Production Specialist
TLDR
Prepare and manage validation protocols and coordinate corrective actions to ensure compliance in pharmaceutical manufacturing processes.
- Prepare and manage validation protocols, reports, and study documentation, monitor validation progress through completion.
- Identify, document, and investigate deviations; prepare investigation reports and coordinate root cause analysis with manufacturing plants.
- Initiate and track corrective and preventive actions (CAPA) against investigations; monitor implementation and ensure timely closure.
- Prepare manufacturing process batch cards and cleaning batch cards (product changeover, periodic, and general cleaning) based on R&D and pilot reports.
- Initiate and manage change controls for manufacturing processes and product changeover cleaning batch cards through the tracking system.
- Coordinate with plants, dispatch, batch card preparation teams, and engineering departments to ensure smooth implementation of CAPA and batch card updates.
- Monitor and follow up on batch cards, cleaning protocols, and deviation closure to ensure on-time completion and compliance.
Qualification: MSC- Chemistry
Experience: 3-5 Years
Preferred Industries: API / Pharma
Make Your Mark with TAPI
Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!
TAPI is a global leader in the production and supply of active pharmaceutical ingredients (APIs), partnering with 80% of the top 50 pharmaceutical companies worldwide. With a strong portfolio of over 350 products and custom CDMO services, TAPI is dedicated to advancing health through innovation and collaboration across its 13 state-of-the-art facilities globally.