17 Archival Research Jobs nearby Vellore

Job Title: Videography and Video EditorLocation: Koregaon Park, Poonawala Fincorp Corporate Office, PuneJob Type: PermanentWork Mode: Work from Office (WFO)Timing: General Shift (MonSat)Notice Period: Immediate JoinerExperience: 3-5 yearsVideography :- Role RequirementsExperience: 35 years in videography, ideally for podcasts, social media content, or brand shootsTechnical Proficiency: DSLR/mirrorless cameras, lenses, stabilizers, lighting, and audio equipmentSkills: Strong sense of framing, lighting, camera movement, and on-set coordinationWork Hours: 6-day working schedule (details discussed during the interview)Key ResponsibilitiesShoot podcasts, interviews, B-roll, events, and behind-the-scenes contentSet up and manage lighting, audio, and camera framing for professional outputCapture dynamic visuals with creative angles and smooth camera movementsOrganize, label, and back up all footage systematicallyProvide raw footage to the editing team for post-productionCollaborate with the creative team on shot lists, storyboards, and visual directionEnsure footage is captured in the right formats and resolutions for multi-platform useProduce 4 fully edited podcast episodes per month (3060 minutes each)Produce 45 short-form videos per week (15120 seconds) for social media (Reels/Shorts)Contribute creative input on titles, thumbnails, and content strategyCore CompetenciesStrong visual storytelling and creative eyeTechnical expertise with camera and lighting equipmentReliability and timeliness in delivering footageCollaborative mindset with editors and content creatorsAdaptability and creativity in fast-paced shoot environmentsWhy Join Us Work at the intersection of mental wellness and purposeBe part of a growing, collaborative, heart-led teamContribute to meaningful impact in peoples healing journeysLearn, grow, and bring your authentic self to work every day Video Editor :-Role Requirements      Experience: 35 years in video editing; experience with social-first content and podcasts is a plus      Software Proficiency: Adobe Premiere Pro, After Effects, Final Cut Pro, or similar      Audio & Visual Skills: Strong grasp of pacing, transitions, audio balancing, and color correction      Work Mode: Full-time, in-office role at our Koregaon Park centre      Work Hours: 6-day working schedule (details during the interview)Key Responsibilities Video Editing         Edit raw footage into polished final deliverables using industry-standard tools         Enhance video through sound design, color grading, transitions, and text overlays         Add royalty-free music, subtitles, sound effects, and voiceovers where required         Export and optimize files for various platforms (MP4, MOV, vertical/horizontal formats)         Provide up to 3 rounds of revisions per video when needed On-Site Videography Support (as needed)         Assist in shooting content including podcasts, b-roll, interviews, and behind-the-scenes         Support with lighting setup, camera framing, and capturing dynamic visuals         Manage footage organization, labeling, and backup for easy access Content Deliverables         4 fully edited podcast episodes per month (3060 minutes each)         45 short-form videos per week (15120 seconds) for social media (Reels/Shorts)         Creative title and thumbnail suggestions when collaborating on content strategy         Provide project files on request for archival or future editing needsCore Competencies to Evaluate During Interviews         Creative Storytelling Ability to communicate messages through thoughtful visuals         Eye for Detail Clean edits, sharp transitions, consistent branding         Technical Proficiency Strong command of video editing tools and audio balancing         Timeliness Deliver content within tight timelines without compromising quality         Team Collaboration Work closely with content, marketing, and production teams         Adaptability Open to feedback, revisions, and evolving creative directions

Role Overview As a Clinical Research Documentation Specialist, you will play a critical role in supporting the Head of the Ethics Committee (EC) Division by ensuring all clinical research documentation is accurate, compliant, and audit-ready. You will manage end-to-end documentation processes in alignment with ICH-GCP, institutional, and ethical standards and support cross-functional needs across departments when required. Key Responsibilities - Regulatory Document Management - Maintain and update essential trial documents in compliance with ICH-GCP guidelines. - Prepare, organize, and manage Investigator Site Files (ISFs) and Trial Master Files (TMFs). - Ensure timely and accurate submission of study protocols, amendments, and informed consent forms to the Ethics Committee. - Ethics Committee Coordination - Assist in preparing EC meeting agendas, presentations, and minutes. - Track and manage approvals, re-approvals, and continuing reviews of studies. - Maintain precise documentation of EC decisions, communications, and correspondence. - Protocol & SOP Compliance - Ensure all activities adhere to Standard Operating Procedures (SOPs), protocols, and applicable regulatory standards. - Maintain documentation for audit and inspection readiness. - Communication & Liaison - Act as a liaison between the clinical research teams and the Ethics Committee. - Coordinate with investigators, sponsors, and regulatory bodies for documentation and submission needs. - Audit & Inspection Readiness - Support internal and external audits by providing organized and accurate documentation. - Implement Corrective and Preventive Actions (CAPA) in response to audit observations. - Training & Documentation Support - Conduct or assist with training sessions on documentation standards, GCP, and EC processes. - Contribute to drafting, reviewing, and updating SOPs related to EC documentation. - Archival & Record Management - Manage secure archival and retrieval of all EC and trial-related documents. - Ensure adherence to document retention and confidentiality policies. Educational Qualification - Mandatory Qualification: Doctor of Pharmacy (Pharm D) - Preferred Candidates: Male candidates only - Must be willing to sign a 2-year service agreement - Must be comfortable working in rotational shifts Skills & Competencies - Strong understanding of ICH-GCP and clinical research regulations - Excellent documentation and organizational skills - Proficiency in MS Office and document management systems - Strong attention to detail and accuracy - Effective communication and coordination skills - Ability to work cross-functionally and manage multiple priorities - Knowledge of audit and inspection processes - High level of confidentiality and ethical integrity Additional Notes As a cross-functional support role, you may assist other divisions or departments as required. This position contributes to ensuring all EC and clinical research documentation is audit-ready, compliant, and aligned with institutional goals.,

As a skilled Technical DevOps Manager - Linux system administrator (SA) at LSEG Post Trade Solutions division - Acadia, you will be responsible for the following: - Effective monitoring for platform efficiency and escalation of issues - Log analysis and data gathering for root cause analysis - First level remediation and escalation of operational issues - Need to be subject matter experts in the underlying technologies You must be self-motivated with the ability to prioritize workload efficiently. Role Responsibilities: - Automated provisioning, installation/configuration, operation, and maintenance of software-defined infrastructure - Participating in technical research and development for process improvements and maximum uptime - Proactively improving service for clients - Managing an environment consisting of Jira tracking, Cisco Nexus, Meraki networking, VMware vSphere, Windows desktop, Windows Server, Ubuntu Server, relational, and document data stores - Utilizing enterprise monitoring tools such as Prometheus, Data Dog, System Centre, or Splunk - Installing new/rebuilding existing servers and configuring hardware, peripherals, services, settings, directories, storage, etc. - Developing and maintaining installation and configuration procedures - Contribution to and maintenance of system standards - Performing daily system monitoring, backup operations, file archival, and purges - Creating, changing, and deleting user accounts per request - Repairing and recovering from hardware or software failures - Applying OS patches and upgrades, and upgrading administrative tools and utilities - No staff oversight but a strong team member with no budget responsibility Experience And Qualifications Required: - Technical experience as a systems administrator - Bachelor's degree in a technical major like engineering or computer science - Good communication skills - Willingness to adopt a Hybrid working mode and work in the Bangalore Office - Experience in the Financial or investment banking environment - Familiarity with financial products and terms - Excellent analytical skills, attention to detail, and problem-solving abilities - Ability to communicate clearly and concisely to IT and business teams and senior management In addition to the job role, London Stock Exchange Group (LSEG) is a leading global financial markets infrastructure and data provider dedicated to driving financial stability, empowering economies, and enabling sustainable growth. The company values Integrity, Partnership, Excellence, and Change, which guide decision-making and actions every day. Working at LSEG will allow you to be part of a dynamic organization across 65 countries, where individuality is valued, and new ideas are encouraged. LSEG offers a range of benefits and support, including healthcare, retirement planning, paid volunteering days, and wellbeing initiatives.,

As a biostatistician at SJRI, you will be responsible for statistical work on various research projects associated with nutrition, public health, health technology, including longitudinal, interventional, observational, cohort studies, randomized control trials, and qualitative studies. **Roles and Responsibilities:** - Preparing study designs and statistical analysis plans for research studies. - Conducting biostatistical analyses of large complex datasets. - Cleaning datasets from completed research studies and managing databases. - Developing final publishable-quality tables and figures for manuscripts. - Writing and documenting SPSS, SAS, or R programs for data cleaning, maintenance, and analysis. - Managing data-related aspects of research projects. - Designing and conducting statistical analyses for grant applications and research manuscripts. - Assisting in electronic data archival. - Performing qualitative data analysis. **Qualifications Required:** - M.Sc. in Biostatistics, Statistics, or a related field (e.g., Epidemiology, Data Science). - 2 years of experience in applying statistical methods to real-world data, clinical trials, public health, and biomedical research. If you are interested in this position, please send your resume to the Principal Investigator of CRC 1 Project at SJRI. The salary offered for this role is Rs. 40,000-45,000 per month based on experience. The preferred languages for communication are English and Kannada. The deadline to apply is 14th December 2025.,

As a Senior Manager, Trial Master File (TMF) Operations at Bristol Myers Squibb, you will play a crucial role in leading and providing strategic direction across R&D functions to ensure high-quality TMF end-to-end processes for in-house and outsourced studies. Your responsibilities will include: - Leading and providing strategic direction across R&D functions for high-quality TMF end-to-end processes - Managing TMF Process Leads and TMF System and Business Lead - Defining TMF migration strategies in collaboration with business stakeholders - Ensuring document management and archival processes are of high quality and in line with industry standards - Leading global, cross-functional projects for the optimization of the Quality Management System and the end-to-end TMF process - Maintaining global processes, procedures, and training materials for inspection readiness - Supporting the development and governance of global processes for TMF - Driving and supporting BMS audit/inspection readiness activities - Defining a control framework for in-house and outsourced studies - Utilizing metrics and trend analyses to identify and prioritize process improvements - Building and maintaining industry intelligence and process expertise through training and participation at conferences - Participating in benchmarking initiatives with peers externally Qualifications required for this role include: Education/Degree(s): - A minimum of a Bachelor's Degree (or equivalent degree) is required, with a degree in a life science, natural science, or business preferred Experience: - Minimum of 10 years of clinical operations, regulatory, pharmacovigilance, or other relevant biopharmaceutical industry experience - At least 5 years in TMF management and inspection readiness or related position - Strong program and project management experience Skills/Abilities: - Demonstrated influential leadership and expertise with senior level interactions - Ability to work in a matrixed organization and influence areas not under direct control - Strong teamwork, interpersonal, and communication skills - Strategic thinking capability with a focus on execution of decisions - Change agility in leading others through change and ambiguity - Ability to provide innovative ideas that create value and seek new information without compromising compliance If you believe you possess the required qualifications and skills for this role, we encourage you to apply. Your work at Bristol Myers Squibb has the potential to transform patients" lives through science and offer you a fulfilling and challenging career opportunity.,

As a Research Associate (RA) in the project sponsored by the Indian Council for Social Science Research (ICSSR) at Mahindra University, you will be working on a Major Research Project entitled "Yadadri: A Devotional Capital, Diasporic Networks and a 21st Century Telugu Identity in the Making". The project aims to study the intersections of global capital, diasporic networks, and religion in Hyderabads urban growth, focusing on its dual role as an IT hub and a devotional capital for the 21st century. **Key Responsibilities:** - Conduct archival and ethnographic research to contribute to the project's objectives. - Travel within South India to conduct fieldwork and gather relevant data. - Demonstrate excellent communication, writing, and translation skills in English and Telugu. **Qualifications Required:** - A Masters degree in History, Anthropology, English Literature, Mass Communication, Cultural Studies, or any Social Science discipline. - Prior experience in archival and ethnographic research will be an added advantage. - Proficiency in English and Telugu languages for effective communication. - Willingness to travel and conduct fieldwork within South India. If shortlisted, you will be offered a fellowship of Rs 20,000/- per month along with coverage for travel and field expenses. The project duration is 2 years. Interested candidates are encouraged to send their CV and a cover letter detailing their research experience to nisha.mathew@mahindrauniversity.edu.in. Don't miss the opportunity to be part of this exciting research project that explores the evolving dynamics of Hyderabads urban landscape and cultural identity. Shortlisted candidates will be notified for an interview on campus by August 21, 2023.,

As a Data Archival Designer at NTT DATA, you will play a crucial role in envisioning and developing high-quality data migration solutions that align with architectural standards and meet the organization's needs. You will collaborate with various teams to ensure projects are completed on time, within budget, and with the desired level of quality. Additionally, you will act as a mentor to foster a culture of continuous improvement within the team. **Key Responsibilities:** - Conduct thorough data analysis of source systems to understand data structures, quality, and dependencies. - Identify data quality issues and develop strategies for cleansing and standardizing data prior to migration. - Design comprehensive data migration plans, including data mapping, transformation rules, and loading procedures. - Create detailed data mapping documents and develop data cleansing and transformation logic. - Work with testers to develop and execute data migration test plans, including unit testing and user acceptance testing. - Collaborate with business stakeholders to understand data requirements and migration objectives. **Qualifications Required:** - Knowledge of computer technology, network infrastructure, systems and applications, security, and storage. - Proficiency in Microsoft Office Suite, particularly Excel. - Experience with Informatica ILM, AWS, Abinitio, and Database Concepts (SQL/NoSQL). - Ability to collaborate effectively with cross-functional teams. NTT DATA is a global innovator of business and technology services, serving 75% of the Fortune Global 100. Committed to helping clients innovate, optimize, and transform for long-term success, NTT DATA has experts in more than 50 countries. Services include business and technology consulting, data and artificial intelligence, industry solutions, as well as the development, implementation, and management of applications, infrastructure, and connectivity. As a leading provider of digital and AI infrastructure, NTT DATA is part of the NTT Group, investing over $3.6 billion annually in R&D to drive organizations and society confidently into the digital future. Visit us at us.nttdata.com.,

As an Associate Creative Producer at MotorInc in the Content department, you will be responsible for assisting with all aspects of pre-production, production, and post-production of audio programs. Your role will be crucial in contributing to the success of radio show segments and episodes. Your organizational skills, audio production knowledge, and ability to thrive in a fast-paced environment will be essential for this role. It is important to have knowledge and interest in cars, bikes, tech, travel, and possess decent writing skills. Key Responsibilities: - Assist in planning, researching, and developing radio show segments and episodes - Research topics, prepare briefing materials for hosts, assist with script development and writing - Schedule and coordinate guest appearances, interviews, and hosts calendar planning - Edit and mix audio content using industry-standard software - Manage and coordinate production calendars and timelines - Contribute creative ideas for new segments and show concepts - Source and clear music, sound effects, and archival audio - Maintain production databases and digital assets - Assist with social media content related to radio programming - Provide day-of-show support during live broadcasts - Coordinate with other departments including app, marketing, and social Qualifications Required: - Bachelor's degree in communications, journalism, media studies, or related field - 3+ years of experience in radio, podcasting, or audio production - Proficiency with digital audio workstations - Strong research and fact-checking skills - Excellent written and verbal communication abilities - Strong attention to detail - Ability to meet tight deadlines in a fast-paced environment - Demonstrated problem-solving skills - Highly disciplined and performance-focused Additional Company Details: - Experience working in a radio environment is preferred - Knowledge or basic understanding of video/still production - Knowledge and interest in current events, news, automotive, and cultural trends - Experience with remote recording setup and troubleshooting - Familiarity with content management systems - Experience with field recording equipment - Understanding of audience development and metrics - Engagement with viewers through replies to comments and maintaining a positive sentiment - Providing constant feedback to marketing and management on listeners" needs and choices Physical Requirements: - Ability to sit for extended periods - Occasional moving of equipment - Occasional travel for remote broadcasts - May require flexible hours To Apply: Please submit your resume, cover letter, and relevant work samples or portfolio to jobs@motorinc.com with the subject line "Associate Creative Producer - Your Name." Make sure to visit MotorInc's content channel on YT and other social platforms before applying.,

As an integral part of Amgen, you will be responsible for the implementation and adoption of the data governance framework, playing a crucial role in modernizing Amgen's data ecosystem and positioning the company as a leader in biopharma innovation. By leveraging cutting-edge technologies such as Generative AI, Machine Learning, and integrated data, you will provide exceptional support for Amgen's data governance framework. Your collaboration with business stakeholders, data analysts, Product Data Owners, and data leaders will ensure the successful implementation and adoption of the data governance framework, ultimately increasing trust and data reuse across Amgen. **Roles & Responsibilities:** - Implement and adopt the data governance framework for a specific domain of expertise within Amgen (Research, Development, Supply Chain, etc.). - Operationalize the Enterprise data governance framework and align the broader stakeholder community with their data governance needs, including data quality, data access controls, privacy and security compliance, master data management, data sharing, communication, and change management. - Work with Enterprise MDM and Reference Data to enforce standards and promote data reusability. - Drive cross-functional alignment in your domain(s) of expertise to ensure adherence to Data Governance principles. - Develop policies for data, metadata, privacy, lineage, access, security, retention, and archival. - Maintain documentation on data definitions, standards, flows, legacy data structures, common data models, and data harmonization for assigned domains. - Ensure compliance with data privacy, security, and regulatory policies for the assigned domains. - Collaborate with Technology teams, business functions, and enterprise teams to define specifications for the development and implementation of data foundations. - Cultivate strong relationships with key business leads and partners to address their needs effectively. **Functional Skills:** **Must-Have Functional Skills:** - Proficiency in technical skills (Advanced SQL, Python, etc.) with knowledge of Pharma processes and domain specialization. - Extensive experience working with or supporting systems related to data governance frameworks like Collibra, Alation. - Thorough knowledge of data management, common data models, metadata management, data quality, master data management, data stewardship, and data protection. - Experience in the data products development life cycle, enabling data dictionaries, and business glossaries for increased data products reusability and data literacy. - Customer-focused with excellent written and verbal communication skills for seamless collaboration with internal stakeholders and external partners. - Ability to manage scrum teams effectively. **Good-to-Have Functional Skills:** - Experience working with data governance councils or forums. - Familiarity with Agile software development methodologies such as Scrum. **Soft Skills:** - Excellent analytical skills. - Effective collaboration with global, virtual teams. - Successful management of multiple priorities. - Team-oriented mindset with a focus on achieving collective goals. - Ability to build strong business relationships and comprehend end-to-end data use and requirements. - Outstanding interpersonal skills and people management abilities in both matrix and direct line functions. - Strong verbal and written communication skills. **Basic Qualifications:** - Master's degree with 8 - 10 years of experience in Data Science, Artificial Intelligence, Computer Science, or related fields OR - Bachelor's degree with 10 - 14 years of experience in Data Science, Artificial Intelligence, Computer Science, or related fields OR - Diploma with 14 - 16 years of hands-on experience in Data Science, AI/ML technologies, or related technical domains.,

As a Java Developer at this company in NYC, NY, your role will involve providing comprehensive technical expertise across multiple technology areas. You will be responsible for solving high-impact, complex business and system issues, as well as developing methodologies and standards for application analysis and testing. Additionally, you will manage resources, mentor junior analysts, and ensure high-quality deliverables. It will be important for you to liaise with QA and support teams to ensure post-release success, while also assessing risk and maintaining compliance with Citis policies and standards. Key Responsibilities: - Providing comprehensive technical expertise across multiple technology areas - Solving high-impact, complex business and system issues - Developing methodologies and standards for application analysis and testing - Managing resources, mentoring junior analysts, and ensuring high-quality deliverables - Liaising with QA and support teams to ensure post-release success - Assessing risk and maintaining compliance with Citis policies and standards Qualifications: - 10+ years of experience in an Applications Support role - Subject matter expertise in one or more Apps Support domains - Strong communication, problem-solving, and leadership skills - Ability to manage multiple priorities and work independently or in teams Additionally, you will need to have technical skills in: - UNIX - Tableau - WebLogic - Tibco - WebSphere - Ab Initio - MHub - Appian - Oracle - Big Data - Autowatch - Control Center environment setup/maintenance - SAN/NAS - Load Balancing - Data Archival - Backup & Restore - Upgrade and Vulnerability Patching (Note: No additional details about the company were provided in the job description.),

As a biostatistician at SJRI, you will be involved in statistical work on various projects related to nutrition, public health, and health technology. Your responsibilities will include: - Preparing study designs and statistical analysis plans for various studies. - Conducting biostatistical analyses of large complex datasets. - Cleaning datasets from completed research studies and managing databases. - Developing final publishable-quality tables and figures for research manuscripts. - Writing and documenting SPSS, SAS, or R programs for data cleaning, maintenance, and analysis. - Managing data-related aspects of research projects. - Designing and conducting statistical analyses for grant applications and research manuscripts. - Assisting in electronic data archival. - Performing qualitative data analysis. Qualifications required for this position include: - M.Sc. in Biostatistics, Statistics, or a related field (e.g., Epidemiology, Data Science). - 2 years of experience in applying statistical methods to real-world data, particularly in clinical trials, public health, and biomedical research. Please note that the salary for this position ranges from Rs. 40,000 to Rs. 45,000 per month, based on experience. The preferred languages for this role are English and Kannada. If you are interested in this position, please send your resume to the Principal Investigator of the CRC 1 Project at SJRI. To apply, please email your cover letter and curriculum vitae to sayeeda.af@sjri.res.in and cc hr@sjri.res.in by 14th December 2025.,

Role Overview: You will provide medical expertise for site identification, study feasibility, study design, conduct, analysis, and reporting. Your responsibilities will also include the generation of integrated databases, pooled analyses for efficacy and safety, ISE and ISSs, as well as dossiers for regulatory submissions for market authorizations of new medicinal products, diagnostics, and devices. Key Responsibilities: - Define regulatory strategies for submission of clinical trial applications, approval, and marketing trial applications in targeted regions such as India, U.S, and EU. - Prepare and review regulatory documents, dossiers containing technical, preclinical, and clinical data in suitable formats, responses to questions and inquiries from health authorities, QA audit plans, quality systems management plans, clinical amendments, and safety reports, as well as data provided for the regulatory approval process. - Interact and liaise with sponsors in the preparation of initial regulatory dossiers, health authorities through telephone contacts, teleconferences, meetings, and submissions, Incyte scientists on unique scientific/regulatory issues impacting drug development, and provide regulatory support to interdepartmental project teams. - Maintain archival systems for all regulatory submissions and contact logs, regulatory guidance documents, regulations, information, QA, clinical, and other SOPs. Qualifications/Experience: - Bachelor's or advanced degree (MD, Ph.D., or Pharm.D.) in scientific/life sciences or related field. - A minimum of 5 years of experience in regulatory affairs with at least 8 or more years of drug development experience. - Strong knowledge of regulations/guidelines governing the development of pharmaceuticals and experience in working with international regulatory agencies.,

Role Overview: You will be responsible for preparing consistent and high-quality technical documents related to Pharmaceutical Research and Development for Formulation at Teva. Your role will involve executing all functions in accordance with current FDA regulations, ICH guidelines, USP methodologies, cGMPs, and SOPs. Maintaining open communication with R&D members to ensure timely delivery of high-quality documents independently with minimal supervision will be a key aspect of your responsibilities. Key Responsibilities: - Prepare documents and facilitate documentation management in R&D while ensuring correctness, completeness, and clarity following established guidelines. - Prepare documents such as Manufacturing Batch Records, Study Protocol and Reports, Stability Protocols, Product Development Report, Quality Overall Summary, response to regulatory queries based on scientific input from the Formulation team. Knowledge of QBD & DOE is essential. - Prepare high-impact presentations including graphs and charts. - Submit documents for signatures, coordinate their flow, archival, and retrieval to ensure timely flow and publish monthly performance metrics. - Continuously improve documentation systems to increase efficiency and compliance with cGMP and/or other regulatory requirements. - Perform other duties as assigned or delegated. - Comply with FDA guidelines/Company Policies of Data Integrity. Qualifications Required: - Education: A minimum of a master's degree (M.Pharm) or a PhD in Pharmacy is required. - Industry Experience: Minimum 12 to 15 years of Formulation R&D experience with solid oral dosage forms for regulated markets. Knowledge of other dosage forms will be an added advantage. - Demonstrated knowledge and understanding of quality and regulatory guidance for SOD products for regulated markets. - Demonstrated knowledge and working understanding of basic concepts of Good Manufacturing Practices (GMP), regulatory documentation required. Additional Company Details: Together, Teva is on a mission to make good health more affordable and accessible worldwide. As the world's leading manufacturer of generic medicines, Teva is dedicated to helping millions enjoy healthier lives. With a presence in nearly 60 countries and a diverse workforce, Teva is always looking for new ways to make a difference and welcomes individuals who share the same mission. Note: The job description did not include any additional details about the company.,

Role Overview: As a AQA Microbiology Reviewer at Syngene, you will be responsible for reviewing and approving various activities related to Quality control Microbiology and QC Biologics. Your core purpose will include Microbiology laboratory QMS review, issuance of logbooks and archival, review and approval of trends and reports, participation in investigations, conducting audits, and interacting with clients. You will also be required to review and approve various documents and ensure compliance with EHSS policies and Good hygiene practices. Key Responsibilities: - Review and approval of trends, protocol, and reports related to EM, water, and samples - Review and approval of SOP, EOP, IOP, specification, CSV protocols, and qualifications documents - Conducting audit trails and regular GMP rounds - Interaction with clients and cross-functional team members - Review and closure of Laboratory incident reports - Supervising the shift analyst activities and working in shifts as required - Ensuring compliance with safety protocols and following environment, health, and safety (EHS) requirements - Issuance of logbooks, documents, forms, and archival of related documents - Review and approval of data in ELN and LIMS - Undertaking other responsibilities related to AQA Microbiology as per requirement Qualifications Required: - Experience: 9-12 years - Education: M.Sc. Microbiology, Biotechnology Additional Company Details: Syngene (www.syngeneintl.com) is an innovation-led contract research, development, and manufacturing organization offering integrated scientific services from early discovery to commercial supply. The company values safety at its core and expects all employees to adhere to safety guidelines, procedures, and SOPs to ensure safe operations and compliance with quality standards. Syngene emphasizes a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Employees are expected to demonstrate alignment with the core values of Excellence, Integrity, and Professionalism. Equal Opportunity Employer. Role Overview: As a AQA Microbiology Reviewer at Syngene, you will be responsible for reviewing and approving various activities related to Quality control Microbiology and QC Biologics. Your core purpose will include Microbiology laboratory QMS review, issuance of logbooks and archival, review and approval of trends and reports, participation in investigations, conducting audits, and interacting with clients. You will also be required to review and approve various documents and ensure compliance with EHSS policies and Good hygiene practices. Key Responsibilities: - Review and approval of trends, protocol, and reports related to EM, water, and samples - Review and approval of SOP, EOP, IOP, specification, CSV protocols, and qualifications documents - Conducting audit trails and regular GMP rounds - Interaction with clients and cross-functional team members - Review and closure of Laboratory incident reports - Supervising the shift analyst activities and working in shifts as required - Ensuring compliance with safety protocols and following environment, health, and safety (EHS) requirements - Issuance of logbooks, documents, forms, and archival of related documents - Review and approval of data in ELN and LIMS - Undertaking other responsibilities related to AQA Microbiology as per requirement Qualifications Required: - Experience: 9-12 years - Education: M.Sc. Microbiology, Biotechnology Additional Company Details: Syngene (www.syngeneintl.com) is an innovation-led contract research, development, and manufacturing organization offering integrated scientific services from early discovery to commercial supply. The company values safety at its core and expects all employees to adhere to safety guidelines, procedures, and SOPs to ensure safe operations and compliance with quality standards. Syngene emphasizes a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Employees are expected to demonstrate alignment with the core values of Excellence, Integrity, and Professionalism. Equal Opportunity Employer.

As an OnBase Developer, you will be responsible for: - Analyzing system specifications and developing OnBase applications to support information systems processes - Preparing detailed specifications from which complex programs will be written - Designing, coding, testing, debugging, documenting, and maintaining programs written from specifications - Formulating scope and objectives through research to develop or modify complex systems - Understanding of application/development, quality assurance and integration methodologies - Hands on experience in OnBase Document Retrieval, Onbase workflow modification, OnBase Document Management, OnBase Document Archival System, and ShareBase Search (Guidewire Accelerators and OnBase Accelerators) - OnBase System Administration experience for installation builds, maintenance, and enhancements of the application - Background in creating Web Services - Nice to have Onbase certified - Able to manage & technically guide the team Qualifications required for this role include: - 3+ years of experience in OnBase development - Knowledge and experience in OnBase Document Retrieval, Onbase workflow modification, OnBase Document Management, OnBase Document Archival System, and ShareBase Search - Understanding of OnBase System Administration for installation builds, maintenance, and enhancements - Experience in creating Web Services - OnBase certification would be a plus Please note that the additional details of the company were not provided in the job description.,

You will be responsible for providing technical assistance and laboratory support to Professor Nigel and his group, focusing on multiple aspects of spatial biology, such as spatial transcriptomics, cancer immunology, and personalized medicine related to Pancreatic Cancer. The role involves supporting the smooth and effective running of the Jamieson Spatial Biology group at the Wolfson Wohl Cancer Research Centre. - Provide technical, archival, and administrative support to the Jamieson Spatial Biology group within the School of Cancer Sciences (SCS). - Contribute to the efficient running of the lab by carrying out tissue-based laboratory work, database management, and archival work. - Keep clear and accurate records of outputs, produce concise written summaries of results, and propose technical solutions to practical problems. - Maintain laboratory areas, ensure equipment is appropriately stocked and maintained, and provide guidance to service users. - Stay updated with advances in the relevant discipline and apply knowledge to enhance technical activities. - Collaborate with colleagues, participate in team meetings, and contribute to wider College activities. - For appointment at Grade 4: Scottish Credit and Qualification Framework level 5 or 6 [National 5 or National 6/Highers, Scottish Vocational Qualification level 2 or 3] or equivalent, and experience of personal development in a similar role. - For appointment at Grade 5: Scottish Credit and Qualification Framework level 7 [Advanced Higher / Scottish vocational Qualification level 3, Higher National Certificate] or equivalent, and experience of personal development in a similar role. As a valued member of the team, you can expect a warm welcoming and engaging organizational culture, flexible working approach, and a commitment to support your health and wellbeing, including a free 6-month UofG Sport membership. The University promotes equality, diversity, and inclusion, welcoming applications from all communities, particularly from under-represented groups. The University endorses the principles of Athena Swan and holds bronze, silver, and gold awards. Visit the University's website for more information on available job opportunities.,

As a Specialist in Industrial IoT, your role will involve strong technical knowledge on Empower and other CDS Systems. You will be responsible for maintaining and supporting the current CDS system, providing end-user issue support, troubleshooting, and resolution. Additionally, you will handle the administration of the CDS system and server maintenance. Your tasks will include performing backup, archival, restore, and periodic system review, as well as supporting in the deployment/installation of CDS applications. Your responsibilities will also include managing user administration of lab applications, coordinating with instrument vendors during application/instrument setup and qualification, and providing training and support to site SMEs in Empower operations and implementations. Experience in working in Pharmaceuticals, Chemical Manufacturing, or regulated environments will be beneficial. You will be required to validate all laboratory and instrument software, including maintenance of the Master Validation Plan, functional requirements, risk assessments, and execution of validation protocols. Ensuring data integrity and compliance with 21 CFR Part 11 and GxP standards will be crucial, along with preparing, drafting, and finalizing SOPs and compliance documents. Qualifications: - Strong technical knowledge on Empower and other CDS Systems - Experience working in Pharmaceuticals, Chemical Manufacturing, or regulated environments - Familiarity with Labvantage, LabWare, SampleManager, StarLIMS, Empower, Lab Management Systems, Caliber LIMS, and AR/VR/MR Please note that the above responsibilities and qualifications are essential for the role of a Specialist in Industrial IoT.,