595 Technology Transfer Jobs - Page 4

Dr. Reddys is looking for Manufacturing Scientists or senior scientists specialized in cell therapy (CAR-T) programs to join their Manufacturing facility team. As a Manufacturing Scientist, you will collaborate with Research and Product Development teams to support GMP Manufacturing operations, Technology transfer, quality assessments, and process validation of the CAR-T process for various Cell therapy programs. Your responsibilities will include designing and executing experiments to develop robust manufacturing processes for cell therapy products, leading and training a team of cell process scientists/engineers, managing T-cell culture and differentiation, documenting experimental procedures and results, supporting the development of SOPs and batch records, and reviewing production batch records for deviations and investigations. You will also be responsible for communicating progress, identifying critical issues affecting supply and timelines, collaborating within departmental teams, contributing to deliverables, serving as a technical subject matter expert for technology transfers, and aligning with leadership to develop a strategic roadmap on continuous medium optimization. To qualify for this role, you should have a PhD/MSc/BSc in biotechnology, biology, immunology, Cell Biology, or a related life-science discipline, along with 5-12 years of industry experience in Cell and gene therapy, biologics manufacturing, or product development functions. Experience in aseptic processing, cell culture, automated equipment, T-cell culture processes, GMP requirements, and DOE is required. Strong organizational, communication, and decision-making skills are essential to succeed in this role. If you are a dynamic individual who can work in a fast-paced environment, collaborate effectively with teams, and drive successful outcomes in manufacturing processes, this position offers an exciting opportunity to contribute to cutting-edge cell therapy programs at Dr. Reddys.,

Exciting Opportunity for Research associate - Alternate Vendor Development in Formulation & Development(PDR) We are looking for a skilled professional with 3-5 years of experience in alternate vendor development for diverse markets like US, EU, ROW, Domestic, WHO. Key Requirements: - B.Pharm/M.Pharm qualification - 3-5 years of relevant experience - Familiarity with various market guidelines - Expertise in technology transfer - Exposure to shopfloor operations is advantageous - Worked in R&D Department /Formulation Department Planning and execution of Alternate Vendor batches for product development

Assist in formulation development of Solid Oral Dosage form. Perform literature & patent search, pre-formulation studies, documentation, data compilation & ensure SOP/GMP compliance for global market products. Required Candidate profile Execution of process evaluation, optimization,scale-up and exhibit batches/Meeting product development timelines/literature survey/ICH guidelines/Solid Oral- Share CV- stuti.naik@enaltec.com

Responsible for managing formulation development of Solid Oral dosage forms for global markets. Oversees pre-formulation, patent search, documentation, compliance, and team guidance as per regulatory standards. Required Candidate profile Pharma professional with 7–10 years in formulation development, strong regulatory knowledge, documentation, data analysis & proven team leadership skills. Share CV- stuti.naik@enaltec.com

Overview Leading seasoning development across multiple snack brands and products for the PepsiCo India region. The role includes flavor ideation, seasoning development or reformulation, ecosystem partnerships with flavor and ingredient houses, seasoning scale up and seasoning qualification. Responsibilities Lead innovations and seasoning reformulation to drive human sustainability, Productivity, Competitive Advantage for brand Kurkure and Premium Support Chef and culinary engagements to build a future pipeline Collaborate/Partner with Internal (PD, Marketing, Consumer insights, Sensory and consumer product insights, Quality etc.) and external stakeholders (Seasoning suppliers) to leverage their tools/expertise and deliver business targets against the briefs. Support creation, update and approvals of specifications through online tools Support the Internal project governance process Risk Management: Identify potential technical risks associated with future strategies and develop mitigation plans Collaborate with Nutrition and Regulatory functions and accurately implement guardrails and targets in advance of project delivery. Display an advanced level of understanding in these areas Rigorously implementing basic Project management and seasoning functionality tools during development process Qualifications Masters of Food Science/Food technology preferred. Project management with 5-7 Years experience in product development and/or seasoning development activities, processes, and systems . Good understanding on sensory evaluation processes, sensory discernment and capable to share constructive feedback on product/Flavor attributes.

Key Responsibilities: Handle end to end scale up activities from Lab to Pilot to Commercial Scale . Absorb the process from the PELAB / R & D and study the same and come out with queries considering the plant constraints and ask to modify the same if not feasible in the Plant. To observe the lab demo batches in PE Lab / R & D and identify Critical requirements of the process and provide the same. To select the equipment's for scale up & discuss with R & D and Production and finalize it. To act as a tool between Production, QC, QA with R & D / PELAB to absorb the technology from Lab to Plant. To observe the initial scale up batches critically & debottleneck the problems faced in the Plant. To have a complete Material, energy balance & Effluent data for the scale up batch to have the complete information about the process. To prepare Dos & donts for the process and give it to Production for regular batches. To conduct HAZOP study and implement the suggestions. To Review the Batch Process Record and Sampling Plan prepared by Production To prepare the PFD, checklist for Documents submitted &To assist QA in preparing Validation protocol. To Plan for DMF validation batches in Plant and ensure that CGMP compliance is adhered while doing the DMF validation batches. To check the ML or aqueous layer for product carry over and try to recover the same by extraction or by distillation techniques. To ensure that Safety system is in position or intact in the Plant. To impart training to Shift in charges, Chemists & subordinates about the process criticality and how to keep them in control especially in case of exothermic reactions. To design system for emergency venting and emergency handling. Key Competencies (Technical, Functional & Behavioral) Excellent verbal and written communication, persuasiveness, inter-personal skills, adaptability, foresight, understanding of business processes.

Job Title: Dy Manager Technology Transfer Location : Mumbai Location Industry: Pharma Industry Experience: Minimum 2 years . Division: API Key Role & Responsibilities: Able to scale up technology from R&D to Kilo scale/ pilot scale/ commercial scale Coordination with R&D team for generating negative study data, concluding to optimize process parameters Observe R&D demo batches & preparation of demo batches report Identify & propose ideas/ technology to improve process efficiency, effective utilization for unit process & operations Preparation of BFD, PFD, P&ID, mass balance, energy balance sheets Skills: Technology Transfer, Process, Scale-up, optimization, validation, PFD, P&ID, BFD, troubleshooting, Process improvement, Technical services, debottlenecking, yield improvement, Data interpretation Kilo lab, Piloting, Equipment selection, mass balance, HAZOP study, MS-Office interested candidates can share cv to hr3@sarthee.com or call at 9033033650

As a part of this role, you will be responsible for overseeing the scale-up and technology transfer of pharmaceutical processes. Your primary focus will be on ensuring the successful transition of processes from the laboratory to full-scale production. This will involve collaborating with cross-functional teams to optimize processes, troubleshoot any issues that may arise during scale-up, and ensure that all activities are carried out in compliance with regulatory requirements. Additionally, you will play a key role in identifying opportunities for process improvements and implementing solutions to enhance efficiency and productivity. The successful candidate will have a strong background in pharmaceutical process development, excellent problem-solving skills, and the ability to work effectively in a fast-paced environment.,

As a Consultant in Intellectual Property & Technology Transfer within the Lifesciences sector, you will be responsible for reviewing and drafting research collaboration agreements, IP licensing agreements, and other partnership documents. Your role will involve assessing the techno-commercial merit of IPR and invention disclosures, as well as conducting technology licensing, technology evaluation, and identifying potential partners. Additionally, you will be creating collaterals/technology briefs for outreach and managing reach-out for transaction closure. Furthermore, you will be tasked with organizing IP and technology transfer related trainings and programs, along with conducting patent claims review and IP analytics. The ideal candidate for this role should hold a Life Science Graduate qualification with a Post Graduation in IPR being preferred. A minimum of 2 years of experience in technology transfer activities is required, along with excellent communication skills. Being a team player with a positive and sincere work attitude is also essential for success in this position. If you are passionate about technology transfer in the Lifesciences industry and possess the necessary educational background and experience, we encourage you to apply for this exciting opportunity based in Hyderabad.,

Job Purpose Culture Anchor:Work Hard - Consistently puts in effort. plans and tracks daily progress to achieve targetsExecute with Rigor - Takes responsibility for meeting targets with focus and effortOwn It - Maintains honesty and fairness in all interactions in line with organizations policiesAct with Integrity Duties and Responsibilities Implementation of Credit Policy and continuous evaluation to ensure adherence to the Policy and compliance with the Authority Matrix at branches in the area assigned.-Credit appraisal for BL & Doctor Loans files for the assigned location-Keeping delinquency under control-Compliance of policy and processes-Reporting of location metrics like Login, Approval, Disbursal, Rejection, Deviation on monthly basis as per prescribed format-Market Research and Feedback for new product launch.-Feed back on credit policy based on market conditions. Required Qualifications and Experience Chartered Accountant /MBA Finance with 2-3 years of relevant experience.

Hiring for Principal Scientist for a leading Pharma MNC at Pune. Role & responsibilities Reporting to : Associate Director Job Summary : To develop synthesis processes of highly potent and/or cytotoxic ADC drug-linkers and transfer processes to internal/external clients and collaborate with manufacturing teams to deliver robust chemical processes that are suitable for commercial-scale manufacturing, while ensuring safety and regulatory compliance. Key Responsibilities: 1. Detailed technical evaluation of project enquiries received from the customers/ BD team. 2. Literature search, scouting the appropriate routes, and Drug-linker process optimization. 3. Execution of Bioconjugation Chemistry in lab and GMP manufacturing on Lab scale. 4. Collaborating with synthetic/analytical chemists, bioconjugation scientists, biologics development team, engineers, PM, DQA, IPMG, BD, PE/TT, manufacturing units, and regulatory teams to develop and support the commercialization of ADCs. 5. Support for kilo lab batches and during commercial campaigns to achieve the QOTIF. 6. To help grow the ADC teams capabilities, research facilities, and enhance the ADC's portfolio. 7. Thorough drug-linker process development and support regulatory submissions, often with compressed timelines. 8. When appropriate, mentor, train, and supervise junior team members in this role. 9. Help drive internal facilities growth to support highly potent and/or cytotoxic material handling. 10. Manage multiple projects and/or material deliveries simultaneously. 11. Monitor and implement safety in the laboratory. 12. Troubleshoots technical challenges during scale-up & tech transfer, monitors schedules, and manages documentation in line with GMP guidelines. Preferred candidate profile Required Qualifications and Experience: MSc organic chemistry with 13+ years of relevant industrial experience in the process development/optimization of ADCs or PhD/post-doctorate in synthetic organic chemistry with experience in ADC drug-linkers. Key Competencies: Problem solving. Conflict resolution. Decision making. Communication skills. Leadership. Negotiation. Collaboration. Cross-functional collaboration. Technical Skills: Proficient in using MS Office. Knowledge of ADCs, Knowledge of High-potent API, Knowledge of working in GMP set-up, organic/process chemistry & safety API process development, tech transfer & manufacturing, proficient analytical skills for small as well as large molecules. to apply please share Resumes with Puja.k@maxisclinical.com Regards Puja

Job Overview: The PDL Scientist - Injectable will be responsible for the development, optimization, and scale-up of sterile injectable formulations and manufacturing processes. The role demands expertise in injectable formulation science, process engineering, and compliance with regulatory and quality standards. Role & responsibilities Formulation Development: Design and optimize sterile injectable formulations, including solutions, emulsions, and suspensions. Perform compatibility and stability studies of active pharmaceutical ingredients (APIs) with excipients. Process Optimization: Develop robust, scalable manufacturing processes for injectable formulations. Define and optimize critical process parameters (CPP) and quality attributes (CQA). Sterility Assurance: Establish aseptic processes and ensure compliance with sterility requirements. Perform filtration studies, autoclave cycle development, and validation. Analytical Support: Collaborate with the analytical team for the development and validation of testing methods. Conduct particle size analysis, pH, and osmolarity evaluations, and other critical tests. Regulatory Compliance and Documentation: Prepare technical reports, batch records, and regulatory submissions in compliance with GMP, ICH, and FDA guidelines. Support regulatory inspections and audits with comprehensive process documentation. Technology Transfer: Facilitate the transfer of processes from lab-scale to manufacturing-scale environments. Work closely with cross-functional teams, including production, quality assurance, and regulatory affairs. Preferred candidate profile 3 - 5 years of experience in injectable formulation and process development. Hands-on experience with lyophilization, sterilization techniques, and aseptic manufacturing processes. Strong knowledge of GMP, ICH, and regulatory guidelines. Proficiency in using laboratory equipment such as autoclaves, lyophilizes, and HPLC systems. Excellent technical writing and documentation skills.

Coordinate technology transfer activities for (OSD) formulations from R&D to manufacturing sites, Support scale-up, exhibit, and validation batches, participate in investigations, deviation handling, and change control activities.

Lead end-to-end tech transfer of OSD products from R&D to commercial manufacturing sites, conduct scale-up and process validation activities, and provide technical support during regulatory audits and inspections.

Role & responsibilities 1. Capacity Planning of New / Existing Products 2. Solvent Recovery improvements 3. Process monitoring for yield improvement & failure investigation. 4. Process monitoring, process data collection, trend data preparation and discussion with concern department. 5. New product technology absorption 6. Trouble Shooting of Equipments & Processes 7. Utility calculation for cost reduction & Energy Conservation. 8. Plant Equipment modification as per Process requirement. 9. PFD, P&ID & Plant Layout Preparation 10. Material & Energy balance calculations 11. Equipment specification data sheet preparation, Techno-commercial preparation for procurement. 12. Equipment sizing, selection & Design calculation. 13. Capex & OPEX preparation 14. Should take active participation in equipment qualification activities such as DQ, IQ & OQ

JOB DESCRIPTION: Pupose:Deliver formulations in defined timeframe to meet product delivery goals for I&D Development of different formulations either as generic or differentiated generics. To demonstrate successful stability and scale up at manufacturing site. Core Job Responsibilities . Development of formulation using scientific rationale in use of excipients to create a reproducible prototype formulation. . Ensure Proper documentation of every trial in the log note books and then using the information for creation of the Product Development Report for use in dossier for filing. . Use of QbD wherever required for Product and process optimization. . Ensure proper upkeep, maintenance and calibration of the equipment. . Ensure scale up of the developed formulation works at engineering batch level. Key Deliverables: . Literature/Patent search to create drug profile . Prototype development with rationale use of excipients . Preformulation study as may be required for formulation development . Conduct 6 months accelerated stability studies to ensure stable formulation . Proof of concept studies to demonstrate BE or comparative PK as the case may be . Scale up studies at 1/10th scale or engineering batch . Technology transfer and manufacturing of Bio/Clinical batch Job Title: Jr Research Scientist Formulation Job Function: Innovation & Development Location: Mumbai (Andheri MIDC) Reporting to:Sr Group Leader Formulation Critical Success Factors: Functional/ Technical: Functional / Technical: 1. Formulation and Product Development a. Schedule and follow all the steps to deliver the drug as per QTPP b. Select the suitable polymers / excipients based on either properties or scientific rationale c. Evaluation of CQA of drug / excipients and estimate its implications for product development d. Designs the process which is reproducible and scalable with higher yield, cost effective, and environment friendly 2. Design of Experiments a. Executes the experiments as per DOE to optimize product and process 3. Pharmaceutical Development Report (PDR) a. Prepares PDR as per Common Technical Document (CTD) module 3 requirements b. Complies with regulatory requirements as defined in QTPP 4. Project Management a. Is able to plan and prioritize multiple project deadlines to meet product delivery goals Education & experience: . M. Pharm/Ph. D. . 5 to 7 yrs The base pay for this position is N/A In specific locations, the pay range may vary from the range posted. JOB FAMILY: Product Development DIVISION: EPD Established Pharma LOCATION: India Mumbai : BKC Building ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Not specified MEDICAL SURVEILLANCE: Not Applicable SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

Vibonum Technologies Pvt Ltd (Althera Groups) is hiring Assistant or Deputy Manager - Technology Transfer Executive for its OSD Pharma manufaturing plant at Nanjangud, Mysore. Role & responsibilities Review of Technology data package and preparation of Gap analysis document. Preparation of technology transfer protocol and report. Co-ordination with FD for smooth Tech Transfer. Monitoring of validation batches at production site. Perform Feasibility trials, Product evaluation trials to understand critical process parameter for smooth transfer and process understanding. Review of MPCR and protocol. Planning for Execution of Process design, Process qualification batch. Coordination with Production, Quality assurance, Quality control, Engineering, Regulatory Affairs, SCM and warehouse for the TT activities. Should be part of handling deviation, change control and failure investigations. Process manufacturing parameters for Qualification batches Vs Commercial batches. Preparation and reviewing of intended batch documents for regulatory submission. Trouble shooting of existing products and process improvement to increase output or to reduce processing time or to improve the quality of products. Preferred candidate profile required from OSD pharmaceutical Executive - TT: Exp required: 08 to 12 years with M. Pharm Candidate should be willing to relocate/work in Nanjangud, Mysuru Plant. Benefits: Free canteen facility Free transport facility Medical Insurance All Statutory benefits etc.

Roles and Responsibilities Team lead for upstream for day to day planning and co ordination Develop processes for recombinant DNA technology, fermentation techniques, and product intermediate processing. Design and execute experiments to optimize process parameters for scale up and commercial production. Collaborate with cross-functional teams to transfer technologies from lab to pilot plant and manufacturing scale. Troubleshoot issues related to process development, optimization, and operation.

About The Role Job description Job title: Data, Personal Loan Location: Head Office Mumbai Grade M3 Number of Position 1 Job Responsibilities: Monitor portfolio delinquencies at micro level, identification of segments, locations, channels, profiles and proposing policies/ strategies to enable business and control risk Proficient in coding and working experience in creating risk monitoring dashboards like vintage charts, KPIs, business trends, etc. Managing portfolio with data driven insights using Demog and Bureau data and recommend necessary alteration in policy when required Experience on creating features using bureau/demog/banking variables and creating insights Handled cross functional projects to develop new product/program Knowledge about policy framework pertaining to personal loan product/Unsecured product Monitoring loss in the business in different segments and highlight the reason for breach in threshold if any. Automating crucial reports, testing and verifying the correctness of the same. Co-ordinating with different stockholder for risk and policy related data and recommendation. Job Requirements: Minimum 3-8 year of experience Work experience with MNC on risk/data analytics field is preferable Proficiency in SAS/Python/DEX for risk management and policy implementation. Ability to debug, troubleshoot and resolve issues related to risk and policy. Use analytical skill to identify root causes of problem and recommend effective solution. Experience in creating features and running decision tree/cluster analysis to identify segments will be an added advantage. Good problem solving skills and clear communicator. Education qualification: Btech or Grad/Post Grad in statistics - Preferred Certification in coding languages like SAS/SQL/Python Preferred

Develop and implement process optimization strategies to improve efficiency and performance. Conduct process analysis and audits to identify areas for improvement. Collaborate with cross-functional teams to develop and execute process improvement initiatives. Monitor and report on process performance, providing insights and recommendations for continuous improvement. Provide training and support to staff on process improvement methodologies and best practices. Stay updated with the latest advancements in process optimization technologies and methodologies.

Mega Lifesciences is looking for an Asst. Manager - Quality Assurance (QA) to work closely with General Manager - Quality Assurance in a fast-paced environment that will offer ample opportunities to learn and expand your experience and expertise. Job Summary Conduct thorough audits of API and FP manufacturing facilities Evaluate suppliers for compliance with cGMP Develop and execute the FP supplier audit calendar, analyze observation trends for Mega products, and evaluate suppliers based on Megas quality policy and guidelines. Coordinate and compile Annual Product Quality Review (APQR) for Megas portfolio Review APQRs in alignment with Megas QMS system Preparation of risk assessment Provide documentation review and support during technology transfer activities Actively contribute in a supportive role within cross-functional teams to ensure smooth transitions between manufacturing sites or processes Qualification Experience Bachelors Degree or Masters Degree in Pharmacy Minimum 8 to 12 years of experience in Plant Quality Assurance or Corporate Quality Control or Corporate Quality Assurance Well versed with related International guidelines Skill Knowledge - The ideal candidate will possess fluency in both written and spoken English, a strong background in pharmaceutical quality assurance (QA), and well-developed analytical and problem-solving skills.

Job Description Position: Junior research scientist (JRS)/Research scientist (RS) Job Location: - Plot No. 214, Borsad - Tarapur Road, Ta: Petlad, Dist: Anand, Gujarat, India. Department: R&D / Formulation Experience: 3-6 years in Nutraceuticals Formulations. Industry: Nutraceutical / Food / Pharma Manufacturing Reports To: Manager FRD. Job Type: Full-Time Company Profile: - Pharmanza Herbal Pvt. Ltd. is one of the few companies which is focusing on standardizing and proving the efficacy of Herbal products. Our strong supplier base, fully equipped R&D facility, FDA approved manufacturing facility, infrastructure for conducting human trials as well as our formulations unit provides a one stop solution to our valued customers. Pharmanza Herbal Pvt Ltd. is one of the leading research-oriented companies, manufacturing herbal extracts used in the Ayurvedic and nutraceutical segment. Our journey began in 1997 with Pharmanza India, our group company located in Khambhat, India, where we started producing herbal extracts. While Pharmanza India primarily focuses on veterinary allopathic formulations, we leveraged its facilities to manufacture herbal products such as Garcinia cambogia, Commiphora Mukul, and Withania somnifera from 1997 to 2004. As the business expanded, and we began exporting our products to countries like the US, Japan, and Germany. Pharmanza Herbal was established in Dharmaj, India, to continue our commitment to quality and innovation in herbal solutions. The facility is certified by Food safety authority of India (FSSAI), Food and drug Administration, India (Gujarat office) with NSF-GMP International. Current certifications include ISO9001:2015, ISO22000:2018, NSF-GMP, NSF-SPORT,USP-GMP,USP Ashwagandha,Bosewelia with Kosher and Halal and USDA/APEDA organic certifications for products. Additionally, we are also certified SEDEX 4 Pillers and ECOVADIS. Job Overview: - We are seeking a highly motivated and detail-oriented Formulation Scientist with 2-4 years of experience to join our team. The ideal candidate will have expertise in formulation development and optimization, along with a strong understanding of dosage forms, excipients, and manufacturing processes. As a key member of our R&D department, you will be responsible for designing and developing solid, semi-solid, or liquid dosage forms, performing stability studies, and ensuring regulatory compliance throughout the formulation process. Responsibilities and Duties: - 1. Research & development along with optimization of formulations for Nutraceutical and Health Supplement as per the organization requirements. 2. Development of solid, semisolid, and liquid dosage forms for herbal and nutraceutical ingredients for domestic, and regulated markets like US, EU, Brazil, and Canada. 3. Ensure adherence to regulatory requirements and customer expectations during product development. 4. Collaborate with cross-functional teams, including Analytical Development, Quality Control, and Manufacturing, to ensure smooth transition from development to production. 5. Contribute to total product development activity from material procurement to stability studies and technology transfer to the manufacturing units. Troubleshooting as required during these operations. 6. Handling different equipment, performing experiments, and documenting the results in a prescribed format. 7. Pre-formulation and excipient compatibility studies, assist in research activities as instructed. 8. Preparation of literature search, patent search, prepare product development reports, stability protocol, process validation protocol, reports and SOPs. 9. Responsible for inventory management and lab management ensuring GDP during documentation and fulfilment of GLP requirements during routine lab work. 10. Troubleshoot formulation-related issues during clinical trials and commercial production. 11. Data compilations and record maintenance. 12. Any other responsibility, as assigned by management. Qualifications: - Education level: Bachelor's or Masters degree in Pharmaceutical Sciences, Chemistry, or a related field Experience: 3-5 years Personal characteristics: Hands-on experience with various formulation techniques, Strong knowledge of drug delivery systems, excipient selection, and stability studies, Familiarity with regulatory guidelines (USFDA, EMA, ICH) and industry standards. Ability to work collaboratively in a fast-paced, team-oriented environment. Salary Range: - Competitive Computer Competency: -Efficient Skills: - Excellent problem-solving and analytical skills with keen attention to detail, Strong written and verbal communication skills Benefits: Competitive salary package. Subsidized food facility. Free Transportation facility from Vadodara location. Medi-claim facility. Opportunities for professional development and growth. A dynamic and collaborative work environment committed to sustainability. Join our dynamic team and contribute to the success of our mission to provide high-quality nutraceuticals and dietary supplements that positively impact people's health and well-being. If you possess the required qualifications and share our passion for quality, we encourage you to apply for this exciting opportunity as an JRS/RS in our manufacturing unit. Company Website: - www.pharmanzaherbal.com Company Email id: - hrm@pharmanza.com

Exciting Opportunity for Research associate - Alternate Vendor Development in Formulation & Development(PDR) We are looking for a skilled professional with 3-5 years of experience in alternate vendor development for diverse markets like US, EU, ROW, Domestic, WHO. Key Requirements: - B.Pharm/M.Pharm qualification - 3-5 years of relevant experience - Familiarity with various market guidelines - Expertise in technology transfer - Exposure to shopfloor operations is advantageous

Responsible for R&D functions, Process development, scale up, Technology Transfer, Trouble shooting, Lab experiments, Documentation,Products Literature search, Preparation of samples, Compliance of EHS/ISO standards etc. in Speciality Chemical plant Required Candidate profile M.Sc. with 10 to12 yrs relevant exp in speciality chemical mfg industry. Sound exp of handling lab instruments like HPLC, GC, KF, IR, UV, Spectrometer, Analyser, Auto Titrator,, Viscometer etc is must Perks and benefits Negotiable

Role & responsibilities Manage end-to-end technology transfer of OSD formulations to commercial sites. Drive process validation, optimization, and evaluation in line with regulatory standards. Ensure accurate documentation and compliance with global regulatory requirements. Coordinate cross-functional activities and respond to regulatory deficiencies. Preferred candidate profile Qualification: M.Pharm Experience: 1015 years in formulation technology transfer (OSD). Strong expertise in process validation, optimization, site transfers & commercial validation