Apitoria Pharma (Aurobindo) – Job Openings for Quality Control

Key Points at a Glance

• Company: Apitoria Pharma Private Limited (Aurobindo Pharma Limited Subsidiary)
• Location: Pydibheemavaram, Srikakulam, Andhra Pradesh
• Role: QC – LCMS
• Experience: 10-15 years
• Designation: AM / DM / Manager
• Qualification: M.Sc / M.Pharmacy
• Key Responsibilities: LCMS analysis with ESI & APCI, troubleshooting, GMP documentation
• Preferred Background: Experience in Manufacturing/R&D with LCMS exposure
• Application Email: arunkumar.komshetpally@apitoria.com

Exciting Opportunity at Apitoria Pharma for QC – LCMS Specialists!

Are you ready to elevate your career with one of the leading names in the pharmaceutical industry? Apitoria Pharma Private Limited, a proud 100% subsidiary of Aurobindo Pharma Limited, is on the lookout for experienced professionals to join our dynamic team in the API Division. Based in the picturesque Pydibheemavaram, Srikakulam, Andhra Pradesh, we are seeking a highly skilled individual to take on the role of QC – LCMS.

About Apitoria Pharma

Apitoria Pharma Private Limited is a renowned Indian multinational pharmaceutical manufacturing company. Headquartered in HITEC City, Hyderabad, we are dedicated to producing high-quality generic pharmaceuticals and active pharmaceutical ingredients. As a subsidiary of Aurobindo Pharma Limited, we share a legacy of excellence and innovation in the pharmaceutical industry.

The Role: QC – LCMS

In this pivotal role, you will be responsible for managing LCMS (Liquid Chromatography-Mass Spectrometry) analysis, employing cutting-edge techniques such as ESI (Electrospray Ionization) and APCI (Atmospheric Pressure Chemical Ionization). This position requires a meticulous approach to handling complex analytical processes and ensuring the accuracy and reliability of our pharmaceutical products.

Key Responsibilities

• Exclusive LCMS Analysis: You will be the go-to expert for all LCMS-related analyses, utilizing ESI and APCI techniques to ensure precision in our pharmaceutical formulations.
• Troubleshooting: Your role will involve diagnosing and resolving technical issues related to LCMS instrumentation and processes.
• GMP Documentation: You will be responsible for maintaining meticulous documentation in compliance with Good Manufacturing Practices (GMP), ensuring all procedures are followed accurately.

Ideal Candidate Profile

We are seeking candidates with 10-15 years of experience in LCMS analysis, preferably with a background in manufacturing or R&D environments. Ideal candidates will hold an M.Sc or M.Pharmacy degree and have a strong grasp of GMP documentation practices. Experience with LCMS exposure in a manufacturing or R&D setting will be highly advantageous.

Why Join Us?

At Apitoria Pharma, we offer a vibrant work environment where innovation and excellence are at the forefront. Joining our team means becoming part of a global pharmaceutical leader with a commitment to quality and advancement. You will have the opportunity to work with cutting-edge technology, contribute to impactful projects, and grow professionally in a supportive and dynamic setting.

How to Apply

If you are passionate about LCMS analysis and meet the qualifications outlined above, we encourage you to apply! Please send your resume and a cover letter detailing your relevant experience to arunkumar.komshetpally@apitoria.com.

Don’t miss this chance to advance your career with Apitoria Pharma. We look forward to your application and the possibility of welcoming you to our dedicated team of professionals!

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Embrace this opportunity to make a significant impact in the pharmaceutical industry with Apitoria Pharma. Apply today and take the next step in your career with a company that values innovation and excellence.