Teyro Labs Is Hiring for IPQA Manager/Deputy Manager (Sterile Manufacturing) in Chennai

Teyro Labs Pvt. Ltd., a fast-growing, USFDA-registered generic pharmaceutical company headquartered in Chennai, India, specializes in the development and manufacture of IP-led niche finished dosage formulations and APIs, with a strong focus on oncology, hormones, and high-potency products.

Operating a world-class facility in Oragadam, Kanchipuram, with a capacity of 10 million vials & PFS per annum, Teyro leverages advanced technologies like isolator-based aseptic processing and BOSCH filling lines. We are hiring an IPQA Manager/Deputy Manager (Sterile Manufacturing) with 10–15 years of experience to ensure quality in our sterile production processes. Join us to contribute to global healthcare innovation!

Position Details

• Job Title: IPQA Manager/Deputy Manager (Sterile Manufacturing)
• Department: In-Process Quality Assurance (IPQA)
• Location: Teyro Labs Pvt. Ltd., Plot No. A-9/1, SIPCOT Industrial Growth Centre, Oragadam, Kanchipuram Dist., Tamil Nadu-601301, India
• Application Email: hr@teyro.com
• Company Website: Teyro Labs
• Note: The posting is active as of May 19, 2025, 11:36 AM IST. Apply promptly as positions may fill quickly.

Job Description

The Position

The IPQA Manager/Deputy Manager (Sterile Manufacturing) will oversee quality assurance during sterile production at Teyro’s Oragadam facility, which specializes in injectables (vials, PFS) and OSD formulations for oncology and non-oncology products. This role ensures compliance with cGMP, USFDA, and ICH guidelines through meticulous oversight of manufacturing and packing processes, focusing on sterility and regulatory standards.

Key Responsibilities

• Perform line clearance procedures for manufacturing and packing to ensure no cross-contamination.
• Conduct in-process checks during sterile production (e.g., compounding, filtration, filling).
• Manage sampling for in-process (IP), finished product (FP), and validation samples per SOPs.
• Review batch records (BMRs/BPRs) for accuracy and compliance with cGMP.
• Oversee media fill/aseptic process simulation to validate sterility assurance.
• Lead process validation and cleaning validation to ensure consistent quality and cleanliness.
• Facilitate visual inspectors’ qualification for optical testing of injectables.
• Conduct Product Quality Reviews (PQR) to assess product performance and compliance annually.

Qualifications

Education

B.Pharm, M.Pharm, B.Sc., or M.Sc. in a relevant discipline (e.g., Chemistry, Microbiology, Biotechnology).

Experience

10–15 years in a sterile manufacturing facility, with hands-on experience in IPQA for injectables (vials, PFS, lyophilized products). Exposure to USFDA audits and aseptic processing is mandatory.

Skills

• Expertise in cGMP, SOPs, data integrity, and 21 CFR Part 11 compliance.
• Proficiency in media fill, aseptic process simulation, and validation protocols.
• Strong knowledge of isolator technology and aseptic filling lines (e.g., BOSCH).
• Ability to lead line clearance, in-process checks, and batch record reviews.
• Excellent communication and leadership skills to manage cross-functional teams.

Candidate Requirements

• Documents to Submit: Updated CV highlighting sterile manufacturing and IPQA experience, photocopies of educational certificates (B.Pharm/M.Pharm/B.Sc./M.Sc.), Aadhar card, PAN card, one passport-size photograph, last 3 months’ pay slips or CTC proof, and experience letters.
• Application Tip: Emphasize your experience with USFDA inspections, media fills, and validation activities in your CV.
• Note: Candidates without sterile manufacturing experience will not be considered.

How to Apply

• Send Your CV: Email your updated CV to hr@teyro.com with the subject line “IPQA Manager/Deputy Manager (Sterile Manufacturing) Application – Oragadam”.
• For More Info: Visit Teyro Labs for details on our facility and operations.
• For Queries: Contact hr@teyro.com.

Why Join Teyro Labs Pvt. Ltd.?

• Global Reach: Contribute to pharmaceuticals supplied across multiple geographical entities, with recent USFDA approval for Capecitabine Tablets (LinkedIn updates, 2025).
• Advanced Facility: Work in a USFDA-registered facility (FEI No. 3021389808) with isolator/CRAB technology and a Martin Christ Lyophiliser for sterile production.
• Innovation-Driven: Be part of a company focused on Quality-by-Design (QbD) principles for product development and regulatory filings.
• Specialized Focus: Engage in oncology and high-potency product manufacturing, a niche area with global demand.
• Career Growth: Join a fast-growing company with opportunities to lead quality initiatives in a regulated market.

Important Notes

• No Recruitment Fees: Teyro Labs does not charge fees for recruitment. Report suspicious activities to hr@teyro.com.
• Eligibility: Only candidates with 10–15 years in sterile manufacturing and relevant qualifications should apply.
• Work Environment: The Oragadam facility supports 10 million vials/PFS annually, with a filling range of 1ml to 50ml, and includes lyophilization and OSD production.

Apply now to join Teyro Labs Pvt. Ltd. as an IPQA Manager/Deputy Manager (Sterile Manufacturing) in Chennai and ensure quality in sterile pharmaceutical production! Email your CV to hr@teyro.com to seize this opportunity in pharmaceutical quality assurance jobs.