QC Logistics Technician

Highly Competitive Salary
  1. Contract
  2. Laboratory Technician
  3. United States
Marietta, Pennsylvania
Posting date: 09 Aug 2019

Proclinical is currently recruiting for an QC Logistics Technician for a pharmaceutical company located in Marietta, PA. Successful candidate will follow and work in accordance with company policies, SOPs and cGMP standards to ensure compliance with all applicable regulations.

Job Responsibilities:

  • Perform utility sampling as per established procedures.
  • Generate all paperwork and labels associated with sampling to meet SOP requirements. Collect PEMS data.
  • Responsible for maintaining and ordering enough reagents and supplies. Performing routine laboratory tasks such as preparation of autoclaving materials, performing glassware-washing and stocking supplies, etc.
  • Assure that all required documentation including records and logs, is complete and accurate according to the current GMPs. File and archive laboratory records and data in accordance with GMPs and SOPs. Reviewing of QC logbooks and equipment logbooks.
  • Communicate and report status of operations as well as variances to supervisors. Take appropriate actions and escalate issues immediately.
  • Process QC paperwork, archiving, documentation of QC paperwork, etc.
  • Escort QC vendors for routine and non-routine work orders.
  • Perform routine laboratory tasks such as Utility/EM sample collections, execution of equipment work orders, glass-ware cleaning and stocking, etc. Perform tasks associated with ordering laboratory supplies and maintaining laboratory equipment.

Skills and Requirements:

  • High school degree; AS or BS preferred.
  • Prefer 2 years GMP laboratory experience (retain, components, chemistry) or AS or BS with 1+ years' GxP experience.
  • Computer skills required in Excel and Word.
  • Ability to follow written procedures and document results in a neat and precise manner.
  • Must be well organized, flexible, open-minded and dynamic.
  • Must have demonstrated self-direct work habits and strong communication skills.
  • Must be a committed team player prepared to work in and embrace a team-based culture.
  • Maintain attention to detail, while completing multiple or repetitive tasks.
  • Demonstrate a serious commitment to accuracy and quality while meeting goals or deadlines.
  • Maintain a high level of integrity while balancing multiple priorities and responsibilities.
  • Demonstrated ability to perform all job duties with limited supervision.
  • Demonstrated familiarity with cGMP's, facility regulatory guidelines and standard operating procedures.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Sarah Beshara at (+1) 267-477-3355 or upload your resume on our website - www.proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.