- The individual carries out a variety of activities to support manufacturing operations becoming familiar with site processes, procedures, and policies as individual develops knowledge aligned with cGMPs and Health Authority regulations.
- The role will support the review and approval of qualification activities, change controls, batch records, auxiliary forms, investigations, procedures, and other quality related documentation.
- The successful candidate will support aseptic operations on shift, including auditing of classified (Grades A/B/C) areas which also includes getting certified for Grade A/B gowning.
- The role follows cGMP and routinely makes decisions using cGMP/process knowledge.
- Previous Experience in the pharmaceutical industry.
- Previous experience supporting aseptic operations or sterile product, experience in Quality Assurance/Engineering role or Technical role.
- Previous experience in food or pharmaceutical environment in regulatory/inspection role.
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Quality Specialist - Elkton, United States - Collabera
Description
Job Description
Job DescriptionResponsibilities:
Qualifications:
Education Requirement: Bachelor's Degree in Science, Health Science, Engineering, or related discipline with 1-3yrs industry experience.
Company DescriptionCollabera is a Global Digital Solutions Company providing Software Engineering Solutions for the world's most tech-forward organizations in the areas of Engineering, Cloud and Data/AI. With its roots serving the engineering needs of the world's most recognized businesses in Technology, Financial Services, Telecom and Healthcare, Collabera today operates across 60 locations in 11 countries, serves 30% of the Fortune 500, and has exceeded the industry growth rate by 3-4x for several years.
