drjobs Quality Specialist - I Assistant

Quality Specialist - I Assistant

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1 Vacancy
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Job Location drjobs

Elkton, MD - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Qualifications Education Minimum Requirement: Bachelor s degree in Science Health Science Engineering or related discipline with 13yrs 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 SAPMEDS etc. Additional: Beta Lactam screening required for this role. Shift Requirements: This will be a rotating shift role with the following hours: 6:30a3:30p and 1:30p10:30p. The successful candidate will support aseptic operations on rotating shift.
Responsibilities 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.
Comments/Special InstructionsCSP Chrissy
System Location: Manufacturing (Z007) Required
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CWR Type: W2 Required

Employment Type

Full Time

Company Industry

About Company

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