Statistical Programmer Job 2026 in Ahmedabad | SAS & CDISC Jobs at Veeda CR

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Statistical Programmer Job 2026 in Ahmedabad | SAS & CDISC Jobs at Veeda CR (Statistical Programmer Job 2026 in Ahmedabad) Introduction If you are planning to build a career in clinical data science, SAS programming, or biostatistics, this Statistical Programmer job at Veeda Clinical Research (Veeda CR) in Ahmedabad is an excellent opportunity. With the increasing demand for professionals skilled in clinical data management and regulatory standards, this role provides a strong foundation in pharmaceutical data science and clinical research. Looking for the best multivitamin? Here is the top recommendation: πŸ‘‰ HealthKart Multivitamin – Best for Daily Energy πŸ‘‰ Buy Now on Amazon (Best Price) About The Company  Veeda Clinical Research (Veeda CR) is a well-established Clinical Research Organization (CRO) headquartered in Ahmedabad, India. Founded in 2004, the company has built a strong reputation in bioequivalence studies, clinical trials, and data management services. Veeda...

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"Zydus MedTech Hiring Senior Executive – R&D (Medical Devices) in Surat | Apply Now"

"Zydus MedTech Hiring Senior Executive – R&D (Medical Devices) in Surat, Gujarat"








(Zydus MedTech Hiring Senior Executive)







Introduction

The Indian medical device industry is rapidly expanding, creating strong demand for skilled professionals in research and development. Recently, Zydus MedTech Pvt. Ltd. has announced a new vacancy for Senior Executive – R&D (Medical Devices) at its Surat, Gujarat facility.

This opportunity is ideal for professionals with 2–4 years of experience in medical device research and development who want to work in a highly regulated, ISO and FDA-compliant environment. If you are looking for a stable, growth-oriented medical device R&D job in Gujarat, this role offers excellent long-term career prospects.


About the Company (Zydus MedTech)

Zydus MedTech Pvt. Ltd. is a leading Indian medical technology company focused on developing innovative and high-quality medical devices for global markets. The company operates as part of the broader Zydus ecosystem and is dedicated exclusively to the MedTech and medical device segment.

Company Highlights (Approximate):

  • Founded: 2021 (as a dedicated MedTech entity)

  • Headquarters: Ahmedabad, Gujarat, India

  • Industry: Medical Devices & Healthcare Technology

  • Employees: 1,000+ (across manufacturing, R&D, and corporate functions)

  • Core Focus: Cardiovascular devices, interventional products, and advanced medical technologies

  • Regulatory Compliance: ISO 13485, ISO 14971, MDR, FDA QSR

Zydus MedTech is known for its strong compliance culture, innovation-driven R&D teams, and global regulatory exposure, making it an attractive employer for medical device professionals.


Job Overview Summary

The Senior Executive – R&D (Medical Devices) role at Zydus MedTech involves hands-on participation in medical device design, development, testing, and documentation. The position plays a key role in ensuring that products meet international regulatory and quality standards while progressing smoothly through the product lifecycle.

This is a full-time, on-site role based in Surat, Gujarat, and is suitable for professionals who want to build deep expertise in design controls, risk management, and regulatory documentation.


Vacancy Details

  • Job Title: Senior Executive – R&D (Medical Devices)

  • Company: Zydus MedTech Pvt. Ltd.

  • Department: Research & Development

  • Location: Surat, Gujarat

  • Employment Type: Full-time, On-site

  • Experience Required: 2–4 years

  • Industry: Medical Devices / MedTech


Responsibility Explanation

As a Senior Executive in Medical Device R&D, you will be responsible for supporting the complete development lifecycle of medical devices. Your work will involve transforming design concepts into compliant, manufacturable products.

Key responsibilities include executing design and prototyping activities, preparing and maintaining technical documentation such as DHF files, and supporting design verification and validation testing. You will actively participate in risk management processes, including hazard analysis and FMEA, to ensure patient safety and regulatory compliance.

The role also requires close coordination with Quality Assurance, Regulatory Affairs, Manufacturing, and external suppliers. Additionally, you will support audits, design transfer activities, and post-market lifecycle updates in line with MDR and FDA expectations.


Eligibility Criteria (Official)

Educational Qualification

Candidates must hold a Bachelor’s or Master’s degree in one of the following disciplines:

  • Biomedical Engineering

  • Mechanical Engineering

  • Polymer / Materials Science

  • Life Sciences

  • Or any related technical discipline

Experience Requirement

  • 2–4 years of experience in Medical Device R&D or other regulated industries

  • Hands-on experience in design documentation, testing, and risk management

  • Exposure to cardiovascular or implantable medical devices is an added advantage


Skills Required

To succeed in this role, candidates should possess:

  • Strong understanding of ISO 13485, ISO 14971, MDR, and FDA QSR

  • Experience in medical device testing, validation, and documentation

  • Ability to prepare technical reports, protocols, and DHF documents

  • Excellent analytical and problem-solving skills

  • Strong technical writing and documentation abilities

  • Team-oriented mindset with cross-functional collaboration skills

  • close attention to detail anda  compliance-focused approach


Salary Estimate

The estimated salary for this position ranges between ₹6,00,000 to ₹10,00,000 per annum (CTC), depending on experience, skill level, and interview performance. Professionals with prior exposure to regulated medical devices and global standards may receive higher compensation.


Interview Details

  • Interview Mode: Technical + HR rounds (online or on-site)

  • Selection Process: Resume screening → Technical interview → HR discussion

  • Interview Focus: Medical device R&D knowledge, design controls, ISO/FDA compliance, and problem-solving skills


Required Documents

Candidates should keep the following documents ready:

  • Updated resume/CV

  • Educational certificates and mark sheets

  • Experience letters from previous employers

  • Government ID proof

  • Any relevant certifications (if available)


How to Apply

Interested candidates can apply online through the official job posting:

Apply Link:
https://www.linkedin.com/jobs/view/4364318315

Applicants are advised to apply as early as possible, as positions may close once suitable candidates are shortlisted.


FAQs – Zydus MedTech R&D Jobs

Q1. Is this role suitable for pharma professionals shifting to medical devices?
Yes, candidates with life sciences or regulated industry experience can transition if they have relevant R&D exposure.

Q2. Is this a work-from-home job?
No, this is a full-time, on-site position based in Surat, Gujarat.

Q3. What regulatory standards are required for this role?
ISO 13485, ISO 14971, MDR, and FDA QSR knowledge is essential.

Q4. Does Zydus MedTech offer long-term career growth?
Yes, the company provides strong growth opportunities in medical device R&D and global regulatory exposure.


Final Conclusion

The Senior Executive – R&D (Medical Devices) position at Zydus MedTech is an excellent opportunity for professionals seeking growth in India’s expanding MedTech sector. With strong exposure to international regulatory standards, hands-on product development, and a compliance-driven work culture, this role offers both professional stability and long-term career advancement.

Candidates with a passion for medical device innovation and quality-focused development should not miss this opportunity.

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