43 Vaccines Jobs - Page 2

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!

Job Title: Executive / Manager/Senior Manager Quality Control Department: Quality Control (QC) Company: Greensignal Bio Pharma Pvt Ltd Location: Gummidipoondi, SIPCOT, Chennai Position Overview: The Manager/Senior Manager of Quality Control (QC) at Greensignal Bio Pharma Pvt Ltd is responsible for developing, implementing, and managing quality control strategies and activities. This role ensures that all quality control processes are compliant with industry regulations and align with organizational goals. The individual will lead various quality control activities, such as sampling, testing, inspection, and documentation, while ensuring compliance with regulatory standards. Key Responsibilities: Develop and implement quality control strategies that align with organizational goals and regulatory standards (e.g., FDA, EU, WHO). Collaborate with cross-functional teams to ensure alignment of quality control objectives across departments. Oversee quality control activities, including sampling, testing, inspection, and documentation, ensuring compliance with internal and external standards. Ensure all quality control activities meet required regulatory standards (e.g., FDA, EU, WHO), and implement corrective actions when needed. Develop, maintain, and review quality control procedures, policies, and documentation to ensure consistency and compliance. Conduct internal audits to evaluate compliance with quality control procedures and identify areas for improvement. Collaborate with the regulatory affairs team to ensure timely and accurate submission of quality control documentation for regulatory filings. Provide training, guidance, and coaching to team members, ensuring they possess the necessary skills to perform quality control tasks effectively. Communicate quality control results, non-conformances, and corrective actions to cross-functional teams in a timely manner. Identify opportunities for continuous improvement in quality control processes and implement initiatives to improve efficiency and compliance. Minimal Qualifications: Education: Masters degree in Microbiology, Life Sciences, Pharmacy, or a related field (M.Sc. Microbiology preferred). Experience: Minimum of 8 years of experience in quality control, preferably in the pharmaceutical or biotechnology industry. Knowledge: Strong understanding of regulatory requirements (e.g., FDA, EU, WHO), microbiology, instrumentation, EMP, failure investigation, and related documentation. Skills: Excellent leadership and project management abilities. Strong written and verbal communication skills. Ability to collaborate effectively with cross-functional teams. Preferred Qualifications: Experience with global regulatory filings and compliance audits. Certification in Quality Management Systems (e.g., ISO 9001, Six Sigma). Expertise in advanced microbiological testing techniques. Personal Attributes: Strong problem-solving skills with keen attention to detail. Proactive and able to thrive in a fast-paced, dynamic environment. Ability to motivate, inspire, and develop team members. To Apply: Please submit your resume and cover letter detailing your qualifications and experience to the following contact details: Email: hr@gsbpl.com Mobile: 8778926365

Position Upstream Scientist , Role Description As an Upstream Scientist , you will be responsible for planning and execution of experiments, analyzing data and preparing reports. Your contribution will be critical in advancing our vaccine programs. Candidate must be able to Design and execute process development studies to develop a thorough understanding of operating and performance parameters Perform hands on work in a cell culture lab, specifically cell culture expansion (insect as well as mammalian systems, adherent/ suspension), cell bank preparation, bioreactor operation in fed-batch and perfusion modes, optimization of media components, feeding control strategy Lead activities of vaccine production as well as process scale up with proper method development reports. Perform and analyse Design of Experiment (DOE) studies to develop or optimize processes to ensure a phase-appropriate, consistent, high-yielding and scalable upstream process from shake-flask to 200L scale bioreactor. Support in PPQ activities and scale-down model establishment, Support process characterization studies and tech transfer process. As needed, support process validation, including validation protocol writing, execution and report writing. Ability to think critically, demonstrate troubleshooting and problem-solving skills. Communicate with internal and external stakeholders through meetings and clearly written emails, reports, and presentations. Identify and leverage external capabilities that complement internal core competencies. Review and apply learnings from academic literature, patent filings and public domain information, to long and short-term in-house process development, on an ongoing basis Contribute to our intellectual property portfolio Contribute to Company-wide efforts to promote a safe work environment. Qualifications PhD with 3-8 years or Masters degree with 10-12 years in an industrial upstream process development role. Previous experience with fermentation matrices is strongly preferred. Should have experience handling various bioreactors, adherent and/or suspension cell cultures Knowledge of engineering principles related to scale-up of fermentation processes Culture process development experience such as cell passaging, formulation of media, aseptic technique processing, and managing reagents is a must Ability to thrive in a fast-paced environment Additional Considerations Previous experience in the following areas are all pluses: Working at a start-up or small company. Multi-year industrial fermentation experience with vaccines/biologics is preferred; direct experience with virus-derived recombinant products and/or viral particles is a plus. Familiarity with regulatory requirements for manufacturing vaccines. Authoring or contributing to SOPs. Managing junior engineers, research assistants, and technicians If interested and meet 80% of the criterion connect with us Intelli Search 9071129990 and email profiles@intellisearchonline.net

Candidate having 7-10 Years experience with any Science Graduate. Should be responsible for the Business Development, having experience in Pharma industry - Vaccines / Formulations / Poultry/ Veterinary / Human, having rapport with Government Departments as well as e-tendering. Roles & Responsibilities Meet with customers/clients face to face or Virtual. Develop relations with customers/ clients Liaise with the finance team, warehousing and logistics. Negotiations Sales forecasts and analysis and present your findings to senior management Sales and marketing strategy e-tendering and purchase procedure of State Govt / Co-operatives / Central Govt / Ministry

Job description Brief Job Description -Research associates conduct desk-based research (incl. clinical, scientific, regulatory, commercial, etc.) on assigned topics and generate a concise summary of findings. They are expected to keep abreast of new developments in their assigned therapeutic area/s and report new events/updates to their respective team members. They are also strongly encouraged to include critical and analytical thinking into their deliverables. Candidate - Highly enthusiastic and committed individuals with strong desk-based research skills are sought for this position Candidates are expected to be meticulous, thorough and well organized. They should be quick learners, have an excellent work ethic and should be willing and able to work in a rapidly evolving role/environment Candidates are expected to possess excellent communication skills, both written and oral The position offers a rare opportunity to be mentored by seasoned industry professionals within Vyuhgenics. Responsibilities - This is a full-time, desk-based job in our Bangalore, India office The primary focus will be on collection, collation and curation of scientific, clinical, regulatory and commercial evidence about therapeutic areas, products, markets, companies and customers of relevance to the global biopharmaceutical industry Travel to scientific and clinical symposia and conferences may be offered to promising candidates Additional skills - Excellent English language skills and working knowledge of MS Office (Word, Excel, PowerPoint) or Google Docs.

Role & responsibilities Responsible for Drup Product Manufacturing Ensure compliance to Current Good Manufacturing Practices (cGMP)& documentation thereof for various production activities. Filling line in built CIP, SIP operations Knowledge of Isolator VHP, Blending vessels- CIP, SIP Good at QMS Regulatory inspection exposure WHO-PQ, USFDA, EU GMP, TGA,ROW Experience in O RABS, Isolator filling lines Lyophilizers - ALUS, Manual operations Blending of viral, bacterial vaccines Media fill activities , TRS 1044 updates Responsible for preparing production plan in consultation with PPIC department and execution thereof with effective planning and utilization of Men, Materials and Machineries for quality linked productivity. To approve the instructions relating to production operations and to ensure their strict implementation. To ensure that products are produced and stored according to the appropriate documentation in order to obtain the required quality. To ensure that the production records are evaluated and signed by an authorized person. Review investigation of Quality Management System (QMS) including market complaint, Out of Specification (OOS), change controls of manufacturing, risk assessment, Corrective Action and Preventive Action (CAPA) etc. To ensure the qualification and maintenance of department, premises and equipment. Ensure compliance to master formula and process provided in the Batch Manufacturing Record (BMR). To ensure that the appropriate validations are done. Reviewing document like of Standard Operating Procedures (SOPs), Batch Manufacturing Record (BMR), Batch Packing Record (BPR), Master Formula Record (MFR)etc. and compliance reports thereof with training of personnel on the same. Ensure appropriate inventory of Consumable in the Department for smooth functioning. Responsible for Co-ordination with Technical Services, Quality Assurance / Quality Control, Finance, Purchase, Warehouse and Administration Departments for effective management of Production targets. Ensure wastage control and optimization of yield at various stages of manufacturing and packaging operations. Ensure compliance to various In-process control guidelines provided in the batch documents. Ensure periodic preventive maintenance of plant and machineries as per schedule worked out by Engineering for optimum performance. Ensure that personnel follow basic safety guidelines during operations. Responsible for the preparation of training calendar for employees and to ensure that the required initial and continuing training of department personnel is carried out and adapted according to need on cGMP and various operational activities. Responsible for preparation of accurate and timely reports of various production activities showing performance and shortcomings against agreed/planned parameters (monthly presentation, work in progress (WIP) statement yield report, monthly planning, expense budget stationary, housekeeping material, production item &capital budget etc). Preferred candidate profile M.Pharm/ B.Pharm / MSc ; Experience- 18 to 25 years Candidate Must have exposure of regulatory Audits should be willing to relocate with family to ahmedabad

-Engage in the sales and promotion of medical devices, specifically targeting major corporate hospitals. -Conduct meetings with healthcare professionals, including doctors and paramedical staff. -Candidates can share their cv at 8178034533

-Engage in the sales and promotion of medical devices, specifically targeting major corporate hospitals. -Conduct meetings with healthcare professionals, including doctors and paramedical staff. -Candidates can share their cv at 8178034533

-Engage in the sales and promotion of medical devices, specifically targeting major corporate hospitals. -Conduct meetings with healthcare professionals, including doctors and paramedical staff. -Candidates can share their cv at 8178034533

Job Description 1. As a Regional Sales Manager you will based at Hyderabad HQ to handle Sales & Business Development of Pediatrics Vaccines Business covering entire AP & Telangana for reputed Pharma listed company. 2. You will ensure achievement of Target, new product launches and scientific/ Medical promotion of Vaccines to Pediatric Development of team of ABM's & MR's and achieving high PCPM and target achievement. 3. You will conduct marketing activities and will ensure effective implementation of strategies. 4. You should be good in Man/ Management and Administrative Control on Field Force and will lead team of ABMs and MRs. Required Candidate Profile 1. You should be B.Sc or Science or Pharmacy Graduate with 10-15 years experience in Pharma Sales out of which 2-3 years as a Regional Sales Manager handling Sales & Business Development to Pediatrics Vaccines covering AP & Telangana for reputed Pharma listed company. 2. You should be good in Man/ Management and Business Development. 3. You should have good experience in scientific / medical promotions , launching new products and effective implementation of strategies. 4. You should be good in Maintaining Administrative Control on Filed Force and helping them to achieve target and incentive Thanks and Regards Ashwini Devendra HRD House Mumbai (Div - Pharma Talent Search) Mulund East. Mumbai 400081. Mobile Number : 8879666426 Email Id : ashwini@hrdhouse.com

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

Brief Job Description - Consultants coordinate desk-based research (incl. clinical, scientific, regulatory, commercial, etc.) on high-importance topics and generate reports which incorporate critical and analytical thinking. They are expected to keep abreast of developments in their assigned therapeutic area/s and continuously assess the impact of any new events/findings. They should have experience in handling clients, mentoring, attending/covering healthcare conferences and project planning. Candidate - Highly enthusiastic and committed individuals with deep knowledge of the biopharmaceutical space and strong analytical skills are sought for this position Candidates are expected to be meticulous and well organized. They should be quick learners, have an excellent work ethic and should be willing and able to work in a rapidly evolving role/environment Candidates are expected to possess excellent communication skills, both written and oral Responsibilities - This is a full-time, desk-based, job at our office in Bangalore, India. The primary focus will be on creating well structured reports, containing in-depth analysis and accurate facts. They will also be expected to take a lead role in collecting scientific, clinical, regulatory and commercial evidence about therapeutic areas, products, markets, companies and customers of relevance to the global biopharmaceutical industry. Travel to scientific and clinical symposia and conferences will be necessary Other responsibilities include project planning, mentoring team members and client interaction Additional skills - Excellent English language skills and working knowledge of MS Office (Word, Excel, Powerpoint) or Google Docs.

Conduct routine physical exams, Vaccinations and screenings for infants & children's. Diagnose and treat a variety of illness and conditions, from minor to complex. *MD in Pediatrics. *Valid KMC Medical License to Practice. * 2+ Years of Experience. Perks and benefits Performance Bonus Based on Individual Performance.

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