42 Tga Jobs

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...

Required Skills and Qualifications: Collect and maintain hashtag#structureddata from global hashtag#regulatoryauthorities (e.g., hashtag#EMA , hashtag#FDA , hashtag#TGA ), hashtag#HTA agencies (e.g., hashtag#NICE , hashtag#HAS , hashtag#CADTH ) and pricing bodies (e.g., hashtag#DMD , hashtag#CODAGE , hashtag#PBS ) • Masters degree in hashtag#pharmacy . • Strong interest or foundational knowledge in hashtag#pharmaceuticaldrug development, hashtag#regulatory affairs, or hashtag#clinical trials. • Excellent attention to detail and ability to work with hashtag#structured data sets . • Proficiency in using hashtag#MS Excel , hashtag#Word , and hashtag#basic data tools.

Required Skills and Qualifications: Collect and maintain hashtag#structureddata from global hashtag#regulatoryauthorities (e.g., hashtag#EMA , hashtag#FDA , hashtag#TGA ), hashtag#HTA agencies (e.g., hashtag#NICE , hashtag#HAS , hashtag#CADTH ) and pricing bodies (e.g., hashtag#DMD , hashtag#CODAGE , hashtag#PBS ) • Masters degree in hashtag#pharmacy . • Strong interest or foundational knowledge in hashtag#pharmaceuticaldrug development, hashtag#regulatory affairs, or hashtag#clinical trials. • Excellent attention to detail and ability to work with hashtag#structured data sets . • Proficiency in using hashtag#MS Excel , hashtag#Word , and hashtag#basic data tools.

Skill Required Roles and Responsibilites 1. Media fill and qualification summary preparation knowledge. 2. To maintain track of qualification and validation activities. 3. To prepare and review the protocols and reports. Execution of various qualification / validation activities. 4. To review correctness of the technical documents received from the supplier (DQ/OQ/IQ/PQ,FAT). 5. Co-ordinate with production and other user department for qualification/validation activities 6. Timely compile and review of qualification validation reports. 7. To review the equipment documents like calibration reports and ensure correctness of documents. 8. To perform FAT. 9. To co-ordinate with outside agencies ...

As an Account Manager at Waters, you will play a crucial role in supporting the successful growth of the business across South India (Karnataka, Tamil Nadu & Kerala). Waters, the world's leading specialty measurement company, values inclusion and diversity, and is dedicated to delivering innovation and customer success in the life, materials, and food sciences. By engaging with the talented and diverse workforce, you will contribute to evolving and improving products to meet customer needs. Your responsibilities will include addressing new and existing customers in diverse markets such as Polymer, Composites, Chemical materials, Food, Environmental, Clinical, and Academia. You will maintain ...

Walk In Drive For Quality Control In Formulation Division @ MSN Formulation Unit -II , Kothur . Department :- Quality Control Formulations Experience:- 2 to 8 Years Skills :- Formulation QC - HPLC | GC | GC MS | LIMS | LCMS | ICPMS | Dissolution | IP/FP | Stability | Method Validation | Method Development | Method Transfer | E&L | | Proficiency with Equipment | Method Development & Optimization | Understanding of Regulations | Data Analysis | Testing and Inspection | Process Improvement | Regulatory Compliance | Equipment Maintenance | Training and Support | Root-cause analysis | Method development and validation | (OSD & Injectables) | USFDA | Regulatory Approvals Division :- Formulation In...

Experienced QA person managing multiple projects involving implementation. Ensuring set norms & laws are met. Excellent knowledge of QA processes of risk management, clinical data management, electronic data management.

About The Role o Responsible for personal discussion of cases as per the laid down policies & procedures and maintain strict adherence to quality. o Adhere to agreed SLAs and timelines in completing the activities assigned. o A skill set of underwriting, disbursements, collateral, coordination with cross function sales operation function o Responsible for protecting company assets through proper evaluation of all credit requests, establishing credit limits and ensuring that all loans granted are adequately documented and secured by the appropriate collateral o Ensure proper communication of credit decisions to Stakeholders. o Responsible for improving underwriting efficiencies while ensuring...

You will be joining a leading innovation-driven organization in India, known for its advanced solutions in paints, adhesives, and construction chemicals. This company is currently enhancing its research and development capabilities and is in search of an experienced specialist to take charge of product development and scale-up initiatives. Your main responsibilities will include leading the research and development of water-based acrylic emulsions for various applications, designing and optimizing polymerization processes for new product formulations, overseeing the synthesis and scale-up of polymers for paints, adhesives, and construction chemicals, collaborating with cross-functional teams...

You will be the NPQ Lead for Metallurgy & Metrology at Ather, based in IBC, Bangalore. Aligned with the Lead of New Product Quality, you will be a member of the New Product Quality team. Your primary responsibilities will include establishing Metrology and Metallurgy labs, leading and managing the labs to ensure faster and accurate test data, and developing measurement methods for components. You will be responsible for approving material, process, heat treatment of parts, and surface modification techniques based on application requirements. Additionally, you will work on application engineering of parts, ensuring the right selection of materials and processes without compromising on fit, f...

Role & responsibilities Preferred candidate profile

You are a highly motivated and technically skilled Manager/Assistant Manager Sales & Marketing for the Plastic Department in Gurgaon. With over 14 years of experience in polymer technology, automotive plastics, business development, and technical marketing, you will be responsible for managing key OEM and Tier 1 accounts, driving market expansion, and ensuring customer satisfaction through technical expertise and strategic sales initiatives. Your key responsibilities will include developing and implementing sales strategies to expand market share in automotive and non-automotive plastics, identifying new business opportunities, and acquiring key OEM and Tier 1 accounts. You will conduct mark...

Requirement Experience in API Regulatory Affairs Routine job skill: Good conceptual, analytical, problem solving, reasoning and organizational skills. Should be change agile and have ability to work in highly matrixed environment. Attention to detail and accuracy required. Must be able to prioritize with independently/minimal guidance. Ability to handle multiple projects with good prioritization skills. Willingness to complete the work as per the committed timeline. Technical Skills: Sound understanding of drug development regulatory processes and requirements for defined market(s) and able to interpret and apply to projects. Ability to identify inconsistencies and deficiencies in technical ...

Department Commercial Banking- MFI business - Risk Location Mumbai Kotak Infinity/ Bengaluru/ Lucknow Reporting Relationships Vice President Number of Positions 5 Position Grade M3/M4 Control Assessment for Branches and HO for MFI business for JLG, Micro LAP and Individual Loan. Responsible for assessing fraud/ operational and financial risks in Tier II, III cities , District/ Tehsil level( MFI branches) Responsible for assessing regulatory and internal policies and process adherence at MFI branches. Responsible for co-ordination with other support & control functions and business team. Responsible for managing MIS/Risk Analysis/Fraud Analysis/improvement/Operational Loss reduction Job Requi...

Role & responsibilities Develop and implement regulatory strategies to support research projects and product development initiatives. Monitor and interpret regulatory requirements and guidelines related to scientific research, including USFDA, Europe (EMA), UKMHRA, Canada (Health Canada), Brazil (ANVISA), China (NMPA), Australia (TGA), New Zealand (MMDSA) Japan (PMDA) and other relevant international standards. Prepare and submit regulatory filing agency queries with gap analysis, including API DMFs, eCTD details, and other relevant documents, ensuring accuracy and compliance with regulatory requirements. Collaborate with cross-functional teams to integrate regulatory considerations into pro...

The candidate should be M.Sc. (Preferably Microbiology) / M.Pharm/Quality Assurance) with at least 10 /12 years of relevant experience in medical devices industry. IPQA, QMS, Validation, compliance , QA related to its processes and strategy.

Position: Site Head (Sr. Manager) - Production Location: Ranjangaon, Near Pune Reporting To: Head - Manufacturing Operations Industry: Pharmaceutical Manufacturing Experience: 15+ years in Plant leadership roles, preferably in pharmaceutical or manufacturing industries About Fresenius Kabi At Fresenius Kabi, we are driven by a commitment to improve the quality of lives: We are Committed to life. We strive for continuous innovation with our outstanding manufacturing capabilities, unique channel access, and customer proximity. With our four complementary business areas BioPharma, Pharma (primarily IV drugs and infusion therapy), Medical Nutrition, and MedTech; Fresenius Kabi plays a vital role...

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile and Allergy Therapy Products, and Generics Solid Dosage Formulations. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma which is subsidiary to Jubilant Pharmova Limited. Jubilant Generics have 2 manufacturing sited at Roorkee, Uttarakhand and Salisbury, Maryland, USA engaged in manufacturing of Tablets and Capsules. The m...

As a System Sales Account Manager (TA INSTRUMENTS) at Waters, you will play a crucial role in supporting the successful growth of the business across (INDIA EAST). Waters, the world's leading specialty measurement company, values inclusion and diversity and focuses on delivering innovation and customer success in the life, materials, and food sciences. By engaging with our talented and diverse workforce, we continuously evolve and improve our products to meet the needs of our valued customers. Your responsibilities will include preparing business plans, territory plans, reports, tender documents, and relevant product solution documents for customers. You will collaborate with demo lab specia...

Dear All, We are looking for an experienced and highly motivated Material characterization Scientist to join our team. In this role, you will be responsible for the development, validation, and review of material characterization techniques, including X-ray Diffraction (XRD), Polarized Light Microscopy (PLM), Inductively Coupled Plasma Mass Spectrometry (ICP-MS), Atomic Absorption Spectroscopy (AAS), Surface Area Analyzer, Rheometer, Differential Scanning Calorimetry (DSC), Thermogravimetric Analysis (TGA), Ion Chromatography (IC), Particle Size Distribution(PSD) and Gas chromatography mass spectrometry (GC-MS/MS). You will play a key role in advancing the capabilities of these techniques, e...