Job Tag: Pharma Jobs in gurgaon

  • Regulatory Affairs Intern Vacancy | Philips

    Regulatory Affairs Intern Vacancy | Philips

    Philips hiring Regulatory Affairs Intern in Gurgaon. sophie rain instagram Life Sciences & Biotechnology students eligible. Apply now for Sep-Dec 2025 internship.


    Philips, a global leader in health technology, is offering an exciting internship opportunity in Regulatory Affairs for students in Life Sciences and Biotechnology. This is a unique chance for students to gain hands-on experience with regulatory processes, compliance, and healthcare technology regulations in India. The internship will be based in Gurgaon and requires commitment from September to December 2025.


    Company Overview

    Philips is a renowned multinational health technology company dedicated to improving people’s health and well-being through meaningful innovation. With a legacy spanning over 130 years, Philips has transformed the healthcare industry by focusing on prevention, diagnosis, treatment, and home care solutions. Philips India continues to be a pioneer in medical devices, imaging technologies, and health systems that contribute to better healthcare access across the nation.


    Job Role & Responsibilities

    As a Regulatory Affairs Intern, you will work closely with the regulatory team to support compliance and monitoring processes for medical devices. Your key responsibilities will include:

    • PC & PNDT Regulations: Tracking and establishing processes at District/State levels for sale, supply, or demonstration of medical devices under the Pre-Conception & Pre-Natal Diagnostic Techniques (PC&PNDT) regulations.
    • AERB Regulations: Monitoring and establishing compliance procedures under Atomic Energy Regulatory Board (AERB) guidelines for medical devices that fall under PC&PNDT regulations.
    • Regulatory Affairs Activities: Consolidating, reviewing, and supporting compliance activities under the Regulatory Affairs function of Philips India Ltd (Health Systems division).

    This internship will provide valuable exposure to regulatory frameworks, compliance protocols, and healthcare technology governance in India.


    Eligibility / Qualifications

    • Education: Currently pursuing a degree in Life Sciences, Biotechnology, or related fields.
    • Commitment: Available for the period September to December 2025, 5 days per week.
    • Location: Candidates must be based in Delhi/NCR region, with mandatory 3 days in-office presence at Gurgaon.

    Relevant Courses: B.Sc. Life Sciences, M.Sc. Biotechnology, B.Tech Biotechnology, B.Pharm, M.Pharm, Clinical Research, Regulatory Affairs courses.


    Location & Salary

    • Job Location: Gurgaon, Haryana (Hybrid – 3 days office, 2 days remote).
    • Stipend: Competitive internship stipend (details to be shared during selection process).
    • Benefits: Exposure to global healthcare technology projects, mentorship from industry experts, and career development opportunities within Philips.
    Regulatory Affairs Intern Vacancy | Philips Gurgaon 2025
    Regulatory Affairs Intern Vacancy | Philips Gurgaon 2025

    Application Process

    Interested candidates can apply directly via the Philips career portal:
    👉 Apply Here

    📅 Applications are open now — apply early to secure your spot for this limited-duration internship!


    Why Join Philips?

    • Gain hands-on experience in regulatory affairs and compliance in the healthcare sector.
    • Work with a global leader in health technology with 130+ years of expertise.
    • Contribute to projects that improve healthcare access and quality worldwide.
    • Exposure to PC&PNDT and AERB regulations, essential for careers in medical device compliance.
    • Build your career path in regulatory affairs, clinical research, or quality assurance.

    FAQs

    1. Who can apply for this internship?
    Students pursuing Life Sciences or Biotechnology degrees are eligible.

    2. Is prior experience required?
    No, this is an internship role for freshers currently studying.

    3. What is the duration of the internship?
    September to December 2025 (4 months, full-time).

    4. Is the internship paid?
    Yes, Philips provides a competitive stipend.

    5. What is the mode of work?
    Hybrid – 3 days office presence in Gurgaon and 2 days remote.

    6. Will this lead to a permanent role?
    Outstanding interns may be considered for future opportunities at Philips India or global offices.


    ⚡ **Apply before

  • Syneos Health Pharmacovigilance Jobs | Safety & PV Specialist I

    Safety & PV Specialist I | Life Sciences Graduates | Gurgaon

    Apply for Safety & Pharmacovigilance Specialist I at Syneos Health, Gurgaon. Open for Life Sciences, Pharmacy, and Nursing graduates.

    Syneos Health, a global leader in biopharmaceutical solutions, is hiring Safety & Pharmacovigilance (PV) Specialists in Gurgaon. This is a golden opportunity for life sciences and pharmacy graduates eager to begin or advance their career in pharmacovigilance and drug safety. Join an organization that has contributed to 94% of FDA-approved drugs and 95% of EMA-authorized products over the past five years.


    Company Overview

    Syneos Health® is one of the world’s most trusted integrated biopharmaceutical companies, dedicated to accelerating customer success through clinical development, medical affairs, and commercial solutions. With a global workforce of over 29,000 employees across 110 countries, Syneos Health partners with top pharma and biotech organizations to bring life-saving treatments to patients faster.

    Their Total Self Culture fosters diversity, inclusivity, and authenticity in the workplace—empowering every team member to contribute meaningfully to the advancement of global healthcare.


    Job Role & Responsibilities

    As a Safety & PV Specialist I, you will play a crucial role in managing safety data, literature review, and case processing to ensure compliance with international pharmacovigilance regulations. Key responsibilities include:

    Literature Search & Data Management

    • Conduct systematic and ad-hoc literature searches in global biomedical databases (PubMed, Medline, Embase).
    • Extract and summarize key safety data relevant to ICSRs (Individual Case Safety Reports).
    • Create and validate literature search strategies for pharmacovigilance use.
    • Manage data entry in PVG quality and tracking systems for ICSR receipt and tracking.

    ICSR Processing

    • Triage ICSRs and evaluate data for accuracy, completeness, and regulatory reporting compliance.
    • Enter data into safety databases and perform MedDRA coding of events, history, and medications.
    • Generate accurate narrative summaries and resolve data queries efficiently.
    • Assist in expedited safety reporting as per GVP and ICH guidelines.

    Quality & Compliance

    • Perform quality control (QC) and validation of ICSR data and literature reviews.
    • Support global and local literature search compliance with regulatory standards.
    • Maintain safety documentation in the Trial Master File (TMF) or Pharmacovigilance System Master File (PSMF).
    • Participate in audits and ensure alignment with company SOPs, GVP, ICH, and GCP standards.

    Technical Systems & Collaboration

    • Work with internal teams and external stakeholders to manage drug safety deliverables.
    • Utilize database tools and software for data capture, coding, and tracking (e.g., Argus, ARISg).
    • Contribute to ongoing safety database maintenance, SPOR/IDMP activities, and duplicate ICSR management.

    Eligibility / Qualifications

    • Education: Bachelor’s or Master’s degree in Life Sciences, Pharmacy (B.Pharm, M.Pharm, Pharm.D), Nursing, Biotechnology, or related disciplines.
    • Experience: Fresh graduates or candidates with prior pharmacovigilance exposure are encouraged to apply.
    • Technical Skills:
      • Knowledge of safety databases and medical terminology.
      • Proficiency in Microsoft Office (Word, Excel, PowerPoint).
      • Familiarity with clinical trial processes, ICH-GCP, GVP, and pharmacovigilance regulations.
    • Soft Skills:
      • Strong attention to detail and accuracy.
      • Excellent written and verbal communication.
      • Time management and multitasking abilities.
      • Team collaboration and analytical problem-solving mindset.

    Location & Benefits

    Location: Gurgaon, Haryana, India
    Job Type: Full-Time, On-Site
    Work Mode: Collaborative environment with opportunities for global exposure.

    Why Join Syneos Health?

    • Opportunity to work with a company contributing to global drug development.
    • Professional growth through career progression, technical training, and mentoring.
    • Recognition through performance programs and global career opportunities.
    • Inclusive culture under the Total Self framework – empowering authenticity at work.
    syneos-health-safety-pv-specialist
    syneos-health-safety-pv-specialist

    Application Process

    Interested candidates can apply directly via the official Syneos Health career portal using the link below:

    👉 Apply Here

    Pro Tip: Apply early to secure your spot – applications may close once sufficient candidates are shortlisted!


    FAQs

    Q1. Who can apply for this position?
    Candidates with Life Sciences, Pharmacy, Nursing, or Biotechnology degrees are eligible.

    Q2. What are the key skills required?
    Strong attention to detail, medical terminology understanding, database handling, and regulatory knowledge.

    Q3. Is prior experience necessary?
    Experience is preferred but not mandatory. Fresh graduates with relevant academic knowledge can apply.

    Q4. What is the work environment like?
    A professional, collaborative, and inclusive environment promoting innovation and growth.

    Q5. How does Syneos Health ensure employee growth?
    Through structured training programs, mentorship, and access to global opportunities.


    Summary Table

    Category Details
    Company Syneos Health
    Vacancies Safety & PV Specialist I
    Required Education Life Sciences, Pharmacy, Nursing, Biotechnology (B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, B.Tech, M.Tech)
    Experience Freshers / Experienced candidates with PV knowledge
    Location Gurgaon, Haryana
    Apply Link Apply Here
  • Fresher Pharmacovigilance Jobs | Safety & PV Trainee at Syneos Health

    Fresher Pharmacovigilance Jobs | Safety & PV Trainee at Syneos Health

    Safety & PV Trainee at Syneos Health, Gurgaon – 2025 Vacancies beaniebaby999 www.only-fans.com beanie baby

    Apply for Safety & PV Trainee at Syneos Health, Gurgaon. Eligibility: Pharma graduates. 2025 vacancies open for freshers and experienced.

    Syneos Health, a leading fully integrated biopharmaceutical solutions company, is seeking passionate individuals to join as Safety & PV Trainees in Gurgaon, Haryana. This role offers an excellent opportunity to contribute to global clinical research and pharmacovigilance initiatives while growing your career in a dynamic environment.

    Company Overview

    Syneos Health® is renowned for accelerating customer success by translating unique clinical, medical affairs, and commercial insights into actionable outcomes. With a workforce of 29,000 employees across 110 countries, Syneos Health has collaborated on over 200 studies, supporting 94% of all novel FDA-approved drugs and 95% of EMA-authorized products. The company emphasizes a Total Self culture, encouraging authenticity, diversity, and inclusivity while fostering career development and peer recognition.

    Why Work Here?

    • Opportunities for career progression and technical training.
    • Collaborative, supportive, and inclusive work culture.
    • Exposure to global pharmacovigilance, clinical trials, and regulatory practices.
    • Recognition through total rewards programs and peer acknowledgment.

    Job Role & Responsibilities

    As a Safety & PV Trainee, you will be responsible for supporting pharmacovigilance activities and ensuring compliance with global safety regulations. Key responsibilities include:

    • Entering and tracking Individual Case Safety Reports (ICSRs) in PVG quality and tracking systems.
    • Assisting in processing ICSRs according to SOPs and project-specific safety plans.
    • Evaluating ICSR data for completeness, accuracy, and regulatory reportability.
    • Coding adverse events, medical history, concomitant medications, and laboratory tests.
    • Compiling comprehensive narrative summaries and identifying queries for resolution.
    • Supporting timely reporting of expedited reports in line with regulatory requirements.
    • Performing literature screening and drug coding, maintaining drug dictionaries, and MedDRA coding.
    • Managing duplicate ICSRs and validation/submission of xEVMPD product records.
    • Participating in audits and maintaining compliance with SOPs, GCP, ICH guidelines, and GVP regulations.
    • Collaborating professionally with internal and external project teams.

    Eligibility / Qualifications

    • Educational Background: B.Pharm, M.Pharm, Pharm.D, Life Sciences, Biotechnology, or related courses.
    • Experience: Freshers are welcome; relevant internship or project experience in pharmacovigilance is an advantage.
    • Skills Required:
      • Knowledge of pharmacovigilance principles and clinical research.
      • Familiarity with ICSR processing, MedDRA coding, and safety databases.
      • Strong attention to detail and analytical skills.
      • Effective communication and teamwork capabilities.

    Location & Salary

    • Location: Gurgaon, Haryana, India (Hybrid model)
    • Salary: Competitive, based on qualifications and experience. Additional benefits provided per company policy.
    Fresher Pharmacovigilance Jobs | Safety & PV Trainee at Syneos Health
    Fresher Pharmacovigilance Jobs | Safety & PV Trainee at Syneos Health

    Application Process

    Interested candidates can apply directly via the Syneos Health career portal: Apply Here. Ensure your resume highlights relevant education, skills, and any pharmacovigilance experience to increase selection chances. Apply now to secure your opportunity!

    FAQs

    Q1: Can freshers apply for this role?
    A1: Yes, freshers with a relevant degree and interest in pharmacovigilance are encouraged to apply.

    Q2: What qualifications are required?
    A2: B.Pharm, M.Pharm, Pharm.D, Life Sciences, Biotechnology, or related fields.

    Q3: Is the role hybrid or remote?
    A3: The position is hybrid, with a requirement to work from the Gurgaon office as per schedule.

    Q4: What is the application link?
    A4: Candidates can apply here.

    Q5: Are there any specific skills needed?
    A5: Attention to detail, knowledge of pharmacovigilance, MedDRA coding, and database handling are essential.

    Q6: How many vacancies are available?
    A6: Multiple vacancies are open; candidates are encouraged to apply promptly.

    Why This Role Matters

    Joining Syneos Health as a Safety & PV Trainee offers a strategic career start in pharmacovigilance, contributing to patient safety, regulatory compliance, and healthcare advancement. The experience gained in clinical trials, safety reporting, and regulatory affairs ensures long-term growth in the pharmaceutical industry.

    Take the first step in your pharmacovigilance career and apply today!


    Vertical Summary Table

    Category Details
    Company Syneos Health
    Vacancies Multiple (2025 openings)
    Required Education B.Pharm, M.Pharm, Pharm.D, Life Sciences, Biotechnology, related fields
    Experience Freshers or relevant internship/project experience

    Apply now to join Syneos Health and accelerate your career in pharmacovigilance!