Quality Assurance Specialist
Recipharma
About the Role
The Quality Assurance Specialist is a full-time, on-site role based in Bengaluru. This role is responsible for monitoring and maintaining compliance with internal quality standards and external regulatory requirements across manufacturing and related operations.
Key Responsibilities
- Reviewing batch records and documentation
- Supporting deviation and CAPA investigations
- Performing internal audits
- Verifying adherence to Good Manufacturing Practice (GMP)
- Collaborating with cross-functional teams to implement quality improvements
- Supporting qualification and validation activities
- Assisting in training personnel on quality procedures
- Preparing quality reports
- Participating in inspections
- Ensuring that products consistently meet defined specifications before release
Requirements & Tech Stack
- Proficiency in documentation, data analysis, and use of standard office and quality management software tools.
Qualifications
- Strong foundation in Quality Assurance and Quality Management, with experience implementing and maintaining quality systems.
- Hands-on experience in Quality Control activities, including review of test results, documentation, and product release processes.
- Demonstrated knowledge of Good Manufacturing Practice (GMP) principles and their application in pharmaceutical or related industries.
- Experience in Quality Auditing, including planning, executing, and reporting internal or supplier audits.
- Bachelor’s degree or higher in Pharmacy, Chemistry, Life Sciences, Engineering, or a related discipline.
- Ability to interpret regulatory guidelines, SOPs, and technical documentation with strong attention to detail.
- Effective communication and collaboration skills, with the ability to work in cross-functional teams and support training initiatives.
- Prior experience in a regulated manufacturing environment (pharmaceutical, biotech, or similar) is highly beneficial.


