Role Description This is a full-time Instrumentation Engineer role located on-site in Ahmedabad. The Instrumentation Engineer will be responsible for maintenance, troubleshooting and calibration of Lab Instruments such as HPLC. LCMSMS, Centrifuge, Evaporators, Oven, Incubator, Utility support, etc.... Qualifications Diploma or Bachelor's degree in Instrumentation, Electronics Engineering or related field Having 1-3 years of experience in Maintenance of Process instruments, Calibration of instruments, Instrumentation, and Troubleshooting skills Electronics Engineering and Calibration expertise Strong problem-solving abilities Excellent communication and teamwork skills Experience with Process control instrument or Calibration industry is a plus Company Description Veeda Lifesciences is an Integrated, Tech-driven & Global CRO that supports the development of biotherapeutics and small molecules by blending scientific expertise with advanced technology. With a presence in 9 countries and sites across 26 geographies, we offer global reach and local expertise. Our services span the entire drug development lifecycle, including preclinical studies, BA/BE Studies, early and late-phase clinical trials, bioanalytical services, and biopharma solutions. Interested candidate send resume at Arjun Vithlani ; Maulik Dholakia Show more Show less

Job Description Job Title Company Secretary Experience: 5-6 Years Location Ahmedabad We are seeking a qualified Company Secretary to manage compliance for our company. Key Responsibilities Ensure compliance with RBI/FEMA, ROC, MCA regulations. Handle compliance with SEBI, RBI, NSE, BSE, and RTA. Liaise with Directors, Promoters, Shareholders, Investors, and external agencies (PEs, IPO professionals, lawyers, etc.). Draft and review corporate Minimum 5 years of experience in a listed company (BSE/NSE Mainboard). Strong knowledge of corporate compliance and regulations. Excellent communication skills. Ability to work independently and manage complex compliance tasks. Good Interpretation skills of any Good skills towards drafting/ reviewing of legal agreement/ contracts. Exposure towards fund raising, acquisition of foreign units, IPO exposure, dealing with Bankers, legal counsels. (ref:iimjobs.com) Show more Show less

#hiring - Remote Opportunity Veeda Lifesciences looking for "Clinical Research Physician" About the Role: The Clinical Trial Physician is responsible for providing medical input within the organization as well as to external partners and performing medical review tasks within the context of clinical trials. Furthermore, the Clinical Trial Physician is responsible for undertaking scientific/medical writing tasks within the organization. Responsibilities: All study related documents that fall under the Clinical Science Department scope (e.g., Study Protocols, ICFs - in collaboration with other departments e.g., Clinical Operations, Regulatory, as required -, Pharmacy Manuals, Medical Review Plans, etc.) Scientific presentations and manuscripts Medical training material (i.e. therapeutic area and study protocol training material) Delivers internal and external study protocol and therapeutic area training courses Provides medical expertise and consultation within the Company on key therapeutic areas of the clinical development program Provides guidance to all involved departments on the medical and scientific aspects of the assigned clinical trials/projects Responds to medical queries from all involved parties in assigned clinical trials (e.g., CRAs, Project Managers, Clinical Operations Managers, Investigators) and collaborates with all concerned staff in maintaining an up-to-date study-specific Q&A log Is available 24/7 to respond to urgent medical/protocol related issues derived from an Investigational Site, as applicable Performs periodic medical review of the data from clinical trials according to the study-specific Medical Review Plan requirements (e.g., review of eligibility, review of efficacy and safety data) Performs real-time medical review on urgent medical and safety issues, as needed Collaborates with and provides medical input to the Data Management staff to ensure the successful development of the study-specific eCRF Attends Investigator Meetings and Conferences, as applicable Complies with the Company's Quality and Information Security Management Systems and applicable national and international legislation, including legislation for data protection and ICH GCP requirements Qualifications: MD (After MBBS) Experience Required: 4 - 8 Years Working Hours: European working hours Pay range and compensation package: Up to 30 LPA Show more Show less

Role & responsibilities Journal Voucher booking - Booking all Journal Vouchers in system on timely basis after scrutinizing the supporting and as per the SOP decided and resolve any issues pertaining to it. Proper booking of all expense in respective cost centre has to be ensured. Collating all data received from different dept and accordingly need to pass journal entries into the system which are as follows: Provision Booking Insurance Expenses - Employee, Subject, Facility & Others Vehicle Hire Expenses All Facility Rent Expenses All Facilty Electricity Expenses Contract ( Phlebotomis, Nurs & Doctor ) Staff Salary Capital Fixed Asset working& Booking Subject Payment Booking for( Cheque& Cash Payment Expenses) Mehsana Facility. All type JVs are to be booked on time basis with accuracy. 2. FAMS Entry to be accounted accurately and on timely basis also match with Tally Dat Preferred candidate profile . 3. Audit- Calculation & Booking - Prepaid Expenses calculation & Booking Debtors & Valuation working & Booking Assisting in Audit - Providing & arranging all requested invoices/ documents during Internal audit. All data and information to be provided on time with accuracy for Finance audit & Company audit. 4. Daily Cash Payment/expenses Booking - Ensuring Daily cash payment booking of all expenses- Cash Payment to employees as per Expense Claim Form & booking of Expenses. Verification of expense claim form as per SOP. Payment to Employees are done after checking and settlement of any earlier imprest/dues. 5. Other Task which will be alloted from Higher Authorities. 6. Email Communication as an when required and suggested by the concern person. 7. Follow up from Concern department for booking of Expense as per Instruction given by the concern person.

Key Responsibilities: 1-Legal Expertise & Documentation: * Minimum 3 to 4 years of experience in a corporate legal environment. * Well-versed with court procedures. *Draft and review legal documents, including CDA, MSA, lease agreements notices, and customer communications. 2-Liaison & Legal Coordination: * Engage with lawyers, police, government officers, and insurance companies. * Coordinate with third parties for claim settlements when necessary. * Interpret and apply various laws to defend the company’s interests, including interactions with government authorities. * Prepare and maintain a monthly tracker of legal events/claims and submit it to the Reporting Authority/Board. 3-Accounting & Compliance: * Preferably have knowledge of accounting software Tally. * Ensure compliance with applicable company laws and regulations. 4-Skills & Requirements: * Proficiency in English, Hindi, and Gujarati. * Strong command of Microsoft Office applications. * Excellent communication and negotiation skills.

Main Duties & Responsibilities: − Maintains the various computer systems owned or operated by the company. − Windows and/or Linux systems, scripting (e.g., Bash, PowerShell), and proficiency in Python for automation and system integration tasks. − VMware / Hyper-V − Provides end-user support, resolves technical issues and provides technical assistance for all operating systems and applications − Provides in-person and remote support through use of the telephone or remote access − Provides new employees with required hardware and appropriate access to the company’s − computer systems − Maintains business software applications − Configures monitors and troubleshoots existing and new operating systems and applications − Ensures that architecture principles and technology standards are consistently applied and updated as appropriate − Co-operates with database programmers, analysts or other system administrators as needed − Tests and installs operating systems and applications security/performance patches − Collaborates with third-party vendors who may be involved in diagnosing and correcting system related issues and assisting with solutions − Assists in utility account maintenance − Supports management with IT requests and potential new implementations − Surveys new IT services/vendors with management as needed for cost containment − Supports Management with tracking of computer/printer devices for asset controls − Ensure that end users have proper computer resources including enough memory and the set up needed to be able to work efficiently − Complies with the Company's Quality and Information Security Management Systems and applicable national and international legislation, including legislation for data protection Education Requirements − Required: BSc in Computer Engineering, alternative BS in Science with at least one certification in system administration from a large vendor

Skills Required Proficiency in organizing and communicating clinical information Scientific writing, Protocols, CT writing, Drugs. Excellent attention to detail, consistency, clarity and scientific rigor Continuous improvement and growth mindset Ability to work in a fast-paced and changing environment Accountable, focused, precise attitude Customer-service mentality and can-do attitude Exceptional command of written and spoken English at a professional level with the ability to write clear, concise and grammatically flawless medical/scientific content. Job Responsibilities Works closely with cross-functional project teams to independently author scientifically accurate, comprehensive and compliant documents, including but not limited to clinical study reports, clinical study protocols, manuscripts, informed consent forms, patients’ narratives, abstracts, posters, oral presentations, etc Manages the collection, consolidation and integration of comments/feedback from internal and external reviewers to efficiently finalize assigned writing projects Performs thorough quality control checks, including copyediting, proofreading, and cross-verification of data within clinical documents and against source TFLs to ensure accuracy, consistency, and compliance with regulatory standards. Ensure that the assigned deliverables strictly adhere to regulatory guidelines (e.g., ICH-GCP, EMA/FDA requirements), publication guidelines (ICMJE, GPP, journal/congress-specific requirements), client specifications, and Veeda's quality standards for content, format, and structure. Streamline the review process by identifying and mitigating potential conflicts early, enabling the timely completion of high-quality deliverables. Provide supervision and technical advice to other medical writers in the team and new writers joining the team, as required. Apply broad therapeutic knowledge to adapt writing style and content for different disease areas and target audiences Conduct literature reviews on assigned therapeutic areas and provide scientific support across departments throughout the clinical study lifecycle, ensuring adherence to timelines and project requirements. Quickly assimilate new therapeutic area information to support emerging project needs Maintain awareness of evolving guidelines and standards across relevant therapeutic fields Provide support to Medical Writing department activities as needed

Associate - Legal Responsibilities Legal Expertise & Documentation: Minimum 3 to 4 years of experience in a corporate legal environment. Well-versed with court procedures. Draft and review legal documents, including CDA, MSA, lease agreements notices, and customer communications. Liaison & Legal Coordination Engage with lawyers, police, government officers, and insurance companies. Coordinate with third parties for claim settlements when necessary. Interpret and apply various laws to defend the company's interests, including interactions with government authorities. Prepare and maintain a monthly tracker of legal events/claims and submit it to the Reporting Authority/Board. Accounting & Compliance Preferably have knowledge of accounting software Tally. Ensure compliance with applicable company laws and regulations. Skills & Requirements Proficiency in English, Hindi, and Gujarati. Strong command of Microsoft Office applications. Excellent communication and negotiation skills. Qualification : Bachelors degree in law. (ref:iimjobs.com)

Main Duties & Responsibilities :. Maintains the various computer systems owned or operated by the company. Windows and/or Linux systems, scripting (e.g, Bash, PowerShell), and proficiency in Python for automation and system integration tasks. VMware / Hyper-V. Provides end-user support, resolves technical issues and provides technical assistance for all operating systems and applications. Provides in-person and remote support through use of the telephone or remote access. Provides new employees with required hardware and appropriate access to the company's computer systems. Maintains business software applications. Configures monitors and troubleshoots existing and new operating systems and applications. Ensures that architecture principles and technology standards are consistently applied and updated as appropriate. Co-operates with database programmers, analysts or other system administrators as needed. Tests and installs operating systems and applications security/performance patches. Collaborates with third-party vendors who may be involved in diagnosing and correcting system related issues and assisting with solutions. Assists in utility account maintenance. Supports management with IT requests and potential new implementations. Surveys new IT services/vendors with management as needed for cost containment. Supports Management with tracking of computer/printer devices for asset controls. Ensure that end users have proper computer resources including enough memory and the set up needed to be able to work efficiently. Complies with the Company's Quality and Information Security Management Systems and applicable national and international legislation, including legislation for data protection. Education Requirements Required : BSc in Computer Engineering, alternative BS in Science with at least one certification in system administration from a large vendor. (ref:hirist.tech)

Core Responsibilities: 1. Design and Analyze PK Studies o Plan clinical PK studies synopsis and feasibility o Analyze PK data using modeling and simulation tools (e.g., Phoenix WinNonlin, R software). o Interpret PK parameters such as C_max, AUC, T_max, half-life, clearance, and volume of distribution. 2. Support Drug Development o Provide PK and statistical input in clinical development phase studies protocol o Evaluate food effect, drug-drug interactions (DDIs), and bioavailability/bioequivalence studies and provide scientific inputs for study design & protocol preparation o Support dose selection and optimization strategies for pivotal study design. 3. Regulatory Submissions o Deep understanding and knowledge of regulatory guidance (like US FDA, MHRA, EMA, HEALTH CANADA, ANVISA etc) documents pertain to BABE as well as clinical trials o Prepare and review PK-Statistical sections for regulatory documents (e.g., ANDA, IND, NDA, BLA, CTA). o Respond to Health Authority questions related to pharmacokinetics. 4. Cross-functional Collaboration o Work closely with clinical, bioanalytical, statistical and regulatory teams. o Participate in multidisciplinary project teams to inform decision-making. 5. Data Interpretation & Reporting o Summarize findings in study reports and scientific publications (as applicable). o Present PK data to internal teams and external teams (Sponsor, DSMB and other regulatory bodies) o Experience into study design, protocol writing, through knowledge of regulatory guidance for BA/BE studies as well as PK clinical trials.

Client Relationship Management & Business Growth: Manage and nurture existing client relationships across the assigned territories to ensure continued business growth. Proactively generate new business from existing clients and develop strong relationships with new prospects. Represent key national and international events, conferences, and seminars to promote the brand and engage potential clients. Strategic Planning & Market Expansion: Identify and explore new areas of market expansion by conducting market research, utilizing open-source information, and developing business cases for new opportunities. Develop and finalize biweekly travel plans for the assigned regions, ensuring the effective allocation of resources for business development efforts. Proposal & Negotiation Management: Review and assess client requests and develop quotations, proposals, and feasibility reports accordingly. Share proposals, feasibility reports, and negotiate terms with clients, ensuring a clear understanding of project requirements. Follow up with clients to close business deals and finalize project agreements. Collaborate with internal stakeholders to ensure proposals align with client expectations and Veeda's capabilities. Reporting & Performance Tracking: Maintain and update the pipeline, ensuring accurate records in the Management Information System (MIS). Track the progress of business opportunities, provide trend analysis, and report regularly to the Business Development Head Desired Candidate Profile Education: Bachelor's or Master's degree in Life Sciences, Pharmacy, Business Administration, or related field. Experience: 7-10 years' prior industry-related business development experience in CRO CTC: 9 to 15 LPA