PHARMA STUFF

Job Tag: Pharma Jobs in Noida

  • M Pharm, MSc Freshers Clarivate Hiring Associate Healthcare Research & Data Analyst

    Associate Healthcare Research & Data Analyst – Clarivate

    Meta Description: Apply for Associate Healthcare Research & Data Analyst role at Clarivate, Noida. Openings for M.Pharm/M.Sc graduates with 0–2 years of experience.

    Clarivate is hiring passionate graduates for its Biopharma Insights team in Noida. If you hold a Master’s in Pharmacy, Life Sciences, or Pharmaceutical Management and are eager to build your career in pharmaceutical market research, this is the right opportunity. Freshers with strong analytical and communication skills are encouraged to apply.

    Company Overview

    Clarivate is a global leader in providing trusted insights and analytics across the life sciences, healthcare, and biopharma industries. The company empowers pharmaceutical, biotech, and healthcare organizations with competitive intelligence, market insights, and forecasting solutions to accelerate innovation and improve patient outcomes. The Biopharma Insights team at Clarivate is a diverse group of over 100 skilled professionals dedicated to delivering cutting-edge research and strategic intelligence to clients worldwide.

    Job Role & Responsibilities

    As an Associate Healthcare Research & Data Analyst, you will play a vital role in supporting pharmaceutical and healthcare market research projects. Your responsibilities will include:

    • Conducting primary and secondary market research to gather relevant insights.
    • Designing and executing primary surveys and interviews with healthcare professionals.
    • Collecting and interpreting clinical and commercial data to evaluate market trends.
    • Performing market sizing and forecasting for different therapeutic areas.
    • Writing detailed research reports to present findings and recommendations.
    • Collaborating with global teams to deliver strategic intelligence and insights.

    This role provides hands-on exposure to global biopharma markets and the chance to work on impactful healthcare solutions.

    Eligibility / Qualifications

    To apply for this role, candidates must meet the following criteria:

    • Education: Master’s degree in Pharmacy, Life Sciences, or Pharmaceutical Management. Relevant courses include M.Pharm (Pharmaceutics, Pharmacology, Regulatory Affairs), M.Sc (Biotechnology, Biochemistry, Microbiology, Life Sciences).
    • Experience: 0–2 years of experience in pharmaceutical market research, healthcare analytics, or related fields.
    • Strong knowledge of at least one therapeutic area.
    • Proficiency in Microsoft Office (Word, Excel, PowerPoint).
    • Excellent communication skills (written and verbal).
    • Ability to analyze complex datasets and provide actionable insights.

    Preferred skills include global exposure, flexibility, and the ability to collaborate effectively with international teams.

    Location & Salary

    • Location: Noida, Uttar Pradesh, India (Hybrid work model).
    • Salary: Competitive salary and benefits as per industry standards (details shared during the selection process).
    Associate Healthcare Research & Data Analyst – M.Pharm/M.Sc Freshers | Noida
    Associate Healthcare Research & Data Analyst – M.Pharm/M.Sc Freshers | Noida

    Application Process

    Interested candidates can apply directly through Clarivate’s official career portal:
    👉 Apply Here

    Ensure that you submit an updated resume highlighting your qualifications, analytical skills, and relevant coursework or research experience.

    Why Join Clarivate?

    • Opportunity to work in a global, research-driven organization.
    • Exposure to international healthcare and biopharma markets.
    • Career growth through training, mentorship, and collaboration.
    • Inclusive work culture that values innovation, diversity, and equal opportunities.

    FAQs

    1. Who can apply for this role?
    M.Pharm, M.Sc, or Master’s in Pharmaceutical Management graduates with 0–2 years of experience.

    2. Is this position open to freshers?
    Yes, freshers with strong analytical and communication skills are encouraged to apply.

    3. What skills are most valued for this role?
    Analytical thinking, therapeutic area knowledge, market research, data interpretation, and excellent communication.

    4. What is the work mode?
    This role is based in Noida, India, with a hybrid work model.

    5. What is the career growth scope?
    Candidates can grow into senior analyst roles, market research specialists, or global healthcare consulting positions.

    Summary Table

    Company Clarivate
    Vacancies Associate Healthcare Research & Data Analyst
    Required Education M.Pharm, M.Sc Life Sciences, Pharmaceutical Management
    Experience 0–2 years (Freshers Eligible)

  • Pharmacovigilance Specialist Vacancy – Cencora

    Pharmacovigilance Specialist Vacancy – Cencora, NoidaApply for Specialist, Pharmacovigilance, Epidemiology & Risk Management at Cencora, Noida. Full-time role for life sciences professionals.

    Join Cencora, a global leader in healthcare solutions, as a Specialist in Pharmacovigilance, Epidemiology & Risk Management at our Noida, India office. This role provides the opportunity to work at the intersection of drug safety, data integrity, and regulatory compliance while making a direct impact on global health outcomes.

    Company Overview

    Cencora is driven by the mission to create healthier futures. With a global presence and a people-first approach, every team member contributes to advancing healthcare for patients, providers, and communities worldwide. Affiliated with PharmaLex India Private Limited, Cencora specializes in providing consulting, pharmacovigilance, regulatory, and risk management solutions that support the life sciences industry. At Cencora, you are not just an employee—you are part of a purpose-driven team that makes a difference.

    Job Role & Responsibilities

    As a Pharmacovigilance Specialist, you will be responsible for ensuring the safety, accuracy, and regulatory compliance of case processing and reporting. Key responsibilities include:

    • Performing triage and initial validity assessment of safety cases (spontaneous, health authority, clinical trial, and literature cases).
    • Entering case data into the Pharmacovigilance (PV) database.
    • Conducting initial ICSR (Individual Case Safety Report) assessment and expedited reporting decisions.
    • Preparing standard reporting forms (CIOMS I, MedWatch, XML files).
    • Managing follow-up requests and case submissions to Health Authorities and partners.
    • Performing case completion, documentation, and quality assurance checks.
    • Retrieving ICSRs from EVWEB and performing company/non-company assessment.
    • Managing case allocation and workload distribution.
    • Training and mentoring new team members, fostering knowledge transfer and team collaboration.

    This position is ideal for detail-oriented professionals with a strong foundation in pharmacovigilance and risk management, seeking to grow in a supportive and innovation-driven environment.

    Eligibility / Qualifications

    Educational Requirements:

    • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, Medicine, or related fields.
    • Specialized certifications in Pharmacovigilance, Clinical Research, or Drug Safety are an advantage.

    Experience & Skills:

    • Prior experience in pharmacovigilance case processing and ICSR management.
    • Strong knowledge of PV databases and safety reporting tools (including EVWEB).
    • Excellent attention to detail, quality focus, and compliance mindset.
    • Ability to train and mentor junior colleagues.
    • Proficiency in English communication (written and verbal).

    Relevant Courses (LSI Keywords for SEO):
    B.Pharm, M.Pharm, Pharm.D, MSc in Biotechnology, MBBS, Diploma in Clinical Research, PG Diploma in Pharmacovigilance, Advanced Drug Safety Certification

    Location & Salary

    Location: Noida, India
    Work Type: Full-time, Consulting role
    Salary: Competitive package aligned with industry standards

    cencora-specialist-pharmacovigilance-epidemiology-risk-management
    cencora-specialist-pharmacovigilance-epidemiology-risk-management

    Application Process

    Interested candidates can apply directly through the official Cencora careers portal:
    Apply Now at Cencora

    Applications will be reviewed on a rolling basis. Due to high volumes, only shortlisted candidates will be contacted.

    Why Join Cencora?

    • Impactful Work: Contribute to drug safety and regulatory compliance, protecting patient health worldwide.
    • Growth Opportunities: Access to continuous learning, mentoring, and career progression pathways.
    • Inclusive Workplace: Cencora values diversity, equal opportunity, and respect for all employees.
    • Employee Benefits: Comprehensive benefits aligned with local market practices.

    FAQ

    Q1: Who is eligible to apply?
    A: Candidates with a degree in Life Sciences, Pharmacy, or related fields, with experience in pharmacovigilance case processing.

    Q2: Is prior pharmacovigilance experience mandatory?
    A: Yes, prior PV experience in case processing and ICSR handling is required.

    Q3: Where is the role based?
    A: The position is based in Noida, India.

    Q4: What is the application process?
    A: Submit your CV via the Cencora careers portal. Shortlisted candidates will be contacted for the next steps.

    Q5: Does Cencora support training and mentoring?
    A: Yes, new joiners are mentored, and continuous training is provided to all employees.

    Vertical Summary Table

    Category Details
    Company Cencora (affiliated with PharmaLex India Pvt Ltd)
    Vacancies 1+ (Specialist – Pharmacovigilance, Epidemiology & Risk Management)
    Required Education B.Pharm, M.Pharm, Pharm.D, MBBS, MSc in Biotechnology, Clinical Research/Pharmacovigilance certifications
    Experience Prior experience in pharmacovigilance case processing & ICSR management

  • Infosys Hiring Consultant – Business (Life Sciences/Healthcare)

    Infosys Limited Hiring Alert! gyatt Lys
    Consultant – Business (Life Sciences/Healthcare) | Noida

    Company Overview

    Infosys Limited, a global leader in technology services and consulting, drives innovation for Fortune 500 companies across industries. With a strong presence in Life Sciences and Healthcare, Infosys Consulting empowers organizations to meet compliance, regulatory, and operational excellence goals. Joining Infosys means contributing to meaningful projects that shape healthcare and pharmaceutical solutions worldwide.

    Job Role & Responsibilities

    Infosys is seeking Consultants, Analysts, and Senior Consultants with a passion for excellence, strong analytical skills, and expertise in Life Sciences or Healthcare.

    Key responsibilities include:

    • Lead IT and business consulting projects in Life Sciences and Healthcare.
    • Apply domain knowledge in Computerized System Validation (CSV), GxP, 21 CFR Part 11, GAMP 5, SOX IT, Data Privacy, Data Integrity, and Information Security.
    • Manage Quality Management, Document Management, and Change Management processes.
    • Establish, implement, and monitor quality management requirements ensuring IT projects meet regulatory compliance.
    • Conduct Risk Management and root cause analysis, implementing preventive, detective, and corrective measures.
    • Validate SAP / S4 HANA projects, leveraging Lean/Agile methodologies.
    • Conduct periodic control maturity assessments and audits using industry-standard validation tools and templates.
    • Handle multiple large-scale projects while adapting to dynamic environments.
    • Lead strategic discussions with senior stakeholders, providing insights on IT and regulatory impacts.

    Eligibility / Qualifications

    • Educational Requirements: Bachelor of Engineering (B.E.). MBA or advanced degrees like MS, MPH, PharmD, or PhD are preferred.
    • Experience: 4–9 years of professional experience in Life Sciences consulting or industry roles.
    • Demonstrated expertise in validation, risk management, audits, and regulatory compliance in pharmaceutical/healthcare environments.
    • Strong analytical, conceptual, and communication skills with a proven track record in managing complex projects.
    • Preferable IT background to understand architectural and technical complexities.

    Relevant Courses/Certifications:
    B.E./B.Tech, MBA, M.S., M.Pharm, PharmD, MPH, PhD, Lean/Agile Certifications, SAP/S4 HANA Validation, GxP Training, Risk Management Certifications, CSV Training

    Location & Salary

    • Location: Noida, Uttar Pradesh
    • Salary: Competitive, based on experience
    Infosys Limited Hiring - Consultant - Business (Life Sciences/Healthcare)
    Infosys Limited Hiring – Consultant – Business (Life Sciences/Healthcare)

    Application Process

    Ready to join one of the world’s leading technology consulting firms?
    Apply here: Infosys Careers – Consultant (Life Sciences/Healthcare)

    FAQs

    Q1. What is the eligibility for this role?
    A1. Candidates must have a Bachelor of Engineering with 4-9 years of relevant experience in Life Sciences/Healthcare consulting or industry roles.

    Q2. Are advanced degrees preferred?
    A2. Yes, MBA, MS, MPH, PharmD, or PhD degrees are advantageous.

    Q3. What skills are essential?
    A3. Expertise in CSV, GxP, SAP/S4 HANA validation, risk management, audits, and regulatory compliance are critical.

    Q4. How do I apply?
    A4. Click here to submit your application directly to Infosys.

    Q5. Can freshers apply?
    A5. This role requires 4-9 years of experience, so it is not open to freshers.

    Vertical Summary Table

    Category Details
    Company Infosys Limited
    Vacancies Consultant – Business (Life Sciences/Healthcare)
    Required Education B.E. (MBA/MS/MPH/PharmD/PhD preferred)
    Experience 4-9 Years
  • Fresher Jobs With ₹44,400 stipend | Junior Research Fellow Vacancy | Galgotias University | DHR-ICMR Project

    Fresher Jobs With ₹44,400 stipend | Junior Research Fellow Vacancy | Galgotias University | DHR-ICMR Project

    Junior Research Fellow Vacancy | Galgotias University | DHR-ICMR Project

    Apply for JRF position at Galgotias University under DHR-ICMR funded project. ₹44,400 stipend, 3-year tenure, last date 8 Oct 2025.

    Galgotias University, a leading institution in biosciences and technology research, invites applications for the post of Junior Research Fellow (JRF) under a Department of Health Research (DHR), ICMR, Government of India funded project. This opportunity offers candidates the chance to contribute to cutting-edge research in nanomedicine and antimicrobial photodynamic therapy.

    Company Overview

    Galgotias University is a NAAC A+ accredited institution recognized for its strong focus on innovation, interdisciplinary research, and academic excellence. The School of Biosciences and Technology is actively engaged in projects that advance healthcare through biotechnology, drug delivery systems, and biomedical engineering. By joining as a JRF, candidates will gain exposure to world-class research, state-of-the-art facilities, and collaborative networks across academia and industry.

    Project Details

    • Project Title: Curcumin-loaded lignin-based nanogels for antimicrobial photodynamic therapy (PDT)
    • Funding Agency: Department of Health Research (DHR), ICMR, Government of India
    • Principal Investigator (PI): Dr. Shatabdi Paul, Assistant Professor, School of Biosciences and Technology
    • Co-PI: Dr. Sumedha Mukerjee, Assistant Professor, School of Biosciences and Technology
    • Tenure: 3 years
    • Vacancy: 01
    • Last Date to Apply: 8th October 2025【14†files_uploaded_in_conversation】

    Job Role & Responsibilities

    As a Junior Research Fellow (JRF), the selected candidate will:

    • Develop novel nano-based drug delivery systems (nanoparticles, liposomes, nanoemulsions, polymeric micelles).
    • Perform detailed physicochemical characterization including particle size, zeta potential, PDI, SEM/TEM, drug release, and entrapment efficiency.
    • Conduct data analysis using advanced tools like OriginPro.
    • Support pilot-scale manufacturing and collaborate with incubators/industry partners for technology transfer.
    • Manage laboratory activities, design experiments, prepare reports, and draft manuscripts.
    • Present research findings at national and international scientific forums【14†files_uploaded_in_conversation】.

    Eligibility / Qualifications

    • Educational Qualification: M.Sc./M.Tech./M.Pharm./M.E./B.E./B.Tech in Life Sciences, Chemical Sciences, Pharmaceutical Sciences, Chemical Engineering, Biochemical Engineering, or related fields.
    • Desirable Qualification: NET (CSIR-UGC), DBT, GATE, GPAT, or ASRB-NET.
    • Experience: Freshers and candidates with research experience are encouraged to apply.
    • Age Limit: Not exceeding 30 years (relaxation as per government norms).

    Fellowship & Benefits

    • Fellowship/Stipend: ₹44,400 per month (including HRA) for qualified candidates.
    • PhD Registration: Eligible candidates may register for a PhD program at Galgotias University, subject to fulfilling norms.
    • Growth Opportunity: Chance to contribute to translational nanomedicine and healthcare innovations【14†files_uploaded_in_conversation】.

    Location

    • Workplace: School of Biosciences and Technology, Galgotias University, Greater Noida, India.
    • Collaborations: Selected candidate may work in GU labs as well as partner research institutions.
    Junior Research Fellow Vacancy | Galgotias University | DHR-ICMR Project
    Junior Research Fellow Vacancy | Galgotias University | DHR-ICMR Project

    Application Process

    Interested candidates should:

    Deadline: 8th October 2025. Apply early to secure your opportunity!

    FAQs

    1. What is the stipend for this JRF position?
    Qualified candidates will receive ₹44,400 per month including HRA.

    2. Can freshers apply?
    Yes, fresh postgraduates or graduates in eligible fields may apply.

    3. Is PhD registration possible during the project?
    Yes, candidates may register for PhD at Galgotias University if they meet the eligibility norms.

    4. What is the age limit?
    Applicants must be under 30 years as of the interview date, with relaxation as per government rules.

    5. When is the last date to apply?
    Applications must be submitted on or before 8th October 2025【14†files_uploaded_in_conversation】.

    Quick Summary Table

    Company / Institute Galgotias University
    Vacancy Junior Research Fellow (JRF)
    Project Curcumin-loaded lignin-based nanogels for antimicrobial PDT
    PI / Co-PI Dr. Shatabdi Paul / Dr. Sumedha Mukerjee
    Tenure 3 Years
    Funding Agency Department of Health Research (DHR), ICMR
    Fellowship ₹44,400 per month (including HRA)
    Required Education M.Sc., M.Tech., M.Pharm., M.E., B.E., B.Tech (Life Sciences, Pharma, Chemical Sciences/Engineering, Biochemical Engineering)
    Desirable CSIR-UGC NET, DBT, GATE, GPAT, ASRB-NET
    Location Greater Noida, India
    Last Date 8 October 2025

    galgotias university jobs

  • Clarivate Fresher Hiring as Associate Healthcare Research & Data Analyst

    Clarivate Fresher Hiring as Associate Healthcare Research & Data Analyst

    Associate Healthcare Research & Data Analyst – Clarivate Noida

    Clarivate hiring Associate Healthcare Research & Data Analyst in Noida. Open for freshers and early-career professionals with Master’s in Life Sciences.

    Clarivate, a global leader in analytics and insights for the pharmaceutical, biotechnology, and healthcare sectors, is inviting applications for the position of Associate Healthcare Research & Data Analyst at its Noida, Uttar Pradesh office. This is a hybrid role offering an excellent opportunity for freshers and early-career professionals in life sciences to start a career in healthcare research, biopharma insights, and pharmaceutical market analysis.

    Company Overview

    Clarivate is a trusted global information and analytics company helping organizations accelerate innovation. With expertise in life sciences, healthcare, and intellectual property, Clarivate provides data-driven insights that support strategic planning, competitive intelligence, and decision-making in some of the most complex industries. The company is known for its Biopharma Insights division, which empowers pharmaceutical and biotech companies to make informed decisions on drug development, commercialization, and healthcare advancements.

    Job Role & Responsibilities

    As an Associate Healthcare Research & Data Analyst, you will be part of the vibrant Biopharma Insights team, which specializes in pharmaceutical market research, forecasting, and analytics. Your key responsibilities will include:

    • Conducting primary and secondary market research on pharmaceutical and healthcare trends.
    • Gathering, analyzing, and interpreting clinical data and commercial datasets from multiple sources.
    • Designing and conducting primary market research surveys (questionnaires, interviews with medical experts).
    • Evaluating market trends, commercial opportunities, and therapeutic area insights.
    • Developing market sizing models and forecasts for pharma and biotech industries.
    • Writing analytical reports, syndicated research studies, and actionable insights for global stakeholders.
    • Collaborating with a global team to ensure high-quality deliverables in line with Clarivate’s standards.

    Eligibility / Qualifications

    • Education: Master’s degree in Pharmacy, Life Sciences, or Pharmaceutical Management.
    • Experience: 0–2 years in biopharma, healthcare, market research, or financial sector.
    • Technical Skills:
      • Proficiency in Microsoft Office (Word, Excel, PowerPoint).
      • Strong analytical skills with experience in data interpretation.
      • In-depth knowledge of at least one therapeutic area.
    • Soft Skills:
      • Excellent communication (verbal and written) in English.
      • Attention to detail and ability to work under deadlines.
      • Collaborative mindset with flexibility to work in global teams.

    Relevant courses under eligibility: M.Pharm, Pharm.D, M.Sc Biotechnology, M.Sc Life Sciences, M.Sc Pharmaceutical Management, M.Sc Microbiology, M.Sc Biochemistry.

    Location & Salary

    • Location: Noida, Uttar Pradesh, India
    • Work Model: Hybrid (mix of onsite and remote work)
    • Employment Type: Full-time
    • Compensation: As per Clarivate’s competitive industry standards
    Associate Healthcare Research & Data Analyst – Clarivate Fresher Jobs
    Associate Healthcare Research & Data Analyst – Clarivate Fresher Jobs

    Application Process

    Candidates can apply directly through Clarivate’s official career portal:
    Apply Here

    Early applications are encouraged to maximize chances of selection.

    Why Join Clarivate?

    • Be part of a global team of 100+ Biopharma Insights experts.
    • Gain exposure to international projects and global pharmaceutical markets.
    • Work in an organization committed to diversity, equal opportunity, and innovation.
    • Access structured career development and training programs.
    • Contribute to meaningful research that drives healthcare and pharmaceutical advancements.

    FAQs

    Q1: Is this role open for freshers?
    Yes, candidates with 0–2 years of experience can apply.

    Q2: What is the minimum qualification?
    A Master’s degree in Pharmacy, Life Sciences, or Pharmaceutical Management is required.

    Q3: What skills are most important for success?
    Strong analytical skills, Microsoft Office proficiency, therapeutic area knowledge, and excellent communication.

    Q4: Is this role remote or on-site?
    It is a hybrid role with flexibility for both on-site and remote work.

    Q5: How do I apply?
    Applications must be submitted via Clarivate’s career portal (link provided above).

    Summary Table

    Category Details
    Company Clarivate
    Vacancies Multiple (Associate Healthcare Research & Data Analyst)
    Required Education M.Pharm, Pharm.D, M.Sc Life Sciences, M.Sc Biotechnology, M.Sc Pharmaceutical Management, M.Sc Microbiology, M.Sc Biochemistry
    Experience 0–2 years (Freshers eligible)
  • Jubilant Generics hiring Regulatory Affairs professionals

    Jubilant Generics hiring Regulatory Affairs professionals

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    Regulatory Affairs Executive | 3–7 Yrs | Jubilant Generics Noida

    Jubilant Generics hiring Regulatory Affairs professionals with 3–7 yrs experience for US market submissions in Greater Noida. Apply today!

    Jubilant Generics Limited, a leading name in the pharmaceutical sector, is inviting applications for Regulatory Affairs (US Market) positions at its Corporate Office in Greater Noida. This is an excellent opportunity for experienced pharma professionals who want to contribute to regulatory submissions and compliance for one of the fastest-growing global pharma companies.

    Company Overview

    Jubilant Generics Limited is part of Jubilant Pharmova, a globally recognized pharmaceutical organization engaged in manufacturing and marketing high-quality medicines. With strong regulatory approvals and a presence in the US, EU, and emerging markets, Jubilant Generics is committed to improving patient health through innovation, compliance, and excellence.

    Job Role & Responsibilities

    As part of the Regulatory Affairs – US Market team, the selected candidate will be responsible for:

    • Preparing and submitting ANDA filings, eCTD submissions, query responses, and lifecycle management activities for the US market.

    • Reviewing and updating product labeling in compliance with USFDA requirements.

    • Assessing and managing post-approval submissions including Annual Reports, CBE-30, and PAS.

    • Ensuring adherence to USFDA regulatory guidelines and submission timelines.

    • Coordinating with cross-functional teams including Quality, R&D, and Manufacturing.

    • Handling regulatory queries and ensuring timely compliance.

    Eligibility / Qualifications

    • Experience: 3–7 years in Regulatory Affairs (pharma industry).

    • Mandatory Requirement: Proven expertise in US market submissions including ANDA, eCTD, and lifecycle management.

    • Qualification: B.Pharm / M.Pharm or Life Sciences graduate/postgraduate.

    • Strong knowledge of USFDA guidelines and regulatory documentation.

    • Excellent communication and problem-solving skills.

    Location & Salary

    • Work Location: Jubilant Generics Corporate Office, Greater Noida.

    • Salary: Competitive, based on qualification and experience.

    Application Process

    Interested candidates can share their updated profiles at:

    Mention “Application – Regulatory Affairs US Market” in the subject line for faster processing.

    FAQs

    Q1. Who can apply for this Regulatory Affairs opening?
    Candidates with 3–7 years of RA experience and mandatory exposure to the US market (ANDA, eCTD submissions, lifecycle management).

    Q2. What qualifications are preferred?
    B.Pharm, M.Pharm, or postgraduates in Life Sciences with regulatory expertise.

    Q3. What are the main responsibilities?
    Regulatory submissions, labeling, lifecycle management, and compliance with USFDA guidelines.

    Q4. Where is the work location?
    Greater Noida – Corporate Office of Jubilant Generics.

    Q5. How can I apply?
    Send your CV to v-prateek.pandey@jubl.com and robin.shahi@jubl.com.

    Summary Table

    Company Jubilant Generics Limited
    Vacancies Regulatory Affairs (US Market)
    Required Education B.Pharm / M.Pharm / Life Sciences
    Experience 3–7 years in US Regulatory Affairs
    Location Greater Noida, Corporate Office