Documentation Control Associate Sharp Clinical Services - 2.6 Allentown, PA Job Details Full-time 23 hours ago Qualifications Pharmaceutical regulatory compliance Spreadsheets Drug regulation High school diploma or GED Productivity software FDA regulations Full Job Description SUMMARY The major functions of this job include maintaining the SOP harmonization process between both sites, maintain updated Training database for both facilities, Handle the entire SOP (Standard Operating Procedure) process and maintain the component specification process.

ESSENTIAL DUTIES AND RESPONSIBILITIES

include the following. Other duties may be assigned. Assist in the SOP harmonization project for multiple Sharp facilities. Create, revise and obsolete SOPs and coordinate those activities with Managers and Directors in both sites. Responsible for ensuring SOPs approval process is streamlined and current. Work with IT to ensure SOPs are posted on Sharp intranet and the necessary security surrounding their control. Create, revise and obsolete component specifications. Responsible for entering and maintaining individual training files for all Sharp employees for both facilities. Update SOP table of contents, distribute SOPs and update appropriate QA folders and Audit Packet for both facilities. Send notices for required training to all Sharp departments. Maintain temporary agencies employees Master Signature Log page and for all permanent employees. Keep track of all permanent employees' background check Assist Quality Assurance department during customer and governmental audits. Other duties may be assigned as appropriate.

SUPERVISORY RESPONSIBILITIES

No direct supervision. Candidate's personal decisions can result in compliance decisions that may have regulatory and financial impact on the company.

QUALIFICATIONS

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. General knowledge of DEA (required) and FDA (plus) regulations. Excellent detail skills as they apply to documentation review and compliance. Good written and oral communication and interpersonal skills Good organizational and planning skills Out-going, assertive and detail-oriented person Knowledge of Microsoft Office Suite and Excel EDUCATION and/or

EXPERIENCE

High School Degree is required. College degree is preferred however, experience and college courses may be substituted for the degree. One to two years related experience and/or training; or equivalent combination of education and experience is preferred. Experience in pharmaceutical or related industry is desired.

LANGUAGE SKILLS

Possess the ability to respond to common inquiries from external customers and the ability to respond to inquiries from peers and superiors.

WORK ENVIRONMENT

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is normally required to sit at a desk or periodically go onto the shop floor. The working environment is clean and not normally subject to hazardous environment or conditions