"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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“Dr. Reddy’s Laboratories Hiring Team Member – Analytical Quality Assurance (AQA) | Pharma Jobs in Hyderabad”

"Dr Reddy’s Laboratories Hiring: Team Member – Analytical Quality Assurance (AQA) at Hyderabad"




(Dr Reddy’s Laboratories Hiring Team Member)



Dr Reddy’s Laboratories, one of India’s most respected global pharmaceutical companies, is inviting applications for the position of Team Member – Analytical Quality Assurance (AQA) at its Hyderabad facility. This opportunity is ideal for experienced pharmaceutical professionals who have a strong background in Quality Control (QC) or Analytical Quality Assurance and are looking to advance their careers in a world-class pharma organisation.

For professionals aiming to work in a regulated environment with global exposure, advanced analytical systems, and strict compliance standards, this role offers excellent long-term career stability and growth.


About Dr Reddy’s Laboratories:-

Dr Reddy’s Laboratories is a globally recognised pharmaceutical company committed to providing affordable, innovative, and high-quality medicines to patients across the world. The company was founded in 1984 and is headquartered in Hyderabad, Telangana, India.

With a strong global footprint across multiple countries and regulated markets, Dr Reddy’s has built a solid reputation in research & development, quality systems, regulatory compliance, and sustainable healthcare solutions. The organisation employs over 24,000 professionals worldwide, working across manufacturing, R&D, quality, regulatory affairs, and commercial operations.

Dr Reddy’s Laboratories follows high ethical standards, scientific excellence, and continuous improvement practices in all its pharmaceutical activities. Working at Dr Reddy’s means being part of a professionally driven, innovation-focused culture that values learning, compliance, and quality-driven processes while contributing to global healthcare improvement.


Job Overview – Team Member (Analytical Quality Assurance):-

The Team Member – Analytical QA role is a critical position within the quality framework of Dr Reddy’s Laboratories. The selected candidate will ensure the accuracy, integrity, and compliance of analytical data generated by the Quality Control department.

This role involves reviewing analytical reports, managing deviations, handling electronic systems, and ensuring compliance with cGMP and cGLP guidelines. Professionals working in this position directly contribute to maintaining global quality standards and regulatory readiness.


Vacancy Details:-

  • Job Title: Team Member – Analytical Quality Assurance (AQA)

  • Department: Analytical QA / Quality Control

  • Employment Type: Full-Time

  • Work Location: Hyderabad, Telangana

  • Industry: Pharmaceutical Manufacturing


Key Responsibilities – Analytical QA Role:-

Selected candidates will be responsible for a wide range of analytical quality assurance activities, including:

  • Reviewing and approving analytical test data generated by the Quality Control department

  • Handling electronic systems such as LIMS, Empower, and SAP for data analysis and reporting

  • Providing Level-2 electronic signatures for Chromatography Data Station (CDS)

  • Reviewing validation, method transfer, and analytical test reports

  • Monitoring instrument calibration and qualification records

  • Managing deviations, incidents, OOS/OOT investigations, and ensuring CAPA implementation

  • Ensuring strict compliance with cGMP / cGLP guidelines

  • Verifying specifications, analytical procedures, worksheets, and reports

  • Reviewing compiled stability data and supporting batch sampling activities

  • Supporting Robotic Process Automation (RPA) initiatives in chromatography data review

This role requires strong analytical understanding, documentation skills, and attention to regulatory compliance.


Eligibility Criteria:-

Candidates applying for this position must meet the following eligibility requirements:

  • Educational Qualification: Bachelor’s or Master’s degree in Pharmacy, Chemistry, Chemical Engineering, or a related discipline

  • Experience: Minimum 3–7 years of relevant experience in Quality Control or Analytical Quality Assurance within the pharmaceutical industry


Skills Required:-

To succeed in this Analytical QA role, candidates should possess:

  • Strong understanding of analytical quality assurance processes

  • Practical knowledge of cGMP, cGLP, and data integrity requirements

  • Hands-on experience with LIMS, Empower, CDS, and SAP systems

  • Ability to handle OOS, OOT, deviations, and CAPA investigations

  • Good documentation, data review, and compliance skills

  • Analytical mindset with attention to detail

  • Ability to work independently and in cross-functional teams


Salary Estimate:-

The estimated salary for this position ranges between ₹6,00,000 to ₹12,00,000 per annum, depending on the candidate’s experience, skill set, and interview performance. Dr Reddy’s Laboratories also offers additional benefits such as medical insurance, learning programs, and career development support.


Interview & Selection Process:-

  • Interview Mode: Company selection process (screening + interview)

  • Work Location: Hyderabad, Telangana

  • Application Method 

Shortlisted candidates will be contacted by the recruitment team for further interview rounds.


Documents Required:-

Candidates should keep the following documents ready during the selection process:

  • Updated resume/CV

  • Educational certificates and mark sheets

  • Experience letters from previous employers

  • Last drawn salary slips (if applicable)

  • Valid photo identity proof


Why Join Dr Reddy’s?

At Dr Dreddy’s Laboratories, employees are empowered to drive innovation and deliver quality medicines to patients worldwide. With a strong focus on research, technology, and compliance, the company offers unmatched career growth opportunities for pharmaceutical professionals.

Frequently Asked Questions (FAQs):-

Q1. Is this job suitable for freshers?
No. This role requires 3–7 years of prior experience in QC or Analytical QA.

Q2. Is experience with LIMS or Empower mandatory?
Yes, hands-on experience with analytical systems like LIMS or Empower is highly preferred.

Q3. What is the work location for this job?
The position is based in Hyderabad, Telangana.

Q4. Does Dr Reddy’s offer long-term career growth?
Yes, Dr Reddy’s Laboratories provides excellent learning opportunities and long-term career development.


Final Conclusion:-

If you are an experienced pharmaceutical professional with expertise in Analytical Quality Assurance or Quality Control, this opportunity at Dr Reddy’s Laboratories can significantly boost your career. With strong exposure to global quality systems, advanced analytical tools, and a professional work culture, this role offers both stability and growth.

Apply early to secure your chance to work with one of India’s most trusted pharmaceutical organisations.


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