Titan Labs Hiring QA Officer/Executive (Documentation & IPQA) | Mahad

Titan Laboratories Pvt. Ltd., a reputable pharmaceutical company, is seeking a dedicated and experienced QA Officer or Executive to join our Quality Assurance team in Mahad. This role will primarily focus on Documentation and In-Process Quality Assurance (IPQA) activities. If you have a strong understanding of pharmaceutical quality systems and a passion for ensuring compliance, we encourage you to apply.

Join Titan Laboratories’ Quality Assurance Team in Mahad

At Titan Laboratories, we are committed to maintaining the highest standards of quality in our pharmaceutical products. As a QA Officer/Executive specializing in Documentation and IPQA, you will play a critical role in ensuring that our manufacturing and quality processes adhere to regulatory guidelines. We offer a professional and growth-oriented work environment where your expertise will be valued.

About Titan Laboratories Pvt. Ltd.

Titan Laboratories Pvt. Ltd. is a pharmaceutical company dedicated to the development, manufacturing, and marketing of high-quality pharmaceutical products. We are committed to excellence in all aspects of our operations and strive to meet the healthcare needs of our patients effectively.

Position: QA Officer – Executive – Documentation & IPQA

We are currently hiring for the position of QA Officer or Executive with a focus on Documentation and In-Process Quality Assurance (IPQA) at our Mahad location.

Key Responsibilities

As a QA Officer/Executive – Documentation & IPQA, your key responsibilities will include:

Conducting IPQA activities in manufacturing and packing areas to ensure adherence to quality standards.
Managing qualification and calibration documentation for equipment and instruments.
Investigating out-of-specification (OOS) and out-of-trend (OOT) results, ensuring thorough root cause analysis and corrective actions.
Handling stability studies and managing all related documentation.
Supporting internal and external audits, as well as regulatory inspections.
Ensuring compliance with current Good Manufacturing Practices (cGMP) and Good Laboratory Practices (GLP).

Candidate Profile

We are looking for candidates who meet the following criteria:

**Education:** Bachelor of Pharmacy (B.Pharm), Master of Pharmacy (M.Pharm), or Master of Science (M.Sc) in a relevant field.
**Experience:** 2-4 years of proven experience in Analytical Quality Assurance within the pharmaceutical industry.
**Knowledge:** Strong understanding of regulatory requirements including ICH (International Council for Harmonisation), WHO (World Health Organization), and other relevant guidelines.
**Skills:** Good documentation practices and a readiness to apply them effectively.

How to Apply

Interested candidates who meet the above qualifications are encouraged to apply immediately by sending their Curriculum Vitae (CV) to shweta.m@tiapharma.