QC API Vacancies at Apitoria Pharma Vizag

Apitoria Pharma Private Ltd; Visakhapatnam; Presencial; INR 420.000 - 700.000; Jornada completa

Descripción de la vacante

Apitoria Pharma Private Limited, a subsidiary of Aurobindo Pharma, invites QC professionals for API division in Visakhapatnam.

This role centers on analytical testing, GMP/GLP compliance, and robust data integrity in a high-volume API setting. Candidates should have B.Pharmacy or MSc Chemistry with 3–5 years API QC experience and hands-on instrument skills.

Formación

• Hands-on analytical testing in bulk drug manufacturing environments.
• Experience with GMP/GLP and data integrity is required.
• B.Pharmacy or MSc Chemistry with 3–5 years API QC experience.

Responsabilidades

• Perform analysis of raw materials, intermediates, and finished API products.
• Operate and interpret data from analytical instruments such as HPLC and GC.
• Support microbiological testing as per approved procedures.
• Ensure compliance with GMP, GLP, and data integrity requirements.
• Maintain accurate laboratory documentation and analytical records.
• Participate in investigations related to OOS, OOT, and deviations.
• Support internal audits and regulatory inspections.
• Follow SOPs, pharmacopeial standards, and quality guidelines strictly.

Conocimientos

Analytical testing

Documentation

Regulatory compliance

GMP/GLP awareness

Educación

B.Pharmacy

MSc Chemistry

Herramientas

HPLC

GC

Microbiology testing

Descripción del empleo

Apitoria Pharma hiring QC professionals for API division in Visakhapatnam. B.Pharm, MSc Chemistry.

Apitoria Pharma Private Limited, a 100% subsidiary of Aurobindo Pharma Limited, has announced hiring for experienced Quality Control professionals for its API division in Visakhapatnam, Andhra Pradesh. This opportunity is targeted at professionals with hands‑on analytical experience in bulk drug manufacturing environments and strong exposure to advanced laboratory instruments.

API Quality Control plays a critical role in ensuring the purity, safety, and regulatory compliance of active pharmaceutical ingredients supplied to global markets. Apitoria Pharma is strengthening its QC team to support high-volume API manufacturing, analytical accuracy, and compliance with international regulatory standards. For experienced QC professionals, this role offers technical depth, regulatory exposure, and long‑term career stability in the bulk drugs segment.

Company Overview

Apitoria Pharma Private Limited operates as a wholly owned subsidiary of Aurobindo Pharma Limited, one of India’s leading pharmaceutical companies with a strong global footprint in APIs and finished dosage formulations. Apitoria focuses on the development and manufacturing of active pharmaceutical ingredients, catering to regulated markets across the US, Europe, and other international regions.

Job Role & Responsibilities

As a Quality Control professional in the API division, you will be responsible for analytical testing, documentation, and compliance activities related to bulk drug manufacturing. The role demands strong technical expertise and adherence to GMP and regulatory guidelines.

Key Responsibilities

• Perform analysis of raw materials, intermediates, and finished API products
• Operate and interpret data from analytical instruments such as HPLC and GC
• Support microbiological testing as per approved procedures
• Ensure compliance with GMP, GLP, and data integrity requirements
• Maintain accurate laboratory documentation and analytical records
• Participate in investigations related to OOS, OOT, and deviations
• Support internal audits and regulatory inspections
• Follow SOPs, pharmacopeial standards, and quality guidelines strictly

This role is ideal for QC professionals who want to deepen their expertise in API analytical testing and regulatory compliance.

Required Education

Candidates must possess one of the following qualifications:

B.Pharmacy, MSc Chemistry

Experience Requirement

• Minimum 3 to 5 years of relevant Quality Control experience
• Prior exposure to API or bulk drug manufacturing is strongly preferred

Technical Skill Requirements

• Strong working knowledge of HPLC and Gas Chromatography (GC)
• Exposure to microbiology testing in pharmaceutical environments
• Understanding of GMP, GLP, and regulatory compliance standards
• Experience with analytical documentation and laboratory investigations

Location & Salary

Job Location

• Visakhapatnam (Vizag), Andhra Pradesh

Salary Details

Salary is not disclosed and will be offered based on:

• Relevant API QC experience
• Technical expertise and instrument handling skills
• Interview performance and company norms

Email ID

Email ID: [e-mail]

Frequently Asked Questions (FAQs)

Who can apply for this Apitoria Pharma QC role?

Candidates with B.Pharmacy or MSc Chemistry and 3–5 years of API QC experience can apply.

Is API experience mandatory?

API or bulk drug manufacturing experience is strongly preferred.

What analytical skills are required?

Hands‑on knowledge of HPLC, GC, and basic microbiology testing is required.

Where is the job location?

The role is based in Visakhapatnam, Andhra Pradesh.

How can candidates apply?

Eligible candidates must email their resume to the official Apitoria Pharma email ID provided.