59 Vaccines Jobs - Page 2

Job role Details: (Just same as a Medical Representative)Role & responsibilities Preferred candidate profile Key Responsibilities: Responsible for Infant Nutrition products medical detailing to the Doctors and Health Care Professionals (HCPs) in the territory. Responsible of ensuring recommendation for the Infant Nutrition product range within the scope of the Indian Code & Infant Milks Substitute Code. Responsible of ensuring quality execution in terms of detailing/ conducting symposiums etc. as per the company guidelines Ensuring the visibility and availability of the product in the market by collaborating with the sales team. Qualification Bachelors Degree in Science (Bsc- Biology, Zoology, Microbiology, Botany, Chemistry, Biotechnology, Biochemistry, Nursing, Home Science, Nutrition & Dietetics or Bpharma ) Experience: Min 1 7 years of experience in field sales role in either Nutrition or Pharma Industry Key Skills: Candidates to have high level of integrity & honesty, hardworking, self-motivator and passionate about enhancing quality of life and contributing to healthier future Good in communication and to possess high learning agility Being able to work effectively in a team and have an ability to build strong and sustainable relationships Trustworthy and be able to work independently within the company policy & guidelines Nestl is committed to the accessibility of its recruitment process. If you require an adaptation during the recruitment process, please talk to your recruiter so we can support you effectively. All information will be treated confidentially. Nestl 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

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.

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

Dear Aspirant , Greetings From Eugia Pharma Specialties Limited (Aurobindo Group)!!!! We glad to inform you all that we planned Walk In Interviews for below vacancies in our Manufacturing unit. Department : Quality Assurance (IPQA) No. of Vacancies : 30 Education Qualification : B. Pharmacy / M Pharmacy Experience : 2-5 Years Designation : Executive Required Skills : Aseptic Area Monitoring / Environmental Monitoring / Aseptic behavior / Media Fill / Gowning Practices / Sterility Assurance/ In Process checks in Injectable Work Location : Eugia Unit -3, Pashamylaram Walk In Details: Date : 29.06.2025 Time : 09 AM - 02 PM Venue : Aurobindo Pharma Limited - Unit - 3 Sy. No. 313, Bachupally, Hyderabad, Telangana 500090 Google Map : https://maps.app.goo.gl/qoL8vZ6EwDm5GcWb8 Contact : Mr Prabhakar / Ms Rama

Role & responsibilities The position is responsible for Moisture and Thiomersal estimation and ensuring GMP practices Physical observation of vaccines and diluents Formulation Verification Record maintenance Maintenance of Live and Inactivated FG samples and register Maintenance of Pullet ND samples at R&D in coordination with production Moisture estimation of Live vaccines, stability & record keeping and R&D testing To Fill records & BTR Regarding Moisture Determination RM - pH, viscosity, density, specific gravity, refractive index, LOD, water Egg sampling and record maintenance Maintenance of retain samples of RM Preferred candidate profile Should have technical knowledge in GMP, GLP, ISO, IS, IP, BP guidelines, MS office Good in communication, inter-personal relationships Job Location: Kadi,Gujarat ( Bus facility available from Ahmedbad,Kalol & Kadi)

Role & responsibilities Vaccine Manufacturing (Cell Culture) Responsible for cell revival, subculture, cell counting of MRC-5 cells. Preparation of MCB/WCB. Experience in handling Roller bottles, Cell stacks, TCFs. Quality Control (Bacterial/Viral) Candidate should have good knowledge of Product testing techniques like : Biochemical, Chromatography, Electrophoresis, Immuno assay, Cell culture & Molecular techniques. Experience in handling HPLC, Dionex, UV-Spectrophotometer, Multimode plate reader and ELISA. Shall be well versed with Biochemical assays (Protein, O-acetyl) immuno-chemical assays and electrophoresis, Education: - Post-Graduate M.Sc. in Biochemistry, Biotechnology, Microbiology, Lifesciences. Experience: - 1-6 years of hands-on experience in relevant field, preferred Vaccine/Biotech background.

Good knowledge and understanding of proteins. Sound knowledge on Good laboratory practices. Hands-on experience on LC based analysis/developments for recombinant protein (mAbs/Biosimilars) required Good team player. Good written and oral communication Role & responsibilities Should have sound knowledge of ICH/USP/EP/IP guidelines, including the writing and review of developmental protocols and reports. Will be part of ADL- The team works on- new method developments, qualifications, process development quality analysis, R&D stabilities Will carry out LC based developments for various quality evaluations of recombinant proteins (Example- RP, IEX, Glycans) Will carry out CE based developments for various quality evaluations Will carry out various analysis for supporting different process stages from clone selection to upstream and downstream process optimizations. Will be responsible for carrying out method qualifications and transfers either to manufacturing quality control or any outsourced labs Will plan/ carryout stability studies for R&D batches. Should be able to assess stability trends and draw conclusions Should be able to plan out experiments and activities for day-to-day functioning Will be responsible Co-ordinate with external labs for outsourced activities Maintenance of equipment logs and documentation in the lab. Will be responsible for routine experimental data compilations and reviews

BUILD CAREER WITH CHIRON ! WALK IN INTERVIEW On 29 June 2025, Sunday TIME: 10:00 AM to 2:00 PM MANUFACTURING Qualification: M.Sc / B.Sc (Micro, Biotech, Virology, Biochemical) / B.Tech / Diploma/ BE Experience 0 5 Years Production: Drug substance Qualification: M.Sc / B.Sc (Micro, Virology, Biochemical) / B.Tech / Diploma Sterile aseptic operation Autoclave /DHS operation Automated CIP/SIP operation Cell culture Aseptic operation Zonal Centrifuge operation Facility commissioning QMS/ Deviation/ Change control/ CAPA/ Investigation of deviation

Formulation/ Vaccine Drug Product Qualification: M.Sc / B.Sc (Micro, Virology, Biochemical) / B.Tech / Diploma Autoclave operation Formulation Filling (Vials , BFS, PFS) Vial Washing, Depyrogenation C- Rabs, O-Rabs, Isolator Sterile aseptic operation Sealing & Capping BMR/ QMS

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.

Achieve Sales Targets: Meet or exceed monthly and quarterly sales targets for assigned territory. Product Promotion: Promote vaccine portfolio to doctors, pediatricians, and healthcare professionals through effective product detailing and scientific communication. Customer Relationship Management: Build and maintain strong relationships with healthcare professionals (HCPs), distributors, and stockiest. Market Intelligence: Gather and report insights on market trends, competitor activity, and doctor feedback to the reporting manager. Coverage & Reach: Ensure regular doctor visits as per the coverage plan and maintain frequency norms for HCP engagement. Inventory & Secondary Sales Monitoring: Coordinate with distribution channels to ensure product availability and support in driving secondary sales. Compliance & Reporting: Maintain proper documentation, submit daily call reports, and adhere to organizational compliance, ethical guidelines, and SOPs. Field Coordination: Work closely with SM/ZBM and cross-functional teams to execute territory-wise strategies effectively.

Job Description Purchase and Coordinator: Coordination: Has to coordinate with the Suppliers. Has to takes best rates from supplier Has to do negotiation with suppliers. Has to give quotation to the Clients. Has to coordinate with the dispatch team. Instruct the dispatch team according to the purchase order. To ask for purchase invoice from the suppliers and check it properly. Purchase: Has to check for the timely deliver for goods. Maintain the documentation like purchase orders, purchase invoice. Has to make excel for enquires from the customers. Has to update purchase rates according to the products on daily basis Maintain good relations with the suppliers. Collect documents like COA, GMP, MD-5 License and Manufacturing License.

Perform well-child visits, Diagnose and treat illnesses, injuries and other health conditions, Give vaccines, communicate with patients and their parents and caregivers, offer health advice to parents, refer families to specialists as needed.

Egg Handling Pre-incubation Egg Candling Allantoic Fluids/Embryo Harvesting Inactivation Aseptic Handling and Sampling cGMP Practices Documentation

Process Maintenance Management Ensure the proper operation and maintenance of equipment used in the production of vaccines and injectable, including sterile systems, filling lines, and aseptic processing equipment. Develop and implement preventive maintenance programs that adhere to GMP standards to minimize downtime and ensure continuous production. Manage maintenance activities for critical production and utility systems, including HVAC, autoclaves, sterilization systems, and other aseptic equipment. Lead troubleshooting efforts for any process or equipment failures, ensuring prompt corrective actions are taken while complying with safety and regulatory standards. Instrumentation and Control Systems Supervise the installation, calibration, and ongoing maintenance of all instrumentation and control systems in the plant, including those that monitor and control critical manufacturing parameters. Ensure compliance with GMP, FDA, and other regulatory standards for instrumentation used in the production of vaccines and injectables. Collaborate with quality assurance (QA) and validation teams to validate control systems and instrumentation for accuracy, reliability, and compliance with regulatory requirements. Lead troubleshooting and maintenance activities for any failures in instrumentation, ensuring immediate corrective action and minimal impact on production. Water Systems Management Oversee the operation, maintenance, and monitoring of water systems, including water for injection (WFI) systems, ensuring that they meet the required pharmaceutical-grade quality and regulatory standards. Ensure compliance with regulatory requirements for water quality, including microbial control and endotoxin levels. Manage water treatment and distribution systems, coordinating routine cleaning, sanitization, and validation of these systems. Ensure water systems are maintained to prevent contamination and safeguard product quality. Utility Systems Management Manage and maintain critical utility systems, including steam, compressed air, HVAC, and cooling systems, ensuring they meet stringent pharmaceutical manufacturing standards. Implement and maintain energy efficiency and sustainability practices, in line with regulatory standards and corporate sustainability goals. Oversee the maintenance and calibration of systems used in temperature and humidity control, which are critical for sterile production environments. Regulatory Compliance & WHO Audits Lead preparation for WHO audits, FDA inspections, and other regulatory audits, ensuring all maintenance practices, systems, and equipment are fully compliant with GMP and regulatory requirements. Ensure the engineering and maintenance documentation, including calibration logs, preventive maintenance records, and validation documents, are accurately maintained and ready for audit. Collaborate with the QA team to support the resolution of audit findings and the implementation of corrective actions. Stay up to date on the latest regulatory changes and industry standards, ensuring the plant operates in full compliance at all times. Validation and Qualification Oversee the qualification and validation of critical equipment, systems, and processes to ensure they meet all required regulatory and operational standards. Work closely with the validation team to develop, execute, and maintain qualification protocols for equipment, systems, and utilities. Ensure that all maintenance activities are aligned with the requirements of the validation master plan (VMP) and that any changes are appropriately documented and validated.

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.