"Syneos Health Hiring Safety & PV Coordinator in Hyderabad | Pharmacovigilance Jobs"

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"Syneos Health Hiring Safety & PV Coordinator in Hyderabad | Pharmacovigilance Jobs" (Syneos Health Hiring Safety & PV Coordinator in Hyderabad) Introduction Candidates looking to build a strong and long-term career in Pharmacovigilance (PV) and Drug Safety have an excellent opportunity at Syneos Health , a globally recognized biopharmaceutical solutions organization. Syneos Health is currently hiring for the position of Safety & PV Coordinator at its Hyderabad office . This is a full-time, office-based role , ideal for professionals who have experience or exposure in pharmacovigilance submissions, safety reporting, regulatory compliance, and clinical research processes . Working with a global organization like Syneos Health provides exposure to international safety regulations, cross-functional teams, and structured career growth . About The Company – Syneos Health Syneos Health® is a fully integrated biopharmaceutical solutions organization that supports pha...

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"FDA Approved Pharma Companies in USA Hiring Indians (2026-27 Guide)"

"FDA-Approved Pharma Companies in the USA Hiring Indians (2026-27 Guide)"



(FDA Approved Pharma Companies in USA 2026-27)



INTRODUCTION

Working with an FDA-approved pharmaceutical company in the USA is a dream for many Indian pharma and life science professionals. These companies follow the highest global standards in drug manufacturing, research, quality control, and regulatory compliance. With the continuous expansion of the US healthcare and pharmaceutical industry, many FDA-regulated pharma companies actively hire skilled Indian professionals across multiple roles.

This article provides a clear, practical, and updated guide on FDA-approved pharma companies in the USA hiring Indians, eligibility requirements, job roles, and how to prepare for such opportunities.


ABOUT FDA APPROVAL & ITS IMPORTANCE

The US Food and Drug Administration (FDA) is responsible for regulating pharmaceutical manufacturing, drug safety, clinical trials, and quality systems in the United States. Companies approved or regulated by the FDA must comply with strict guidelines, such as:

  • cGMP (Current Good Manufacturing Practices)

  • Data integrity norms

  • Quality assurance systems

  • Regulatory documentation standards

Indian professionals with experience in WHO-GMP, USFDA audits, or regulatory affairs are highly valued in such organizations.


FDA APPROVED PHARMA COMPANIES INTHE  USA HIRING INDIANS

Many US-based and multinational pharmaceutical companies regularly recruit Indian talent, especially those with strong academic backgrounds and compliance knowledge.

Well-Known FDA-Approved Companies:

These companies operate under FDA regulations and often hire Indians for technical, regulatory, and commercial roles.


JOB OVERVIEW SUMMARY

Indian candidates are hired across manufacturing, quality, regulatory, research, clinical, and business functions. Roles may vary depending on qualification, experience, and visa eligibility.


COMMON JOB ROLES AVAILABLE

  • Regulatory Affairs Associate

  • Quality Assurance Officer

  • Quality Control Analyst

  • Clinical Research Associate

  • Validation Engineer

  • Manufacturing Supervisor

  • Pharmaceutical Scientist

  • Medical Affairs Executive

  • Supply Chain Analyst

  • Sales & Business Development (Healthcare)


ELIGIBILITY CRITERIA

Educational Qualifications:

  • B.Pharm / M.Pharm

  • B.Sc / M.Sc (Life Sciences, Biotechnology, Microbiology, Chemistry)

  • Pharm.D

  • MBA (Healthcare / Pharma Management)

  • PhD (for R&D roles)

Experience Requirements:

  • Fresher (limited roles via internships or traineeships)

  • 1–5 years (QA, QC, RA, Manufacturing)

  • 5+ years (Senior, managerial, leadership roles)


SKILLS REQUIRED

  • Knowledge of USFDA regulations

  • GMP, GLP, GCP understanding

  • Documentation & SOP writing

  • Data integrity compliance

  • Analytical and problem-solving skills

  • Strong English communication

  • Cross-functional teamwork


SALARY ESTIMATE (USA – APPROXIMATE)

(May vary by role, state, and experience)

  • Entry-level: $55,000 – $75,000 per year

  • Mid-level: $80,000 – $120,000 per year

  • Senior roles: $130,000 – $180,000+ per year

Indian professionals with USFDA experience often receive competitive packages.


VISA & WORK AUTHORIZATION INSIGHT

Most companies prefer candidates with:

  • H-1B Visa

  • OPT / STEM OPT

  • Green Card / PR

  • Internal company transfer (L-1 Visa)

Some pharma companies sponsor visas for high-skill roles, especially in regulatory affairs, R&D, and compliance.


HOW INDIANS CAN APPLY (PRACTICAL STEPS)

  1. Create a US-style resume (ATS-friendly)

  2. Highlight USFDA / GMP experience

  3. Apply through official company career portals

  4. Use LinkedIn job search & referrals

  5. Avoid fake consultancy promises

  6. Gain certifications in:

    • Regulatory Affairs

    • Clinical Research

    • Validation & Quality Systems


FAQs 

Q1. Can freshers from India get jobs in FDA-approved US pharma companies?
Freshers may enter through internships, traineeships, or higher education pathways in the USA.

Q2. Is USFDA experience mandatory?
Not mandatory but highly preferred. WHO-GMP experience is also valuable.

Q3. Which role is best for Indians abroad?
Regulatory Affairs, Quality Assurance, Clinical Research, and Manufacturing roles have strong demand.

Q4. Are Indian pharma degrees accepted in the USA?
Yes, but role eligibility depends on licensing, experience, and company policies.


FINAL CONCLUSION

FDA-approved pharmaceutical companies in the USA offer excellent career growth, global exposure, and high earning potential for Indian professionals. With the right qualifications, compliance knowledge, and strategic preparation, Indians can successfully build long-term careers in the US pharmaceutical industry.

If you are serious about working in FDA-regulated pharma companies, start building skills, documentation expertise, and international-standard profiles today.


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