About Teyro Labs Private Limited :
Headquartered in Chennai, India, Teyro Labs is a fast-growing generic pharmaceutical company with a major focus on the development and manufacture of IP-led niche finished dosage formulations and Active pharmaceutical ingredients (APIs).
Teyro Labs is involved in the Research & Development, Manufacturing and Supply of pharmaceuticals across different geographical entities around the globe.
We are always building on our company’s core strengths of vertical integration in the fields of discovery, research, process chemistry, active pharmaceutical ingredient production, formulation development and regulatory filings. Teyro Labs is committed to achieving its vision and mission of invariably becoming the most innovation-led transnational pharmaceutical company.
Inseminating quintessential aspects into our system to satisfy a wide array of criteria, Teyro Labs always strives to be more and thereby aspire to be the best. Our partnership philosophy with our customers has helped deliver incremental value to both our company and partners.
Fulfilling the demands of the world markets – Teyro Labs aim at building on our strong global footprint, we are committed to fulfilling the demands of the world markets by anticipating future needs and pioneering strategic new in-roads into the commercial pharmaceutical sector.
Also, we focus on building an enterprise that generates value for all its stakeholders. We are focused on fulfilling the demands of the world markets through different business segments.
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About Teyro Labs Private Limited Jobs:
TEYRO LABS PRIVATE LIMITED Multiple Pharma Job openings in Tamilnadu.
Positions | Educational Qualification | Experience | Job Description |
---|---|---|---|
Executive QMS | B Pharmacy / M Pharm/ BSc / MSc | 2 to 6 Years | Experience in QMS activities of Finished Dosage Formulation operation both sterile and non-sterile. Candidates preferred exposure to Regulated markets like USFDA, EUGMP, UKMHRA, etc… |
Sr. Executive Quality Assurance -Validation | B Pharmacy /M Pharm /BSc / MSc | 4 to 8 Years | Working knowledge in Qualification, Validation of Equipment, Utilities, Cleanroom, and Water Systems relating to Finished Dosage Formulation operations both sterile and non-sterile. Candidates preferred with working experience in Regulated environments like USFDA, EUGMP, UKMHRA, etc. |
Manager Quality Assurance -Validation | B Pharmacy / M Pharm / BSc / MSc | 10 to 15 Years | Relevant experience overseeing the Qualification, Validation of Equipment, Utilities, Cleanroom, and Water System activities relating to Finished Dosage Formulation operations, both sterile and non-sterile. Exposure to regulated markets like USFDA, EUGMP, and UKMHRA is essential |
Executive Quality Assurance IPQA-Non- Sterile | B Pharmacy / M Pharm /BSc / MSc | 2 to 6 Years | Working Experience in Solid Orals Finished Dosage Formulations of Regulated environments like USFDA, EUGMP, and UKMHRA. Adequate Knowledge in IPQA activities like line clearance, process, and cleaning validation sampling, qualification, Intermediate, bulk & FG sampling. |
Executive Quality Assurance IPQA-Sterile | B Pharmacy /M Pharm / BSc / MSc | 2 to 6 Years | Working Experience in Sterile Injectable Finished Dosage Formulations of Regulated environments like USFDA, EUGMP, and UKMHRA. Adequate Knowledge in IPQA activities like line clearance, process, and cleaning validation sampling, qualification, Intermediate, bulk & FG sampling. |
Executive/Sr. Executive FDD-Non-Sterile | B Pharm/ M Pharm | 04 to 08 years | The idle candidate has relevant Experience in Research & Development of Finished Dosage Formulations of Oral Solids, and exposure to working in regulated environments like USFDA, EUGMP, and UKMHRA is preferred. |
Asst. Manager FDD- Non-Sterile | B Pharmacy / M Pharm | 8 to 12 Years | The idle candidate has relevant Experience in Solid Orals Formulation Development for the Regulated Markets of the USA and EUROPE. Hands-on experience in handling different dosage forms of OSD. |
Executive FDD-Sterile Injectable | B Pharm/M Pharm | 2 to 6 Years | Relevant work Experience in Injectable Formulation Development for Regulated Markets like USA and EUROPE is preferred. Hands-on experience in handling different dosage forms of Injectable formulations. |
Application process; Interested candidates, please post your updated resume to: career@teyro.com; sureshbabu@teyro.com
Plant Address: Formulation Division: Plot No. A-8/1, SIPCOT Industrial Growth Centre, Oragadam, Sriperumbudur, Kanchipuram-001 301 API Division: C17, SIPCOT Industrial Complex, Chidambaram Road, Cuddalore, Tamil Nadu – 605 005

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