Quality Specialist
•2 days ago
Hours | Full-time, Part-time |
---|---|
Location | Elkton, Virginia |
About this job
Quality Specialist
12 months
Elkton, VA 22827
Shift Requirements: 8am-5pm.
Qualifications:
Education Minimum Requirement:
Bachelor's Degree in Science, Health Science, Engineering, or related discipline with 1-3yrs industry experience.
Required Experience and Skills:
Previous Experience in the pharmaceutical industry.
Preferred Experience and Skills:
12 months
Elkton, VA 22827
Shift Requirements: 8am-5pm.
Qualifications:
Education Minimum Requirement:
Bachelor's Degree in Science, Health Science, Engineering, or related discipline with 1-3yrs industry experience.
Required Experience and Skills:
Previous Experience in the pharmaceutical industry.
Preferred Experience and Skills:
- 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.
- Previous experience in project management, process data analysis. Lean Six Sigma Certification Previous Experience with SAP,MEDS, etc. Additional: Beta Lactam screening required for this role.
- The successful candidate will support aseptic operations.
- 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. May perform quarantine functions and accountability reviews. Supports special projects as assigned.
- The role follows cGMP and routinely makes decisions using cGMP/process knowledge.
- May work with customers to resolve problems and to satisfy quality and production needs.
- Follows site safety requirements. Authors, reviews, and approves data/ documents such as methods, procedures, and/ or protocols.
- Performs all work and completes assignments in a timely manner and is an active member of 1 or more teams. The individual tracks/reports metrics as needed. May provide training/ presentations as needed. May help with regulatory inspections.
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Full-time Jobs Part-time Jobs Gig Jobs Posting ID: 935651100 Posted: 2024-05-04 Job Title: Quality Specialist