Explore high-paying R&D jobs at Teyro Labs in Oragadam, Chennai. Openings for M.Pharm/M.Sc. candidates in Formulation & Analytical Development. Work on oncology formulations for USFDA/MHRA markets. Apply by June 30, 2025.
🧪 Teyro Labs R&D Jobs 2025 – Formulation & Analytical Development Roles in Chennai (Apply by June 30)
Teyro Labs Private Limited, a cutting-edge USFDA-approved pharmaceutical manufacturer, is expanding its Research & Development team in Oragadam, Chennai. If you’re passionate about oncology formulations, regulatory R&D, and working with advanced pharmaceutical technologies, this opportunity is tailored for you.
With a global focus on high-potency oncology drugs and regulated markets (US/EU), Teyro Labs offers world-class infrastructure, a collaborative environment, and exposure to ANDA filings and regulatory audits. Be part of a team developing life-saving formulations that matter.
🏢 About Teyro Labs
Based in Chennai, Teyro Labs is a generic pharmaceutical company specializing in IP-led niche formulations and API development. The company’s 11-acre manufacturing facility at Oragadam is equipped with isolator-based sterile processing, CRABS technology, and BOSCH automatic filling lines – fully aligned with USFDA, MHRA, and WHO standards.
As part of the Accord Group, Teyro Labs focuses on oncology and high-potency drug development, making it a pioneer in India’s growing pharma innovation ecosystem.
📌 Job Openings – R&D Formulation & Analytical Development
🔬 Open Positions:
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Formulation Development (OSD)
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Analytical Development (QC & Stability Testing)
| Position | Details |
|---|---|
| Roles | Formulation Development / Analytical Development |
| Department | Research & Development (R&D) |
| Experience | 1 to 5 years |
| Qualifications | M.Pharm (Pharmaceutics/Tech), M.Sc. (Chemistry/Biotech) |
| Location | Oragadam, Chennai – SIPCOT Industrial Growth Centre |
| Work Mode | Fully Onsite |
| Last Date to Apply | June 30, 2025 |
🔧 Key Responsibilities
🧪 Formulation Development (OSD – Tablets/Capsules)
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Develop oral solid dosage forms for global regulated markets (USFDA, MHRA).
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Prepare Technology Transfer Documents (TTD) for exhibit and commercial batches.
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Execute scale-up, optimization, and exhibit batch manufacturing.
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Assist regulatory team in preparing dossiers and product submissions.
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Support cGMP audit readiness and participate in inspections.
🧫 Analytical Development
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Conduct method development using HPLC, GC, UV-spectroscopy, and wet chemical techniques.
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Perform drug-excipient compatibility, dissolution, and stability testing.
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Prepare Standard Test Procedures (STPs) and method validation reports.
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Ensure instrument calibration and compliance with ICH guidelines.
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Provide analytical support to formulation teams during development.
🎓 Eligibility & Qualifications
| Requirement | Details |
|---|---|
| Educational Background | M.Pharm (Pharmaceutics/Pharmaceutical Technology) or M.Sc. (Chemistry, Biotech) |
| Experience Range | 1 to 5 years in pharmaceutical R&D or QC |
| Core Skills | HPLC, GC, ICH Q3, dissolution, cGMP, STP preparation |
| Industry Exposure | Regulated markets (USFDA, MHRA, EU), ANDA filings, validation processes |
| Work Traits | Attention to detail, teamwork, documentation accuracy |
🌟 Why Work with Teyro Labs?
✅ USFDA-Approved Facility: Work in a state-of-the-art R&D lab using isolator-based containment and BOSCH lines.
✅ Oncology & High-Potency Focus: Be a part of niche therapeutic areas with global impact.
✅ Career Advancement: Training in regulatory submissions, participation in audits, and technology transfer projects.
✅ Global Exposure: Opportunity to contribute to ANDA filings for US, EU, and RoW markets.
✅ Innovative Environment: Access to advanced technologies, stability chambers, and controlled environments.
✅ Company Culture: Small, high-impact teams with rapid decision-making and a focus on scientific excellence.
💰 Compensation & Benefits
| Benefit | Details |
|---|---|
| Salary Estimate | ₹3–6 Lakhs per annum (as per Indeed) |
| Growth Path | Scale to R&D Lead, Regulatory Affairs, or Site QA roles |
| Learning Opportunities | Hands-on with ANDA filings, ICH guidelines, and high-potency molecule R&D |
| Recognition | Performance-based appraisals, audit exposure, and cross-functional learning |
📬 How to Apply
📧 Send your updated CV to: hr@teyro.com
📞 Contact: +91-9790979646
📝 Email Subject Line: “R&D Application – Formulation/Analytical Development”
❗ Important:
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Mention your desired role and years of experience clearly.
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Attach resume in PDF or Word format.
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Application Deadline: June 30, 2025
🧠 Application Tips
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Showcase HPLC, GC, analytical validation, or OSD formulation exposure.
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Highlight experience with regulatory audits (USFDA, MHRA).
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Mention any knowledge of ICH Q8–Q12 guidelines or exposure to ANDA development.
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Include any project or dissertation relevant to oncology or formulation tech.
📘 Helpful Link: ICH Guidelines for R&D Reference
🏭 Work Environment Snapshot
| Aspect | Details |
|---|---|
| Location | SIPCOT Industrial Complex, Oragadam, Chennai (45 km from city center) |
| Work Setting | Fully onsite in a regulatory-grade R&D facility |
| Team Size | 175+ employees with dedicated R&D, QA, and regulatory teams |
| Certifications | USFDA, MHRA, WHO-compliant facility with sterile manufacturing |
🌍 Equal Opportunity Commitment
Teyro Labs promotes inclusivity and equal opportunity across all hiring. We welcome professionals from diverse academic and regional backgrounds who are passionate about innovative pharmaceutical science.
🚀 Take the Next Step in Your Pharma Career
Don’t miss this chance to work with a next-generation pharma innovator. Join Teyro Labs and contribute to global oncology solutions, regulatory innovation, and scientific excellence.
📅 Last Date to Apply: June 30, 2025
📍 Location: Oragadam, Chennai
👉 Build your R&D career where science meets global impact.
