Quality Specialist in Brentwood, NC at Volt

Date Posted: 6/28/2019

Job Snapshot

  • Employee Type:
    Contingent
  • Location:
    Brentwood, NC
  • Job Type:
  • Duration:
    48 weeks
  • Date Posted:
    6/28/2019
  • Job ID:
    185377
  • Pay Rate
    $15.0 - $20.0/Hour
  • Contact Name
    Volt Branch
  • Phone
    (919) 829-1660

Job Description

Volt has been a leader in the Staffing Industry for 60 years and currently has more than 100 branches nationwide to serve both our clients' and candidates' needs. We connect office professionals with leading employers in the area. Whether you are looking for a contract/temporary position or a direct hire, we are here to serve you. Find out more about us by visiting www.volt.com.

Volt is an Equal Opportunity Employer.

We have 3 exciting Quality Specialist positions with a growing pharmaceutical company headquartered in North Raleigh.

Position 

The Quality Specialist formats and revises GMP documents including but not limited to SOPs (Standard Operating Procedures) and specifications.

Key Responsibilities

  • Revises and reformats SOPs and specifications in accordance with company requirements.
  • Ensures accuracy of the documents created.
  • Liaises with functional groups within the facility to assist in the revision of site procedures and other GMP documents, as required.
  • Reviews documents for correctness in terms of grammar, outline, and references.
  • Completes assigned work in a timely manner, with minimal supervision.

Requirements

  • High School Diploma or Equivalent
  • Min. Associates Degree in English or similar area of study, Bachelor’s degree preferred
  • Strong computer skills, especially in MS Word
  • Strong writing and editing skills
  • Fluent in English
  • 1-2 years of experience in the Pharmaceutical or other FDA regulated environment a plus
  • Flexible schedule with the ability to work evenings and weekends, as necessary
  • Demonstrates excellent written and verbal communication skills
  • Strong organizational and follow-up skills required for quick response to document status change, ensuring that all critical documents are readily retrievable and are current.

Physical Requirements of the Role

Position is exposed to a number of environments, office, lab, outside, plant floor, etc.  This role is continuously sitting and typing.  Frequently talking and using eye and hand coordination.  Occasionally requiring lifting and carrying less than 10 lbs. Standing, walking, bending over, and repetitive use of legs are done occasionally.  

Any person shown at any time (either by medical examination or supervisory observation) to have an apparent illness or open lesions that may adversely affect the safety or quality of drug products shall be excluded from direct contact with components, drug product containers, closures, in-process materials, and drug products until the condition is corrected or determined by competent medical personnel not to jeopardize the safety or quality of drug products. All personnel shall be instructed to report to supervisory personnel any health conditions that may have an adverse effect on drug products.

This job description is intended to describe the general nature and level of work being performed by the person assigned to this position.  The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.  This job description does not state or imply that the above are the only duties and responsibilities assigned to this position.  There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.  All requirements are subject to possible modification to reasonably accommodate individuals with a disability.