Quality Specialist

Review and approve batch records to ensure compliance with quality standards and regulatory requirements.Document and investigate deviations, ensuring timely resolution and implementation of corrective actions.Manage change controls and ensure all changes are properly documented and reviewed.Collaborate with cross-functional teams to facilitate quality improvement initiatives.Support the preparation and maintenance of quality documentation.If extended beyond 6 months, assist in training for batch record release work.Qualifications: Education:Bachelor's degree in Life Sciences, Pharmaceutical Sciences, or a related field (preferred).Experience:4-8 years of experience in Quality Assurance within the pharmaceutical or biotechnology industry.Demonstrated experience in batch record review, deviation management, and change control processes.Skills:Strong understanding of cGMP regulations and quality standards.Excellent attention to detail and ability to analyze complex data.Strong written and verbal communication skills for effective documentation and collaboration.Ability to work independently and as part of a team.Additional Requirements:Manager references required to validate experience and performance.Candidates must be flexible and able to adapt to changing priorities.