2 LEELABITE FOOD PRODUCTS JOBS

As a SAP Order to Cash Lead, you will be responsible for providing expert guidance and leadership in designing, implementing, and optimizing SAP solutions related to the order to cash process. You will collaborate with cross-functional teams to ensure the efficient flow of information and goods from order creation to cash collection. This is a strategic role that will help realize the global businesses goals across all regions (NAFTA, EMEA, APAC, and LATAM).Duties and ResponsibilitiesSAP OTC Process Optimization: Analyze existing order to cash processes, identify areas for improvement, and develop and implement SAP solutions to optimize efficiency and effectiveness.System Integration: Collaborate with IT functional teams to integrate SAP Order to Cash modules with other SAP modules and external systems.Configuration and Customization: Configure and customize SAP OTC modules to meet business requirements, including pricing, billing, and credit management.End-to-End Project Management: Lead SAP OTC implementation projects from inception to completion, including gathering requirements, designing solutions, and overseeing the deployment.User Training and Support: Provide training and support to end-users, ensuring they can effectively use SAP OTC functionalities.Documentation: Create and maintain comprehensive documentation related to SAP OTC configurations, processes, and solutions.Quality Assurance: Conduct thorough testing and quality assurance to ensure SAP OTC solutions meet business needs and are free of errors.Continuous Improvement: Stay up to date with SAP best practices and industry trends to recommend and implement improvements continually.Stakeholder Collaboration: Collaborate with cross-functional teams, including sales, finance, and logistics, to align order to cash processes with business goals.Responsible for communicating business related issues or opportunities to next management level.Performs other duties assigned as needed.QualificationsMinimum of 7+ years’ experience with SAP SDMedical Device industry or medical field is a plusBachelor's degree in Business, Information Technology, or a related field. Master's degree is a plus.Minimum of 8 years of experience as an SAP Order to Cash Consultant.In-depth knowledge of SAP Order to Cash modules, and integration with other SAP modules such as MM, FI, WMS, and TMS.Proven experience in SAP implementation projects, with a track record of successful delivery.Strong analytical and problem-solving skills.Excellent communication and interpersonal skills.Ability to work independently and lead cross-functional teams.SAP certification is a plus.Experience with EDI integration for Sales and DistributionExperience with Interfaces (IDOCS, BAPIs, SAP PI, etc.)Experience with master data migration and conversationAbility to work independently and effectively in a fast-paced and dynamic environment.Experience with SAP S/4HANA.Experience with SAP Firori.

Location: Bangalore, India#16 Salarpuria Premia (Opp. Cessna Business Park), Sarjapur Outer Ring Road (ORR), Bangalore 560103Working Type: OnesiteAt ASP, we believe in you. We believe in your potential — your ability to learn, grow, and contribute in meaningful ways. We believe in the power of great people working together to innovate and solve problems no one could solve alone. We build enduring partnerships with our customers and take on their challenges and opportunities as our own.Applies advanced Quality Engineering/Scientific Method techniques and principles to all tasks and activities with a focus on software development projects. Applies relevant regulations, standards, GxP requirements, and industry best practices to all assignments, identifying risks to projects and product developments. Acts as a subject matter expert in Quality Engineering and scientific matters. Develops and leads key strategic Quality Engineering/scientific initiatives throughout the organization. Regularly partners with R&D team members and other cross-functional teams to deliver high quality products to our customers with prioritization on patient safety.Your ImpactHere’s where you’ll demonstrate your competencies: Assure compliance with software procedures, identify task dependencies, guide teams on appropriateness of the development life cycle, and assure development and maintenance efforts are effective and compliant.Provide software quality engineering principal expertise, both external (Regulations) and internal (MD&D and ASP standards and procedures), including leading both internal and external audits for software quality systems.Provide training to software development teams, staff, contractors and business partners on ASP software quality engineering procedures. Leverages software experience and technical knowledge to lead compliance and risk management activities for software projects or software portion of systems projects.Continually improve software quality engineering processes based on industry trends and best practices. Improve software technical expertise and understanding of regulatory requirements. Assure that robust, reliable and compliant systems are transferred to users with a prioritization on patient safety.Assure that project software change control is compliant with all quality procedures and work instructions.Implements systems to address changing regulations.Represents SWQE function during regulatory inspections. Recommends issue resolution to senior management for significant capability and compliance issues.Resolves and seeks consensus across affected business areas. The individual will ensure that all applicable Quality System Regulation, including FDA and ISO (i.e. QSR 21, CFR 820, ISO13485, IEC 02304, ISO 14971.), security, records retention, Sarbanes-Oxley laws and applicable statutory/regulatory (e.g. FDA and ISO) compliance are considered and emphasized in all computer Systems Validation plans and actions. Will ensure that documented evidence exists to provide a high degree of assurance that specific design and processes will consistently and continually produce a product that meets specifications and critical to quality attributes. Will establish and recommend changes to standard operating procedures in all areas related to Computer Systems Validation and be responsible for providing Quality System Regulatory interpretation, consulting, training, and assessment to ensure project teams are aligned with current regulatory requirements, standards, and current industry trends (FDA QSR 21 CFR 820 / ISO13485 quality system requirements). Will ensure and/or develop appropriate methodologies, policies and procedures to deliver business solutions consistent with the company and department Vision and Mission, will lead continuous improvement of the Software Development Lifecycle Management process and clarify business needs and turn them into solution designs and will serve as the technical subject matter and expert and communicates to auditors and investigators on Computer Systems Validation process.Will serve as the technical expert for the organization (worldwide) in the application of Software Development Lifecycle Management advanced theories, concepts, principles, and processes for an assigned area of responsibility (i.e., subject matter, function, type of facility, or equipment, or product). Responsible for communicating business related issues or opportunities to next management level.Performs other duties assigned as needed.Our NeedsHere’s what we’ll need from you: Bachelor’s degree (or equivalent) in Engineering (software, computer, computer science or electrical) AND 5 or more years of relevant experience OR Graduate degree AND 3 or more years of relevant experience. ASQ CQE, CQM, CQA; Process Excellence yellow, green or black belt optional.Experience working in a regulated environment (Medical Device, Aerospace, etc.). This includes knowledge of, and experience with, applicable standards, GxP requirements and applicable regulations.Development experience with any or all: imbedded product software, ATE, customer/product data management, product connectivity.Strong knowledge of system development methodologies and software program metricsExperience with system/software Quality Engineering methods, techniques and principles. Thorough understanding of GxP standards and medical device regulatory and compliance environment including: ISO 13485, 21 CFR Part 820 and 21 CFR Part 11. Thorough knowledge of and in-depth experience with system development configuration management and change control processes, testing (V&V), issue tracking and defect management.Experience with cyber security and data integrity requirements, methods and implementationExperience managing projects, and demonstrating project leadership abilities. Experience with a proven track record of implementing appropriate risk mitigation w/in-depth knowledge of ISO 14971 Risk Management and IEC 62366 Software Development ProcessesExperience with GxP data collection.Demonstrated ability to perform “hands on” troubleshooting and problem solving.Working knowledge of failure investigation processes, computer code static analysis methods and tools.Clear and effective communicator (presentation, technical writing, verbal)Strong understanding of either embedded software systems or cloud applications (SaaS). Leadership ability in developing achievable high-quality computer Systems Validation in partnership with various departments, such as R&D, Operations, Service etc. and managing the implementation and execution of these SDLC goals is strongly preferred.Ability to effectively manage external development partners, consultants and contractors desired. Strong knowledge of Product Software Lifecycle Development process required. A working knowledge of Microsoft office products (MS Word, Excel) and other Testing Software tools is required.Strong working knowledge of FDA QSR 21 CFR 820 / ISO13485 quality system requirements and the ability to provide an expert knowledge of both regulatory requirements and other complianc3e areas to minimize risk across franchise required.Extensive Quality Engineering experience with working knowledge of product design verification, as well as product and project validation activities required.Excellent both written and verbal communication skills and capable of working independently and in a team setting.Strong Project Management and leadership skills required.Demonstrated competence in change management preferred.Project management methodologies required.

This position supports remote work. We have offices in Bangalore, Mumbai and Chennai in India.Position SummaryThis position is responsible for enhancing customer satisfaction for all customers of Advanced Sterilization Products. The responsibilities include support of the global complaint handling process through timely evaluation, investigation and closure of product complaints in accordance with established company procedures and worldwide regulations and standards. The role requires completion of complaint investigations and escalation of trends and product problems.Duties and ResponsibilitiesReviews Incoming Complaints and Completes Good-Faith Effort to Collect Additional Information as RequiredAuthors Clear, Technical, and Accurate Reports Describing Complaints and Investigations for Compliance Files Independently Completes Low Complexity Complaint Investigations within Required TimelinesCoordinates Initiation of Company Issue Escalation Process as RequiredParticipates in Improvement InitiativesMaintains Compliance to Applicable Foreign and Domestic Regulations Governing the Management and Processing of Medical Device Related Complaints including Protected Health Information (PHI) and Patient Privacy LawsResponsible for communicating business related issues or opportunities to next management levelPerforms other duties assigned as neededEducationBachelor’s degree is preferredYears of Related ExperiencePrefer 2 years’ experience in the Medical Device industry.Knowledge, Skills, Abilities, Certifications/Licenses, and AffiliationsCritical thinking and investigation skills are required.Ability to multitask, including ability to understand customer requirements, retrieve relevant information, and provide responses satisfactorily and with immediacy is required. Employee must be able to effectively prioritize and manage multiple activities and responsibilities.Ability to understand and follow complex written procedures is required. Candidates should be familiar with general quality management system concepts, including good documentation practice (GDP), corrective and preventive action (CAPA), and document change control practices.Ability to function in a team environment and deliver on team objectives is required. Ability to influence and drive change is preferred. Prefer project management and/or process mapping experience.Strong written and verbal communication skills are required. Must be highly proficient in reading, writing, and speaking the English language. Prefer developed presentation skills.Professional demeanor on the phone and in email is required. Technical writing is a routine part of this position. Strong attention to detail is required.Familiarity with computers and Windows-based PC applications. Ability to learn and manipulate complex computer system applications is required. Ability to type at least 50 words per minute (WPM) is required. Experience with word processor software (e.g. Microsoft Word) and internet browsers (e.g. Internet Explorer) is required. Prefer experience with Complaint Management Systems.Normally receives no instructions on routine work, but all work is reviewed and approved. Receives general instruction on new tasks. Detailed initial training on procedures and software is provided.Prefer prior medical device complaint handling experience, or knowledge of medical device regulations.Prefer working knowledge of sterilization and/or high-level disinfection technologies.

Company Description We suggest you enter details here Role Description This is a full-time on-site role for a Graphic Designer at GREEN PLANET BIO PRODUCTS in Jalandhar. The Graphic Designer will be responsible for creating visual concepts, using computer software or by hand, to communicate ideas that inspire, inform, and captivate consumers. The role involves designing logos, marketing materials, social media graphics, and more. Qualifications Proficiency in graphic design software such as Adobe Creative Suite (Photoshop, Illustrator, InDesign)Strong creative abilities and a keen eye for aestheticsExcellent communication skills to collaborate with team members and clientsAbility to manage multiple projects and meet deadlinesUnderstanding of design principles, typography, and color theory