Optimus Pharma Hiring DQA – API Executive (R&D Centre, Hyderabad)

Optimus Pharma, a dynamic and growing pharmaceutical company committed to [mention company’s focus if known, e.g., innovation and quality in API development], is seeking an experienced and detail-oriented **Executive** to join their **Drug Quality Assurance (DQA) team** at their **API Research and Development (R&D) Centre in Hyderabad**. If you have a strong background in API quality assurance and are looking for a challenging role in a research-driven environment, we encourage you to apply.

Career Opportunity: DQA – API Executive at Optimus Pharma R&D Centre, Hyderabad

As a DQA – API Executive at Optimus Pharma’s R&D Centre, you will play a crucial role in ensuring the quality and compliance of our Active Pharmaceutical Ingredients (APIs) throughout the research and development process. This position offers an excellent opportunity to contribute to the development of high-quality pharmaceutical products and work within a team dedicated to scientific excellence.

About Optimus Pharma

Optimus Pharma is a [Insert brief description of the company if known – e.g., leading pharmaceutical manufacturer specializing in the development and production of high-quality APIs]. We are committed to [Insert company’s mission or values if known – e.g., delivering innovative and affordable healthcare solutions]. Our R&D Centre in Hyderabad is at the forefront of our efforts to develop and refine our API portfolio.

Job Title

Executive – DQA – API (R&D Centre)

Requirements

**Experience:** 2 to 4 Years of relevant experience in API Quality Assurance.
**Gender:** Male candidates are preferred.
**Qualification:** Masters of Science (M.Sc.) in Chemistry or a related field.
**Essential Knowledge:** Should have prior experience working with Active Pharmaceutical Ingredients (API).

Job Description

As a DQA – API Executive, your responsibilities will include:

Review of equipment qualification/calibration/validation reports (IQ, OQ, PQ) related to all analytical instruments.
Should have knowledge on review of Specifications & Standard test procedures.
Review of reference standard and impurity COA’s and characterization data.
Should have knowledge of GTI & Nitrosamines risk assessment.
Responsible for issuance and archival of documents.
Should have good knowledge of ICH guidelines, USP general chapters.
Should have knowledge of QMS activity (Incidents, Change controls).
Responsible for maintaining GLP & GDP at the workplace.

Interested?

If you meet the above requirements and are interested in this exciting opportunity at Optimus Pharma’s R&D Centre in Hyderabad, we encourage you to send your CV and Portfolio to apply today at:

[email protected]

We look forward to receiving your application and exploring how your expertise can contribute to our team!