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Teyro Labs Pvt. Ltd., a USFDA-approved Indian pharmaceutical company established in 2016, is a fast-growing leader in oncology and specialty formulations. Part of the Accord Group, Teyro Labs excels in R&D, manufacturing, and global supply of niche pharmaceutical products, with a strong presence in the USA, EU, and emerging markets. We are hiring Quality Control (Senior Executive/Executive/Jr. Executive) professionals for our world-class facility in Chennai, Tamil Nadu. Join us to drive excellence in pharmaceutical quality control!
Note: Candidates must have experience in pharmaceutical formulations, preferably in oncology or sterile/non-sterile products. API-only experience may not be sufficient.
Job Details
- Department: Quality Control (QC)
- Designation: Senior Executive / Executive / Jr. Executive
- Location: Teyro Labs Pvt. Ltd., Old No. 29, New No. 13, Tilak Street, T. Nagar, Chennai – 600017, Tamil Nadu
- Qualification: B.Pharm / M.Pharm / M.Sc (Chemistry, Analytical Chemistry, or related fields)
- Experience: 2-8 Years in pharmaceutical quality control (experience in oncology or sterile/non-sterile formulations preferred)
Key Responsibilities:
- Perform analysis of raw materials, packing materials, in-process samples, and finished products.
- Conduct chromatographic analysis using HPLC and GC with proficiency in software like Empower or Chromeleon.
- Operate and troubleshoot analytical instruments (e.g., UV, FTIR, dissolution apparatus, KF titrator).
- Perform instrument calibrations and preventive maintenance as per SOPs.
- Execute analytical method validation and method transfer activities for assays, related substances, and dissolution.
- Manage stability chamber operations and analyze stability samples per ICH guidelines.
- Prepare and review QMS documents (e.g., SOPs, STPs, specifications, validation protocols).
- Ensure compliance with cGMP, USFDA (21 CFR Part 210, 211), and ICH guidelines.
- Support regulatory audits and handle OOS, OOT, deviations, and CAPA documentation.
Key Skills:
- Hands-on experience with HPLC, GC, and other analytical instruments.
- Strong knowledge of analytical method validation, method transfer, and stability studies.
- Familiarity with GLP, GMP, and regulatory compliance for formulations.
- Detail-oriented with strong documentation and problem-solving skills.
Why Join Teyro Labs?
- Global Leader: Work with a USFDA-approved company specializing in oncology and high-potency formulations, with a growing global footprint.
- Innovative Environment: Contribute to cutting-edge R&D and manufacturing at a world-class facility in Chennai.
- Career Growth: Access training and career advancement opportunities within the Accord Group.
- Benefits: Competitive salary, health insurance, and a collaborative work culture.
Learn more about our mission at Teyro Labs and industry standards at USFDA or ICH.
How to Apply
- Email Application: Send your updated CV to hr@teyro.com. Mention “Quality Control [Designation] Application” (e.g., “Quality Control Senior Executive”) in the subject line.
- Contact: For queries, call +91 9790979646.
- Requirements: Include CV, educational certificates, last 3 months’ salary slips, and a cover letter highlighting your QC experience in formulations.
- Stay Updated: Follow #PharmaJobs and #ChennaiJobs on X.com for the latest pharmaceutical career opportunities.
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Important: Teyro Labs does not charge any fees for job applications. Beware of fraudulent invitations requesting payment. Contact hr@teyro.com for verification.
Join Teyro Labs to drive quality and innovation in pharmaceutical manufacturing!