Quality Assurance Admin - Temp To Perm Opportunity

Sheffield Pharmaceuticals is an OTC, drug, and medical device manufacturing company regulated by the FDA. Our products include a variety of creams, ointments, nasal products and toothpastes to promote wellness and first aid relief for our customers.

At Sheffield Pharmaceuticals our mission is to help improve the health and wellness of humankind. Every team member from manufacturing to quality programs to development and facility services are critical components to this effort. We believe our people are our greatest assets and are committed to providing our employees with an environment that supports personal and professional growth. We take pride in knowing our efforts are helping countless customers for years to come.

We are currently seeking a detail oriented, integral, and driven Quality Assurance Administrator who will be responsible for overseeing and assuring compliance with various current good manufacturing practices (cGMP) activities. The administrator will collaborate with internal and cross departmental team members to ensure the highest of quality and compliance to product specifications, processes, and procedures.

Responsibilities:

• Performs reviews of batch records and associated data for product release and determines if records are within range of internal and cGMP regulations.
• Independently investigates, trouble shoots, and rectifies issues as a result of QA analysis though deviation investigations using root cause analysis tools.
• Provides QA oversight and performs real time, on-the-floor documentation review and inspections during manufacturing operations.
• Collects data from multiple quality systems and composes data into metric reports.
• Supports Company Quality Training Program
• Maintains document retention policy and organization of paper files
• Regular and reliable attendance on a full time basis [or in accordance with posted schedule]
• Embodies Sheffield's cultural values and aligns daily actions with department goals and company culture.

Qualifications/Attributes:

• Working knowledge of good documentation practices and cGMP Regulations 21 CFR Part 210, 211, and 820 strongly preferred.
• Excellent attention to detail and communication skills required
• Ability to prioritize tasks in a fast paced environment
• Experience with Word, Excel, and PowerPoint

Education:

Minimum High School Diploma required.

Sheffield Pharmaceuticals is an Equal Employment Opportunity employer. We provide equal opportunity to employees and applicants for employment without regard to race, creed, color, religion, sex, age, national origin, physical or mental disability, sexual orientation, marital or familial status, genetic information, protected veteran status, or other basis protected by law.