43 Vaccines Jobs

Requirements: 1-3 years of experience in Injectable Plant production. Expertise in sterile manufacturing. Strong understanding of regulatory compliance & quality standards Educational qualification in Pharmacy, Biotechnology, or related fields.

Position Title : Senior Scientific Officer/Scientific Officer Grade : E - 7 Reporting To : Section Manager Natureof Position : Permanent EducationalQualification : M.Sc. / M.Tech (Biotechnology/Microbiology) Experience : 4 to 7years Locationofwork : Lalru Roles and Responsibility: 1. Knowledge about the updated cGMP guidelines 2. Knowledge about Cleaning, Operation, documentation and maintenance of chromatography systems (AKTA series) and water bath. 3. Responsible for online documentation as per cGMP along with routine log book management of production activity and equipment. 4. Knowledge of qualification (IQ/OQ/PQ) of chromatography systems (AKTA series), TFF systems, and refrigerators, cold rooms, HVAC/UDAF and tanks. 5. To ensure the entire downstream processing activity to be carried out as per compliance and process requirement 6. Knowledge for preparation and implementation of SOP/BMR/Protocols 7. Knowledge of adsorption, desorption, depth filtration, coarse and micro filtrations, centrifugation, ultrafiltration systems, Ion exchange, size exclusion and affinity chromatography. 8. Responsible for the execution of the purification modification with project team as and when required. 9. Knowledge of column packing 10. To ensure the effective cleaning and sanitation of the Core area, and systems as per schedule. 11. To ensure GMP compliance as per the applicable National and International rules and guidelines Such as Schedule M and World Health Organization (WHO). 12. Well versed with UNICORN software and integrity tester 13. Well versed with handling of QMS elements 14. Media fill, sterile filtrations, online particle counter and chartless temperature recorder 15. Hand on in MS word and excel 16. Calibration and verification of weighing balances, pH meters and spectrophotometer. 17. Knowledge of vNPC monitoring Competencies Required: 1. Thorough knowledge and understanding of column chromatography, column packing and TFF systems . 2. Understand Aseptic Behavior aseptic handling, aseptic working & aseptic cleaning. 3. Must understand Sterile Operations, Scientific practices & process criticalities of Vaccine manufacturing. 4. Analytical approach – Good in trend analysis, data evaluation & process calculations. 5. Adequate, Timely & Quality deliverance/ Output within stipulated timeframe. 6. Effective Communicator 7. Understanding of different room grades and area monitoring. 8. Motivate Team and Enable High Performance 9. Effectively Manage Absenteeism / Vacancy 10. Effective Performance Reviews of the Team and their Training responsibilities Preferred candidate profile

Amneal is coming in your city Hyderabad this 07th & 08th Jun 2025 for Walk In Drive Hiring for Projects & Engineering and Peptide expereince : Walk-In Interview Drive #Hyderabad We are coming to your city for a walk-in interview drive! If you're looking to build a rewarding career with a growing Global Pharmaceutical Company, dont miss this opportunity. Day 1: Saturday, 07th June 2025 Time: 9:00 AM to 5:00 PM Venue: Lemon Tree Premier Plot No. 2, Survey No. 64, HITEC City, Madhapur, Hyderabad 500081, Telangana Day 2: Sunday, 08th June 2025 Time: 9:00 AM to 5:00 PM Venue: Vivanta Hyderabad, Begumpet 1-10-147 & 148, Mayuri Marg, Begumpet, Hyderabad 500016, Telangana Opening in Engineering Department for the following opening : Designation : Sr Executive / Manager Yrs of Exp : 5-12 Yrs Qualification : M.Tech / B.E Expereince into Electrical : Experienced in electrical project execution, compliance, and commissioning, with strong knowledge of HT and LT electrical systems and a solid understanding of pharmaceutical equipment requirements. Expereince into Instrumentation Skilled in automation and instrumentation of equipment and utility systems, with hands-on experience in regulatory compliance, calibration, temperature mapping, and thermal validation. Expereince into Civil Civil engineer overseeing site execution, quality assurance, regulatory compliance, cross-functional coordination, and project documentation in pharmaceutical projects. Expereince into Mechanical Mechanical project scope includes HVAC systems, utility services, regulatory compliance, project timelines, and cross-functional coordination. In-depth knowledge of process equipment used in injectable pharmaceutical plants experience in the installation, commissioning, and qualification of water systems. Expereince into Process Strong expertise in equipment used for injectable manufacturing, with preferable knowledge of isolator systems. Experienced in the installation, commissioning, qualification, and documentation of process equipment Interested candidates who are unable to attend interview, can share their CV on below mentioned Email Id with subject line Application for Falcon indiacareers@amneal.com

Sterile Operations Trainer Grade: G8 Designation: Deputy General Manager Location: Halol 1 Job Description: Education: B. Pharm / M. Pharm Overall responsibility of Aseptic Training Academy (ATA), Baska To plan, develop, and execute training at Aseptic Training Academy (ATA) - Sterile Operations for Sun Global Operations (SGO) Training. Creation of simplified training modules for technicians, scheduling and execution of training Creation of training evaluation and/or feedback systems Course creation according to levels (Level 1 - Technicians, Level 2 - Supervisors and above, Level 3 - Managers and above) pertaining to sterile operations Planning, scheduling & execution of technical training program relevant to sterile operations for new recruits/for existing employee by self/internal or external facility Identification of Certified trainer at various locations (sterile operations) based on additional training need of respective location Coordination with location head and Subject Matter Expert (SME) for conducting the additional training program according to training calendar on monthly basis pertaining to sterile operations To prepare and submit SGO training score card for sterile operations on monthly basis after plant review to Corporate Quality Policy and Training department (CQPT) To maintain the training records of training Periodical review of technical courses along with business units for site specific course and the head of course for suitable course content / design and pedagogy up gradation To coordinate in technical course scheduling and publishing of calendars and facilitate visiting faculty/guest faculty in course delivery Any other work assigned by superiors from time to time

Regulatory Affairs Job Opportunity! Desired Experience : 3- 15 years Job Location : Genome Valley, Shameerpet, Hyderabad Preferred Industry : Vaccines / Biotech Designation: Senior Manager/ Manager/ Deputy Manager/ Assistant Manager/ Senior Executive/ Executive Qualification: M. Pharmacy/ M. Sc/ B. Pharmacy Job Responsibilities: Responsible for Regulatory submission to Indian NRA, Emerging Markets, Regulated Markets and World Health Organization. Experienced in handling, management and expansion of product portfolios, markets/ territories. Experienced in the preparation, review and submission of applications/ response to RCGM vide IBSC. Expertise in preparation, compilation and submission of Indian NRA applications (Eg: Form CT 10, 16, CT18, 40, 10, Export NoC, etc., but not limited) Well versed with Indian NRA submission portals, IBKP, SUGAM, NSWS, ODLS/ ONDLS, etc. Author, review and compilation of Regulatory Packages like Briefing documents, Scientific package, Pre-IND packages, Clinical Trial, Expedited request, Pre-qualifications, etc. Author, review, compile and submission of Marketing Authorization Applications (CTD/ ACTD/ eCTD) in India, Emerging Markets, Regulated Markets and Vaccine Prequalification Dossier to WHO. Application for Post Approval Change(s), Variations and Comparability packages Author, review and submission of responses to India, EM, WHO and Regulated markets.. Hands-on experience with MS office tools, PDF, Track Wise, DMS, Veeva Vault, Lorenz/ Pharma ready, etc.. Handling the Health Agency audits for India, EM, Regulated and WHO inspections Coordination with cross functional departments like QA, QC, Production, Warehouse, Distribution, Marketing and various teams (Internal & External). Review of Artworks (Labels and Package Insert) and Pack Profiles. Any other regulatory support required by the organization per submission need. Interested Candidates having relevant experience can send in their CVs to HR.Intern4@biologicale.com by mention the subject as Applying for "Regulatory Affairs"

Walk-In Drive Hyderabad | June 1, 2025 Join our growing team at OneSource The new way to CDMO We're hiring for multiple roles across our R&D and Manufacturing facilities in Bengaluru. Walk-In Interview Details: Date: Sunday, June 1, 2025 Time: 9:00 AM 4:00 PM Venue: Oakwood Residence, 115/1, Road No. 2, Financial District, Gachibowli, Hyderabad, Telangana 500032 Open Positions: Process Development Lab (Unit 1, Bommasandra) Research Associate | Sr. Research Associate | Scientist Qualification: B.Tech / M.Tech (Biotechnology) Experience: 2 – 12 years Drug Substance Manufacturing (Unit 2, Doddaballapura) Executive | Sr. Executive Qualification: MSc / B.Tech / M.Tech (Biotech, Microbiology) Experience: 2 – 8 years Drug Product Manufacturing (Unit 2, Doddaballapura) Executive | Sr. Executive | Team Leader Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm Experience: 2 – 12 years in sterile injectables

Biological E. Limited (BE) invites both experienced professionals and fresh diploma holders, as well as graduates and self-driven individuals, to join its Speciality Injectables Business located in Shamirpet, Hyderabad. The available positions are listed below: QUALITY ASSURANCE (IPQA) : Designation : Executive & Senior Executive Qualification : B. Pharm / M. Pharm / M.Sc. Experience : 3-9 Years Required Skills : Providing line clearances during the manufacturing activities like Dispensing, Manufacturing, Visual inspection, Packing and Dispatch activities, Collection and submission of in process samples, finished product samples, stability samples, control samples, cleaning samples and other samples as described in respective procedures/batch manufacturing records and packing records/protocol, Performing AQL inspection and periodic inspection of control samples, Review of the executed batch manufacturing records, batch packing records and protocols, Preparation and evaluation of the visual inspection defect set, test set and qualification of Visual inspectors, Person should have exposure on QMS elements (CAPA,Change control,Deviation). PRODUCTION PHARMA: Designation : Officer & Senior Officer Qualification : Diploma / B. Sc. Experience : 2-6 Years The candidate should possess the following skills: Hands on experience in Operation & Cleaning of Vial Washing machine, Depyrogenation Tunnel, Automatic,Terminal sterilization, Vial Filling and Vial Sealing machine & Automatic PFS filling machine. Hands on experience in Operation & Cleaning Lyophilizers with Auto Loading & Unloading Systems (ALUS). Exposure in Aseptic process activities, Aseptic Techniques, Aseptic filling & sealing activities and Media fill activities. Execution Knowledge on manufacturing and compounding activities. PRODUCTION PHARMA: Designation : Executive & Senior Executive Qualification : M. Pharmacy / B. Pharmacy /M.Sc Experience : 2-7 Years The candidate should possess the following skills: Hands on experience in Manufacturing, filtration, Filling, Lyophilization, Sealing, Pre & post Manufacturing activities. Planning and Execution of Batch Manufacturing Activities, Filling Activities, Lyophilization, sealing activities & filter Integrity. Experience on monitoring of NVPC and trending. Hands on experience in Documentation activities in shop floor. Planning & Execution of Aseptic Media Fill simulation activities & Execution of Interventions. Quality Control: Designation : Executive Qualification : B. Pharm / M.Sc. Experience : 3-6 Years (Injectables) Required Skills: Handling of HPLC/GC with empower Software is mandatory,Ion chromatograph with chromeleon software for DS & DP injectable, UV Visible Instrument, KF and Potentiometer with Tiamo Software, Analysis of In-process, Finished Product, Stability samples of injectable formulation, Knowledge on e-LIMS analysis is preferable, Analysis of AMV/AMT Activities, Analysis of diluent compatibility studies is preferable. Microbiology: Designation : Executive Qualification : M.Sc (Microbiology/Biotechnology) Experience : 3-6 Years Required Skills (EM) : Environmental Monitoring in aseptic areas, Water Sampling, Utility Monitoring, Trend Preparation. Required Skills (Testing): Culture handling , Bacterial Endotoxin Test , Sterility testing , Microbial method suitability (Sterility & BET) , Container closure integrity test , Microbial Limit testing , Water testing , Media preparation and sterilization , Regulatory Audit exposure , Good communication skills , Willing to work on shifts Engineering: Designation : Officer/Sr.Officer/Executive/Sr.Executive Qualification : Diploma/B. Tech. Experience : 3-8 Years The candidate should possess the following skills: Utilities: Candidates with the ability to handle utility equipment such as air compressors,Industrical chillers, and boilers. Candidates should also possess sound knowledge of documentation practices and Quality Management System (QMS) elements. Exposure to regulatory audits/inspections by authorities such as USFDA, MHRA, and other global agencies. HVAC: Candidates should have a strong background in the operation and maintenance of HVAC systems in a sterile/regulated environment. Experience in handling equipment such as AHUs, chillers, cold chambers, LAFs ,DPB,Walkin incubators and SPB. Strong understanding of documentation practices and Quality Management System (QMS) elements. Exposure to regulatory audits/inspections by authorities such as USFDA, MHRA, and other global agencies. Water system: Candidates must have hands-on experience with CSRO, HSRO, WFI, and PSG systems, along with knowledge of routine monitoring and GMP documentation. Familiarity with QMS elements and exposure to regulatory audits (USFDA, MHRA, etc.) is essential. Process Instrumentation - Injectables regulatory : Candidates with the ability to handle Lyophilizer, vial line, PFS line, auto claves and compounding equipments, PFS & Vial line related packing equipments. Candidates should have knowledge on SCADA,HMI and PLCs. Should have exposure in regulatory audits. Should work in shifts and should able to handle periodic activities & documentation and qualifications. Process Instrumentation API regulatory : Should handle shift instrumentation activities and have experience on handling automations that includes PLC & SCADA in API equipment. Should have experience on troubleshooting of Lyophilizer. Should handle periodic activities like data backups etc. should have exposure in regulatory audits. BMS & Outside Instrumentation: Should handle field instruments, SCADA (Honeywell) and PLC during BMS trouble shooting. Should handle shift activities for BMS & IBMS monitoring and trouble shooting. should able to handle periodic activities & documentation and qualifications. Interested Candidates may Walk-in with an updated Resume, latest increment letter, and payslips for the last 3 months on Sunday, Jun 01, 2025 from 09:00 am to 02:00 pm at Hotel Kinara Residency, Utsav Banquet Hall, 2nd Floor, 2-62/2, S.R. Chambers, beside BSNL building, Chandanagar, Hyderabad, Telangana -500050. PS: Candidates who are unable to walk-in may send in their CVs by mention subject as Applying for Department Name to careers@biologicale.com . If an individual has already attended the interview in the past 6 months or has already been offered a position with us, please do not share the profiles. - Human Resources

Job role Details: (Just same as a Medical Representative) The ethical promotion of Nestle's infant nutrition products in their territory by clearly communicating with Health Care Professionals (HCPs) about Nestle's Infant Nutrition products, their features, advantages, benefits and their appropriate use, within the Code of Ethics Nestle's instructions and keeping in mind, mother's milk is best for Babies. Ensuring recommendation for the Nestle Nutrition product range within the scope of the Indian Code, detailing against homemade Paps and bovine milk. Being a reliable source of information on infant nutrition and infant feeding practices. Ensuring quality execution in terms of detailing/ conducting scientific symposiums etc. as per the company guidelines. Who can apply: Candidates who are graduates with at least 1 year of experience in nutrition or pharmaceutical industry. Candidates with high level of integrity & honesty, hardworking, self-motivator and passionate about enhancing quality of life and contributing to healthier future. Being able to work effectively in a team Ability to build strong and sustainable relationships High Learning agility Trustworthy and be able to work independently within the company policy & guidelines Nestle is committed to providing equal opportunities without any discrimination on the grounds of age, color, disability, origin, nationality, religion, race, gender, or sexual orientation. We are an equal opportunity employer, and we value diversity at our company. For any reasonable accommodation in the recruitment process for persons with disabilities, kindly reach out to your recruiter. Reasonable accommodation includes any appropriate modifications to ensure that persons with disabilities are provided an equal platform in the recruitment process's.

Inspection and verification of In-process activity in Manufacturing Area. Monitoring of Handover Activity of ARM/Bulk. Verification of Packing and Dispatch activity for Final ARM/Bulk. Issuance of Cell Bank / Issuance of Reference standard.

Role- AGM- International Business development- LATAM; East Europe / Russia CIS Company- A leading Biopharmaceutical Company Location- Bangalore Reporting To- VP- BD Roles and Responsibilities This role requires a dynamic individual with excellent analytical skills, strategic thinking, and the ability to manage complex projects and partnerships across semi-regulated markets, including Emerging Markets Latin America, Europe, . Expertise in sales and marketing within these regions is essential. Develop international business strategies to drive growth in overseas markets. Identify new opportunities for product launches and market expansions. Analyze market trends, competitor activity, and customer needs to inform business decisions. Deep & hands on understanding on the Documentation, Regulatory ecosystem/landscape, Dossier preparation to submission, facilitation at target market Identify and evaluate opportunities for in-licensing and out-licensing of Plasma Derived Products / Critical Care / Oncology / Vaccine / Biohpharma products across semi-regulated markets. Manage relationships with key customers, distributors, and partners. Will be responsible for managing International BD for regions such as- LATAM; East Europe / Russia CIS Desired Skills Post Graduation Degree in Business Management or Life Sciences. Total 15+ years of relevant pharmaceutical industry experience. Strong background in bio-pharmaceutical international business, particularly in semi-regulated markets such as Latin America, Europe, Emerging Market Expertise in sales and marketing within these regions. Sound knowledge of the global pharmaceutical industry (Biologics (Biopharm; Oncology. Critical Care, Vaccines. Strong analytical skills with advanced knowledge of Excel and PowerPoint. Excellent verbal and written communication skills with the ability to network effectively.

WALK-IN INTERVIEW FOR EXPERIENCED PROFESSIONALS Job Location: Hyderabad Experience: 2 to 10 Years Qualification: ITI / Diploma / B.Sc / B.Pharmacy / M.Sc Designations: Operator Sr. Operator Jr. Executive Executive Sr. Executive Openings in the Following Areas: 1. Drug Substance (Bioprocess) Roles & Responsibilities: Upstream Process: Cell Culture Fermentation Autoclave Operation Downstream Process: Virus Culture Centrifugation Tangential Flow Filtration (TFF) Purification Chromatography 2. Drug Product (Formulation & Filling) Roles & Responsibilities: Formulation Activities Filling (Vials, BFS, PFS) Operating Equipment in: Closed RABS (C-RABS) Open RABS (O-RABS) Isolators Sealing and Capping Vial Washing & Autoclaving 3. Packing & Visual Inspection Roles & Responsibilities: Primary and Secondary Packing Operations Handling Track and Trace Systems Operating Labeling and Cartonator machine Documentation & SAP Entries Visual Inspection of Vials & Pre-Filled Syringes (PFS) Note: Candidates with relevant experience in regulatory and compliance environments (USFDA, EU GMP, etc.) will be preferred. Please bring: Updated resume, latest salary slips, passport-size photo, and original certificates.

Job role Details: (Just same as a Medical Representative) The ethical promotion of Nestle's infant nutrition products in their territory by clearly communicating with Health Care Professionals (HCPs) about Nestle's Infant Nutrition products, their features, advantages, benefits and their appropriate use, within the Code of Ethics Nestle's instructions and keeping in mind, mother's milk is best for Babies. Ensuring recommendation for the Nestle Nutrition product range within the scope of the Indian Code, detailing against homemade Paps and bovine milk. Being a reliable source of information on infant nutrition and infant feeding practices. Ensuring quality execution in terms of detailing/ conducting scientific symposiums etc. as per the company guidelines. Who can apply: Candidates who are graduates with at least 1 year of experience in nutrition or pharmaceutical industry. Candidates with high level of integrity & honesty, hardworking, self-motivator and passionate about enhancing quality of life and contributing to healthier future. Being able to work effectively in a team Ability to build strong and sustainable relationships High Learning agility Trustworthy and be able to work independently within the company policy & guidelines Nestle is committed to providing equal opportunities without any discrimination on the grounds of age, color, disability, origin, nationality, religion, race, gender, or sexual orientation. We are an equal opportunity employer, and we value diversity at our company. For any reasonable accommodation in the recruitment process for persons with disabilities, kindly reach out to your recruiter. Reasonable accommodation includes any appropriate modifications to ensure that persons with disabilities are provided an equal platform in the recruitment process's.

Walk-in-Interview Biological E. Limited invites experienced, dynamic, and self-motivated professionals with 2 to 10 years of experience to apply for the following positions in its Vaccine and Pharma SGI businesses, located in Shamirpet, Hyderabad. Production (Injectables): Designation: Sr. Executive/ Executive/Sr. Officer/Officer Qualification: M Pharmacy/ B Pharmacy/ M Sc/ Diploma / B. Sc. Job role: Experience in Manufacturing, Compounding, filtration, Filling, Washing, Lyophilization, Sealing, Pre & Post Manufacturing activities. Isolators experience will be preferable. QA - In Process Quality Assurance (IPQA): Designation: Dy. Manager/Asst. Manager/Sr. Executive/Executive Qualification: M. Pharmacy/ B. Pharmacy/ M.Sc. (Lifesciences) / B. Tech/M. Tech (Biotechnology) Job Roles: Drug Product: To execute Fill-Finish activities. review of SOPs, batch records, validations and media fills; line clearance for filling operations; change controls, deviations, OOS investigations, and trend analysis. Drug Substance: To execute activities for Bulk Viral Antigen production, line clearance, dispensing. review and approval of batch records, SOPs, PV, CV, and APS documents; QMS management; trending and batch release activities; control and reconciliation of Master and Working Cell Banks. Quality Assurance (Validation): Designation: Sr.Executive/Executive Qualification: M. Pharmacy/ B. Pharmacy/ M.Sc. / B. Tech Job Roles: Experience in Preparation and review and Execution of Qualification/Validation protocols and reports for its compliance, Responsible for review of Engineering related Preventive maintenance schedules, Calibration schedules, Calibration certificates, Validation protocols and log books. Quality Control (Biologics/Vaccines): Designation: Asst. Manager/Sr. Executive/Executive Qualification: M.Sc. (Lifesciences) / B. Tech/M. Tech (Biotechnology) Job Roles: Biochemical Assays: - Estimation of components in polysaccharides, along with biochemical analyses such as protein, nucleic acid, aluminium content, and composition analysis. Analytical method validation, adherence to ALCOA principles,OOS and OOT investigations. Instrumentation Testing: - Analytical instruments such as HPLC and IC, along with performing instrument-based assays including molecular size, aggregates, purity, and composition analysis. Basic troubleshooting, 21 CFR Part 11 and Audit trial review practices, ALCOA principles, OOS, OOT systems and investigations. Virology: Experience in in-vitro viral testing of Starting material, Raw material, In-process, Final bulk, Final lot and Stability samples for Viral vaccines. review testing for QC release of products/RM/stability studies of Viral Vaccines/New projects/Products. Interested candidates may walk-in with an updated CV, latest increment letter and the last 3 months payslips on 25th May, 2025 i.e., Sunday from 09:30 am to 03:00 pm at Hotel Vivanta, 147, 53, SG Highway, opposite Bhagwat Vidhya Peeth, Sola, Ahmedabad, Gujarat - 380061. PS: Candidates who are unable to walk-in may send in their CVs by mention subject as Applying for Department Name to careers@biologicale.com . If an individual has already attended the interview in the past 6 months or has already been offered a position with us, please do not share the profiles. - Human Resources

A pediatrician's job description involves caring for infants, children, and adolescents, encompassing preventative care, diagnosis and treatment of illnesses, and monitoring growth and development

Role & responsibilities Expertise in batch manufacturing and preparation related activities. To observe & follow all rules and regulations of the production department. Must be from Parenteral background & exposure to Aseptic vial / Bottle filling process is desirable. To be aware and responsible for achieving quality objective and fulfilling the requirements of applicable quality procedures. Technical exposure and expertise on filling & Autoclave machine. Exposure of USFDA audits. Preferred candidate profile Candidate should have relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliance) organization. Perks and benefits As Per Company Norms.

Job description Job role Details: (Just same as a Medical Representative) The ethical promotion of Nestle's infant nutrition products in their territory by clearly communicating with Health Care Professionals (HCPs) about Nestle's Infant Nutrition products, their features, advantages, benefits and their appropriate use, within the Code of Ethics Nestle's instructions and keeping in mind, mother's milk is best for Babies. Ensuring recommendation for the Nestle Nutrition product range within the scope of the Indian Code, detailing against homemade Paps and bovine milk. Being a reliable source of information on infant nutrition and infant feeding practices. Ensuring quality execution in terms of detailing/ conducting scientific symposiums etc. as per the company guidelines. Who can apply: Candidates who are graduates with at least 1 year of experience in nutrition or pharmaceutical industry. Candidates with high level of integrity & honesty, hardworking, self-motivator and passionate about enhancing quality of life and contributing to healthier future. Being able to work effectively in a team Ability to build strong and sustainable relationships High Learning agility Trustworthy and be able to work independently within the company policy & guidelines Nestle is committed to providing equal opportunities without any discrimination on the grounds of age, color, disability, origin, nationality, religion, race, gender, or sexual orientation. We are an equal opportunity employer, and we value diversity at our company. For any reasonable accommodation in the recruitment process for persons with disabilities, kindly reach out to your recruiter. Reasonable accommodation includes any appropriate modifications to ensure that persons with disabilities are provided an equal platform in the recruitment process's s

ROLE PROFILE Position Title : International Business Development Job Level (HR use only) Department International Business Development Location Corporate Office Sub Department NA Reports to VP- Sales & Marketing Role Purpose We are seeking a highly experienced and deliberate AGM for our International Business Development team. The ideal candidate will have a strong background in pharmaceutical international business, with a focus on in-licensing, out licensing, mergers & acquisitions, and market intelligence. This role requires a dynamic individual with excellent analytical skills, strategic thinking, and the ability to manage complex projects and partnerships across semi-regulated markets, including Emerging Markets Latin America, Europe, . Expertise in sales and marketing within these regions is essential. Principal Accountabilities and Key Activities 1. Business Development: Deep & hands on understanding on the Documentation, Regulatory ecosystem/landscape, Dossier preparation to submission, facilitation at target market Identify and evaluate opportunities for in-licensing and out-licensing of Plasma Derived Products / Critical Care / Oncology / Vaccine / Biohpharma products across semi-regulated markets. Explore early launch and tactical opportunities to fill gaps in the start-plan. Identify long-term, niche, and complex opportunities that align with the company's strategic goals. 2. Partner/Alliance Management: Manage existing partnerships and identify new opportunities for products or markets. Conduct commercial negotiations, contract closures, and presentations to cross-functional teams (CFT) and executive leadership teams (ELT). Oversee end-to-end deal management from opportunity identification, commercial negotiation, due diligence, contract negotiation, to deal closure and support for launch activities. 3. Market and Competitive Intelligence: Generate competitive intelligence (CI) data for peers, partners, products, and markets. Analyze market competition and pricing using various methodologies and databases such as IQVIA, import/export data, Global data, and clinical trials. Monitor qualitative market events and generate monthly reports summarizing key events, including new approvals, filings, PIV listings, new launches, product line extensions, combinations, and EXIM data. 4. Performance Analysis: Track competitor activities and generate monthly reviews of their implications for the company using IMS, export/import, and other relevant databases. Benchmark the company's performance and productivity against competitors based on available data. Work closely with business teams and the BD/portfolio team to provide analyses and reports based on pharmaceutical audits and other secondary data. 5. Sales and Market Analysis: Analyze sales, market, competitor, and market research data to provide business insights. Publish weekly/monthly product performance updates and analysis. Generate insights based on secondary or primary research data. 6. People Management: Lead and manage a team, fostering a collaborative and high-performance work environment. Ensure effective communication and coordination among team members and other departments 7. International Travel: Travel internationally as required to manage business development activities and partnerships. Internal Stakeholders External Stakeholders Functional Heads Business Development Sales and Marketing Regulatory Affairs Research and Development Finance & Accounts Legal SCM Pharmaceutical Companies Regulatory Bodies Healthcare Professionals Patients and Patient Associations Market Research Firms Distributors and Wholesalers Industry Associations Academic and Research Institutions Third Party / Liaison Agency Knowledge, Experience and Qualification Technical Knowledge and Understanding of: Education & Experience: Skills & Ability: Sound knowledge of the global pharmaceutical industry (Biologics (Biopharm; Oncology. Critical Care, Vaccines. Strong analytical skills with advanced knowledge of Excel and PowerPoint. Excellent verbal and written communication skills with the ability to network effectively. Strategic thinker with an analytical approach to problem-solving. Proven track record in commercial negotiations and contract management. Ability to work with cross-functional teams and manage complex projects. Post Graduation Degree in Business Management or Life Sciences. Total 15+ years of relevant pharmaceutical industry experience. Strong background in bio pharmaceutical international business, particularly in semi regulated markets such as Latin America, Europe, Emerging Market Expertise in sales and marketing within these regions. Strong understanding of market research methodologies and competitive intelligence. Ability to generate and interpret CI data and market analysis reports.

Job Title: Manager/Senior Manager QA Regulatory Affairs Company: GreenSignal Bio Pharma Pvt Ltd Location: Gummidipoondi, Chennai, Tamil Nadu Experience: 8-15 years in Quality Assurance and Regulatory Affairs, specifically within the Vaccine, Injectable, and Sterile Industry Educational Qualification: M.Sc in Biotechnology, Microbiology, or a related field Bachelor’s or Master’s in Pharmacy Additional qualifications in life sciences or pharmaceutical sciences are a plus Job Overview: As the Manager/Senior Manager – QA Regulatory Affairs , you will play a pivotal role in ensuring that our vaccine , injectable , and sterile pharmaceutical products meet global regulatory requirements and quality assurance (QA) standards. You will oversee regulatory strategies, regulatory audits, and the management of Quality Management Systems (QMS) to ensure our products comply with industry-specific standards. This role demands extensive experience in regulatory affairs , particularly within the vaccine and sterile manufacturing domains, including handling CDSCO , EU GMP audits, and other regulatory matters. Key Responsibilities: Regulatory Strategy & Compliance: Develop and execute regulatory strategies to ensure compliance with global standards for vaccine , injectable , and sterile products . Maintain a strong understanding of global regulatory requirements, including FDA , EMA , WHO , and local regulations like CDSCO to guide product approvals and market entry. Ensure alignment of product development and manufacturing processes with Good Manufacturing Practices (GMP) , Good Laboratory Practices (GLP) , and other relevant GxP standards. Audit & Inspection Management: Coordinate and manage regulatory audits (e.g., CDSCO , EU GMP ) for vaccine , injectable , and sterile products, ensuring full compliance and readiness across all departments. Lead the preparation for regulatory inspections related to CDSCO and EU GMP , working closely with relevant teams to ensure effective corrective actions and continuous compliance. Manage responses to audit findings and ensure the implementation of corrective actions in line with industry standards. Quality Management System (QMS): Oversee the implementation and management of the Quality Management System (QMS) to ensure product quality and regulatory compliance. Lead the development and review of Standard Operating Procedures (SOPs) , ensuring that they align with current regulatory requirements for vaccine and sterile product manufacturing. Monitor and ensure compliance with the QMS framework across all departments to maintain consistent product quality. Regulatory Submissions & Documentation: Oversee the preparation, compilation, and submission of regulatory dossiers and eCTD documents to regulatory bodies (e.g., FDA , EMA , CDSCO ). Ensure that all required documentation and records are properly maintained and comply with regulatory standards, ensuring smooth regulatory approvals for vaccine , injectable , and sterile products . Risk Assessment & Mitigation: Conduct regulatory risk assessments to identify potential issues related to product development, manufacturing, and compliance. Develop and implement risk mitigation strategies to ensure uninterrupted production and compliance with regulatory standards. Cross-Functional Collaboration: Collaborate with internal teams such as R&D, Production, and Quality Control to ensure regulatory compliance throughout the product lifecycle, from development to post-market surveillance. Provide regulatory guidance and training to cross-functional teams, ensuring awareness of applicable QA practices and regulatory requirements . Corrective and Preventive Actions (CAPA): Lead the implementation of Corrective and Preventive Actions (CAPA) to address audit findings, non-conformities, and deviations, ensuring continuous improvement in compliance and quality practices. Key Skills and Competencies: Expert Knowledge of Regulatory Guidelines : Extensive knowledge of global regulatory requirements (e.g., FDA , EMA , WHO ) with specific expertise in vaccines , injectables , and sterile product manufacturing . Regulatory Submissions & Documentation Expertise : Strong experience in preparing regulatory dossiers and eCTD submissions in compliance with regulatory standards for vaccines and sterile products . Audit & Inspection Management : Hands-on experience managing CDSCO and EU GMP audits, including preparing for inspections, addressing findings, and implementing corrective actions. Quality Management System (QMS) Oversight : Expertise in implementing and maintaining QMS in compliance with GxP , FDA , EU , and WHO guidelines, ensuring product quality and regulatory compliance. Risk Management & Mitigation : Proven ability to conduct regulatory risk assessments and implement mitigation strategies to prevent non-compliance and product issues. Strong Leadership & Project Management : Demonstrated ability to lead cross-functional teams, manage multiple projects, and meet regulatory deadlines while ensuring alignment with quality and regulatory expectations. Corrective & Preventive Action (CAPA) Implementation : Experience in managing CAPA processes, addressing non-compliance issues, and ensuring the effective resolution of audit findings and regulatory observations. Excellent Communication Skills : Strong verbal and written communication skills, with the ability to liaise with internal teams, regulatory bodies, and external stakeholders in a professional and clear manner. About GreenSignal Bio Pharma Pvt Ltd: GreenSignal Bio Pharma Pvt Ltd is a leading pharmaceutical company specializing in vaccine , injectable , and sterile products . Our commitment to quality, compliance, and innovation has made us a trusted partner in the healthcare industry. We are looking for experienced professionals to contribute to advancing our vaccine and biologics portfolio while adhering to the highest regulatory standards. For more information, please visit: www.gsbpl.com How to Apply: Interested candidates can apply via email at: hr@gsbpl.com For inquiries, please contact us at: +91 8778926365 Join Our Team and make a significant impact in the vaccine and sterile product industries

Job role Details: (Just same as a Medical Representative) The ethical promotion of Nestle's infant nutrition products in their territory by clearly communicating with Health Care Professionals (HCPs) about Nestle's Infant Nutrition products, their features, advantages, benefits and their appropriate use, within the Code of Ethics Nestle's instructions and keeping in mind, mother's milk is best for Babies. Ensuring recommendation for the Nestle Nutrition product range within the scope of the Indian Code, detailing against homemade Paps and bovine milk. Being a reliable source of information on infant nutrition and infant feeding practices. Ensuring quality execution in terms of detailing/ conducting scientific symposiums etc. as per the company guidelines. Who can apply: Candidates who are graduates with at least 1 year of experience in nutrition or pharmaceutical industry. Candidates with high level of integrity & honesty, hardworking, self-motivator and passionate about enhancing quality of life and contributing to healthier future. Being able to work effectively in a team Ability to build strong and sustainable relationships High Learning agility Trustworthy and be able to work independently within the company policy & guidelines Nestle is committed to providing equal opportunities without any discrimination on the grounds of age, color, disability, origin, nationality, religion, race, gender, or sexual orientation. We are an equal opportunity employer, and we value diversity at our company. For any reasonable accommodation in the recruitment process for persons with disabilities, kindly reach out to your recruiter. Reasonable accommodation includes any appropriate modifications to ensure that persons with disabilities are provided an equal platform in the recruitment process's.

Role & responsibilities: Media preparation, media suitability test, growth promotion test. Water sampling and testing. Maintenance of stock cultures, sub culturing and culture suspension preparation. Environment monitoring program (passive air sampling, Active air sampling and surface sampling). Sterility Testing, Bacterial endotoxin test, bioburden testing. Testing of Total organic carbon (TOC) in water samples. Endotoxin testing through KTA method and Gel Clot method. Testing of media fill samples. Enumeration of biological indicators. Preparation of trends and compilation summery for water and environmental monitoring. Establishment of alert and action limits for water and environmental monitoring. Establishment of Limit for bioburden samples. Identification or microorganisms by Vitek 2 Identification system. Container closure integrity test. Preservative efficacy test. Disinfectant Validation. Handling of Change controls, deviation, Out of Specification and writing of audit justification reports. Preparation of sops, protocols and reports aligning as per quality standards, cGMP documents as per pharmacopeias. Audits faced USFDA,WHO, MHRA, ANVISA,customer audits, etc.. Training of team members in SOP, Analyst qualification, Quality documents Preferred candidate profile: Posses the quality of good Team Leader. Believe in team work. • Should have exposure to day-to-day routine microbiological activities like media preparation, culture handling, Plating etc. *Relevant experience must be for working in microbiology lab. *Must have experience of working into sterile area.

JOB DESCRIPTION: Hands on experience in Injectable formulation and exposure to biotech/ Biopharma Formulations in any reputed biotech or vaccine based companies. Sales experience in injectable and biotech/ biopharma ingredients. Position is to be based in Mumbai with travel pan India. Self- motivated, driven and keen interest in networking with good communication and presentation skills. Technical people who want to get on the commercial side can apply.

1. Animal Health and Welfare: - Monitor and maintain the overall health of the farm animals. - Develop and implement disease prevention and control measures. - Ensure animal welfare standards are met. 2. Disease Diagnosis and Treatment: - Conduct regular check-ups and diagnose diseases. - Develop and implement treatment plans. - Monitor treatment efficacy and adjust plans as needed. 3. Vaccination and Immunization: - Develop and implement vaccination schedules. - Ensure timely vaccination of animals. - Monitor vaccine efficacy and adjust schedules as needed. 4. Reproductive Health and Breeding: - Monitor reproductive health of breeding animals. - Develop and implement breeding programs. - Ensure optimal reproductive performance. 5. Nutrition and Feed Management: - Collaborate with nutritionists to develop and implement feeding plans. - Monitor feed quality and ensure optimal nutrition. 6. Biosecurity and Hygiene: - Develop and implement biosecurity protocols. - Ensure proper hygiene practices are followed. 7. Mortality and Morbidity Management: - Monitor and investigate mortality and morbidity cases. - Develop and implement strategies to reduce mortality and morbidity. 8. Record Keeping and Reporting: - Maintain accurate and up-to-date records. - Prepare and submit regular reports on animal health, disease incidence, and other relevant metrics. 9. Training and Capacity Building: - Provide training and guidance to farm staff on animal health and welfare. - Collaborate with other experts to stay updated on best practices. 10. Compliance with Regulations and Standards: - Ensure compliance with relevant laws, regulations, and industry standards.

Job role Details: (Just same as a Medical Representative) The ethical promotion of Nestle's infant nutrition products in their territory by clearly communicating with Health Care Professionals (HCPs) about Nestle's Infant Nutrition products, their features, advantages, benefits and their appropriate use, within the Code of Ethics Nestle's instructions and keeping in mind, mother's milk is best for Babies. Ensuring recommendation for the Nestle Nutrition product range within the scope of the Indian Code, detailing against homemade Paps and bovine milk. Being a reliable source of information on infant nutrition and infant feeding practices. Ensuring quality execution in terms of detailing/ conducting scientific symposiums etc. as per the company guidelines. Who can apply: Candidates who are graduates with at least 1 year of experience in nutrition or pharmaceutical industry. Candidates with high level of integrity & honesty, hardworking, self-motivator and passionate about enhancing quality of life and contributing to healthier future. Being able to work effectively in a team Ability to build strong and sustainable relationships High Learning agility Trustworthy and be able to work independently within the company policy & guidelines Nestle is committed to providing equal opportunities without any discrimination on the grounds of age, color, disability, origin, nationality, religion, race, gender, or sexual orientation. We are an equal opportunity employer, and we value diversity at our company. For any reasonable accommodation in the recruitment process for persons with disabilities, kindly reach out to your recruiter. Reasonable accommodation includes any appropriate modifications to ensure that persons with disabilities are provided an equal platform in the recruitment process's.

Role & responsibilities Equines diagnosis, treatment, vaccination, perform minor surgeries and assist in major surgeries Preferred candidate profile B.V.Sc., preference will be given to M.V.Sc. in Clinical subject. Last date for applying for the position 21.03.2025. Perks and benefits Best in Industry

Job Description Company: GreenSignal Bio Pharma Pvt Ltd Location: Gummidipoondi, Chennai, Tamil Nadu Experience: 1-12 years above in production, preferably in the Bio-Pharmaceutical industry, specifically in vaccine manufacturing Educational Qualification: MSc Microbiology/Biotechnology/B. Pharm/B.Tech with more than 8 years of experience in vaccine biologicals and injectables Job Title: Senior Manager / Manager / Executive- Production Job Summary: The Senior Manager /Executive - Production will oversee daily vaccine manufacturing operations, ensure compliance with regulatory guidelines, manage production staff, and drive continuous improvement to enhance operational efficiency and product quality within the pharmaceutical industry. Key Responsibilities: Production Planning and Coordination: Plan, coordinate, and optimize end-to-end vaccine production activities to meet quality standards, timelines, and cost targets while ensuring resource availability. Oversee Manufacturing Operations: Supervise day-to-day manufacturing operations, including formulation, filling, packaging, and storage processes, ensuring efficient workflow and compliance with production protocols. Compliance: Ensure adherence to Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMP), and regulatory guidelines (FDA, EMA, WHO). Issue Resolution: Troubleshoot and resolve production-related issues to minimize downtime and ensure batch integrity. Team Management: Lead and manage production staff, providing training on safety, quality, and operational protocols specific to vaccine manufacturing. Performance Monitoring: Track key production metrics, implement strategies to improve batch yields, and reduce material wastage. Safety Enforcement: Enforce workplace safety protocols to prevent accidents, contamination, and ensure bio-safety compliance. Risk Management: Identify risks in production processes, such as contamination risks or equipment failures, and develop contingency plans. Material Handling: Ensure safe handling, storage, and disposal of biological materials, vaccines, and hazardous chemicals following industry best practices. Process Improvement: Drive continuous improvement initiatives to enhance production efficiency and product quality. Equipment Management: Oversee the maintenance, calibration, and validation of production equipment to ensure optimal performance. Documentation and Reporting: Ensure accurate documentation of production activities and prepare reports for regulatory compliance and internal audits. Skills and Competencies: Strong leadership and team management abilities in vaccine manufacturing environments In-depth knowledge of GMP, regulatory compliance, and vaccine production protocols Proficient in production planning, batch processing, and process optimization Excellent problem-solving and troubleshooting skills within pharmaceutical production settings Strong communication and interpersonal skills for effective team coordination Risk assessment and mitigation capabilities specific to biological production Commitment to bio-safety, product quality, and continuous improvement About GreenSignal Bio Pharma Pvt Ltd: GreenSignal Bio Pharma Pvt Ltd is a leading pharmaceutical company dedicated to delivering quality healthcare solutions, with a strong focus on vaccine manufacturing and biological products. Our commitment to innovation, compliance, and operational excellence drives our success. For more information, please visit our website: www.gsbpl.com How to Apply: Interested candidates can apply at: hr@gsbpl.com Contact us at: 8778926365 Apply Now to join our team and contribute to impactful pharmaceutical and vaccine innovations!