92 Solid Orals Jobs - Page 4

Role & responsibilities *Operate and maintain tablet compression machines, ensuring they run efficiently and produce tablets that meet quality standards. * Monitor the compression process to ensure tablets are produced according to specifications, conducting regular checks for weight, thickness, and hardness. * Identify and resolve any mechanical or process issues that arise during production to minimize downtime and maintain productivity. Preferred candidate profile ITI / Diploma or Graduate with 2-8 years of experience Perks and benefits Relocation allowance Travel allowance Initial accommodation Virtual Interview (Online Interview)

Job Title - Research Associate / Scientist (Formulations) Dosage Forms : Oral Solids Oral Liquids Markets Handled : Regulated, India / ROW Job Location - Kandivali, Mumbai Job Requirements - M Pharm candidate having minimum 3 years experience in formulation research for Regulated / ROW market Job Responsibilities - Literature, Pharmacopeial and patent search, review, discussion and documentation. Application for NOC, test license, import license, mfg license. To raise indent and coordinate for APl, RM, PM and tooling. Execution of pre-formulation and trial batches for formulation development. Design of experiments and optimize the formulation development Preparation and management of stability batches. Apply for licenses to concerned authority for manufacturing, Pilot BE batches and importing of reference product. initiate activities such as generation of item code, product code, product clearance and indenting innovator samples. Preparation of new SOP's and JSA and revision of existing SOP's. Preparation of MMD,BOM,EPO and coordinating with documentation officer. Coordination with other departments such as AD, RA, QA, Production QC, Purchase and Location for smooth execution of products.

Role & responsibilities Analytical Development Laboratory (ADL) Position: Executive Experience: 03-08 Years Qualification: M.Pharm / M.Sc Job/ Skill Set HPLC/GC/IC method development, feasibility, verification, equivalency, validation for API, complex OSD products, oncology products, topical products having exposure to regulated, Semi Regulated & India markets Comparative evaluation of methods with alternative vendor methods versus existing primary vendor and regulatory impact analysis Dissolution development, comparative dissolution, multimedia dissolution and statistical evaluation and report preparation Good understanding and hands on experience of analytical instruments like HPLC,IC, GC etc. NI/GI & NDSRI with LCMS/GCMS expertise, Solid state characterization and API sameness study Hands on experience on in-vitro Studies, E&L, Solid State characterization, IVPT/IVRT, Impurity characterization, sameness study Welversed with USP/EP/BP/IP and various current regulatory guidelines (ICH/EMEAVFDA) Pertorm maintenance and calibration of lab instruments / equipment Contact Details: Email : nitinsingh@torrentpharma.com, devalmodi@torrentpharma.com, vilshashah@torrentpharma.com

Job Title: Research Scientist - P.HD (Formulation-OSD) Location: Dholka (Ahmedabad) Experience: 2-3 Education: M.Pharm + P.HD Job Description To develop Stable & Bioequivalent for solid oral products for Europe, ROW & Domestic Markets. Technology transfer of developed products to plant level, this includes all TTD-related works. To collect and compile all data and submit to respective regulatory agencies. To address DCGI/ regulatory agency queries as per requirement. To extend support to plant for any commercial trouble shooting. Interested candidate can share there CV on disha.bhalani@cadilapharma.com

1. Good Documentation Practices, Compliance for Standard Operating Procedures, Quality Management Systems shall be followed. 2. Review and understanding of product related technicalities for smooth transfer of products to Internal Manufacturing facility of Strides or External Facility. 3. Co-ordination and collection of technical documents from internal sites. 4. Review of Tech pack documents and sharing (MFR, MPR, Spec/STP, BMR, BPR, Tool drawings layouts etc.) to Internal or external manufacturing sites. 5. Review of Master documents before initiating validation batches at Internal or external manufacturing sites. 6. Handling of Investigation related to OOS/OOT/Deviation occurred/reported for New Products and Site Transfer Projects. 7. Conducting/Monitoring of Feasibility trials/ Scale up trials at R&D or Manufacturing site. 8. To be involved in cost improvement program for identified product, to change the formula and improvise the process as required. 9. Handling of Product Robustness Projects and related activities like conducting the trials at R&D, Execution and Monitoring of Optimization batches and Registration/Commercial batches for PR projects. 10. Handling of Trouble shooting to improve the product quality attributes. 11. Review of APQR, RCI, CAPAs, PDR and other related documents. 12. Handling of QMS events (CC/Deviations) in Trackwise. 13. Ensure Test license availability at R&D & Plant. 14. Ensuring Toolings and RMs availability for execution of lab trial batches, PO/PE/Scale up batches and monitoring the batches during execution. 15. Preparation and Review of Trial Reports, and Investigational Summary Reports. 16. Preparation and Review of Documents i.e. MFRs, BMRs, BPRs, Protocols/Reports, QRM for Trial/Feasibility, PO and New Products, various batch sizes and subsequent revisions of all kinds. 17. Review & Approval of PVP & PVR. 18. Preparation and review of stability protocol for experimental batches. 19. Initiation/approval of the test request for the analysis. 20. Process optimization activities for internal/external products as identified and assigned. 21. GMP, GDP, Quality Management systems and SOP shall be followed to ensure the continuous compliance.

Dear All, We are seeking a highly motivated and talented Formulation R&D Scientist to join our innovative team. The ideal candidate will have a strong foundation in formulation development and you will play a crucial role in developing new and improved formulations, ensuring product quality, and meeting regulatory requirements. Location: Hyderabad(Dulapally) Required Experience: 6-8 Years Job Responsibilities: 1. Plan and execute Pre-formulation and formulation activities and ensure the timely execution of project related tasks in coordination with team members. 2. Actively participate in the literature search and preparation of formulation development strategy. 3. Coordinate with QA department for getting forms and logbooks 4. Follow good laboratory practices, good documentation practices (online LNB writing) and maintain the logbooks and forms for equipment/instruments 5. Coordination and participation of internal department audits / sponsor or client audits 6. Coordination with purchase/sourcing department for procurement of materials 7. Participation in qualification of equipments/instrument pertaining to the department 8. Compilation, interpretation and review of analytical results and stability data 9. Submission of documents and coordination with liaison personnel for procuring required licenses for carrying out the development work 10. To initiate the project and allot the product identification codes 11. Preparation of Master formula card (MFC), scale up BMR, process evaluation plan, exhibit batch protocols, stability protocol, Dissolution profiling report, Assessment report, Tablet sub division study summary report and all documents related to Formulation development. 12. To drive all concerned documents from formulation development to exhibit batches and then to commercialization through document management system. 13. Coordinate to prepare the specifications for raw materials, in-process and finished product. 14. Preparation of product development reports (PDR) 15. Preparation of summary reports for exhibit and process evaluation batches. 16. Initiation of Change controls. 17. Initiation of document/ mandatory revision/withdrawal control form. 18. Initiation of departmental incidents. 19. Conducting departmental trainings. 20. Calibration of instrument/equipment pertaining to the department. 21. Preparation and processing of department SOPs/Guidelines/Operating instructions. 22. Preparation of summary reports for exhibit and process evaluation batches Note: Interested candidates can share their resumes to raghuveera.vutla@aizant.com and Immediate joiners are more preferable

Cross-Functional Collaboration: Collaborate with R&D, manufacturing, and marketing teams to integrate regulatory considerations into the product development and commercialization processes. Regulatory Submissions: Oversee the preparation and submission of all necessary regulatory new dossier filings, and variations, to relevant health authorities in the targeted regions. Market Intelligence: Monitor and analyze evolving regulatory landscapes and market trends to proactively identify opportunities and challenges. Stakeholder Engagement: Build and maintain strong relationships with regulatory agencies, industry associations, and key stakeholders to facilitate smooth regulatory processes. Team Leadership: Lead and mentor a diverse team of regulatory professionals, promoting a culture of excellence, compliance, and continuous improvement. Compliance Oversight: Ensure all regulatory activities adhere to internal policies and external regulations, managing audits and inspections effectively.

-We are looking out candidates for different sections and positions in Quality Assurance department. Such as IPQA, QMS, Lab QA, AMV QA. Interested candidates can share their resumes on a.salunkhe@v-ensure.com & n32admin@v-ensure.com Role & responsibilities 1) IPQA - In process Checks. - Line clearance - Review of BMR, BPR 2) QMS - Handling and review of Change control, deviations, CAPA of different departments. - Document issuance, archival, retrieval. - Facing the Audits. 3) Lab QA & AMV QA - Managing Analytical QA activities. - Review of documents related to QC i.e. Raw material, finished products, stability. - Review of documents of Method validation, Assay. Preferred candidate profile - Candidates must have experience in Pharma formulation plant. - Must have good communication skills. - Candidates from Regulatory plant will be given preference. - Immediate joiners will be preferred. Perks and benefits Best in the industry

Role & responsibilities Should have an experience of minimum 20 years from a reputed pharma industry and out of that at least in one organization is biologicals/Biosimilars/Monoclonal antibody Manufacturing facility . Should have experience in handling Fermenters/Bioreactors, all utilities related to Biological production, Drug Substance and Drug Product, Validations and related documentation. Should have experience in Break down maintenance and Preventive maintenance of all equipment. Should have experience in handling all Statutory audits.

Job Area: Engineering Group, Engineering Group > Systems Engineering General Summary: About The Role :Qualcomm is the largest fabless design company in the world. Qualcomm provides hardware, software and related services to nearly every mobile device maker and operator in the global wireless marketplace. Our chipsets power a variety of products; tablets, smartphones, e-readers and other devices, and our digital design team is at the core of all of them. Depending on your technical area, you will be responsible for becoming a subject matter expert and go-to person for other members of your team. The environment is fast-paced and requires cross-functional interaction on a daily basis so good communication, planning and execution skills are a must. Qualcomm's Adreno Graphics Research Team is responsible for research, prototyping, profiling, analysis and optimization of emerging 3D Computer Graphics algorithms such as Ray Tracing, Mesh Shading, NERFs and Gaussian Splatting. The team works at the intersection of Computer Graphics and GPU architecture, identifying architectural inefficiencies in existing Adreno GPU hardware (HW) and proposing next-generation GPU HW architectural improvements. Position Overview:- Develop, analyze and optimize emerging graphics workloads.- Build functional models and microbenchmarks to obtain a deeper understanding of underlying GPU HW and make recommendations based on analysis.- Identifying and quantifying performance bottlenecks and resolving the same through either HW or SW (e.g. GPU Compiler or Driver) optimizations.- Work closely with HW Architects to develop new features to define Next Gen GPU Architecture.- Contribute to Adreno GPU intellectual property (IP) advancement, for example, by publishing research articles and blogs- Explore emerging algorithms in 3D Graphics domain including literature survey, competitive analysis, research on short comings and propose new changes that benefit Adreno GPU's performance, power and/or functionality. Minimum Qualifications: Bachelor's degree in Engineering, Information Systems, Computer Science, or related field and 4+ years of Systems Engineering or related work experience. OR Master's degree in Engineering, Information Systems, Computer Science, or related field and 3+ years of Systems Engineering or related work experience. OR PhD in Engineering, Information Systems, Computer Science, or related field and 2+ years of Systems Engineering or related work experience. Minimum Qualifications - Bachelor's or higher degree in Computer Engineering, Computer Science, Electrical Engineering, or related field. 12+ years Systems Engineering or related work experience Preferred Qualifications:- Master's or higher degree in Computer Engineering or Computer Science. 7+ years of relevant GPU System Engineering or Research experience. Applicants :Qualcomm is an equal opportunity employer. If you are an individual with a disability and need an accommodation during the application/hiring process, rest assured that Qualcomm is committed to providing an accessible process. You may e-mail disability-accomodations@qualcomm.com or call Qualcomm's toll-free number found here. Upon request, Qualcomm will provide reasonable accommodations to support individuals with disabilities to be able participate in the hiring process. Qualcomm is also committed to making our workplace accessible for individuals with disabilities. (Keep in mind that this email address is used to provide reasonable accommodations for individuals with disabilities. We will not respond here to requests for updates on applications or resume inquiries). Qualcomm expects its employees to abide by all applicable policies and procedures, including but not limited to security and other requirements regarding protection of Company confidential information and other confidential and/or proprietary information, to the extent those requirements are permissible under applicable law. To all Staffing and Recruiting Agencies :Our Careers Site is only for individuals seeking a job at Qualcomm. Staffing and recruiting agencies and individuals being represented by an agency are not authorized to use this site or to submit profiles, applications or resumes, and any such submissions will be considered unsolicited. Qualcomm does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to our jobs alias, Qualcomm employees or any other company location. Qualcomm is not responsible for any fees related to unsolicited resumes/applications. If you would like more information about this role, please contact Qualcomm Careers.

Roles and Responsibilities Conduct pilot plant scale up activities to commercialize new products. Ensure successful transfer of technologies from lab to production scale. Develop formulations for solid oral products using OSD technology. Troubleshoot issues related to formulation development and scaling up. Collaborate with cross-functional teams for tech transfer projects.

Role & responsibilities Relevant Experience : Should have experience of Production for Formulation Plant of Oral Solids (Tablets, granules, powder) & Allied in PHARMACEUTICAL COMPANY / FACTORY. FDA Approval in Tablet Section Pharma Formulation plant would be preferred. 1. Batch Manufacturing Manufacture production batches as per Batch Manufacturing Record (BMR) and Batch Production Record (BPR). 2. BMR/BPR Documentation Complete the online BMR and BPR as per the respective activities. 3. Coordination with QA Coordinate with the Quality Assurance (QA) department for the issuance of monthly formats. 4. Manufacturing Parameters Review Review parameters during manufacturing stages such as compression, filling, and packing for oral dosage products. 5. SOPs and Documentation Prepare, update, and maintain Standard Operating Procedures (SOPs), BMR, and BPR documents. 6. Document Maintenance Ensure proper maintenance of documents, including BMR, BPR, cleaning records, calibration logs, environmental records, and equipment usage logbooks. 7. Manpower Allocation Allocate and manage manpower for the effective utilization of resources. 8. Production and Packing Oversight Oversee and manage the overall manufacturing and packing activities in the oral department. 9. Compliance with cGMP & GDP Monitor and implement Current Good Manufacturing Practices (cGMP) and Good Distribution Practices (GDP) within the department. 10. Quality Management System: Handle the Quality Management System (QMS), including initiating, investigating, and completing change control, deviations, and incidents. 11. Equipment & Area Qualification: Monitor and review equipment and area qualification activities and ensure timely reporting. 12. Validation Activities Coordinate with QA and QC departments for product process validation and cleaning validation activities. 13. Production Target Achievement Ensure daily and monthly production output targets are achieved. 14. Cross-Department Coordination Facilitate coordination between Quality Assurance, Quality Control, Warehouse, and Engineering departments. 15. Material Availability Check Ensure availability of required raw materials (RM) and packaging materials (PM) as per the production plan and schedule. 16. Training & Development Conduct training programs on SOPs, GMP, technical procedures, and identify training needs for department personnel. 17. BMR/BPR Handover to QA Ensure completed BMR and BPR are handed over to the QA department before dispatch activities. Required Candidate profile: 1. 07-10 years of experience in Formulation Pharmaceutical Plant. 2. Relevant Experience in Pharma formulation plant. 3. Computer proficiency in MS Office, Excel, e-mail and internet functions, ERP

Your Responsibilities The job responsibilities include: • Formulation development for Oral Care including new chassis and actives. • Design and reporting of formulation and stability studies. • Use of statistics and digital tools for smart decision making • Summarizing and presenting formulation development work and insights to local and global Oral Care teams. • Contributing personal expertise and skills to building a wider community of Oral Care Global R&D formulators. • Maintaining an up to date understanding of UL and competitor technologies. • Designing and delivering data to enable IP filings. • Monitoring consumer feedback on product launches • Working closely with global CTI & CMI to pick up market insights • Providing support to manufacturing sites for issues related to product & process and carrying out main plant trials • Working on competitor intelligence About You • Have scientific and technical curiosity with a willingness to learn new technical skills. • Good listening and communication skills with stakeholders, peers, and team members • Ability to work to deadlines, planning and managing own time. • Team working across functions and geographies. • Agile and resilient - able to be flexible in meeting team needs. The candidate will have demonstrated: • Excellent understanding of the innovation process and roles and responsibilities Formulator • Experience of applying physical and chemical science knowledge to develop new products and/or measurements. • Ability to design, record and report their own experiments. • Very preferably, experience in use of digital tools and basic statistics in product development. • Ability to working with globally located cross functional teams. • Ability to create concise communications to a wide range of stakeholders and team members. Qualifications & Experience: • Candidate should hold an MSc (Chemistry), B.E. (Chemical Engineering), BPharm/M Pharm degree (or similar qualifications in a closely related subject). • R&D experience part of which should preferably be as a formulator or process scientist. • Preferably, experience in use of digital tools, experimental design and basic statistics • Experience in formulation development in personal care, preferably oral care • Experience in working across sites and geographies. • Fluent written and spoken English.

Job Title Payments - GPP Responsibilities Global Pay Plus Testers. MT MX messaging , SWIFT payments Preferred Skills: Banking->GPP Financial Services Domain->Payments->GPP Generic Skills: Banking Educational Requirements Bachelor of Engineering Service Line Infosys Quality Engineering * Location of posting is subject to business requirements

Job Title Payments - GPP Responsibilities Global Pay Plus - Payments Technical and Professional Requirements: Payments:ISO-20022 standards SWIFT, SEPA, MT messages Preferred Skills: Banking->GPP Financial Services Domain->Payments->GPP Generic Skills: Banking Educational Requirements Bachelor of Engineering Service Line Infosys Quality Engineering * Location of posting is subject to business requirements

Job Title - Platforms Senior Manager Level- Senior Manager- S&C GN-CFO&EV Management Level:06 Senior Manager Location:Gurgaon, Mumbai, Bangalore, Pune, Hyderabad Must have skills:SAP FICO Implementation Good to have skills:Generic FICO, PS+Investment mgt, DRC, FSCM, CO, VIM+FI, OCR, Functional MDG, AFC/FCC, SAP ICMR, Intercompany, SAP CFIN Experience:15-18 years Educational Qualification:MBA(Finance) or CA or CMA Job Summary : Have been part of at least 6 end to end SAP implementations. Out of which 3+ in S4 Understand the SAP roadmap for S/4 HANA and become a trusted advisor for clients in driving their S/4 HANA adoption. Have experience in defining a Business Case for S4 Transformation and RoI calculations. Have worked in the capacity of Solution Architect / Design Authority in Past and have done lot of advisory work for ERP's for e.g. Product selection, Value realization, Fit Gap Assessment etc. Work closely with clients to understand their issues, define IT strategies, architecture solutions, win buy-in for your recommendations. Drive sales pipeline and independently own proposals related to Finance / Multi-function S/4 HANA engagements. Lead and transform the consulting industry by developing some key Assets and Accelerators which can help Clients in their digital transformation journey. Provide direction for complex SAP S/4 HANA issues, and can collaborate with the business and developers and execute on agreed timelines. Provide consulting solutions including how to leverage standard SAP S/4 HANA functionality and how to enable requirements while maximizing the ROI Lead intelligent conversations to guide clients through best-practice project scoping and delivery to ensure overall project success in implementing SAP S/4 HANA Have ability to manage project execution and manage client conversations during assessment, design, implementation, and status reporting Lead the problem solution design and implementation ensuring high quality adhering to the timelines and defined budget Supervision of Accenture Managers, Senior and Junior analysts and consultants and client personnel to drive delivery outcomes. Roles & Responsibilities: Should know how to lead and deliver S/4 HANA engagements across different implementation approaches including excellent understanding of client business processes, pain points, S/4 HANA solution options and organization structure Should know how to drive and build sales pipeline including BDs and Proposals Should be aware of digital finance technologies that drives business processes Should know how to lead business case creation for SAP design to implementation projects Drive continuous improvement capability with regards to methodology, tools, practices and maturity Professional & Technical Skills: MBA from a Tier-1 or Tier-2 B-school. CA or CPA Deep knowledge and experience in Finance and Controlling Org structure and design, S/4 HANA Implementation and rollout point of views, approach and design principles, roadmap, and business case definition. Ability to drive large scale digital finance transformation initiatives during the entire life cycle of the project. 15+ years' experience in SAP S/4 HANA design to implementation projects At least 8+ years of consulting experience in a big4 or similar firms Extensive experience in GTM/Presales and writing proposals. Programme management experience and track record of successful (on-time & on-budget) delivery of large, complex programs in a dynamic environment with numerous and complex stakeholders' groups Active role in the identification of opportunities by farming existing relationships and growing new networks. Ability to work independently with minimal supervision and lead global distributed teams Additional Information: An opportunity to work on transformative projects with key G2000 clients Potential to Co-create with leaders in strategy, industry experts, enterprise function practitioners and, business intelligence professionals to shape and recommend innovative solutions that leverage emerging technologies. Ability to embed responsible business into everything"from how you service your clients to how you operate as a responsible professional. Personalized training modules to develop your strategy & consulting acumen to grow your skills, industry knowledge and capabilities Opportunity to thrive in a that is committed to accelerate equality for all. Engage in boundaryless collaboration across the entire organization. Qualifications Experience:15-18 years Educational Qualification:MBA(Finance) or CA or CMA

- Carry out Formulation and R&D efforts for nutraceutical products - New Product Development across all Oral Solid Dosage Formats (powders, capsules, tablets, gummies, chewables etc) - Preparing NPD documents viz. Technical Dossiers, SOI etc