Overview:
Quality Assurance / Document Control position available at Sciecure Pharma Inc. We are seeking an entry level or partially experienced QA Associate on a permanent basis. Considering local candidates with GMP experience in a manufacturing setting within the QA department.
Job Type: Full-time
Responsibilities:
Assist in the timely completion of Quality Assurance tasks and responsibilities.
Use and manage Quality spreadsheets, tracking sheets and checklists.
Become proficient in the following internal systems and activities: SOP's, Change Controls, Deviations, Corrective Actions, Training records, and record retention.
Process, circulate, review and catalog documents and approvals.
Organize and maintain the electronic storage of cGMP documents.
Provide support during inspections and audits.
Qualifications:
Entry level candidate with some experience in Quality Department (QC or QA).
Bachelor's degree in science or equivalent is required.
3 years of prior work experience in a Biotechnological, Pharmaceutical, or Clinical environment is required.
Some understanding of FDA guidelines and cGMP's.
Superior attention to detail with strong organizational skills.
Must be proficient with Microsoft Office applications.
Has the ability to handle multiple tasks in a timeline-driven environment.
Send resume to:
Sciecure Pharma Inc.
HR Department
11 Deer Park Drive, STE 120
Monmouth Junction NJ, 08852
Email: [email protected] 