25 Compilation Jobs

Amdocs helps those who build the future to make it amazing. With our market-leading portfolio of software products and services, we unlock our customers innovative potential, empowering them to provide next-generation communication and media experiences for both the individual end user and enterprise customers. Our approximately 30,000 employees around the globe are here to accelerate service providers migration to the cloud, enable them to differentiate in the 5G era, and digitalize and automate their operations. Listed on the NASDAQ Global Select Market, Amdocs had revenue of $4.89 billion in fiscal 2023. In one sentence Focuses on non- functional testing with responsibility for segments of test planning, design and execution, meeting planned scope and schedule and maintaining the engagement and relationship with the customer and internal stakeholders. What will your job look like You will oversee and execute test processes, determine the proper prioritization of the testing activities and ensures integrative work and full coverage of test scenarios in accordance with plans and observations from concurrent testing activities. You will develop and implement NF automation procedures and tools. You will create and define test execution plans as well as non-functional requirements for mitigating technical risks. You will design and review test solutions and scenarios, develop NF scripts and automation utilities to be implemented and executed in alignment with the scope determined during test planning, leveraging knowledge and a broad understanding of E2E Business process & requirements You will select and apply appropriate structural design techniques to ensure that tests provide an adequate level of confidence and optimization. The tests are to be based on code and aligned with version requirements, customer needs/use and design scope You will call attention to and focuses on incident assessments. You will provide recommendations for resolution of issues and proposes improvements to the NF aspects of code, system optimization, best sizing and architecture You will ensure that product documentation, testware and work products used in the testing activities are of the highest quality to ensure traceability, correctness and compliance with product requirements and specifications, internal standards and clients' needs. You will maintain and enhance the professional and business relationship with the client/ internal customers. You will provide professional and technical support to team members and keeps them informed of assignment/ project status. Mentors new team members All you need is... 7-10 years experience in performance testing of large scale enterprise systems. Expert in developing test scripts, creating scenario, test execution and analysis usingLoadRunner / Jmeter / Neoload / Blazemeter / SOASTA / Akamai and any monitoring tool. Expert in compiling, analyzing and interpreting performance test results. Knowledge of application monitoring (e.g. HP Diagnostic, Dynatrace, AppDynamics etc.) Attention to detail and good interpersonal and communication skills Ability to understand hardware and software architectures Ability to evaluate open source performance test tools and suggest suitable one for theapplication under test Understanding of throughput, latency, memory and CPU utilization Should be ready to work in an environment which may demand individual contribution as well asa team player. Hands-on knowledge of Knowledge of SQL and PL/SQL query, C, C++, Java, Unix or any otherlanguage Why you will love this job: You will be responsible for Identifying, analyzing and mitigating non-functional issues and technical risks of software systems You will be involved in participating in and/ or leading formal and informal reviews with stakeholders

Responsibilities: * Prepare new DMF, annual reports, respond to customer queries. * Compile sequences with eCTD software, validate, submit. * List NDC drugs to FDA, prepare submissions. Provident fund

Develop procurement plans with business demand-spice commodities Identify, evaluate, onboard reliable spice suppliers - farmers, FPOs, traders, vendors Negotiate pricing, payment & delivery terms Monitor market, seasonal availability, price changes Required Candidate profile Prepare RFQ & issue PO & timely follow up Track inventory & coordinate procurement Coordinate with logistics partners for shipping, customs clearance Track procurement spending & cost cutting

RSM is looking for a dynamic Manager to join our Assurance team. You will have the opportunity to work as a team member on diverse client engagements. Our clients include local, national and internationally recognized companies. RSM s assurance professionals helping companies improve their performance through the most challenging business cycles. Responsibilities Perform Review and Compilation engagements in accordance with firm and professional standards as directed by engagement leaders. Design, develop, and execute analytical procedures to assess financial data and performance metrics. Review and analyze lease agreements to ensure compliance with lease accounting standards (e.g., ASC 842), including calculation of lease liabilities, right-of-use assets, and related journal entries. Responsible for overseeing the accurate and timely preparation of financial statements, including income statements, balance sheets, and cash flow statements, ensuring compliance with accounting standards and regulations. Prepare detailed supporting schedules for financial statement analysis and review, ensuring accuracy and compliance with accounting standards, to facilitate comprehensive reporting and decision-making for managerial review. Revenue recognition procedures to ensure compliance with regulatory requirements and accurately reflect earned revenue, optimizing financial transparency and accountability Required Qualifications Bachelor of Commerce (Accounting) degree or equivalent degree from an accredited university Licensed CPA / Qualified CA 5+ years of current or recent experience in a public accounting environment 7 plus years' experience in Canda Corporate tax return/compilation/review engagement related field Experience leading teams and mentoring associates Understanding of accounting services, with knowledge of review and compilation standards A proven record of building profitable, sustainable client relationships Minimum of 4 years of team lead or in-charge experience overseeing staff on multiple engagements Preferred Qualifications Experience with managing review and compilation engagements including the applicable taxation. A successful record of directing and deploying staff and senior associates on multiple, simultaneous engagement Preparing financial statements, conducting compilations and reviews, and completing Canadian corporate tax returns. empowering you to balance life s demands, while also maintaining your ability to serve clients. Learn more about our total rewards at https://rsmus.com/careers/india.html .

Roles and Responsibilities Prepare dossiers for regulatory submissions, including compilation of data from various sources into a cohesive document. Review and compile dossiers prepared by others to ensure accuracy and completeness. Coordinate with internal departments (e.g., CMC, Non-Clinical Toxicology) and external vendors/consultants to obtain necessary information for dossier preparation. Ensure timely submission of dossiers to relevant authorities (e.g., FDA, EMA). Maintain accurate records of all correspondence with regulatory agencies. Desired Candidate Profile 5-8 years of experience in Regulatory Affairs or related field (B.Pharma / M.Pharma degree required). Strong understanding of drug regulatory affairs, particularly in Europe market. Proficiency in compilation, dossier preparation, and regulatory submissions.

Hello all GNU/Linux fans and geeks! Nakshatra Systems is looking forward to hire a Linux Software Repository maintainer, who can service, maintain, upgrade/udpate and manage the software repository. Job is Work from home and contract based. Looking for immediate joiners. Contract job of 1 year. Candidate will have to sign a legal agreement that will include NDA and NCA. Vacancy : 1 Minimum experience needed : 1 - 2 years Mandatory technical skills : ============================= Compiling and creating software from source code. Ability to create software packages using package creation tools to install/remove software. Creating/Updating packages. Keeping track of software dependencies. creating / providing / managing software patches Monitoring and staying current with CVE's Maintaining Changelogs and other documentation. Providing bug fixes. Reviewing changes. Proficiency in linux commands, filters, bash scripting, C and python. Knowledge of patch command and other similar software management tools. Connect with upstream developer for solutions if needed to get issues resolved. Good troubleshooting skills. Knowledge of Slackware Linux a HUGE plus. As Nakshatra Linux is a clone and a derivative of slackware linux , candidates with knowledge of slackware will be prioritized over to those with knowledge of redhat/debian. Non-technical pre-requisites : ============================== Should be fluent in english with good verbal and written skills Since nature is work from home , a good broadband internet connection (at least 50 mbps) with IPV6 facility is mandatory for remote logins and work. Ability to work in team as well as independently. Should be able to resolve assigned tasks in the specified time-frame/deadlines. Candidates with matching skill set that are shortlisted will be contacted via phone for a technical telephonic interview. This is not a sysadmin profile job.

Role & responsibilities Keen Knowledge on Regulatory guidelines for finished product registration. Dossier compilation as per guidelines. Compilation and review the product dossiers for submission in CTD, ACTD . Gap analysis of the dossier and addressing the gaps before submission to MOH. Handling the customer and MOH queries . Life cycle management of the product. Development report, scale up report , specification, COA, stability protocol and Process validation protocol. Documents review (Specification, STP, Analytical method validations, Development report and validation reports, BMR, BPR, PVP/R and stability). Post approval experience to file the applicable variations timely. Knowledge on EAEU, ICH and EMEA guidelines. Re-registration (Renewal) procedures. Administrative documents requirements (COPP, Mfg. License and Import License) . Registration information management system updates on regular basis.

Role & responsibilities Lead the compilation, analysis, and reporting of global management information systems (MIS) and financial performance, ensuring accuracy and consistency across all regions. Review forward-looking financial plans and forecasts from global entities, comparing them with historical trends and actual performance to highlight key variances and business risks. Conduct comprehensive financial analysis across entities and product portfolios, including profitability, cost structures, and operational performance. Report deviations and key insights to senior global management. Design, implement, and continuously improve global cost allocation models and methodologies to ensure fair and transparent distribution of shared costs. Develop and deliver management reports, dashboards, and insights tailored to the needs of the senior global leadership team. Maintain a centralized database of financial and technical data for key products, including both launched and pipeline products. Support supply chain cost analysis and inventory performance reviews to enhance efficiency and cost control. Collaborate with Group Accounting during month-end close to validate results and provide performance commentary. Prepare high-quality financial reports and presentations for board meetings, shareholder communications, and other executive forums. Participate actively in global finance transformation projects, systems upgrades, and process improvement initiatives. Provide ad-hoc analytical support to the global leadership team, including market research, competitive analysis, and industry benchmarking to inform strategic decisions, legal matters, and investor relations. Qualification Requirements: MBA or MBA with CA or CA with relevant experience in FP&A. At least 5+ years FP&A experience from Pharma or FMCG industries. Experience working with cross-functional and cross-regional teams. Strong proficiency in MS Excel, PowerPoint, and dashboard creation tools such as Power BI. Expertise in global cost allocation, planning systems, and management reporting tools. Working knowledge of SAP ERP systems. Strong analytical mindset, attention to detail, and a proactive approach to problem-solving. Demonstrated ability to meet tight deadlines and prioritize effectively. Fluency in English language is mandatory

Role & responsibilities Extensive Knowledge in Pre-Submission activity and handling new product submissions. Handling of post approval activities (US/EU and ROW) Experience in handling life cycle management Activities. Line Extension and New Submissions. Well versed in applicable regulatory and country specific guidlines.

Immediate Joining | Remote | | Part Time - Visiting Faculty Impart Training Sessions for the students of Drug Regulatory Affairs Weekend Training Sessions Prepare presentations Deliver Training Sessions

Key Responsibilities: Undertaking Audit confirms involving trade reconciliation, by comparing buy and sell trades extracted from in-house applications compared against third party report. Extracting the required notices, documents, information and any other materials from various market platforms as specified by the client. Any other tasks relating to the audit confirmation process as asked for by the client team. Assistance in preparation of monthly and quarterly reporting deliverables; review of 10-K and 10-Q SEC filings, for BDCs of an alternate asset manager. Conducting mathematical accuracy, across financial statements, notes and management discussion analysis sections of filings. Tie out of current quarter by checking against the NAV pack shared by the Finance team and raising comments in the internal platform or system. Performing consistency checks to ensure values read the same across the sections within the filings. Compiling and comparing loan portfolio data across various market players by extracting a schedule of investments. Preparation of fact card based on finance pack, to include key figures like NAV, returns and capital metrics data. Any other task or ad hoc requirement as defined. Requirements: Master’s degree in finance/ CFA L2 cleared / CA (Final), with 0-2 years of experience in the financial service industry would be preferred. Extreme attention to detail with keen observation of numbers and reports. Experience in audit related reconciliation process is an added advantage. Flexibility to stretch and work towards timings around closure of audit filings. Effective communication skills with ability to connect with clients, over phone and email, and understand the requirements and focus on delivery. Strong understanding of financial statements and familiarity and ability to read financial statements. Display strong attention to detail to deliver high level of accuracy and quality. Self-starter and is persistent in executing the workflows to ensure closure until the end. Proven ability to work independently and collaboratively in a fast-paced, dynamic environment.

RSM is looking for a dynamic Manager to join our Assurance team. You will have the opportunity to work as a team member on diverse client engagements. Our clients include local, national and internationally recognized companies. RSM's assurance professionals helping companies improve their performance through the most challenging business cycles. Responsibilities Preparing financial statements, conducting compilations and reviews, and completing Canadian corporate tax returns. Perform Review and Compilation engagements in accordance with firm and professionalstandards as directed by engagement leaders. Design, develop, and execute analytical procedures to assess financial data andperformance metrics. Review and analyze lease agreements to ensure compliance with lease accountingstandards (e.g., ASC 842), including calculation of lease liabilities, right-of-use assets, andrelated journal entries. Responsible for overseeing the accurate and timely preparation of financial statements,including income statements, balance sheets, and cash flow statements, ensuringcompliance with accounting standards and regulations. Prepare detailed supporting schedules for financial statement analysis and review,ensuring accuracy and compliance with accounting standards, to facilitate comprehensivereporting and decision-making for managerial review. Required Qualifications Bachelor of Commerce (Accounting) degree or equivalent degree from an accrediteduniversity. Qualified CA / Licensed CPA 5+ years of current or recent experience in a public accounting environment 7 plus years' experience in Canda Corporate tax return/compilation/review engagement related field. Experience leading teams and mentoring associates. Understanding of accounting services, with knowledge of review and compilationstandards. A proven record of building profitable, sustainable client relationships. Minimum of 4 years of team lead or in-charge experience overseeing staff on multipleengagements. Preferred Qualifications Experience with managing review and compilation engagements including the applicabletaxation A successful record of directing and deploying staff and senior associates on multiple,simultaneous engagement. Preparing financial statements, conducting compilations and reviews, and completing Canadian corporate tax returns

We are seeking a QA-RA Executive to join our dynamic team. The ideal candidate will be responsible for the preparation, compilation, and submission of regulatory dossiers as per CTD/ACTD/eCTD, country-specific regulatory requirements. The role will also involve supporting the QA-RA team in various regulatory tasks and ensuring compliance with applicable regulations and standards. Key Responsibilities: Dossier Preparation and Submission : Responsible for the preparation, compilation, and submission of assigned regulatory dossiers in line with CTD/ACTD/eCTD formats, country-specific requirements for regulatory agencies. Regulatory Compliance : Ensure compliance with regulatory guidelines, ensuring all submissions meet quality standards and deadlines. Additional Tasks : Perform any other tasks as assigned by the reporting manager or senior team members. Backup and Reporting : In the absence of the primary responsible person, handover responsibilities will be managed to a designated colleague. Functional reporting to be done as per the department's organogram. Qualifications: Educational Background : B.Pharma , M.Pharma , B.Sc , or M.Sc in a relevant field. Experience : Minimum 1 year of experience in a regulatory affairs or quality assurance role. Maximum 5 years of experience in a similar position, preferably in the pharmaceutical or healthcare device industry. Technical Skills : Knowledge of Dossier preparation according to CTD/ACTD/eCTD guidelines. Strong understanding of regulatory requirements in healthcare, pharmaceutical, or medical device industries. Desired Skills: Strong attention to detail and high levels of accuracy. Ability to work efficiently under pressure and manage multiple tasks. Excellent communication skills (both written and verbal). Team player with a proactive attitude and problem-solving ability.

Introduction: Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S. Bhartia and Mr. Hari S. Bhartia with strong presence in diverse sectors like Pharmaceuticals, Life Science Ingredients, Contract Research and Development Services, Therapeutics, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Group has global presence employing around 42,000 people across the globe with over 2,400 in North America. Jubilant Pharmova Limited Jubilant Pharmova Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radio pharma, Allergy Immunotherapy, CDMO Sterile Injectable, Contract Research Development and Manufacturing Organisation (CRDMO), Generics and Proprietary Novel Drugs businesses. In the Radio pharma business, the Company is involved in manufacturing and supply of Radiopharmaceuticals with a network of 46 radio-pharmacies in the US. The Company's Allergy Immunotherapy business is involved in the manufacturing and supply of allergic extracts and venom products in the US and in some other markets such as Canada, Europe and Australia. Jubilant through its CDMO Sterile Injectable business offers manufacturing services including sterile fill and finish injectable (both liquid and lyophilisation), full-service ophthalmic offer (liquids, ointments and creams) and ampoules. The CRDMO business of the Company includes the Drug Discovery Services business that provides contract research and development services through two world-class research centres in Bangalore and Noida in India and the CDMO-API business that is involved in the manufacturing of Active Pharmaceutical Ingredients. Jubilant Therapeutics is involved in Proprietary Novel Drugs business and is an innovative biopharmaceutical company developing breakthrough therapies in the area of oncology and autoimmune disorders. The company operates six manufacturing facilities that cater to all the regulated market including USA, Europe and other geographies. Find out more about us at www.jubilantpharmova.com . The Position Organization- Jubilant Pharmova Limited Designation - Deputy Manager / Manager - Regulatory Affairs Location- Nanjangud, Mysore Responsible for following activities of Head -Technical Services, Design and Engineering Department: Preparation/review and submission of new dossiers and updates for global markets. Preparation/review and submission of responses to queries from regulatory authorities/customers. Provide technical regulatory support to CRD for various activities (route of synthesis, starting material designation, specifications design, applied testing methodologies, Analytical method validations) related to new product development and other regulatory issues as they arise. Review of R and D technical packages for new product development (NPD) as well as cost/quality improvement process (CIP/QIP) for regulatory adequacy. Coordination with R and D to discuss on process and product controls, quality, patent and special studies to respond the queries from regulatory authorities/customers. Tracking of activities status to meet the timeline for new Submissions, Responses and Life cycle management of Dossiers. Preparation/review and submission of technical packages and open parts as per customer requirement. Review of technical packages for out sourced starting materials and intermediates for regulatory adequacy.; Review of analytical method validations, characterization data, process validations, analytical data, specifications/test methods, BMRs, packing material details, and stability data etc. w.r.t. regulatory adequacy for dossier compilation. Review of CSO/stability protocols [EDMS] and change controls (track-wise) related to facility, manufacturing process and control of materials etc. for regulatory adequacy. Attending to and lsquo;on the job trainings' and and lsquo;off the job trainings'. Updating health authority new guidelines to Regulatory affairs team. Person Profile. Education Qualification: MSc / M.Pharma,/ B.Tech / M.Tech Chemical Engineering Experienc e Range : 10+ years in API Regulatory Affairs Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. To know more about us, Please visit our LinkedIn Page- https://www.linkedin.com/company/jubilantpharmova/mycompany/

Introduction: Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S. Bhartia and Mr. Hari S. Bhartia with strong presence in diverse sectors like Pharmaceuticals, Life Science Ingredients, Contract Research and Development Services, Therapeutics, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Group has global presence employing around 42,000 people across the globe with over 2,400 in North America. Jubilant Pharmova Limited Jubilant Pharmova Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radio pharma, Allergy Immunotherapy, CDMO Sterile Injectable, Contract Research Development and Manufacturing Organisation (CRDMO), Generics and Proprietary Novel Drugs businesses. In the Radio pharma business, the Company is involved in manufacturing and supply of Radiopharmaceuticals with a network of 46 radio-pharmacies in the US. The Company's Allergy Immunotherapy business is involved in the manufacturing and supply of allergic extracts and venom products in the US and in some other markets such as Canada, Europe and Australia. Jubilant through its CDMO Sterile Injectable business offers manufacturing services including sterile fill and finish injectable (both liquid and lyophilisation), full-service ophthalmic offer (liquids, ointments and creams) and ampoules. The CRDMO business of the Company includes the Drug Discovery Services business that provides contract research and development services through two world-class research centres in Bangalore and Noida in India and the CDMO-API business that is involved in the manufacturing of Active Pharmaceutical Ingredients. Jubilant Therapeutics is involved in Proprietary Novel Drugs business and is an innovative biopharmaceutical company developing breakthrough therapies in the area of oncology and autoimmune disorders. The company operates six manufacturing facilities that cater to all the regulated market including USA, Europe and other geographies. Find out more about us at www.jubilantpharmova.com . The Position Organization- Jubilant Pharmova Limited Designation - Deputy Manager / Manager - Regulatory Affairs Location- Nanjangud, Mysore Responsible for following activities of Head -Technical Services, Design and Engineering Department: Preparation/review and submission of new dossiers and updates for global markets. Preparation/review and submission of responses to queries from regulatory authorities/customers. Provide technical regulatory support to CRD for various activities (route of synthesis, starting material designation, specifications design, applied testing methodologies, Analytical method validations) related to new product development and other regulatory issues as they arise. Review of R and D technical packages for new product development (NPD) as well as cost/quality improvement process (CIP/QIP) for regulatory adequacy. Coordination with R and D to discuss on process and product controls, quality, patent and special studies to respond the queries from regulatory authorities/customers. Tracking of activities status to meet the timeline for new Submissions, Responses and Life cycle management of Dossiers. Preparation/review and submission of technical packages and open parts as per customer requirement. Review of technical packages for out sourced starting materials and intermediates for regulatory adequacy.; Review of analytical method validations, characterization data, process validations, analytical data, specifications/test methods, BMRs, packing material details, and stability data etc. w.r.t. regulatory adequacy for dossier compilation. Review of CSO/stability protocols [EDMS] and change controls (track-wise) related to facility, manufacturing process and control of materials etc. for regulatory adequacy. Attending to and lsquo;on the job trainings' and and lsquo;off the job trainings'. Updating health authority new guidelines to Regulatory affairs team. Person Profile. Education Qualification: MSc / M.Pharma,/ B.Tech / M.Tech in Chemical Experience Range : 6+ years (in API Regulatory only) Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. To know more about us, Please visit our LinkedIn Page- https://www.linkedin.com/company/jubilantpharmova/mycompany/

Role & responsibilities Keen Knowledge on Regulatory guidelines for finished product registration. Dossier compilation as per guidelines. Compilation and review the product dossiers for submission in CTD, ACTD . Gap analysis of the dossier and addressing the gaps before submission to MOH. Handling the customer and MOH queries . Life cycle management of the product. Development report, scale up report , specification, COA, stability protocol and Process validation protocol. Documents review (Specification, STP, Analytical method validations, Development report and validation reports, BMR, BPR, PVP/R and stability). Post approval experience to file the applicable variations timely. Knowledge on EAEU, ICH and EMEA guidelines. Re-registration (Renewal) procedures. Administrative documents requirements (COPP, Mfg. License and Import License) . Registration information management system updates on regular basis.

Hiring for Linux Operating System - Build engineer -Harita Techserv Pvt Ltd Experience : 7 + Years Job Location : Chennai Role : Linux Operating System - Build engineer / OS Build - Engineer Qualifications Bachelors or Master's in CS/CE or related field Strong analytical and problem-solving skills Ability to work independently, learn quickly and be proactive Good communication skills (verbal and written) Key Responsibilities: Build custom Linux OS using Buildroot. Customize and optimize Linux Kernel for different CPU architectures Work with cross-compilation toolchains to build and deploy Linux . UEFI secure boot and Trusted Platform Module (TPM) implementation. Enable device drivers for peripherals. Add security patches to kernel and other packages. Debug and fix system boot issues, kernel panics, and hardware-software integration issues. Document the porting process. Skills and Experience: Hands-on with Buildroot/Yocto, gcc, make Strong experience in Linux Kernel (configuration, compilation, debugging). Debug hardware failures and device driver issues GRUB and UEFI secure boot Experience in bringing up Linux images on QEMU Experience in porting Linux to different ARM cores is preferrable Familiarity with disk encryption Interested candidates can share the updated resume yamuna@harita.co.in Note : Interested candidate should be available for F2F interview must @ Chennai location.

Role & responsibilities 1. Preparation & compilation of dossier in ACTD, CTD & country specific format according to guidelines of various countries. 2. Timely compile documents for license renewals, update and re-registrations. 3. Review of technical documents like BMR, Stability, Spec-STP,PVP-PVR,PDR required for dossier compilation. 4. Collect and co-ordinate information and compile regulatory documentation for submission to regulatory agencies or to commercial partners, advise on the submission strategy. 5. Response to query/deficiency/Notice of Deficiency raised by Drug Regulatory Authority or technical representative. 6. Stakeholder Engagement. 7. Cross-functional Collaboration. Preferred candidate profile M. Pharma (Pharmacy)/B.Pharma ( Pharmacy) Perks and benefits

Work Monitoring & Performance Supervisor Ensure timely task completion & track progress. Identify workflow bottlenecks Conduct audits & ensure compliance with policies Generate reports & optimize workflows Provide feedback & support training

Eugia Pharma is looking for Regulatory Affairs Associates with good experience in US and Canada Market. Job Location : Pashamylaram, Hyderabad Canteen and Transportation facility available JD for US Market Panning, reviewing and submission for assigned ANDA and NDA projects. Excellent drafting skills for FDA Deficiencies with high quality and regulatory standards in response. Evaluation and good interpretation of post approval changes. Submission of Supplements like CBE, CBE-30 and Prior Approval Supplement (PAS), Annual Reports. Review and authorizing regulatory change controls. Knowledge of eCTD, Module 2and 3. Formulate US Regulatory filing strategy for new projects. JD for Canada Market Experience in Dossier compilation (Injectable & OSD dosage forms) & knowledge of regulatory procedures and guidelines (ICH). Planning, execution and assessment of product life cycle management activities and strategies (LCM & Variation) Review technical documents like Protocols, API & Drug product technical packages, Change Controls etc and prepare technical documents to support regulatory submissions Knowledge in query response to agencys questions within assigned timelines

Responsibilities : Assistance in Financial Preparations Compilation & Review of following : Inventory Fixed Asset Trade Payable 3. Assistance to Monthly MIS 4. Accounting & MIS Provision, etc.

Responsibilities Extensive experience in bookkeeping, financial statement preparation, compilations, reviews, and Canadian tax compliance. Prepare corporate income tax returns for Canadian clients (T2), partnership returns and other tax slips. Develop and apply knowledge of International Financial Reporting Standards (IFRS), Generally Accepted Accounting Principles (GAAP) and/or Accounting Standards for Private Enterprise (ASPE). Set-up files for new clients and newly incorporated businesses, manage multiple files simultaneously. Perform accounts receivable, accounts payable, capital asset acquisition and disposition, HST and payroll reconciliations. Summarize current financial status by collecting information and preparing balance sheet, income statements and other relevant reports. Assess appropriateness of audit evidence for Assets, liabilities, expenses, revenues etc. Review, investigate and correct discrepancies and irregularities in financial entries, documents, and reports. Prepare correspondence, technical reports, client summaries and presentations outlining engagement findings, facts, and highlights. Contribute to the development of new ideas and approaches to improve work processes while effectively using RSM internal programs and systems. Taking ownership of assigned tasks and deliverables to ensure service excellence through prompt responses to internal and external clients. Providing timely, high quality client service that meets or exceeds client expectations including coordinating the development and execution of the audit work plan and client deliverables. Understanding RSM and RSM Delivery Center's line of business service offerings and work as a team in providing an integrated service delivery. Ensuring professional development through ongoing education. Participating in a range of projects and open to collaborate and work with multiple teams; demonstrating critical thinking, problem solving, initiative and timely completion of work. Required Qualifications Bachelors in Commerce/MBA Qualified Chartered Accountant / ACCA / CPA 1-2 years of relevant experience Excellent verbal and written communication (English) as the position requires frequent communications with RSM International clients Strong Data Analytical skills including advanced Excel skills (Vlookups, pivot tables, and basic formulas), Word and PowerPoint Preferred Qualifications Experience in Non Assurance services (PCR) preferred. Working knowledge in MS office and caseware experience will be an advantage Qualified CA Freshers' with Articleship Qualified ACCA/CPA Fresher ACCA/CPA Pursuing (half-way through the qualification)

The Director of Overseas Education, Counselling and Admissions will be responsible for providing strategic leadership and direction to the department, overseeing the entire process of student admissions. Required Candidate profile Excellent interpersonal and communication skills. Demonstrated ability to build and maintain relationships with educational institutions and stakeholders.

Greetings from BVR People Consulting!! Position: Regulatory Affairs - Formulation Designation: Executive or Asst. Manager Division: Injectable and Solid oral products Qualification: B. Pharm, M. Pharm and M. Sc (FULL TIME) only Years of Experience: 4 to 8 Years CTC range: 5 to 13 LPA. Job Locations: Bangalore ( Electronic City ) No. of Positions: 04 Job Summary: Compilation and submission of the dossier and query responses as per the EU/UK/ANZ /Israel/Belarus and Ukraine regulatory requirements within stipulated timeframe (for Injectable and Solid oral products ). Interaction with CFTs for product specific requirements and to attend product strategy meetings. Review of final data and technical documents received towards dossier compilation from API team, RnD, IP, PV, QA, Commercial, Packaging and Plant team. Compilation of labelling documents as per current EU/UK/ANZ/Israel/Belarus and Ukraine regulatory requirements. eCTD Publishing of dossiers in DocuBridge software. Product life cycle management for approved Europe products i.e. variation, Renewal and sunset exemption filings. Maintain product database, regulatory files, records and reporting systems. Timely updation and maintenance of RIMS database. Preparation and submission of high-quality national translations for National Phase. Post Approval and Pre approval NOTE: We are looking Notice period 01 month or immediate joiner. Interested Candidates should forward their resume to " ganapathi@bvrpc.com" and also Your Current CTC, Excepted CTC and Notice period. Thanks K Ganapathi Mob. No. 9600387468

BIOS UEFI and Coreboot Bangalore 5 to 8 years Semicon-Embedded Design,Embedded SW Experience in the x86 BIOS/UEFI development Experience with x86 CPU/APU architectures and associated compilation tools Expert in C language Experience with platform bring-up. Familiar with at least one BIOS code base (AMI, Insyde, or Phoenix BIOS) Experience of working with opensource coreboot project & mainboard related porting. Experience of working with Intel FSP codebase and understanding of coreboot & FSP boot flow. Understanding of coreboot & FSP build tools and build processes. Experience of working with different coreboot payloads like edk2, SeaBios, Tianocore etc Ability to read platform Hardware and Processor specifications to understand the coreboot mainboard porting required. Good understanding of UEFI framework concepts to port UEFI code to FSP. Additional Skillset : Working knowledge of Git for code reviews, source code management, and BIOS releases to QA. Ability to juggle tasks and respond to different teams for various requests for custom BIOS requirements. Good understanding of industry standard protocols like PCIe, SPI, eSPI etc. Good understanding of specifications like ACPI, SMM. Good understanding of x86-64 architecture from BIOS developers perspective. Good understanding of UEFI BIOS Boot flow. Basic understanding of Linux Kernel like software development concepts (Kconfig). Academic credentials:- Bachelors degree in computer science engineering from reputed college - Masters degree from reputed university is a big plus