61 Tga Jobs

About The Role - Grade Specific Must Have 1) Strong Informix database Skills (IDS. XPS, 4GL, ESQLC) 2) DB Upgrade and Design for Informix Skills. 3) Design/ Migrations to Informix from old version and XPS to IDS 4) Automation/Scripting skills - python, AI 5) Experience with rewriting SQL queries, stored procedures, triggers, and views. 6) Work on performance tuning and query optimization 7) Well versed with CDC concepts. 8) Experience with Performance tuning and Health Checks 9) Product installation, including Informix 4GL Tools, Informix Server, and Informix Client SDK 10)Informix HDR, ER, CM, RSS, SDS 11)Informix Backup using ontape and onbar

Walk In Drive For Quality Control In Formulation Division @ Corporate Office Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharma Experience:- 2 to 8 Years Division :- Formulation Interview Date:-25-10-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- MSN Corporate, H. No. 2-91/10 & 11 /MSN, Whitefields, Kondapur, 500084 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make healt...

As a Research Associate in the Analytical R&D team within the Peptide Synthesis division, your role will involve supporting the development and execution of analytical methods for peptide characterization. You will collaborate closely with cross-functional teams in R&D and Quality to ensure the quality assessment of peptides. Key Responsibilities: - Assist in developing and performing analytical methods (e.g., HPLC, UPLC, UV, FTIR, KF, LC-MS) for the characterization and quality assessment of peptides - Conduct routine testing of raw materials, intermediates, and final peptide products - Support method validation, transfer, and troubleshooting under the guidance of senior scientists - Docume...

Date: 14 Oct 2025 Location: Bangalore, KA, IN, 560099 Division: Development Services Job Description Designation: Junior Manager QMS EGMP Job Location: Bangalore Department: QC About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development, and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries worldwide. Syngene's clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its more than 4000- strong team of sc...

The opportunity Were looking for Senior Manager with expertise in Life Sciences Regulatory Compliance and Stakeholder Management to join the leadership group of our EY-Regulatory Compliance team. This is a fantastic opportunity to be part of a leading firm whilst being instrumental in the growth of emerging service offering. Your key responsibilities Client Responsibilities Participate and lead Regulatory Compliance engagements Help manage the financial aspects of engagements by organizing staffing, tracking fees, and communicating issues to project leaders Drive-in business development initiatives along with client management and account management Build strong internal relationships within...

Job Description Role:- Team Lead - Polymer (Manager/Sr. Manager) - R&D Key Responsibilities: Lead polymer synthesis and process development projects for CDMO/CMO customers Design and optimize polymerization process (bulk, solution, emulsion, suspension) at lab scale Prepare process packages (Tech Pack) for pilot and tech transfer Maintain compliance with safety protocols, documentation standards, and regulatory guidelines Drive innovation projects in new polymer materials aligned with Novopors growth strategy Competencies: Strong expertise in polymer synthesis, characterization, and modification techniques Hands-on experience with all polymerization methods (free radical, emulsion, solution,...

As a Polymer Specialist at TVS Motor Company, your main responsibility will be to serve as a polymer material expert and play a vital role in selecting the appropriate materials and processes for components of 2W & 3W vehicles, including both ICE & Electric variants. Your tasks will involve collaborating on new technology projects related to polymers, composites, and paints, engaging with suppliers and research institutes to explore innovative ideas. - Conduct polymer parts testing and clearance using various material characterization techniques such as FTIR, DSC, TGA, XRD, SEM/EDS, as well as mechanical testing for all new products. - Coordinate with design teams to gather exact material re...

Role Overview: As an R&D Engineer in the field of Physics and Materials Science at Lucknow, UP, your primary responsibility will be to conduct research on advanced materials, composites, and coatings. This will involve performing laboratory experiments, material synthesis, and characterization using advanced techniques such as XRD, SEM, TEM, FTIR, DSC, and TGA. Your role will also require you to analyze data, interpret results, and provide actionable insights for product/process development. Additionally, you will be involved in supporting the design, fabrication, and testing of prototypes and functional devices. Collaboration with cross-functional engineering teams to integrate materials in...

Job Description We are looking for a motivated and detail-oriented Research Associate to join our Analytical R&D team within the Peptide Synthesis division. The selected candidate will support the development and execution of analytical methods for peptide characterization, working closely with cross-functional teams in R&D and Quality. Key Responsibilities Assist in developing and performing analytical methods (e.g., HPLC, UPLC, UV, FTIR, KF, LC-MS) for the characterization and quality assessment of peptides Conduct routine testing of raw materials, intermediates, and final peptide products Support method validation, transfer, and troubleshooting under the guidance of senior scientists Docu...

Responsibilities: Dossier Preparation & Submission Prepare, compile, and review CTD / ACTD / eCTD dossiers for product registration in global markets. Coordinate for ANDA, DMF, CEP, COS, and other regulatory submissions for APIs and formulations. Ensure accuracy and completeness of Module 15 in line with specific regulatory authority requirements. Regulatory Compliance & Communication Ensure continuous regulatory compliance of products as per cGMP and ICH guidelines. Review and submit annual reports, amendments, variations, and renewals as required. Communicate with regulatory agencies and address queries, deficiencies, and clarifications (Q&A) in a timely manner. Documentation & Data Collec...

Handling the sophisticated scientific instruments. Completion of the sample testing within the stipulated time. Maintaining log registers of the instruments on daily basis. Purchase management of consumables/materials required for Central Instrumentation Facility (CIF) and maintaining the stock register. Handling the administration-related works related to CIF. Keeping the instruments in a good condition and checking the quality of data frequently. Taking corrective measures by contacting the suppliers for servicing/repairing.

In this role, your main responsibility will be XRD analysis, method development, and polymorph quantification. You will also be supporting routine analysis tasks such as PSD, DSC, TGA, etc. Key Responsibilities: - Conduct XRD analysis - Develop methods for analysis - Quantify polymorphs - Support routine analysis such as PSD, DSC, TGA, etc. Qualifications Required: - Bachelor's degree in Chemistry or related field - Experience with XRD analysis techniques - Strong understanding of polymorph quantification - Proficiency in PSD, DSC, and TGA analysis,

As a part of Agratas, a wholly owned subsidiary of Tata Sons, you will be involved in designing, developing, and manufacturing high-quality, high-performance, sustainable batteries for various applications in the mobility and energy sectors, tailored to meet the needs of our customers. Agratas operates as a scale-up business with a start-up mindset, dedicated to green growth and technological advancement, innovating next-generation battery technologies at cutting-edge R&D Innovation Hubs in India and the UK. Key Responsibilities: - Lead the analytical characterization strategy for materials, electrodes, electrolytes, and interfaces to ensure high-performance and reliable Li-ion cells. - Deve...

REQUIREMENT: Exposure of Regulatory Audit minimum 04-05 times Independently (USFDA, TGA, EU, MHRA). Candidate Profile 8-12 yrs. exp. in engineering department (Formulation Plant Only). Good Knowledge and exp. in automated equipment required for Electrical, Maintenance & Utility. Should have a minimum of 8+ years of experience as an Engineering Manager, with independent management of an Engineering department, and substantial exposure to regulatory environments. Ability to effectively manage an engineering team. Must have handled USFDA, MHRA, and TGA & EU Regulatory Audit. Job Description Responsible for maintenance and utility management, project oversight, cost-saving initiatives, manpower ...

As a Senior Officer in Manufacturing at our company, you will play a crucial role in our Manufacturing team, focusing on executing complex production activities, providing technical guidance, ensuring compliance, and supporting the team lead in achieving production goals. Your strong foundation in pharmaceutical unit operations and problem-solving skills will be key in maintaining quality systems. **Key Responsibilities:** - Lead and execute manufacturing processes efficiently including Granulation, Compression, Coating, Filling, Lyophilization, Packaging. - Provide on-floor guidance, supervision, and training to officers & operators. - Review and verify GMP documentation such as BMR, Logboo...

You will be responsible for testing finished products and analyzing them using instruments such as HPLC, GC, and Dissolution apparatus. Your key responsibilities will include: - Conducting finished product analysis - Performing injectables analysis, focusing on physical parameters using HPLC and GC - Operating instruments like HPLC, GC, Auto titrator, IR, and troubleshooting HPLC/GC issues - Participating in audits by regulatory bodies like USFDA, MHRA, TGA It is essential that you possess good communication and documentation skills, as well as an understanding of data integrity concepts.,

Employment Mode : Contract to Hire Offshore OT Analyst Roles and Responsibilities: Good experience working in the Cyber security domain with a minimum of 5 years in the Industrial automation and controls space Strong understanding of various components in the ICS ecosystem, common security issues faced and best practices to be followed from a security standpoint Strong understanding of Industrial control operations and protocols Sound knowledge of the ICS cybersecurity framework IEC 62443 Good understanding of concepts like Industry 4.0, Cyber Physical Systems, Digital Twin Preferable to have hands-on experience working at a Manufacturing plant Demonstrable credentials in the Industrial cont...

Walk In Drive For Quality Control In Formulation Division @ Kothur Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharmacy Experience:-1 to 5 Years Skills :- HPLC | GC | Dissolution | IP/FP | Stability (OSD & Injectables) | USFDA | Regulatory approvals Division :- Formulation Interview Date:-20-09-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur | MSNF-IV, Mekaguda | MSNF-V, RK Puram Venue Location :- Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Car...

vvTGA #ProjectController #FinanceJobs #GeoData #Fugro #Hiring Job Title: Project Controller Location: [Specify Location] Experience: 2–5 Years Qualification: B.Com / CA Inter / MBA Finance About Fugro We’re looking for a Project Controller to strengthen our team. Job Purpose The Project Controller is responsible for accurate financial management of assigned projects. This includes tracking and reporting revenues, costs, overheads, cash flow forecasting, validating invoices, and supporting project managers with financial strategies to meet contractual requirements. Primary Responsibilities Maintain accurate records of revenues and costs for projects. Forecast Earned Value and cash flow; devel...

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com . Job Summary Responsible for auditing Apotex Enterprise sites, Apotex and Apotex Pharmachem...

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com. Job Summary Responsible for auditing Apotex Enterprise sites, Apotex and Apotex Pharmachem ...

Key Responsibilities Lead and manage the Quality Assurance department, ensuring compliance with GMP norms and regulatory requirements of WHO, EU GMP, PICS, TGA, MHRA, USFDA, and other global agencies . Develop, implement, and monitor Quality Management Systems (QMS) across all QA functions. Ensure strict adherence to SOPs and continuous improvement practices in line with regulatory expectations. Oversee handling of rejected materials, market complaints, product recalls, deviations, change controls, CAPA, and CCF . Manage end-to-end Validation and Qualification activities (process validation, cleaning validation, equipment qualification, analytical method validation, etc.). Ensure audit readi...

Job Overview TE Connectivity has Product Analysis & Value Engineering (PAVE) team located at Bangalore, India to support Industrial Solutions Segment business units for product tear down, benchmarking, should costing and value engineering capabilities. As part of the group, incumbent product engineer will be responsible to contribute to cost savings through hardware tear down, material characterization, manufacturing process evaluation, competitor product benchmarking, establish cost target, identify opportunities for cost savings & build value engineering project pipeline. Some of the products engineer will be responsible to support include Relays, Connectors, Sensors, Wire harness, contact...

Job Overview TE Connectivity has Product Analysis & Value Engineering (PAVE) team located at Bangalore, India to support Industrial Solutions Segment business units for product tear down, benchmarking, should costing and value engineering capabilities. As part of the group, incumbent product engineer will be responsible to contribute to cost savings through hardware tear down, material characterization, manufacturing process evaluation, competitor product benchmarking, establish cost target, identify opportunities for cost savings & build value engineering project pipeline. Some of the products engineer will be responsible to support include Relays, Connectors, Sensors, Wire harness, contact...

Date: 1 Sept 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Development Services Job Description Designation: Analyst Special Instrumentation and Method validation Job Location: Bangalore About Syngene At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and syst...