. The IMCD Group realised revenues of EUR 4,443 million in 2023 with more than 4,736 employees in over 116 offices, 145 warehouses and 73 state-of-the-art laboratories across the globe. IMCDs dedicated team of technical and commercial experts work in close partnership to tailor best-in-class solutions and provide value through expertise for around 60,000 customers and a diverse range of 7000+ world class suppliers. IMCD shares are traded at Euronext, Amsterdam (IMCD). IMCD India Established in 2008 and headquartered in Mumbai, IMCD India represents international producers of specialty chemicals and ingredients. Covering a range of market sectors and with an exceptional track record of growth, our team of high caliber technical and commercial specialists advice our customers on function. Formulation and application of products. In our endeavor to seek solutions and not just products for our key, small and medium enterprise customers, our fully equipped technical center based in Mumbai provides vital support to the Asia-Pacific region. Our regional presence, flexible and tailored supply chain infrastructure and compliance to all local laws and regulations, ensures that IMCD is able to trade Pan-India and deliver a world class customer service. Being a part of IMCD B.V., IMCD India has the benefit of an international network, generating know-how, providing expertise on products and applications whilst supporting local customers through product development and R&D projects. IMCD India, with its multicultural team, is a local reliable partner in sourcing, marketing, sales and distribution across the length and breadth of the country. Purpose of Job We are seeking a highly skilled and motivated individual to join our team as a Master Data Management Item Code Creator, to join our Global Master Data Centre and Item Creator in Mumbai, India. This role is responsible for master data management of products within our organization, including the downloading and management of Data Sheets. Main tasks and responsibilities Master Data Management (MDM): Take ownership of maintaining and enhancing the master data quality and integrity for product-related information. Extract data from various documents and accurately input it into designated company applications. Apply data governance policies, standards, and procedures to ensure consistency and accuracy across all data sets. Collaborate with cross-functional teams to define data requirements, classification, and hierarchies to support business processes. Perform data quality checks to identify and resolve discrepancies or inconsistencies in masterdata. Supplier Data Sheet Management: Coordinate with suppliers to obtain and download Safety Data Sheets (SDS) and Technical Data Sheets (TDS) for products. Ensure the timely updating of SDS and TDS in the master data repository. Validate and verify supplier data against internal specifications and requirements to ensure compliance and accuracy. Safety Data Sheet (SDS) Management: Review and interpret SDS to extract and index relevant product information, such as chemical composition, hazards, and handling procedures. Classify and categorize products based on safety and regulatory requirements, such as OSHA, REACH, and GHS-standards. Ensure the availability and accessibility of SDS to relevant stakeholders. Develop and create labels and SDS for assigned products. Technical Data Sheet (TDS) Management: Collect and manage TDS to provide comprehensive product specifications, performance characteristics, and application guidelines. Standardize and organize TDS-information to facilitate product comparisons, evaluations, and selections. Collaborate with product development teams to update and maintain accurate TDS reflecting the latest product features and improvements. Item Creator: Create new product items in the global product catalogue, ensuring all necessary information is included. Critical review of provided information to ensure not only completeness but also accuracy of information provided. Ensure that items comply with relevant industry regulations and standards, and document necessary certifications. Attach relevant documents such as safety data sheets (SDS), product specifications, and others that may be of relevancy.. Document Item Creation processes, data flows, and automation solutions, including technical specifications, user guides, and training materials. Provide ongoing support and guidance to colleagues on item creation processes. Collaborate closely with Product Managers, HSEQR, Group IT and other stakeholders. Key Attributes: Collaborate with team to support key projects. Timely closure of queries/ concerns raised by the customer about the ordered product thereby building enduring and trusting partnerships with customers. Team player with sound verbal/ written communication skills and a customer centric mindset Ambitious, self-motivated, results driven, well-organized and conscientious individual seeking a long-term association with the organization. Ability to identify opportunities for automation and process improvement. Excellent attention to detail and accuracy. Ability to work independently and as part of a team. Effective communication and collaboration skills, with the ability to interact with stakeholders at all levels of the organization. Strong written and verbal communication skills in English. Knowledge of other languages is a plus. Strong attention to detail and commitment to delivering high-quality results in a fast-paced environment. Key Stakeholders: External: Suppliers Internal: Global IMCD Workforce Reporting Structure: Role Reports to: Lead MDM Positions that report into this role: None Essential Experience: Bachelors degree in a relevant field (Science, Engineering, Business) or equivalent experience. Ideally 3+ years of experience in data-entry, data management, or a similar role, proven experience in product master data management, data governance, and data quality management Strong analytical and problem-solving skills. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).

Work Schedule Second Shift (Afternoons) Environmental Conditions Office Job Description Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Are you passionate about making a positive impact on the worldThermo Fisher Scientific Inc. is currently seeking a highly motivated and experienced Product Stewardship Specialist I to join our world-class team. As a global leader in providing scientific solutions, we are dedicated to enabling our customers to make the world healthier, cleaner, and safer. Responsibilities: Determine, implement, and monitor product stewardship programs to ensure compliance with regulatory requirements Provide support to the Global Product Stewardship team by implementing systems, procedures, and completing projects in support of compliance tracking for raw materials and finished products. We are looking for a Hazard Communication Expert to join our Global Product Stewardship Team. Responsible for material introduction (NPI), classifications and labelling (includes dangerous goods classifications with SME inputs). Ensure completion of regulatory and risk management assessment for compliance to applicable regulations including but not limited to GHS, DG, TSCA, OSHA, EPA, EU REACH, ECHA, etc. Authorizing the SDS and Labels for Hazard classification using UL WERCs. Classification of substances/mixtures in accordance with GHS regulation and Experience with good understanding of GHS and applicable regional regulations Interacts with and responds to global customers, suppliers, and other applicable functions in supporting hazard communication and regulatory compliance needs. Develop expertise in relation to the regulations by maintaining current knowledge of the laws and regulations to provide updated information and respond quickly and accurately to customer requests, internal personnel, and suppliers. Collaborate with cross-functional teams to ensure flawless execution of product stewardship initiatives Conduct audits and assessments to identify areas for improvement and successfully implement corrective actions Proactive in developing process improvement plans using Lean methodologies Lead projects related to global Product Stewardship and assist the Supervisor/Manager to meet business objectives and overall compliance and regulatory requirements. Assist in annual product reporting requirements as necessary. Guide and support team members to achieve the goals of the team Requirements: Master of science degree in Chemistry, other life science. 2 or more years experience in Hazard communication, chemical hazard assessment and authoring Safety Data Sheets and labels based on various national, international and global hazard communications Regulatory Affairs, Dangerous Goods is recommended. Good knowledge of current Hazard Communication requirements and other global chemical regulations and/or guidance (e.g. REACH, ECHA, CLP, GHS, TSCA, regional specific experience with Korea, China are preferred). Strong knowledge of Prop 65, OSHA, EMS, and ISO guidelines. Project management experience. Strong systems background in product lifecycle management and any SDS authoring tool Good analytical and problem-solving skills Excellent communication and collaboration abilities What sets this opportunity apart is the chance to work for a company that values diversity and inclusion. At Thermo Fisher Scientific, we believe that a diverse workforce fosters innovation and drives success. We are committed to creating an inclusive environment where all backgrounds, experiences, and perspectives are respected and celebrated.

Task Working as Intercompany buyer Supporting purchasing tasks - RFQ Management / COP / SDS / Tooling tracking Handling complex purchasing tasks and reports Handling simple negotiations Project purchasing - Independent project handling Supporting in development of new tasks Working with couple of team members and train them Assisting team in analyzing defects Driving certain special projects in function Process compliance Timely delivery of tasks per set guidelines Doing self quality check Notifying internal, external defects and working per corrective actions Maintaining task documentation as per guideline Daily timesheet recording Tools/Systems Understand and utilize PU/LOG tools and systems for executing tasks Soft Skill Good Communication skills - Written and Verbal English Intercultural Awareness for USA & Germany IATF 16949 - Awareness Time management , Conflict management, Presentation skills Misc / Others Participate in team and department meetings Maintain 5S of own area

Greething!!! Corro Health is Hiring for Certified Medical Coders..! Designation : Executive / Sr. Executive Location : Banaglore and Noida Specialties: IVR - CIRCC Certification Manadatory Location: Bangalore/ Noida Specialties: E&M OP , EM IP Denails IVR Surgery Cardiology Surgery Cardio-Vascular Surger Cardiothoracic Surgery Ortho and Cardiology (Both Experience is must) NeuroSurgery Location: Noida Experience: 1 to 9 Years Certification: AAPC/AHIMA ( Mandatory ) Salary: Best in the industry ***Preferred Immediate Joiners 15 days to 30 days*** Interested candidates please send your resume to ashrafara.j@corrohealth.com and Ashraf HR 8015364150

Coder is accountable to manage day to day activities of coding the Patients chart & Diagnosis report. Responsibility Areas: Understand the client requirements and specifications of the project. Meet the productivity targets of clients within the stipulated time (Daily & Monthly) Applying the instructions/updates received from the client during production. Coding or auditing charts, based on requirements. Prepare and Maintain reports Good Knowledge on Anatomy & Physiology Excellent Knowledge on ICD & CPT Good Computer Skills Above Average Communication Skills Good Reporting Skills

The Opportunity Avantor is looking for a dynamic, forward-thinking, and experienced Associate - Global Data Compliance, who will be responsible for delivering results against some of the most complex business and technology initiatives. This role will be a full-time position based out of IND- Coimbatore. If you are passionate about solving complex challenges and driving innovation – let’s talk! Our organization is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Job Description The Associate, Global Data Compliance supports Global Product Data Compliance team, ensuring the proper product classification, managing product and quality data on SAP, create/source/upload regulatory compliance documents (COA/SDS/TDS), licensing of regulated chemicals, and manage customer queries/request with respect to product data, documents and certificates. Keeps informed of regulatory changes and implement the necessary changes to maintain company compliance. Entry level position- collect, evaluate, write, and submit data and reports for regulatory bodies. Assist with data gathering and analysis for legal purposes. Coordinate document requests, procedure changes, and other quality projects. Audit and monitor data, systems, and processes for compliance to policies and laws. MAJOR JOB DUTIES AND RESPONSIBILITIES (List in order of importance) Adhere to the workflow instructions/standard operating procedure provided by the business and support product on-boarding, review/classify licensed/restricted regulated materials, source/create/upload compliance documents/certificates ensuring the same is available for the customer Obtains & maintains federal, state and local product & facility registrations, licenses & certifications in accordance with the regulation and any other license necessary to support the business Handle customer queries related to product data and regulatory compliance documents Complete all assigned tasks as per Service Level requirements specified by the business and meet/exceed key performance parameters Liaise with both internal and external customers and provide resolution with a customer centric approach Stays current on applicable regulations and evaluates their impacts on the business, and propose guidance, procedures, programs & policies Recognize important regulations & changes involving compliance Modifies & maintains department work procedures Performs other duties as assigned QUALIFICATIONS (Education/Training, Experience And Certifications) Minimum of a graduate Degree in Chemistry/Life science or an equivalent subject. 0 to 2 years of experience Good knowledge and experience within the chemicals and lab products industry is a must computer skills (Word, Excel and Access, VBA, PowerBi etc) Knowledge, Skills And Abilities Excellent communication skills (verbal and written) Strong organizational skills with exceptional attention to detail and accuracy Efficiency in a deadline-driven environment with multiple concurrent assignments SAP experience considered a plus Strong interpersonal skills Good analytical and problem-solving skills Good organizational skills Strong computer skills including Word, Excel and Access Flexibility to work in shifts. Disclaimer The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor? Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today! EEO Statement We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at recruiting@avantorsciences.com and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. 3rd Party Non-solicitation Policy By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation Show more Show less

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This job is with Organon, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Responsibilities Job Description Order to Cash (OtC) Management OtC Cycle Oversight: Manage the entire Order to Cash cycle, including customer order management, execution, and ensuring timely delivery of products to customers. Alliance Partners and SCM Governance: Collaborate with alliance partners to establish and maintain effective supply chain governance, ensuring compliance and alignment with strategic goals. Order Management: Coordinate order processing for all market customers, ensuring compliance with commercial and quality guidelines/SOPs. Inventory Control: Monitor inventory levels across super distributors (SDs) to prevent obsolescence and ensure product availability aligns with forecasts. Timely Shipment Delivery: Process, monitor, and deliver shipments to respective SDs/customers in a timely manner, maintaining high service levels (On-Time In-Full, Line-Item Fill Rate). Compliance Assurance: Ensure adherence to standard operating procedures (SOPs) and company policies throughout the OtC process, Including all ERP (Athena) transactions. Planning Process Management Demand Planning: Oversee demand planning for India and neighboring markets, ensuring accurate forecasts that align with business objectives. Fulfillment Planning: Manage fulfillment planning for local source supplies & review import supplies, optimizing supply chain efficiency. MRP Cycle Monitoring: Review the Material Requirements Planning (MRP) cycle, communicating net requirements to the respective import teams. Supply Chain Execution Management: Drive initiatives to monitor plan versus actuals, addressing chronic supply issues and updating stakeholders on constraints and potential sales losses. Collaboration with Regulatory : Collaborate with regulatory team to identify impacts on planning & supplies due to regulatory changes. Product Availability Monitoring: Ensure product availability aligns with forecasts at hubs. SD Management : Ensure product availability at Super distributors. Manage inventory across SDs while controlling inventory obsolescence. Key Deliverables Cost to Serve: Monitor and optimize the cost to serve metrics. Inventory Management: Analyze inventory norms based on product contributions and support improvements in inventory planning. Service Levels: Maintain high service levels and ensure compliance metrics are met. Forecast accuracy , On-Time In-Full, Line-Item Fill Rate) Relationship Management Organizational Development: Build and lead a highly effective supply chain organization capable of cross-functional collaboration. Stakeholder Engagement: Cultivate strong relationships with internal and external stakeholders to continuously understand and meet customer requirements. Required Education, Experience And Skills Graduate in Engineering or Supply Chain-related fields. A Master's degree is an added advantage. Experience in Supply Chain (Order to Cash, Planning Process, and Alliance Management). SAP experience 2-8 years - MM Module Secondary Job Description Who We Are: Organon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women's Health, expanding access to leading biosimilars and touching lives with a diverse and trusted portfolio of health solutions. Our Vision is clear: A better and healthier every day for every woman. As an equal opportunity employer, we welcome applications from candidates with a diverse background. We are committed to creating an inclusive environment for all our applicants. Search Firm Representatives Please Read Carefully Organon LLC, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Annualized Salary Range Annualized Salary Range (Global) Annualized Salary Range (Canada) Please Note: Pay ranges are specific to local market and therefore vary from country to country. Employee Status Regular Relocation: No relocation VISA Sponsorship Travel Requirements: Organon employees must be able to satisfy all applicable travel and credentialing requirements, including associated vaccination prerequisites Shift Flexible Work Arrangements: Valid Driving License Hazardous Material(s): Number Of Openings 1 Requisition ID: R534498 Show more Show less

Hi All interview Started For CODERS & QA and offer Relese also Started ED Facility 1 year Above , Denial coders , surgery coder, EM OP coder Location - Chennai, comibatore, pune ONLY WORK FROM OFFICE Certified Must NOTICE Period Acceptable Designation - Medical Coder / QA Shift: Day shift Available Timing from 10.30 am to 6.30 pm Monday to Saturday kowsalya 8122343331 WatsApp and call Send Updated Resume , Recent Photo with the Mentioned Details Your Interview Will Be Scheduled Name - Contact Number - Current Company - Experience - Certification - Take home salary - Expected salary - Certification Number - NOTICE PERIOD - Active Bond - Email ID - Kinldy share this to all friends who in need of jobs in Coding

We are currently seeking an Team Coach/Group Coach for Surgery Medical Coding at Vee Healthtek. Job Description: - Must have over 6 years of experience in Medical Coding - Specialization in Surgery Medical Coding - Experience of 6+ years on Surgery - Designation: Team Coach/Group Coach - Location: Hyderabad/Bangalore/Trichy (Work from office) - Salary: 65K CTC Maximum based on the experience and interview outcome Candidates must have experience in team handling, with a minimum of 2 years in team management, excellent communication skills, and client management abilities. Interested candidates are encouraged to contact us immediately at 9443238706 (also available on Whatsapp) or send your profile to ramesh.m@veehealthtek.com. Best Regards, Ramesh HRD Vee Healthtek

Immediate Job Openings for Surgery Medical Coders @ Vee Healthtek Job Description: 1+ Years of Experience in Surgery Medical Coding. Specialty : Surgery Medical Coding Experience : 2 - 5 Years. Designation : Sr Coder/QA Certification: CPC/COC/CCS/CIC is Must Salary: 45K CTC Max Joining: Immediate Joiners only Location : Chennai/Bangalore/Hyderabad/Trichy/Salem/Pune - WFO Interested Candidate can Call Immediately to 9443238706 (Available on Whatsapp) or forward your profile to ramesh.m@veehealthtek.com Regards, Ramesh - HRD 9443238706 ramesh.m@veehealthtek.com Vee Healthtek

Job Profile for Enzyme Specialist The Enzyme Specialist will be responsible for the research, development, optimization and application of enzymes in various biotechnological, pharmaceutical, agricultural and industrial processes. The role involves enzyme screening, production, purification, characterization and process scaling, with a focus on sustainability and innovation. Qualification & Experience PhD in Biotechnology, Biochemistry, Microbiology, Enzyme Technology or related field. 2–5 years of hands-on experience in enzyme production and application. Strong expertise in molecular biology tools for enzyme engineering (e.g., site-directed mutagenesis, CRISPR, directed evolution). Proficiency in analytical techniques: SDS-PAGE, HPLC, spectrophotometry, LC-MS, etc. Familiarity with bioinformatics tools for enzyme structure-function prediction. Duties & Responsibilities Scope of work includes, but is not limited to the following Design, execute and manage enzyme-related projects, including screening, isolation and production from microbial, plant or synthetic sources. Use molecular cloning, synthetic biology and recombinant DNA technologies to generate optimized gene constructs. Evaluate expression profiles using RT-qPCR, Western blotting or reporter gene assays. Develop and refine methods for enzyme purification, immobilization and stabilization. Characterize enzyme kinetics, substrate specificity, thermostability and pH tolerance. Maintain detailed records and reports for publications, patents, and regulatory compliance. Provide technical support to cross-functional teams and contribute to product development. Key Skills This includes but not limited to the following: Strong analytical and problem-solving abilities. Knowledge of regulatory and safety practices in enzyme handling. Excellent communication and documentation skills. Ability to work independently and in a collaborative environment. Please note that preference will be given to candidates who have relevant research publications, possess knowledge of RT-PCR and are from the northern region. Show more Show less

Bosch Software Engineering, Data Science Bengaluru, Karnataka, India Posted on Jun 17, 2025 Apply now Company Description Bosch Global Software Technologies Private Limited is a 100% owned subsidiary of Robert Bosch GmbH, one of the world's leading global supplier of technology and services, offering end-to-end Engineering, IT and Business Solutions. With over 28,200+ associates, it’s the largest software development center of Bosch, outside Germany, indicating that it is the Technology Powerhouse of Bosch in India with a global footprint and presence in the US, Europe and the Asia Pacific region. For more than 138 years, Robert Bosch GmbH has led groundbreaking innovations across a wide range of industries. As the world becomes increasingly software-driven, Bosch is accelerating its journey to create smarter solutions "Invented for Life." As an integral part of this transformation, Bosch Software and Digital Solutions (SDS) was established as a global technology powerhouse within BGSW, a captive unit of Bosch. Experts in software, sensors, and services, we partner with organizations ranging from leading startups to established industry giants to deliver new-age digitalization. We help reimagine the present and the future of businesses with Smarter Digital solutions. Be a part of a company that's constantly evolving and driving innovation! Stay connected and explore career opportunities by following us on LinkedIn and visiting our website Job Description Roles & Responsibilities : Bosch Software and Digital Solutions is a leading systems integrator and solution provider for technology led business transformation. It is the systems integration arm of Bosch Global and is headquartered in Bangalore. The Chief AI Officer (CAIO) will be responsible for developing and articulating a clear AI vision for SDS and overseeing, implementing and governing SDS’ AI strategy that aligns with business goals. The CAIO will also oversee the development of innovative AI and Gen AI solutions/offerings for further transforming SDS’s offerings portfolio and to support SDS customers with their AI journeys. The CAIO will lead Bosch SDS’s AI-first approach and align SDS’ portfolio offerings to the rapidly evolving needs of our customers. Key Responsibilities Strategic AI Vision and Roadmap Develops and articulate a clear AI vision that aligns with SDS’s short, medium and long-term goals. Creates an AI roadmap that outlines short-term and long-term initiatives. Identifies vital areas where AI can drive business growth and efficiency. AI Strategic Leadership Develop and drive SDS’ AI strategy to align with organization's broader transformation roadmap and business goals. Define overall AI GTM and growth strategy in conjunction with business leaders. AI Product and Solution Development Analyze emerging trends to create AI products/accelerators, frameworks and capabilities in key areas such as predictive analytics, NLP, Computer vision, generative AI, agentic AI, and automation. Define guidelines for AI model development for customers, ensuring ethical, transparent, and responsible AI Use Conceptualize the blueprint of asset to-be developed and collaborate with technical team to execute and implement the same. Co-lead initiatives like hackathons, workshops, and other events to encourage innovation and cross sharing of ideas. AI Strategy Consulting and Advisory Lead customer discussions to understand their existing problem statements and business challenges and assess their existing AI maturity. Define target AI Reference architecture, use case discovery, business case and implementation approach for AI initiatives. Define consulting approach and frameworks and develop AI Consulting proposals, bid defense, and help in acquisition. Manage/Lead AI consulting engagement to define AI strategy, roadmap, and execution plans aligned with business objectives. AI Implementation Oversee the implementation of AI projects for customers, which includes Design and deployment of AI-powered solutions, including machine learning (ML), generative AI, computer vision, NLP, and generative AI solutions for customers. Identify emerging AI trends and technologies to create competitive, scalable offerings. Leverage the existing code base/solutions to ideate and create re-usable assets/IPs. AI Team leadership and Talent Development Build and Lead cross-functional AI teams (Data Scientists, ML Engineers, AI researchers, Gen AI developers, Product Managers, etc.) Foster a culture of continuous learning, innovation, and collaboration. Establish AI training and upskilling programs for employees. Qualifications Qualifications & Experience: Bachelor’s degree in computer science or engineering. Good to have master’s degree/Post-graduate in IT, AI, Data Science, or related fields. 15+ years of experience in AI, data science, or machine learning, with a proven track record in leadership roles Strong knowledge of AI frameworks, Gen AI, cloud AI services, and big data technologies Good understanding of emerging technologies like Gen AI, Agentic AI etc. Experience in leading mid and large-scale AI transformations across domains such as Manufacturing, healthcare, retail, etc. Strong knowledge of AI ethics, governance, and regulatory considerations Excellent communication, leadership, and stakeholder management skills Key Competencies and Skills: Deep understanding of AI technologies, including NLP, Computer Vision, and Generative AI Strategic thinking and strong skills across leadership, collaboration and stakeholder management Ability to drive cross-functional teams towards AI innovation, deal closures and successful project delivery. Additional Information KPIs And Success Criterion AI-driven revenue generation and cost optimization Growth of AI portfolio in Bosch SDS, along with opportunity pipeline and AI Adoption across customers Growth of AI team, employee engagement and retention AI project delivery success rates and business outcomes/customer feedback Apply now See more open positions at Bosch Show more Show less

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. The Environmental, Health and Safety Specialist will be responsible for the development, implementation and management of site programs and policies to ensure compliance with federal, state, and local environmental, health and safety regulations. This individual will work with various cross-functional teams including Operations, Security, Facilities, Engineering, etc. to promote engagement and support of EHS targets, safety and health culture and regulatory compliance. This position supports multiple Manufacturing/R&D sites and reports directly to the Director of Environmental, Health and Safety. You Are Responsible For Managing and performing planning, inspection, reporting, and recordkeeping for all environmental, health, and safety (EHS) compliance programs. Developing and implementing EHS policies and procedures. Maintaining OSHA logs, EHS permits, licenses, and registrations. Investigating EHS-related incidents (including injuries, near misses, and releases) to determine root causes and implementing corrective actions. Managing workers’ compensation claims and the return-to-work program. Performing evaluations and risk assessments of processes to ensure EHS compliance and recommending improvements to reduce or eliminate waste, emissions, and hazards. Collaborating with cross-functional teams on new projects and process development. Conducting industrial hygiene (IH) surveys, job hazard analyses (JHA), and personal protective equipment (PPE) assessments. Performing ergonomic evaluations for office and manufacturing environments. Partnering with the facilities team to manage the Contractor Safety Program. Conducting compliance assessments, EHS inspections, and management system audits. Developing EHS training courses and delivering in-person training on specific EHS topics. Leading EHS Committees and Emergency Response Teams. Maintaining the chemical inventory and SDS database. Managing environmental compliance activities, including hazardous waste handling, SARA 312 reporting, and SARA 313 Toxic Release Inventory reporting. Maintaining EHS Management System requirements. Providing technical guidance to management on EHS issues and regulatory compliance. Interfacing with EHS regulatory agencies. Supporting the Radiation Safety Officer (RSO) in managing site Radiation Safety Programs. Minimum Qualifications Bachelor’s degree in Safety, Environmental Science, or related discipline. 8-10 years experience in EHS Program Management. Working knowledge of EPA and OSHA regulations and industry EH&S standards. Strong knowledge in electrical safety and high voltage including OSHA and NFPA 70E compliance. Demonstrated ability to recognize, evaluate, and recommend controls for workplace hazards. Excellent interpersonal, communication and analytical skills. Strong writing capabilities, especially with writing clear, concise EHS procedures. Proficient in MS Office (Word, Excel, PowerPoint, and Access). Ability to manage multiple projects/tasks and work independently with minimal supervision. Must be able to interface with all levels of the organization. Travel up to 20% when necessary. Preferred Knowledge/Skills, Education, And Experience Certified Safety Professional (CSP) certification, Certified Hazardous Material Manager (CHMM) certification, or equivalent. Experience working with ISO 14001 and ISO 45001 Management Systems. Forklift train-the trainer certification. Fall protection train-the-trainer certification Who we are : We are a team of more than 73,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways. How we work: When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably. To find out more about Siemens Healthineers businesses, please visit our company page here. The Annual Base Pay For This Position Is Min $104,000 - Max $156,000 Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate. If this is a commission eligible position the commission eligibility will be in accordance with the terms of the Company's plan. Commissions are based on individual performance and/or company performance. The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan. life insurance, long-term and short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time. Equal Employment Opportunity Statement: Siemens Healthineers is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law. EEO is the Law: Applicants and employees are protected under Federal law from discrimination. Reasonable Accommodations: Siemens Healthineers is committed to equal employment opportunity. As part of this commitment, we will ensure that persons with disabilities are provided reasonable accommodations. If you require a reasonable accommodation in completing a job application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please fill out the accommodations form here. If you’re unable to complete the form, you can reach out to our HR People Connect People Contact Center for support at peopleconnectvendorsnam.func@siemens-healthineers.com. Please note HR People Connect People Contact Center will not have visibility of your application or interview status. California Privacy Notice: California residents have the right to receive additional notices about their personal information. To learn more, click here. Export Control: “A successful candidate must be able to work with controlled technology in accordance with US export control law.” “It is Siemens Healthineers’ policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.” Data Privacy: We care about your data privacy (https://www.siemens-healthineers.com/careers/recruitment-application-privacy-notice) and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. We ask instead that you create a profile in our talent community where you can upload your CV. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you an alert when relevant positions become open. Register here to get started. Beware of Job Scams: Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons that are currently posing as Siemens Healthineers recruiters/employees. These scammers may attempt to collect your confidential personal or financial information. If you are concerned that an offer of employment with Siemens Healthineers might be a scam or that the recruiter is not legitimate, please verify by searching for the posting on the Siemens Healthineers career site. To all recruitment agencies: Siemens Healthineers does not accept agency resumes. Please do not forward resumes to our jobs alias, employees, or any other company location. Siemens Healthineers is not responsible for any fees related to unsolicited resumes. Show more Show less

In this role, you will Design & Develop, platform components and applications for Hospital Patient Monitoring business category. Your role: Participating in the development of application software Analyzing and understanding the Software/Functional Requirements Specification Owning the detailed design of the system. Comfortable in design, implementation, testing, and documentation Ensure quality by writing developer level tests (unit, component, etc) Debugging defects Performing unit testing of the code. Contributing to Features/User stories for modules/SDS /Test strategy Working with team for the quality and timely deliveries. Creating products according to the specifications and software development process Creating engineering documentations to comply with product development policies, practices and procedures Participates in peer reviews for project artifacts and ensure the quality of deliverables Supporting project estimation, planning and risk management activities Keeping abreast of technical developments in own field through study, technical contacts and propagate it you're the right fit if: 5 - 9 years of experience with good Knowledge of C++ and Python programming languages Good knowledge of serial communication and communication protocols (eg RS232, RS422, USB, SPI etc) Basic knowledge of HW (eg microcontroller, A/D converter, i/o controls) Personal Characteristics Excellent communication and documentation skills. Self-starter, quick learner, ability to work with teams. Software Craftsmanship mindset. Proactive and self-driven, possesses due sense of urgency. Ability to stay focused on the target to deliver in agile manner. Openness to collaborate in interest of project/organization. Shall be very good technically; good problem solving abilities. Working with multisite teams, Quality conscious and Process & customer Oriented. Ability to learn, team orientation and independent Basic knowledge in the field of digital signal processing (optional) Basic knowledge of medical technology and human physiology Strong analytical and problem-solving skills Good programming and debugging experience Experience working with CI/CD pipelines Working experience in Agile/SAFe development methodologies Good communication and documentation skills Ability to stay focused on the target to deliver in agile manner. Openness to collaborate in interest of project/organization Work experience on systems used in healthcare is a plus

In this role, you will Design & Develop, platform components and applications for Patient Monitoring business category. Your responsibilities Participate in the development of application software Analyzes and understands the Software/Functional Requirements Specification Owning the design (high level and detailed) of the system. Should be hands on with design, implementation, testing, and documentation Performing unit testing of the code. Contributes to Features/User stories for modules/SDS /Test strategy Providing technical guidance in a technical, functional/domain area and participates in technical decisions Working with engineers and other team members for the quality and timely deliveries. Participates in peer reviews for project artifacts and ensure the quality of deliverables Supports in project estimation, planning and risk management activities Keeps abreast of technical developments in own field through study, technical contacts and propagate it Guides and coaches the project team in technology and domain Interacts effectively with other functions (verification, Quality, regulatory, project mgmt) for the success of the project You are a part of The Hospital Patient Monitoring business resides in the Connected Care business cluster. MA is a software and solutions business encompassing patient monitoring and its capabilities. Our MA solutions reach more than 370 million people every year. Our advanced intelligence platforms provide clinicians with information when and where they need it so that they can make smart decisions. Our ultimate priority is to enable caregivers, administrators and patients to make decisions that support better health, increase efficiency and control costs. At PIC Bangalore, the team is part of the global Monitoring & Analytics R&D team to drive the business roadmap. To succeed in this role, you should have the following skills and experience 5+ years of experience in software development with hands-on in C#, .Net Core, Angular, REST Api,Web Services, Database(SQL,Postgresql), MicroServices Strong analytical and problem-solving skills Excellent software design skills Good programming and debugging experience Experience working with CI/CD pipelines Working experience in Agile/SAFe development methodologies Good communication and documentation skills Experience with Test Automation using Behavioral Driven Development (BDD) Good communication and documentation skills. Ability to stay focused on the target to deliver in agile manner. Openness to collaborate in interest of project/organization Strong analytical and problem solving skills Knowledge of Privacy & Security Rules , aspects for Software Work experience on systems used in healthcare is a plus. Personal Characteristics Excellent communication and documentation skills. Self-starter, quick learner, ability to work with teams. Software Craftsmanship mindset. Proactive and self-driven, possesses due sense of urgency. Ability to stay focused on the target to deliver in agile manner. Openness to collaborate in interest of project/organization. Shall be very good technically; good problem solving abilities. Working with multisite teams, Quality conscious and Process & customer Oriented.

Job title : Synthetic Chemistry Scientist Job location : Bangalore & Hyderabad About Syngene : At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards always Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose of the Role: Personnel handling this profile will be responsible for conducting reactions and delivering final compounds within a fast turnaround time, meeting the specific requirements of both the project and Syngene. The candidate should be capable of independently solving chemistry problems. He or she should ensure that the experimental observations are recorded contemporaneously and in compliance with the Electronic Laboratory Notebook (ELN) policies of the project and Syngene. Role Accountabilities: Expected to design a synthetic scheme for any given target and to be proactive in identifying rate limiting steps along with the mitigation strategy. The candidate should be well versed in using literature search engines and predictive synthesis tools Perform synthetic chemistry reactions, reaction workups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab equipments Ensure that the samples generated during synthesis are given for analysis and record subsequent results obtained and update the supervisor / group leader on the progress of synthesis and ensure samples are packed appropriately for shipment Record the observations of experiment/reaction, results, utilization of resources and other activities related to the reaction in the laboratory or e-notebook following guidelines and in timely manner and ensure that the same is handled safely and confidentially. The candidate should be capable of meeting Syngene s productivity expectations (# of compounds/month and # of steps/month) without compromising on safety and quality. The candidate should be capable of synthesizing the final compounds at a faster turnaround time The candidate should have excellent analytical interpretation and purification skills Ensure that they know the SDS of the chemicals they are handling and aware of emergency response procedures in case of accidental spillage, leakage or fire and ensure proper waste segregation as per EHS norms Always follow EHS and quality system requirements in the workplace ensuring individual safety and lab safety Attend all mandatory trainings and update training records as and when trainings are completed Always ensure confidentiality Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience 3 - 10 years Skills and Capabilities: Should have deeper knowledge with concepts of organic synthesis and reaction mechanisms Candidate should be capable of solving synthetic problems independently Should be excellent in purification and analytical interpretation skills. Familiar with operations of relevant apparatus - instrument / equipment. Education M.Sc/ M.Pharm/ Ph.D/Ph.D+PD in Synthetic chemistry. Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status regarding public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities

WE ARE HIRING CERTIFIED EXPERIENCED MEDICAL CODERS|| CHENNAI ,HYDERABAD ,NOIDA || HR SWETHA 9030360584 || Specialty: ENM with Denials ENM with Surgery ED Profee+facility OBY/ GYN Surgery IVR SDS MULTI SPECIALTY DENIALS Experience: 2 to 10 years in above mentioned specialties Notice Period: Up to 60 days Package Up to 10 LPA Shift Timings: General shift Work from office Location : Chennai, Hyderabad, Noida Reliving is Mandatory Interested candidates can share your updated resume to HR SWETHA 9030360584 (share resume via WhatsApp ) Refer your friend's / Colleagues NOTE : OPENINGS IS FOR ONLY CERTIFIED EXPERIENCED MEDICAL CODERS ONLY NOT FOR FRESHERS AND NOT FOR HCC CODERS ALSO ONLY ABOVE MENTIONED SPECIALTIES CAN APPLY.

Job Description Perform a variety of activities involving the audit of coding of medical records by ascribing accurate diagnosis and CPT codes as per ICD-10 and CPT-4 systems of Perform Coding and auditing for Outpatient and/or Inpatient records with a minimum of 96% accuracy and as per turnaround time requirements Exceeds the productivity standards for - as per the productivity norms for inpatient and/or specialty specific outpatient coding standards Maintains high degree of professional and ethical standards Focuses on continuous improvement by working on projects that enable customers to arrest revenue leakage while being in compliance with the standards Focuses on updating coding skills, knowledge, and accuracy by participating in coding team meetings and educational conferences Job REQUIREMENTs To be considered for this position, applicants need to meet the following qualification criteria: Graduates in life sciences with 5 - 10 years of experience in for Surgery Experience in Medical Coding Audit and Physician Education, preferably in Surgery Coding, will be a plus Knowledge of Coding Procedures and Medical Terminology in an ambulatory setting Exposure to CPT-4, ICD-9, ICD-10, and HCPCS coding CCS/CPC/CPC-H/CIC/COC certification from AAPC /AHIMA would be a plus Current certification with valid proof of certifications Good knowledge of medical and billing systems, regulatory requirements, auditing concepts, and principles

Role : The role is to secure the telematics solutions are deployed on all vehicles in a quality assured way. This group will play a vital role to effectively utilize the potential of Telematics linked solutions like Uptime Services, Fleet Management, Vehicle Tracking, Navigation etc. , . The Vehicle Connectivity team in Bangalore is an integral part of Global Vehicle Connectivity organization which shall secure connected vehicles supporting the increasing demand for soft products. Connectivity is a key enabler for fleet management, uptime services and advanced vehicle services such as driver assistance, truck specific navigation and fuel reduction, targeting reduced costs as well as increased revenues. Vehicle Connectivity department develops software for on-board telematic systems for several Volvo companies. As a Lead Developer you will gain a good understanding of End to End functions of On-board Telematics sub-system, logical design of End to End functions and develop embedded software working in a global environment. You would make significant contribution to Global Telematics Software platform, joining a team of highly skilled and well organized product development team with colleagues worldwide. The position holder will report to Group Manager, Embedded Software Development, Vehicle Connectivity. Responsibilities : esign, develop, test, maintain, document and release software solutions according to a new Epic/Capability iscuss with the System Leaders/Functional Owners group to get the required specification which need to be analysed and implemented as solutions. esponsible for developing the Low-Level Design of the SW and provide technical guidance to the team to realize the feature/solution reakdown the new Capabilities onto features and write Stories for the team to realize. esponsible for providing estimates for the work packages and technically implementing the solutions. esponsible for a number of software components and competence areas. evelop embedded code in C++ language from software requirement specifications, candidates are expected to have good knowledge of C++ (99, 11, 14 and 17) standards. erform trouble shooting in Application SW, drivers, BSP, OS, middle ware software. evelop unit tests, tests the software to verify functionality using various testing tools. ocument the software code in order to release the software for use in the ECU. ollow the predetermined work processes in order to comply with the standards. uggest and implement improvements in the software development process/environment.

Roles : The role is to secure the telematics solutions that are deployed on vehicles in a quality assured way. This group will play a vital role to effectively utilize the potential of Telematics linked solutions like Uptime Services, Fleet Management, Vehicle Tracking, Navigation etc. , . Connectivity is a key enabler for fleet management, uptime services and advanced vehicle services such as driver assistance, truck specific navigation and fuel reduction, targeting reduced costs as well as increased revenues. Vehicle Connectivity department develops software for on-board telematic systems for several variants. As a Lead Developer you will gain a good understanding of End to End functions of On-board Telematics sub-system, logical design of End to End functions and develop embedded software working in a global environment. You would make significant contribution to Global Telematics Software platform, joining a team of highly skilled and well organized product development team with worldwide colleagues. The position holder will report to Group Manager, Embedded Software Development, Vehicle Connectivity. Responsibilities : Design, develop, test, maintain, document and release software solutions according to a new Epic/Capability Discuss with the System Leaders/Functional Owners group to get the required specification which need to be analysed and implemented as solutions. Responsible for developing the Low-Level Design of the SW and provide technical guidance to the team to realize the feature/solution Breakdown the new Capabilities onto features and write Stories for the team to realize. Responsible for providing estimates for the work packages and technically implementing the solutions. Responsible for a number of software components and competence areas. Develop embedded code in C++ language from software requirement specifications, candidates are expected to have good knowledge of C++ (99, 11, 14 and 17) standards. Perform trouble shooting in Application SW, drivers, BSP, OS, middle ware software. Develop unit tests, tests the software to verify functionality using various testing tools. Document the software code in order to release the software for use in the ECU. Follow the predetermined work processes in order to comply with the standards. Suggest and implement improvements in the software development process/environment.

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Title: Scientist II Job Location: India, Bangalore About Company: About The Company Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. Our Innovative Laboratory technologies & Services makes it easier for customers. About Team: Antibody team The antibody team is involved in engineering and development of antibodies, with a deep focus on reagent quality and specificity. The core activities of team include design, development, purification, conjugation and testing of antibodies in a variety of immunoassay applications using pioneering tools and technologies. The goal of the program is advanced product development and creation of product specific information to promote research use. Role & Responsibilities Role: To be an integral part of an antibody development team with a focus on performance and specificity using innovative molecular, protein, and cell biology methods. Responsibilities: Independent experimental planning and execution to meet program goals and schedules. Timely record keeping of results into data sheets and laboratory note-books. Regular mining of literature and keeping oneself up to date with developments in field of antibody development and protein biology. Ideate effectively to recommend improvements in product development and workflows. Compilation and presentation of data in written and oral formats to different audiences including stakeholders and leadership. Active participation in team meetings. Mentoring junior scientists and provide in-lab supervision. Candidate Requirement: Education & Experience levels: Applicants should have Masters with greater than 5 years relevant experience or PhD with greater than 2 years’ experience in a life sciences field with a strong focus on structural biology, protein design, protein purification, molecular biology, immunology, biotechnology or biochemistry. Nature of experience: Extensive experience and knowledge in protein purification and analysis technologies such as affinity or ion exchange chromatography, SEC, HPLC, and SDS-PAGE. Experience and knowledge of protein affinity measurement platforms. Familiar with working in a cell and molecular biology lab, with experience in assays for in vivo of protein expression, protein-protein interaction (using co-immunoprecipitation) or development of immunoassays. Proficiency in display-based antibody development techniques, demonstrating a strong track record of successful projects. Extensive experience and familiarity with antibody or protein engineering, rational design of mutants, and molecular biology. Experience with structural biology and protein modeling and visualization tools such as Pymol, Shrodinger, Discovery Studio or other such programs. Experience with antigen design for immunizations, analysis and identification of epitopic regions desirable. Familiarity or experience in development of conjugation chemistries or performing antibody conjugation. Theoretical or practical experience in antibody development platforms is desirable. Project or work experience in support of relevant skills such as publications, project reports or thesis work. Proficient in MS Office applications such as Word, Powerpoint, Excel and possess a strong statistical knowledge and familiarity with statistical software such as Prism. The successful candidate will be self-motivated and a self-starter who is excellent at learning and applying new concepts for process or product improvements, possess excellent oral and written communication skills to connect to peers and leadership, and will be an excellent teammate with the ability to work with different colleagues. Thermo Fisher Scientific is an equal opportunity employer and value diversity at our company. All qualified applicants will receive consideration for employment without discrimination basis race, color, religion, sex, sexual orientation, gender, gender identity or expression, national origin, protected veteran status, age, genetics, pregnancy, disability or any other legally protected status. Thermo Fisher Scientific aligns with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! ThermoFisher is committed to crafting a diverse work environment that values and respects individuals from all backgrounds. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Show more Show less

Job Summary Are you passionate about solving customer problems, offering Technical solutions and building deeper business relationships that help drive growth for industry leading Consumer Products customers? Joining science and creativity, we are an international collective of thinkers who partner with customers to bring scents, tastes, experiences, ingredients and solutions for products the world craves. If you are skilled at solving complex problems with elegant technical solutions, and have a collaborative approach to exceeding customer expectations, you could be our next Senior Application Technician! Your Focus As a Senior Application Technician, you will provide technical service to support the Home and Personal Care sales teams in the South Asia, Middle East and Africa regions. You will be part of a global network where our colleagues work across R&D, Application and Commercial functions for our Health & Bioscience business. The role is based in Hyderabad, India and will report to Senior Application Scientist. How You Will Contribute Perform the design, execution, and interpretation of experiments. Prepare and present technical reports, summaries, and protocols. Work closely with other Home and Personal Care (HPC) Application & R&D Labs. Conduct process safety management (PSM) of new equipment, maintaining SDS & Safety of Lab. Troubleshoots service, delivery and customer application problems. Support sales by demonstrating technical applications knowledge of the product and/or technical solutions at the customer. Plan project approaches and routinely formulates work plans. What You Will Need To Be Successful Bachelor`s or Master’s degree in Biochemistry, Biotechnology, Food Technology, Bio Engineering, Agriculture Engineering or any other relevant discipline. Minimum 2-3 years of work experience in detergent, surfactant or chemical industry, preferably in an R&D or Technical Support role. Excellent verbal and written communication skills. Good interpersonal skills and ability to build and maintain relationships. Proactive and self-starting personality. Team player who enjoys working in an international environment. We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability. Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more Show more Show less