629 Biochemistry Jobs - Page 23

This Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance s and defined regulatory strategies. He would even be responsible for the preparation and review of information required for development of regulatory CMC dossiers for commercial products. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world. Your role at our organization is integral to helping the world meet new breakthroughs that affect generations to come, and we re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. Primary responsibilities include, but are not limited to: Regulatory Responsibilities: Provide input to global product and project regulatory strategies by performing assessments of CMC changes, identifying global regulatory requirements and critically evaluating supporting documentation to assess acceptability and identify potential risks. Execute regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support post-approval supplements/variations, annual reports, registration renewals and responses to health authority questions per established business processes and systems. Liaise with global CMC, Our Manufacturing Division and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance. Assess and communicate potential regulatory risks and propose mitigation strategies. Deliver all regulatory milestones for assigned products across the product lifecycle Identify and communicate potential regulatory issues to GRACS CMC management, as needed Technical Skills: Experience in reviewing scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data. Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills. Demonstrated understanding of related fields (eg, pharmaceutical manufacturing, analytical testing, and quality assurance). Proficient computer skills and previously demonstrated ability to operate in electronic document based GMP systems Leadership Skills: Demonstrated ability to generate innovative solutions to problems and effectively work with and communicate to key stakeholders. Demonstrated flexibility in responding to changing priorities or dealing with unexpected events. Capability to handle multiple priorities and balance work to achieve business goals. Demonstrated effective leadership, communication, and interpersonal skills Qualifications & Skills Bachelor s in Science, Engineering, or a related field (advanced degree preferred). Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry Minimum 5 - 7 yrs of Industry Pharmaceutical industry experience out of 4 years experience in managing CMC Regulatory submissions for small molecules/vaccines/biologics The candidate may be required to travel to other CMO sites on a need basis.

This Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance s and defined regulatory strategies. He would even be responsible for the preparation and review of information required for development of regulatory CMC dossiers for commercial products. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world. Primary responsibilities include, but are not limited to: Regulatory Responsibilities: Provide input to global product and project regulatory strategies by performing assessments of CMC changes, identifying global regulatory requirements and critically evaluating supporting documentation to assess acceptability and identify potential risks. Execute regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support post-approval supplements/variations, annual reports, registration renewals and responses to health authority questions per established business processes and systems. Liaise with global CMC, Our Manufacturing Division and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance. Assess and communicate potential regulatory risks and propose mitigation strategies. Deliver all regulatory milestones for assigned products across the product lifecycle Identify and communicate potential regulatory issues to GRACS CMC management, as needed Technical Skills: Experience in reviewing scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data. Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills. Demonstrated understanding of related fields (eg, pharmaceutical manufacturing, analytical testing, and quality assurance). Proficient computer skills and previously demonstrated ability to operate in electronic documentam based GMP systems Leadership Skills: Demonstrated ability to generate innovative solutions to problems and effectively work with and communicate to key stakeholders. Demonstrated flexibility in responding to changing priorities or dealing with unexpected events. Capability to handle multiple priorities and balance work to achieve business goals. Demonstrated effective leadership, communication, and interpersonal skills Qualifications & Skills Bachelor s in Science, Engineering, or a related field (advanced degree preferred). Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry Minimum 10 - 12 yrs of Industry Pharmaceutical industry experience out of 6 years experience in managing CMC Regulatory submissions for small molecules/vaccines/biologics. The candidate may be required to travel to other CMO sites on a need basis.

Job Title: Invivo Pharmacology Scientist Job Location: Bangalore JOB PURPOSE (Briefly describe the objectives of the job) : The individual must possess knowledge on cancer animal models and various screening methodologies in oncology research area. Understanding of full-cycle drug discovery process is required along with hands-on training in handling various rodents for experimental purposes. KEY RESPONSIBILITIES : Responsible to conduct assigned research projects including experiments with utilizing current concepts and recognized standard techniques. Responsible to set up the experimental designs, analysis of data and concluding from the progress. Record laboratory observations information in lab notebooks, database and document the experimental designs. Responsible for data analysis, perform calculations for the result of the experiment. Summarize the research and communicate result of research to the supervisor. EDUCATIONAL QUALIFICATION / WORK EXPERIENCE : M. Pharm Pharmacology / M. V.Sc / M. Sc biochemistry with 1-3 years of experience TECHNICAL /FUNCTIONAL SKILLS : Hands-on experience in execution of subcutaneous tumor xenograft models, orthotopic xenograft model, metastasis models and syngeneic tumor models. Hands-on experience in studies involving IHC and ELISA readouts Will work independently or in association with senior scientists and other associates in the design and execution of in-vivo efficacy experiments using oncology models. Experience in animals handling (rodents and non-rodents) such as dosing by various routes, bleeding by various routes, injections by various routes and surgical modalities which includes cannulation etc Data recordings and entry into the required formats as per the organizational guidelines. Organizational skills and the ability to work in a highly collaborative environment are required. BEHAVIORAL/MANAGERIAL SKILLS : Good communication skills Excellent interpersonal skills Good team player Strong documentation skills Adhere to organizational data integrity practices and ensure documentation in compliance with ALCOA plus principles. Ensure compliance with environment, health, and safety (EHS) processes defined at organizational level to meet safety goals. EQUAL OPPORTUNITY EMPLOYER: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodation for qualified individuals with disabilities.

Role Title- Scientific officer Working with- HOD, COL What the role entails Key accountabilities/ responsibilities Routine maintenance of equipment as defined in SOP. Quality Control procedures as defined in SOP. Specimen processing as per defined SOPs. Completion of allocated test protocol within TAT. Storage of samples before and after investigations performed. Maintaining turn around time. Documentation of Daily QC / Maintenance etc. Regular preview of SOPs (Read & Understood). Follow biomedical waste disposal procedures as per guidelines. Following the safety guidelines strictly as per norms. What we are looking for in you Candidate with prior work experience into pathology is preferred. Excellent people management, communication and analytical skill. Good administration and department handling Skills. What we promise to you- A strong growth prospective. Role Demands (travel)- Travelling not involve Location- Mumbai Education Requirement Essential- Bsc / MSc/DMLT Experience- 5 + years Stakeholder interfaces- All Departments in Metropolis

Job Description The incumbent will be responsible The perform advanced repairs, preventative maintenance and installation for equipment and devices offered by Avantor. Diagnoses and troubleshoots complex systems. Provides technical support and training to customers on operational or maintenance aspects of equipment. Serve as customer contact on technical and service-related problems.. Mentor less-experienced peers and assist supervisors, but does not formally supervise others. What were looking for: Education: M.Sc (Microbiology/Biochemistry/Biotechnology/Biomedical) Experience: Minimum 5 years experience in Technical Services. Experience of people management desirable but not essential. How you will thrive and create an impact: Performs normal day to day duties as a Service Engineer•Leads, motivates and mentors technical service personnel and implements and supports career development programs regarding same•Leads, motivates and mentors Service Engineers and implements and supports career development programs regarding same•Promotes the Equipment and Instrument Service Department and consistently seek out additional revenue streams and opportunities for growth•Forges strong relationships with customers through regular site visits/meetings associated with direct reports in order to understand customer needs and to further develop the associates•Supervises and ensure all faults are resolved promptly and that preventative maintenance is delivered to customer•Provides second level of technical support and advice to on site Engineers in order to resolve faults in a timely and efficient manner•Functions as a technical resource to team members to ensure the customer’s quality requirements and schedules are met•Develops and executes plans to improve processes and operations for better services•Liaises with Region North colleagues and customers/vendors on technical information •Responsible for approving annual leave requests and/or leaves of absence and ensuring all associates use Workday to record same•Ensures timely completion of PMP goals for all team members•Manages training requirements for all associates in team and schedules internal and external training where and when required•Designated point of contact for all associates for escalation of issues if and when they arise•Actively leads and promotes the Avantor ICARE Values•In conjunction with Service Director, sets, agrees and takes ownership of goals as per PMP process•Performs other duties as assigned• Skills, Knowledge & Competencies •Diploma/Degree in Mechanical/Engineering or related discipline•Minimum 5 years experience in Technical Services•Experience of people management desirable but not essential•Full clean driving license•Excellent customer facing skills•Keeps up to date with all technical developments within area of expertise•Strong leadership ability •Ability to cultivate teamwork and collaborate across internal functions•Ability to influence the actions of others and to work in a fast paced field based environment•Ability to work in a matrix structure•Excellent interpersonal and communication skills •Keen negotiation skills •IT Literate – Workday and MS Office applications•Excellent time management skills •Can comfortably deliver a presentation• Regards, Vimal Sharma Email ID: vimal.sharma@avantorsciences.com

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Self Supportive Training ll be provided for Fresher Required Candidate profile UG / PG in Life Science, Medical, Paramedical Dental, Pharmacy, Physio, Nursing, Microbiology, Biochemistry, Biotechnology, Biology, Bio-Medical, Zoology, Bioinformatics, Botony, Nutrition & Dietetics Perks and benefits 12700/- to 14600/- PM Excluding Special Allowances

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Self Supportive Training ll be provided for Fresher Required Candidate profile UG / PG in Life Science, Medical, Paramedical Dental, Pharmacy, Physio, Nursing, Microbiology, Biochemistry, Biotechnology, Biology, Bio-Medical, Zoology, Bioinformatics, Botony, Nutrition & Dietetics Perks and benefits 12700/- to 14600/- PM Excluding Special Allowances

Refer Medical Records and assign ICD-10-CM, CPT, HCPCS Codes Clinical Documentation Review Medical Coding and Medical Billing

As an Associate Content Editor in the Biosis team you will select, analyse, interpret, and summarize scientific research in support of the relevant specialty collections on Web of Science. You should have comprehensive knowledge in a life sciences subject such as biochemistry, microbiology, biotechnology, pharmacology or genetics. Your role will require you to be target-driven and to meet defined quality standards. About You - experience, education, skills, and accomplishments Postgraduate in Biotechnology, Microbiology, Biochemistry, Genetics, Molecular biology, or any related Life Sciences field 1+ years experience of content editing in a science-related field. Good scientific research and analytical skills, with attention to detail. General computer proficiency (MS Office) and ability to quickly learn new software tools What will you be doing in this role? Apply biotechnology, microbiology, pharmacology, molecular biology concepts to curate biology-related data from research articles in line with editorial policies Achieve weekly production volumes and consistently meet quality targets Take active role within the team to ensure targets are met Achieve and maintain consistent quality standards Adheres to editorial publishing schedules and quality standards. Maintain a flexible and adaptable approach towards process change Takes initiative by raising, discussing, and resolving subject matter and production issues Maintains and develops scientific knowledge and skills training as required to complete work and stay current on scientific trends and developments related to the employee s editorial responsibilities To make positive efforts to promote personal safety and that of others by taking reasonable care at work, by carrying out the requirements of the law or following recognized codes of practice provided or advised by management to ensure safe working practices. To undertake any other reasonable duties as requested by your line manager /Manager/Leadership team on a permanent or temporary basis Hours of Work Full time, 9AM to 5 PM IST

Hiring experienced Medical Professionals for our multispecialty hospital in Purnia, Bihar. Accommodation provided. MD (Anatomy, Physiology, Biochemistry, Microbiology, Pathology, Forensic Medicine, Community Medicine, Pharmacology)

Analyze and manage Healthcare data Follow international healthcare regulations Work on healthcare documentation processes with timely submission Assist in the analysis and categorization of medical data for reporting purposes

Long Description Primary Job Responsibilities: Method development, qualification and transfer and data review activity. Analyst training, CSV lab compliance and lab support. Additional Job Responsibilities: Coordination with DQA for compliance and documentation activities. Competencies Collaboration Customer Centricity Developing Talent Innovation & Creativity Process Excellence Result Orientation Stakeholder Management Strategic Agility Education Masters in Biotechnology or Biochemistry Work Experience Candidate with 10-12 years of experience in chromatographic method development and qualification

Job description Labtron Equipment looking for Product Specialist / Product Managers for Hyderabad office. Interested can share their Resumes to Mail id :rasumalla@labo.best / What's App 9963352511 Location: Hyderabad and Mumbai

Title of Project -: Randomized controlled trial of immunosuppressive therapy (ATG+CSA) with Eltrombopag and ATG+CSA with romiplostim in aplastic Anemia & Correlation of therapy response with transcriptomic profiling Project Name-: Project Research Scientist-I (Non-Medical) No. of Vacancy-: One (01) post Emoluments-: 56,000/-+ 27% HRA Essential Qualification-: 1) First Class Post Graduate degree including the integrated PG degrees in science. (Applied Biology, Biotechnology, Life Science Genetics, Biotechnology, Biochemistry, Microbiology) OR 2) Second Class Post Graduate Degree including the integrated PG degrees in Science with Ph.D. in Applied Biology, Biotechnology, Biochemistry, Genetics, Life Sciences, Microbiology) Desirable Qualification-: Experience in Molecular Biology including NGS and Bioinformatics. Candidate should have at least 4 years research experience in relevant area. Age limit-: Not Exceeding 35 years Duration-: One Year, Likely to be extended.(Project Duration 02 years) Posting-: ICMR-NIIH, Mumbai Interested candidates can share their cv on this mail id anchal.g@esolglobal.com.

Experience 2-5 yrs. Location- Mumbai & Bangalore . Qualification DMLT / B.Sc. MLT . Responsibilities – • Observes all laboratory safety precautions in the handling of clinical specimens and running of tests. • Maintains integrity in testing/reporting/confidentiality • Follows the ethics and Quality policy of the organization • Continuously upgrades his knowledge and skills as per the requirement of the job • Ensuring proper maintenance of all equipment’s including daily, weekly and monthly maintenance • Sample receiving as per pre-analytical acceptance criteria and proper segregation of samples.

Greetings from Thyrocare! We are looking Consultant MD Pathology - (Locum) for our Amritsar, Mohali, Kochi Lab of *Thyrocare Technologies Ltd. Only sundays working,and on weekdays as and when required. If any one is interested kindly share your resume : tereza.nerson@thyrocare.com Or whatsaap : +91 83558 89455 Regards, Mrs.Tereza Nerson Contact No: 8355889455 Sr. HR | Talent Acquisition Thyrocare Technologies Ltd.

Hiring SR/AP Professor Ophthalmology Pediatrician General Medicine Surgeon Orthopedic Gynecology Emergency Medicine Anesthesia Community medicine Radiology Pharmacology Forensic Biochemistry Physiology for Medical College in Jaipur & Udaipur

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Self Supportive Training ll be provided for Fresher Required Candidate profile UG / PG in Life Science, Medical, Paramedical Dental, Pharmacy, Physio, Nursing, Microbiology, Biochemistry, Biotechnology, Biology, Bio-Medical, Zoology, Bioinformatics, Botony, Nutrition & Dietetics Perks and benefits 12700/- to 14600/- PM Excluding Special Allowances

PYDAH EDUCATIONAL INSTITUTIONS is looking for Lab Programmers to join our dynamic team and embark on a rewarding career journey Develop software applications based on business requirements and technical specifications Write clean, efficient, and maintainable code Test and debug software applications to ensure they meet quality standards Collaborate with cross-functional teams to design, develop, and deploy new features Troubleshoot and resolve software defects and issues Optimize software performance and ensure scalability Conduct code reviews and provide constructive feedback to team members Stay up-to-date with industry trends and emerging technologies Document software designs, code, and technical specifications Participate in agile development processes and contribute to continuous improvement ,

PYDAH EDUCATIONAL INSTITUTIONS is looking for Lab Assistants (ECE) to join our dynamic team and embark on a rewarding career journey Prepare and set up laboratory equipment and materials for experiments and tests Collect and process samples according to established protocols Conduct routine laboratory tests and procedures, such as preparing solutions, conducting experiments, and performing assays Record and maintain accurate data and records of results Operate laboratory equipment, such as centrifuges and microscopes, and maintain equipment in good working condition Follow established protocols and regulations, including safety guidelines and quality control procedures Maintain a clean and organized laboratory environment, including ordering and stocking supplies Communicate with laboratory supervisors and other team members to provide updates and ask questions Strong technical skills, attention to detail, and the ability to follow precise instructions Good organizational and communication skills ,

PYDAH EDUCATIONAL INSTITUTIONS is looking for Lab Assistants (Pharmacy) to join our dynamic team and embark on a rewarding career journey Prepare and set up laboratory equipment and materials for experiments and tests Collect and process samples according to established protocols Conduct routine laboratory tests and procedures, such as preparing solutions, conducting experiments, and performing assays Record and maintain accurate data and records of results Operate laboratory equipment, such as centrifuges and microscopes, and maintain equipment in good working condition Follow established protocols and regulations, including safety guidelines and quality control procedures Maintain a clean and organized laboratory environment, including ordering and stocking supplies Communicate with laboratory supervisors and other team members to provide updates and ask questions Strong technical skills, attention to detail, and the ability to follow precise instructions Good organizational and communication skills ,

The Associate Field Biologist/Field Biologist/Sr. Field Biologist shall be responsible for Pest Audits of Branch Large / HD Customers (having Third-party Audits- USFDA, AIB, BRC, FSSC, SQF, LEED, etc), Key national customers in various segments - Food & Pharma Mfg, w/h, Large food retailers (excluding QSRs, Fast food chains), Large ITES & MA s, etc. The incumbent will report administratively to the DM & functionally to Opex QA and work as a part of the multi-functional team involving collaboration with the internal & external stakeholders. Job Responsibilities: Carry out Pest Audits of Global accounts, Key designated NK accounts- Food & Pharma units, Food & Pharma warehouses, Large food retailers (excluding QSRs, Fast food chains), Large ITES & MA and Branch accounts - Large HD accounts (Third party Audits- AIB, BRC, FSSC, SQF, LEED, etc.). Specific accounts will be assigned at the time of induction in consultation with BM, DM and OpEx. Responsible for proper, on time completion & submission of all audits with reports as per contract agreement of assigned customers by visiting customer sites due as per iCABs calendar plan at an agreed frequency. Share completed audits with customers and internally for actions within 24 hours, after completion of audit inspection. Support, and guide branch operation team to streamline documentation at Global, NK & LA customer sites assigned. Must Generate service leads based on recommendations during audits. Conduct TPA for technicians handling Global, NK & Branch-HD & LA assigned. Conduct surprise visits at NKA & HD accounts as and when required. Identify key improvement areas of site technicians during an audit, encourage and groom them for better performance in service Leads from the customer sites. Must have a complete understanding of Service Operation i.e. technician, supervisor and admin activity. A clear understanding of various Food standards and SOPs, Pink Notes, Standard Forms, SHE, Atex L 2 and other regulations. Be able to Identify Atex atmospheres during audits and report to Opex/ SHE Know and understand pest identification, especially for uncommon pests; Know and understand about life cycle, classification, morphology, and habitat of uncommon pests. Key Result Areas: 100% Audit completion as per iCABS PMI Frequency for assigned accounts At least one (01) service lead per audited site through the recommendations. 100% TPA & development of assigned technicians handling accounts site Meeting NKA customers and developing relations Promote Heat & Co2 Treatment Competencies (Skills essential to the role): Skills in various PMS, sound knowledge of pest & pest management options (ERDM principle) SHE and SCP operating knowledge Good team player with the ability to collaborate with cross-functions Possess strong communication, analytical, keen observation, report preparation & presentation skills Positive Attitude and take pride in their work Ability to work Independently Negotiation skills for getting work done, persuasive Educational Qualification / Other Requirement: Bachelors or Master s Degree in Agriculture / Botany / Zoology / Biology / Microbiology / Chemistry / Biochemistry / Entomology / Agro-chemicals & Pest Management. Successfully completed RPCI s BPM-2/CBU/IPM/L2 Training Program (for internal candidates only) Excellent computer skills and proficiency in Excel/spreadsheets, word docs, PowerPoint presentation / G slides / GSuite Excellent communication skills in English both verbal and written. Minimum two years of experience in Handling HD Accounts Preferably possess a two-wheeler with a valid driving license, able to ride 2 wheeler with all safety precautions. Agile & flexible to perform on-site inspection and willing to travel extensively. Role Type / Key working relationships: External team - Customers and customer representatives Internal team - Opex, GM/DM/ADM, BM/ABM/Base Manager / Site Incharge, Operations & Sales Colleagues including NKA, Service Planners

Job Description : Job Title - Head- Product & Process Research About us With over 200 brands sold in nearly 180 countries, we re the world s leading premium drinks company. Bring your passion and use your curiosity as you explore, collaborate, and innovate to build brands consumers love. Together with passionate people from all over the world, you ll test new ideas, learn and grow, and unlock a brighter, more exciting future. Join us to create a career worth celebrating. About the Function: Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo s 30,000+ people work in Supply Chain and Manufacturing. It s an intricate and sophisticated operation that s the product of logistical, manufacturing, and technical collaborations. Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We re committed to realising our Society 2030: Spirit of Progress goals, to protect the environment and support our farmers and suppliers. Whatever your skills and experience, we ll help you to thrive in our inclusive culture. Role Responsibilities: Qualification: Ph.D. ( Biochemistry) Experience: Strong industrial research experience (15 years or more) in relevant FMCG (Post Doc: not essential but desired) Skills and capabilities: Strong leadership quality In depth knowledge of process chemistry & biocehmistry of flavour generation from natural raw material processing . Individual must have hands- on experience in the area of Flavour precursor biosysnthesis, enzymatic flavour formation, volatile organic compounds & flavour interactions with matrix . Idividual must have an appreciation for certain areas of process biochemistry in addition to the above. These include Biocatalysis, fermentation technology, bioprocess engineering, Systems biology. Individual must be well-versed with recent technological advancements in all the above areas. Demonstrated experience in achieving research goals Strategic research plan and timely execution for the business growth Responsibilities: S&T Program: Develop S&T Project pipeline ( raw material- grains and agri waste streams, yeast, precursors and enzymes application for flavour block generation across grain and malt spirit, sustanability in operations through water and carbon, value generation from waste streams, distillary digitization) by driving multi-disciplinary actions within various scientific as well as technological areas to fulfil current as well as future business needs Design and deliver S&T Projects OTIF for innovation, productivity, capability and future sustainability of the business Ensure deployment of projects across the various geographies of the business Coach, guide and mentor the team so that projects are completed as per timelines and challenges encountered by the team are tackled Coordinate and work closely with, liquid innovation, sensory and consumer insights, manufacturing, sourcing and innovation to ensure smooth functioning of projects Drive a culture of collaboration by running projects with cross functional teams as well as with external collaborators on exploring open innovation opportunities Productivity initiatives: Maturation Chemistry : Maturation of Spirits - technlogy applications Lead science and scale up program ( also involving new agee technology application) of various spirits maturation projects for Malts and grains For Grains platfom Lead development and running of alcohol yield process improvement projects in lab and demonstrating the Proof of Concept (POC) at pilot level Capability improvements: Analytical methods for assessing various markers of quality of spirits Technology scan and methodology development for analytical markers. Development and standardization of various new age tools and provide analytical guidance to various research and innovation programs Liquid Innovation Projects Responsible for providing S&T based solutions to the Liquid Innovation team during their new liquid Development Open Innovation with External Collaborator (Industry or Academia) Responsible for running projects with external collaborators & evaluation of its progress at every stage of development Scientific inputs to Regulatory and DST renewal Responsible for reviewing regulatory documents and providing inputs Ensure yearly filing of DST returns through new S&T projects Vendor development with Sourcing Support the sourcing function with scientific insights that helps techno-commercial evolution of raw material vendors Flexible Working Statement: Flexibility is key to our success. From part-time and compressed hours to different locations, our people work flexibly in ways to suit them. Talk to us about what flexibility means to you so that you re supported from day one. Diversity statement: Our purpose is to celebrate life, every day, everywhere. And creating an inclusive culture, where everyone feels valued and that they can belong, is a crucial part of this. We embrace diversity in the broadest possible sense. This means that you ll be welcomed and celebrated for who you are just by being you. You ll be part of and help build and champion an inclusive culture that celebrates people of different gender, ethnicity, ability, age, sexual orientation, social class, educational backgrounds, experiences, mindsets, and more. Our ambition is to create the best performing, most trusted and respected consumer products companies in the world. Join us and help transform our business as we take our brands to the next level and build new ones as part of shaping the next generation of celebrations for consumers around the world. Feel inspired? Then this may be the opportunity for you. If you require a reasonable adjustment, please ensure that you capture this information when you submit your application. Worker Type : Regular Primary Location: Bangalore Technical Centre Additional Locations : Job Posting Start Date : 2025-03-05

Long Description Monitor the manufacturing process (Drug Product) and batch trend analysis. Data acquisition, trending and analysis. Preparation / review of documents pertaining to tech transfer like Development report, Tech transfer report, MFR, BMR and BPR w. r. t. drug product. Review aseptic product filling operations such as formulation, filtration, filling, visual inspection and secondary packing operations on shop floor as and when required. Technology transfer of new / existing products from sending unit (R&D) to receiving unit (Manufacturing) or from site-to-site transfer. Responsible for preparation of Process Validation protocols / reports, QRMs, supporting PV on shop floor as and when required. Responsible for writing technical documents such as scientific justification and evaluation. Troubleshooting the problems and investigations using investigation tools for root cause analysis in a holistic manner as and when required. Supporting regulatory for Dossier filing and giving technical inputs in respective sections. Review of process related change controls, co-ordinate the approval process and follow up to close out. Competencies Education Masters Post Graduation in Biotechnology or Biochemistry Work Experience 10 - 15 years

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Self Supportive Training ll be provided for Fresher Required Candidate profile UG / PG in Life Science, Medical, Paramedical Dental, Pharmacy, Physio, Nursing, Microbiology, Biochemistry, Biotechnology, Biology, Bio-Medical, Zoology, Bioinformatics, Botony, Nutrition & Dietetics Perks and benefits 12700/- to 14600/- PM Excluding Special Allowances