Promea Hiring Fresher & Experience – In-Process QA – Jr Executive/Executive

About Promea

Promea Therapeutics is a rapidly growing pharmaceutical company dedicated to manufacturing high-quality medicines and ensuring compliance with global regulatory standards. With a commitment to innovation and quality, Promea provides a great platform for professionals looking to build a rewarding career in the pharmaceutical industry.

Job Overview

Promea is actively hiring for In-Process Quality Assurance (QA) – Jr Executive/Executive roles. This opportunity is open to both freshers and experienced professionals who are passionate about maintaining pharmaceutical quality standards. The selected candidates will be responsible for ensuring that manufacturing and packaging processes comply with regulatory guidelines.

Position: In-Process QA – Jr Executive/Executive
Experience: 0-4 years
Job Type: Full-time
Location: Hyderabad
Industry: Pharmaceutical

Key Responsibilities

Oversee quality assurance processes across warehouse, production, and packaging units.
Ensure compliance with cGMP (Current Good Manufacturing Practices) and other regulatory standards.
Conduct real-time monitoring and verification of manufacturing processes.
Identify and resolve quality-related issues in collaboration with production teams.
Participate in deviation investigations and assist in Root Cause Analysis (RCA) and Corrective and Preventive Actions (CAPA).
Maintain accurate and complete documentation of quality-related activities.
Assist in internal and external audits and support audit response preparations.
Provide guidance and training to production personnel on quality standards.
Stay updated with the latest industry regulations and quality control practices.

Required Qualifications

Education: Bachelor’s degree in Pharmacy, Chemistry, Biochemistry, Microbiology, or related fields.
Experience: 0-4 years in In-Process QA in the pharmaceutical industry.
Strong knowledge of cGMP, quality assurance protocols, and regulatory compliance.
Analytical skills to monitor and assess quality control issues.
Ability to work independently and collaboratively with cross-functional teams.
Excellent documentation and problem-solving skills.
Experience in conducting deviation investigations, RCA, and CAPA is an added advantage.