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Current openings: QA Specialist • Manufacturing Associate I
Title: QA SpecialistDepartment: Quality
Job Description: Candidate will provide quality assurance support for all aspects of Phase I/II clinical product manufacturing. This includes internal audits, area clearance/release and auditing of cGMP related documentation (including Environmental Monitoring, equipment records and batch production records). Candidate will establish and maintain QA equipment, training and document files; review and revise Standard Operating Procedures and other documentation as needed for continuous improvement; as well as other responsibilities as required.
Qualifications: Bachelor's degree in Biology or a related field or the equivalent combination of education and experience required. A minimum of two years of Quality Assurance (QA) experience in a pharmaceutical or biotechnology industry is preferred. Candidates should have the ability to work independently and demonstrate strong organizational skills, including the ability to prioritize workload. Strong technical writing capabilities and a proficient knowledge of GMPs is required. Strong written and verbal communication skills are a plus.
To apply email resume, cover letter, and salary requirements to jobs@omniabio.com