1059 Biochemistry Jobs - Page 15

` Position: Medical Coder HR SHANMUGAPRIYA 8072891550 Job Description: Position: Medical Coder Medical Coding is the process of converting patient health information into alpha numeric codes. Coders take medical reports from doctors, which may include a patients condition, the doctors diagnosis, a prescription, and whatever procedures the doctor or healthcare provider performed on the patient, and turn that into a set of codes, which make up a crucial part of the medical claim. Eligibility: All (UG/PG) Life Science& Paramedical Graduates BDS BPT BHMS BAMS Siddha,Unani,Naturopathy {Dip Bsc Msc} Nursing/GNM {B.E M.E} Biomedical Engineering {B.tech,M.tech}Biotechnology Biochemistry Bioinformatics Microbiology Zoology and Advanced zoology Biology Botany Medical Lab Tech Plant biotechnology Pharmacy(B.Pharm M.pharm) Paramedical Physiotherapy Physician assistant Critical Care Technology Medical Biochemistry Medical Record Science Operation Theatre & Anaesthesia Technology {Bsc Msc Dip} Clinical Nutrition Human Genetics Medical Laboratory Technology Medical Sociology Epidemiology Molecular Virology Biostatistics Blood Banking Technology Regenerative Medicine Optom. Genetic Counseling Radiology & Imaging Technology Medical Biochemistry Medical Microbiology Clinical Care Technology Clinical Care Technology Medical Physics {Bsc Msc Dip} Accident & Emergency Care Technology Audiology & speech Language Pathology Cardiac Technology Cardio Pulmonary Perfusion Care Technology Critical Care Technology Dialysis Technology Neuro Electrophysiology Medical Sociology Nuclear Medicine Technology Operation Theatre & Anaesthesia Technology Optometry Physician Assistant Radiology Imaging Technology Radiotherapy Technology Medical Record Science Respiratory Therapy Fitness and Lifestyle Modifications Accident & Emergency Care Technology Critical Care Technology Nursing Aide Operation Theatre & Anaesthesia Technology Ophthalmic Nursing Assistant Medical Record Science Optometry Technology Radiology & Imaging Technology Medical Lab Technology Cardiac Non Invasive Technology Dialysis Technology Dentist Requirement: Knowledge in Anatomy and Physiology Good communication and interpersonal skills Basic Computer Skills Benefits System based job Weekly 5 days duty Day shift with Sat and Sun off Food and Cab provided by company Incentives based on performance Starting salary 12k to 25k with increment in 6 months for experienced. Abroad opportunities available Bonus for referring friends Medical expenses covered by company Provident Fund will be provided Job Location: Chennai, Coimbatore, Vellore, Trichy, Cuddalore, Pondi Salem, Erode, Namakkal, Thanjavur, Nagercoil, Theni,Dindokal Thiruvannamalai, Villupuram, Karur, Tirunelveli,Kanniyakumari Tirupati, Kerala, AP,Tamilnadu,Telangana Reach us : HR SHANMUGAPRIYA 8072891550 Required candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology GNM DGNM Physician assistant Anesthesia technician Perfusion Technology Medical coder Freshers Medical coding Freshers jobs in chennai Medical coding openings in chennai Wanted Medical coder Freshers jobs Medical coding Medical coder Medical coding Freshers Jobs in chennai Jobs for Passed outs Freshers jobs in chennai Jobs for freshers Nursing jobs for freshers Pharma jobs for Freshers Biotechology Jobs Microbiology jobs Biomedical jobs Bioinformatics jobs Bsc/Msc Jobs Biochemistry jobs Life science jobs in chennai Paramedical jobs in chennai Jobs in Tamilnadu Jobs in Pharmacy Jobs in Hospital GNM STAFF NURSE ANM STAFF NURSE GNM FEMALE STAFF NURSE DGNM FEMALE STAFF NURSE GNM MALE NURSE MALE STAFF NURSE NURSING JOBS IN CHENNAI Perks and Benefits Incentives & Benefits as per Corporate Standards

Job Role: Assistant Professor Location: Gujarat Experience: 1 - 4 Years Salary: 1.50 L/Mo - 1.70 L/Mo; negotiable Accommodation Details (if Provided): Accommodation Provided Gender: Male / Female Required Candidate profile Education: UG: MBBS or equivalent as per NMC rules PG: MD / DNB (Biochemistry) or equivalent Language: Essential: English Desirable: Gujarati / Hindi Perks and benefits Salary Negotiable, Accommodation Provided

Job Role: Associate Professor Location: Gujarat Experience: 4 - 8 Years Salary: 2.40 L/Mo - 3.10 L/Mo; negotiable Accommodation Details (if Provided): Accommodation Provided Gender: Male / Female Required Candidate profile Education: UG: MBBS or equivalent as per NMC rules PG: MD / DNB (Biochemistry) or equivalent Language: Essential: English Desirable: Gujarati / Hindi Perks and benefits Salary Negotiable, Accommodation Provided

They perform a variety of surgical procedures, including both open and minimally invasive techniques, to address a wide range of conditions. General surgeons evaluate patients, review medical history, and determine the need for surgical intervention.

RolE Embryologist Responsibilities: Basic Embryology procedure including ICSI (Minimum 100 case done) Performing Invitro Fertilization Procedures. Conducting regular assessments of health and development of embryos. Maintaining records and samples to ensure testing and laboratory work remains consistent. Monitoring and maintaining quality control. Preferred candidate profile Embryologist Requirements: Degree in Clinical Embryology/Life sciences. Minimum 3 years experience as an Embryologist. minimum 100 ICSI experience Good research skills and handle all embryology work independently Strong interpersonal skills. Competent in data capturing. Solid organizational skills. e & responsibilities

Urgent Requirement of MD/MS doctors for Medical Colleges all over India

Assistant Officer - Nutrition Science and Analytical Services Job Details | Tata Consumer Products Limited Search by Keyword Search by Location Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: Assistant Officer - Nutrition Science and Analytical Services Tata Consumer Products Limited Assistant Officer - Nutrition Science and Analytical Services What are the Key Deliverables in this role? Financial Outcomes Provide timely analytical support to the Regulatory Affairs function to ensure regulatory compliance. Deliver prompt support to the Quality Assurance team to enable informed quality and business decisions based on analytical data. Continuously validate and monitor laboratory performance, while estimating analytical expenses and updating the manager actual expenses and projected budgets. Customer Service Responsible for coordinating with all stakeholders, including Quality Assurance, Regulatory Affairs, Customer Care, NPD, Legal functions, and managing external analytical activities. Must provide timely support to all stakeholders. Internal Processes Coordination with stakeholders for QA-RA analytical support. Capable of responding effectively to rapidly changing requirements, targets, and expectations. Preparation of weekly task reports. Responsible for coordination with external laboratories. Accountable for the release of every final report. Support the team during audits. Assist with purchase order (PO) generation and payment processes. Demonstrate due diligence and maintain a high level of attention in repetitive tasks. Innovation and Learning Continuous skill development in domestic and international regulations related to food analytical specifications and emerging analytical methods. Responsible for developing strong customer care skills. Take initiative to solve problems through small, proactive actions. What are the Critical success factors for the Role? Master s degree in science with a major in Chemistry, Biochemistry, Analytical Chemistry, or related subjects. Minimum of 3 years of experience in a role related to analytical science, preferably in regulatory affairs, QA/QC or R&D functions in food and beverage sector. Experience working in an NABL-accredited laboratory is an asset. Demonstrated knowledge of various testing standards such as IS, FDA and USDA. Skilled in sample handling management. What are the Desirable success factors for the Role? Knowledge of quality and food safety requirement including FSMS requirements, RCA, Training, FSSAI & Legal metrology Good quality and analytical capability Proficiency if Excel, Power Point & word. Good communication skills, ability to grasp new concept and implement.

Position : Sr. Sales Executive (Laboratory Equipment Division) Reports to : Territory Manager Location : Delhi, Hyderabad, Bangalore and Chennai Years of Experience : 3- 6 years of Experience Minimum Qualifications : Diploma in Electronics / Chemical / Instrumentation Preferred Qualifications : BSc. or MSc. In Chemistry / Biology / Physics /Botany/Zoology/ Biotech/Biochemistry or Graduates / Diploma holders in Electronics / Chemical / Instrumentation Engineering Responsibilities: Visit customers and promote Memmert, Preekem, Toshvin, and other Laboratory Equipments Identify new business opportunities through cold calling/visits and phone calls to regular and new customers To update opportunities and daily management through CRM Keep technical knowledge up to date of related products Understand technical specifications of products and offer consultative solutions Need to convince customer for sale of quality products Attend and drive commercial negotiations Build and maintain strong relationships with key decision-makers (end users, lab managers, scientists, procurement heads, etc.) Follow up with customers for orders and payments To work on active cases, co-ordinate with regional head, regional sales team to generate new enquiries and ultimately achieve LED Business targets of assigned territory To coordinate with Toshvin service team for installation and services to customers Need to coordinate with product manufacturer for order booking, shipments and getting service solutions Key Success Behaviours (Key Competencies): The candidate should be sincere, hardworking and target oriented The candidate should have excellent English communication skills Ability to travel and meet customers within assigned territory Learn and improve technical and commercial knowledge continuously for effective product selling Looking for opportunities to build strong relationship with customers

Duration Initially for a period of one year and extendable for one more year or till termination of the project whichever is earlier based on performance evaluation on yearly basis. Money 31000 + 18% HRA per month for candidates with NET or GATE or undergone selection process through National level examination conducted by Central Government Department and their agencies. For other candidates it s 25000 + HRA who do not have NET or GATE as per DST guidelines. Qualification First Class Post-Graduate Degree in Life Sciences (Microbiology/ Biotechnology/ Biochemistry etc). Experience Desirable: Candidates with prior experience in molecular biology techniques including gene cloning and protein purification will be preferred.

Job Role: Senior Resident Location: Gujarat Experience: 0 - 1 Years Salary: 1.10 L/Mo - 1.20 L/Mo; negotiable Language Skills: Essential: English Desirable: Gujarati / Hindi Gender: Male / Female Required Candidate profile Education: UG: MBBS or equivalent as per NMC rules PG: MD/DNB (Biochemistry) or equivalent Eligibility: As per NMC rules Accommodation Details: Accommodation Provided Perks and benefits Salary Negotiable, Accommodation Provided

We Are Hiring | PhD - Biochemistry Location: Gurgaon Industry: Diagnostic / Healthcare Role Highlights Ensure compliance with NABL and other regulatory standards What We’re Looking For: PhD in Biochemistry Experience in diagnostic labs

Receiving and preparing blood samples for analysis; Analysing blood samples using computer-aided and manual techniques; Reviewing initial data that revealsfor examplewhite or red blood cell abnormalities; Making decisions on further haematological analysis; Liaising with other medical professionals to discuss patient treatment plans; Prescribing specific types of treatment for individual patients; Cross-matching blood for use in transfusions; Investigating the biochemistry of blood clotting; Producing quantitative data in the form of reports and providing key information to medical staff about a patients condition; Assisting colleagues in the interpretation of test results; Selecting appropriate techniques for different types of haematological analysis; Maintaining accurate and detailed records.

Greetings from Thyrocare! We are looking Lab Technician (Intern) - for our Head Office Turbhe Lab of *Thyrocare Technologies Ltd. Address- D-37/1, TTC Industrial Area, MIDC, Turbhe, Navi Mumbai - 400703 If any one is interested kindly share your resume Email ID : mitu.jena@thyrocare.com Or whatsaap : +91 9321414235 Regards, Mr. Mitu Jena Contact No: 9321414235 Sr. HR | Talent Acquisition Thyrocare Technologies Ltd.

Role & responsibilities Designation : Quality Executive Department of Work: Quality Qualification : Bsc/Msc- Chemistry, Bio-chemistry Preferred candidate profile

Interested candidates share resume to sanjay.behera@thyrocare.com or whatsapp to 8928285213 Eligibility Requirements: The candidate should be capable of independently managing the lab. Should be able to supervise and manage a small team of 23 technicians. Should be proficient in performing microscopy, particularly in Hematology and Clinical Pathology. Should have a basic understanding of laboratory quality assurance practices.

Summary The senior International Program Regulatory Manager (Sr. IPRM) works under limited supervision of the International Program Regulatory Director to support the design and execution of optimal registration strategies and plans for the assigned portfolio in the assigned International countries. By partnering efficiently with International Program Regulatory Directors, global DU and International (INT) regulatory stakeholders, the Sr. IPRM supports optimal pipeline planning accounting for regional priorities and efficient use of regulatory paths for acceleration in assigned countries. They support the timely execution of registration plans by the relevant line functions and the resolution of high priority topics. The Sr. IPRM uses global, regional and country sources to maintain the relevant databases on country requirements, pipeline information and registration plans across all INT markets and to disseminate relevant information to INT stakeholders. Sr. IPRM supports and implements initiatives to enhance efficiency in ways of working and functional excellence. The Sr. IPRM is a member of the INT RA subteam and may act as deputy of the IPRD on global RA subteams. The Sr. IPRM may lead or contribute to regional cross-functional initiatives and committees. About the Role Key Responsibilities Drives the execution of registration plans as defined in the INT RA subteam and in partnership with the countries, regional roles and global LFs as applicable. Drives the design, up to date maintenance and execution of registration plans for all INT countries in alignment with RA INT and RA DU, including procurement of ancillary document for submission dossier, review of and contribution to responses to Health Authority (HA) questions, follow up on key milestone activities by relevant RA and LF stakeholders. Maintain up to date contact CO contact lists for programs and COs in scope. Supports the IPRD in partnering with DU RA roles to obtain, digest and communicate efficiently pipeline information to relevant stakeholders. Drives updates to the country requirements and registration plans are performed timely and the necessary quality. Sr. IPRM supports and implements initiatives to enhance efficiency in ways of working and functional excellence. Supports the IPRD in the design and execution of plans for Emerging Markets Brands and may interface with the Emerging Markets Brands Center of excellence for assigned projects. Supports the IPRD in designing and executing registration plans for products that target diseases which are predominantly prevalent in INT countries. Partners with GRSS&C LCM group on geographic expansion plans and execution for INT countries. Drives the dissemination of information to and education of global roles on INT country/regional requirements. Support the execution of or act as a region representative in functional or cross-functional initiatives, particularly those with potential impacts on INT RA resources or FTE allocations. May act as deputy of IPRD on assigned programs. Meets objectives as defined in registration plans for the countries and portfolio in scope. Proof of maintenance and communication of country requirements and registration plans for INT countries. Minimum Requirements: Minimum of 6 years in Regulatory, product development, minimum of 1 year s country, regional or global Regulatory Proven track record of HA negotiations, Ability to develop and communicate strategic vision Ability to work in cross-functional environment, Proven expertise in project management Highly committed and team oriented, Proven strong matrix leadership skills Proven track record of early recognition of potential regulatory issues, complex situations, sound risk assessment and overcoming hurdles Strong team player, Proven track record of successful risk assessment, Organizational awareness Ability to travel and represent the organization Degree in Science (e. g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent. Desirable: Advanced degree in Science (e. g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent. Commitment to Diversity and Inclusion: Accessibility and accommodation Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients lives. Ready to create a brighter future together? https://www. novartis. com / about / strategy / people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork. novartis. com/network Benefits and Rewards: Read our handbook to learn about all the ways we ll help you thrive personally and professionally:

Urgent vacancies for, consultant with good experience in medical college at a medical college in Durgapur, WB

Greetings from Thyrocare! We are looking Consultant Biochemist for our Navi Mumbai Lab of *Thyrocare Technologies Ltd. Qualification Required - MD Biochemistry & DNB Shit Timing- 10 PM TO 6 AM Address : D-37/1, TTC Industrial Area, MIDC, Turbhe, Navi Mumbai - 400703 . If any one is interested kindly share your resume : tereza.nerson@thyrocare.com Or whatsaap : +91 83558 89455 Freshers those are passed MD/DNB in 2025 can also apply Regards, Mrs.Tereza Nerson Contact No: 8355889455 Sr. HR | Talent Acquisition Thyrocare Technologies Ltd.

Anatomy Community Medicine Physiology General Medicine biochemistry Pedia pharmacology Skin pathology psy microbiology General Surgery orthopedics Obst & Gyne ENT Opthomolgy

Greetings from Thyrocare! We are looking Lab Technician (ELISA) - for our Turbhe Lab of *Thyrocare Technologies Ltd. Address:D-37/1, TTC Industrial Area, MIDC, Turbhe, Navi Mumbai - 400703 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.

Anatomy Community Medicine Physiology General Medicine biochemistry Pedia pharmacology Skin pathology psy microbiology General Surgery orthopedics Obst & Gyne ENT Opthomolgy

ORGANISATIONAL OVERVIEW Lambda Therapeutic Research is a Global full-service Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK) and Warsaw (Poland), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries. Act as Senior Analyst in Bioanalytical Biosimilar Department Department : Bioanalytical- Proteins & Biosimilars Designation: Executive Location : - Ahmedabad Education : M.SC Biotechnology/ Biochemistry Experience: 4-6 yrs. CTC range : 8-10 Lac/annum Job description: Act as a Senior analyst for method validation and studies for LBA PK methods. Candidate has ability to develop and validate of LBA based bioanalytical PK methods and handling of 2 Project/MV activity together with 2-3 analyst team. Analyze serum samples clinical studies as per respective draft/method SOPs. Independent execution of ELISA / ligand binding assays, Collate, analyze and interpret data. Troubleshoot technical challenges during conduct of MD/MV/Projects. Review or prepare Method SOPs, BA-PBS SOPs, Study Plans, Analytical Reports and Validation Reports. Assist in reconciliation of study or MV raw data, Respond to QA and QC communications for in study or in process audits. Management of inventory for critical reagents or study specific general reagents. COMPETENCIES Accountability Communication Work Ethic Organizational Culture fit Initiative

JOB DESCRIPTION Job Title: Bioassay Analyst - Large molecules Job Location: Bangalore Department - BGRC Analytical About Syngene: Syngene ( www.syngeneintl.com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose of the Role: The candidate shall be responsible to perform the development, validation, and routine testing of bioassay/ELISA for Large Molecules (LMs), especially Monoclonal antibodies (mAbs) and other LMs. The candidate shall be responsible for method development, validation, and stability testing drug substance/drug product. The candidate shall be willing to work in shifts. Role Accountabilities: Shall develop and validate cell-based assays and binding assays (ELISA), SEC and CGE especially for monoclonal antibodies (mAbs), etc. Shall troubleshoot the problems for these methods. Must have strong knowledge of the development of cell-based bioassays for Monoclonal antibodies. Experience in Qualification and Validation of cell-based bioassays Shall have experience on Good documentation/laboratory practices such as ALCOA+ Broad knowledge on analysis of cell-based assays to derive relative potency software s (such as Softmax Pro and PLA) Basic cell culture technics and hands-on experience in maintaining of mammalian cells. Must have experience in handling various cell lines (adherent and suspension cell lines). Preparation of Mammalian cell banks for Bioassays. Experience in handling of primary and continuous cell lines like Revival, maintenance, cell bank preparation, and cryopreservation Shall prepare the raw datasheets, protocols, reports, and SOPs Handling of QMS (Incidents, deviations, Out of Specifications, change controls, etc.) for GMP activities Shall be responsible for procurement and inventory maintenance of Pharmacopeial Standards / Chemicals / Reagents / Consumables / Spares etc., required for the projects Shall adhere to the procedure of GxP/GMP/Safety and as per the procedure defined in the internal standard operation procedure Must have good hold on MS office (word, excel, ppt), outlook, and other essential tools required for routine activity Experience in developing and validating SEC, CGE methods is an added advantage especially for monoclonal antibodies (mAb) is an added advantage Experience in calibration and qualification of HPLC, UPLC, GC, and other QC laboratory instruments is added advantage Good communication and e-mail writing skills are required since the candidate needs to communicate with clients/external users situated overseas Commitment to safety Behavioral Skills Good Interpersonal skills Self-time management Good Team player Polite/Good Communication skills Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience 2-6 years Skills and Capabilities: Development, validation, and routine testing of Bioassay /ELISA, SEC, CGE for Monoclonal antibodies (mAbs) and other Large molecules Qualification and validation of cell-based bioassays Able to follow instructions and perform the tasks under the supervision of the Team leader Preparation and Maintenance of all the documents Experience in developing and validating SEC, CGE and HPLC methods for mAbs is an added advantage Theoretical knowledge in Chromatography and spectroscopy technique Good documentation/laboratory practices such as ALCOA+ Good knowledge of MS-office (word, excel, ppt) and E-mail writing skills Education M. Pharm/ M. Tech/ M.Sc. / B.Sc. (Biotechnology/Biochemistry) with 2-6 years experience in GMP environment (QC) Equal Opportunity Employer:

Career Category Regulatory Job Description Join Amgen s Mission of Serving Patients At Amgen, if you feel like you re part of something bigger, it s because you are. Our shared mission to serve patients living with serious illnesses drives all that we do. Since 1980, we ve helped pioneer the world of biotech in our fight against the world s toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Job Summary: Amgen is seeking a Manager, Regulatory Affairs CMC - Data Automation to shape the future of regulatory affairs by driving digital transformation and automation within CMC submissions. At Amgen, we are committed to innovation and excellence in regulatory science, offering a dynamic work environment where expertise in automation and AI can make a meaningful impact on regulatory efficiency and compliance. Join us in revolutionizing regulatory submissions through cutting-edge data automation! Key Responsibilities: Support the implementation of automation and digital tools to streamline regulatory CMC documentation and submission workflows. Assist in developing standardized templates and structured data formats for consistent and compliant submissions. Contribute to projects focused on the application of AI and structured content/data management (SCDM) for regulatory use cases. Coordinate with cross-functional teams, including Process Development, Quality, and Regulatory Affairs, to ensure alignment on automation and data standards. Monitor industry trends and guidance to maintain up-to-date knowledge on digital and regulatory innovations. Support the design and deployment of automated solutions for data extraction, conversion, and integration with regulatory platforms. Participate in training activities to expand internal capabilities in digital tools and regulatory data automation. Assist in regulatory interactions related to digital transformation, ensuring preparedness for engagement on evolving standards. Basic Qualifications: Doctorate degree OR Master s degree and 3 years of directly related experience OR Bachelor s degree and 5 years of directly related experience Experience managing and leading a team in a regulatory or compliance environment Preferred Qualifications: Degree in life sciences, digital or data science, biochemistry, or chemistry Experience leading global regulatory CMC submissions with knowledge of ICH guidance and global requirements Background or basic experience in digitalization, automation, software development Background in manufacturing, process development, quality control, or quality assurance Hands-on experience with Veeva Vault platforms and regulatory technology solutions. What we expect from you We are all different, yet we all use our unique contributions to serve patients. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers. amgen. com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation .

Dear Sir/Madam, We are urgently looking for Doctors for various Medical Colleges and Hospitals across India. For Medical Colleges, we require the following in all Clinical & Non-Clinical Departments: * Senior Residents * Assistant professors * Associate Professors * Professors * Medical Superintendents * Dean/Principals For Hospitals: Consultants & Surgeons in All Clinical Departments *** Please reply at the earliest to avail the most suitable position *** WEPS is the Topmost Healthcare Recruitment Firm in India. We recruit healthcare professionals for a variety of the Medical Colleges & Hospitals in the country. For further information and to upload your resume, please visit Regards, Tanu Goyal WEPS SCO 12, LGF, Hollywood Plaza, VIP Road, Zirakpur, SAS Nagar, Punjab 140 603 Email: weps.careers@gmail.com Mob: 7015609544 whatsapp@87015609544