Quality Assurance Associate

Quality Assurance Associate In line with current Good Manufacturing Practices (cGMP), the Quality Assurance Associate is entrusted with carrying out a diverse range of assignments within the Quality Assurance department.
Responsibilities and roles: -Collaborate with the Production team to review executed Production Records.
-Provide QA support for manufacturing processes on the production floor.
-Review SOPs, logbooks, and related documentation associated with daily QA activities.
-Conduct internal audits of GMP operations to ensure compliance.
-Offer assistance during external regulatory or partner GMP audits.
-Develop and implement improvements to quality system procedures.
Qualifications: ? Bachelor's Degree and at least one (1) year of QA experience in the pharmaceutical bio industry
? Excellent communication (verbal and written), interpersonal, and teamwork skills
? Ability to be productive and successful in a fast-paced work environment
Preferred Additional Capabilities
? Prior experience in the CDMO industry
? Experience working with GMP compliant / quality-controlled procedures
? Multilingual