117 Compilation Jobs

Responsible for compilation and review of license application documents of Import Licenses, Test licenses, Manufacturing licenses, WHO-GMP, Free Sale Certificate and COPP. Responsible for compilation and review of Form CT-21 Submissions. Responsible for preparation of responses for above said licenses and form CT-21 submission in Indian regulatory agency. Responsible for preparation of supplements and variations for submission in Indian regulatory agency. Location - R & D Center- Turkapally, Shameerpet, Hyderabad

- Design and implement Snowflake data warehousing solutions based on business requirements and best practices. - Create and maintain data models, schemas, tables, and views in Snowflake. - Develop and optimize SQL queries for efficient data retrieval and manipulation. - Work closely with data engineers and architects to ensure seamless integration of data sources into Snowflake. - Collaborate with cross-functional teams to identify and resolve data quality and performance issues. - Monitor and optimize the performance of Snowflake clusters and query execution. - Implement and enforce security measures to protect sensitive data stored in Snowflake. - Stay updated with the latest Snowflake fea...

Dear All, We have opening for Regulatory Affairs (Formulations) - Sr. Executive for Regulatory Market where we are seeking a proactive and detail-oriented Regulatory Affairs professional to join our dynamic team! Role & responsibilities 1. Should be able to compile, review regulatory dossiers independently. 2. Review and respond to customers & ministry queries. 3. co-ordination with all stake holders to collect required documents. 4. Market Reg Market (EU, UK, TGA, New Zealand, South Africa) Education - B.Pharm / M. Pharm Desired Skills Strong understanding of CTD / ACTD, ICH . Proficiency in dossier preparation and compilation of regulatory documents Excellent attention to detail , document...

As a member of Withum, you will be part of a place where talent thrives, and your individuality matters. With endless opportunities for growth and a culture that values entrepreneurial energy and inclusive teamwork, you will experience exponential results. Withum is dedicated to empowering clients and professional staff by providing innovative tools and solutions to address accounting, tax, and overall business management needs. As a nationally ranked Top 25 firm in the US, we are committed to recruiting the best and brightest individuals who have a genuine passion for the business. Your Role Overview: - Lead the engagement team staff in planning and executing audits, reviews, or compilation...

As a Front Desk Executive at our company in Chandigarh, your role involves the following responsibilities: - Maintenance of Office Files - Compilation and Segregation of Files - Maintenance of Case Diary - Handling Accounts - Typing tasks Qualifications Required: - Education: Higher Secondary (12th Pass) preferred - Experience: Minimum 1 year of total work experience required - Language Proficiency: Must be fluent in Hindi, Punjabi, and English Please note that the work location is in person at our office in Chandigarh. If you meet the qualifications and are interested in this Full-time position, please contact us at 9915004500 during office hours only. Kindly note that having your own vehic...

Seeking a motivated US offshore Audit Associate to perform audits & Review Engagements for nonpublic entities. Must have expertise in US GAAP audits, risk assessment, test of details. Proficiency in Excel, Engagement Manager & Audit Software. Required Candidate profile Qualification required: BCom/BBA/BBM/MBA/MCom Skills/Experience in: US Audit, US GAAP, US GAAS, Review and compilation, Audit planning, Financial Statements accounts Audit Procedures and Testing.

- Compilation & review of AMV, PV data - Preparation of CTD and ACTD dossier modules - Complete dossier preparation as per ROW market, Latam - Handling of regulatory queries - Follow up with client's regulatory - Job allocation to the subordinates

In this role as a Sr. Executive Quality Assurance (QA), you will have the following responsibilities: - Device Master File Compliance: Draft the Device Master File in alignment with Indian Medical Device Rule 2017 requirements to ensure full compliance for regulatory submissions and audits. - Clinical Data Collection and Compilation: Collect and compile data on device safety and performance from scientific journals and databases such as EMBASE, PubMed, and Cochrane to support regulatory submissions and product evaluations. - Technical Documentation and Regulatory Compliance: Assist in drafting technical documents like Biological Evaluations, Risk Management, and Usability Reports, complying ...

Purpose/Objective This is executive level position who has to support timely document compilation, form filing, transfer of funds and investment of surplus funds. Also, monitoring of Bank accounts and co-ordination with ABEX to reconcile pending entries are critical tasks. Key Responsibilities of Role Form preparation, filing and compilation of documents for Opening of New Bank Account as well as of Closing of Bank account if not require - Account openings, forms filing and investment and redemptions with Mutual Fund - FD creation - Payment through Liquidice (Online Fund transfer) for fund transfer within timeline - Arrangement of bank advices against payment - Clearing of open BRS entries w...

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) Develop an understanding of the client's business, and become an industry specialist to understand client specific needs Understand and utilize RSM's audit, review and compilation methodologies Function as in-charge facilitating client work by monitoring and reportin...

As a Job Description parser, I have extracted the relevant details from the provided job description: Role Overview: - You will be responsible for studying and analyzing the concept design prepared by the Principal Architect. - Your role will involve compiling all design input data prepared by Architects, Structural, and MEP consultants. - You will be tasked with preparing concept drawings, presentation drawings, submission drawings, working drawings, and detail drawings as per the project requirements. - Your experience should include working on projects in Residential, Commercial, Industrial, Healthcare, and Institutional sectors. Key Responsibilities: - Study and analyze concept design - ...

As a Senior Manager in Regulatory Affairs at our company, your role will involve the following responsibilities: - Act as a regulatory lead and take charge of all regulatory affairs projects - Execute and ensure timely delivery of all regulatory affairs projects - Assist in drafting and compiling dossiers for submission in various markets - Conduct quality checks on all outputs from the regulatory affairs team - Manage and oversee all regulatory submissions made by the team - Communicate project status updates to clients and the Head of Regulatory Affairs - Provide mentorship to less experienced or new team members Qualifications Required: - You should have a total of 10 to 15 years of regul...

Job Title: Manager II – India Regulatory and business Conitnuity Business Unit: R&D1 Regulatory Affairs Job Grade G11A Location Baroda At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Key Responsibilities: To evalua...

Role Overview: Withum is a place where talent thrives, offering endless opportunities for growth and fostering entrepreneurial energy and inclusive teamwork for exponential results. As an Audit Senior in the Withum India office, you will work with an integrated team of US and India-based accounting professionals. Your role will involve all aspects of audit engagements, from planning to completion, including supervision/mentoring of staff and building/maintaining client relationships. Key Responsibilities: - Lead the engagement team staff in planning and executing audit, review, or compilation engagements. - Provide supervision and support to engagement staff, promoting open communication to ...

Key Skills & Requirements Programming: Proficiency in C/C++ with strong understanding of OOP, pointers, and data structures. Development Experience: Hands-on experience in product/software development. Environment: Comfortable working in Linux/Unix environments. Design & Review: Ability to perform design/code reviews and follow best practices. Database & Patterns: Proficient in RDBMS, design patterns, and principles. Debugging: Experience with C/C++ debugging tools, core-dump analysis. Build Process: Knowledge of linking, compilation, and build processes. QA & API: Familiarity with QA tools, API development, and library development. SDLC & Agile: Holistic understanding of software developmen...

Interview For Auto Workshop For Chemical Co in Bhuj on 30-11 Dip/BE Mech/Auto 5 TO 15 YR EXP 17.0 LPA Apply : sdpbharuch@gmail.com Sub: Auto Work Shop Bhuj Only Chemical Co Experience Prefer Free Requirement Required Candidate profile Interview Venue : Bhuj SDP HR Solution 611, Golden Square, Beside DMART, Near ABC Circle, Bholav, Bharuch

Regulatory Affairs Executive : (BKM) is seeking a Regulatory Affairs Executive to join our team. In this role, you will be responsible for getting new products approval from the regulated market. In-depth knowledge of US FDA, EMA, and ICH regulatory frameworks, eCTD/ACTD dossier preparation, compilation and submission. Familiar with regulatory tools like Extedo, Lorenz, Veeva Vault RIM Job Responsibility : Prepare, compile, and review eCTD dossiers for submissions (e.g., ANDA/NDA /MAA/ANDS). Coordinate with cross-functional teams (QA, QC, R&D, Manufacturing, Packaging) for accurate documentation. Submit applications to US FDA, HC, EMA, and other authorities in compliance with regional requir...

We are looking for a highly skilled and experienced Embedded Application Engineer to join our team in the DMS & Vision Systems domain. The ideal candidate will have 3-6 years of experience. Roles and Responsibility Design, develop, and test embedded applications for DMS & Vision Systems. Collaborate with cross-functional teams to identify and prioritize project requirements. Develop and maintain high-quality code using various programming languages. Troubleshoot and debug issues in existing embedded systems. Implement new features and updates in existing products. Participate in code reviews and contribute to improving overall code quality. Job Requirements Bachelor's degree in Computer Scie...

Dear All, We have opening for Regulatory Affairs (Formulations) - Executive / Sr. Executive where we are seeking a proactive and detail-oriented Regulatory Affairs professional to join our dynamic team! Experience of handling M4 & M5 in Regulatory Affairs is must. Role & responsibilities 1) Thorough knowledge of Module 4 & Module 5 2) Preparation of required modules. 3) Document preparation for BE, NOC, TL, Import Permission applications for R&D procurement. 4) Follow up with the CRO for tracking BE study milestones and all other relevant activities. 5) Reviewing of the BE protocol, report. Education - B.Pharm / M. Pharm Desired Skills Strong understanding of CTD Modules 4 & 5 (Non-clinical ...

Manager – Regulatory Affairs & Advocacy Gurugram – Full time About Absolute : Absolute is a bioscience company founded with the idea of a shared future where both people & planet win together. The company’s vision is to build a thriving future for people and the planet by harnessing the power of nature, science & exponential innovation. Today, Absolute’s Bio division has evolved into a generation-defining bioscience company across Agriculture, Human Health & Sustainable Materials. Operating across 30+ countries, Absolute’s Agtech businesses encompass – Climate Solutions, Soil Health testing, Crop Insurance & Tech driven commodities trade. Absolute’s revolutionary businesses are backed by, Xe...

Responsible for planning, compiling, and submitting regulatory dossiers as per country guidelines. Coordinate with QA/QC/R&D for documentation, manage product registrations, renewals, variations, ensure compliance, and maintain regulatory records.

ear Candidate, We are seeking a Senior Executive/ Assistant - Regulatory affairs Europe) to join our team, He/ she will be responsible for Dossier compilation, preparation, Life cycle management, Pre approval, Post approvals. based at Govandi Location. Markets : Europe Dosage Form : OSD/ Sterile Key Responsibilities: Collate/prepare and file dossiers in a timely and accurate manner for formulations/ drug products to get licenses from various targeted markets. Prepare the checklist for documentation for regulatory filings as per current regulatory requirements (country specific). Collate and conduct first-level review/overview of relevant standard technical documentation like stability, TTD, ...

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. RSMs 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 andperformance metrics. Review and analyze lease agreements to ensure compliance with lease accountingstandards (e.g., ASC 842), i...

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) Develop an understanding of the client's business, and become an industry specialist to understand client specific needs Understand and utilize RSM's audit, review and compilation methodologies Function as in-charge facilitating client work by monitoring and reportin...

As an Architectural Assistant, your responsibilities will include: - Studying and analyzing concept designs prepared by the Principal Architect. - Compiling all design input data prepared by Architects, Structural, and MEP consultants. - Preparing concept drawings, presentation drawings, submission drawings, working drawings, and detail drawings as per the project requirements. - Having experience in Residential, Commercial, Industrial, Healthcare, and Institutional projects. Qualifications required for this role: - M. Arch or B. Arch degree. Desired experience: - 3 to 8 years of relevant experience in the field. As an Architectural Assistant, your responsibilities will include: - Studying a...