Quality Assurance / Document Control

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:

• Process, circulate, review and catalog documents and approvals.
• Provide support during inspections and audits.
• Become proficient in the following internal systems and activities: SOP's, Change Controls, Deviations, Corrective Actions, Training records, and record retention.
• Assist in the timely completion of Quality Assurance tasks and responsibilities.
• Use and manage Quality spreadsheets, tracking sheets and checklists.
• Organize and maintain the electronic storage of cGMP documents.

Qualifications:

• Bachelor's degree in science or equivalent is required.
• Superior attention to detail with strong organizational skills.
• Has the ability to handle multiple tasks in a timeline-driven environment.
• Entry level candidate with some experience in Quality Department (QC or QA).
• 3 years of prior work experience in a Biotechnological, Pharmaceutical, or Clinical environment is required.
• Must be proficient with Microsoft Office applications.
• Some understanding of FDA guidelines and cGMP's.

Send resume to:
Sciecure Pharma Inc.
HR Department
11 Deer Park Drive, STE 120
Monmouth Junction NJ, 08852
Email: [email protected]