Quality Associate at Metro Logics Inc
Las Vegas, NV 89115, USA -
Full Time


Start Date

Immediate

Expiry Date

17 Nov, 25

Salary

0.0

Posted On

17 Aug, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Regulated Industry, Documentation Practices, Positive Work Environment, Continuous Improvement, Communication Skills, Interpersonal Skills, Organizational Performance

Industry

Pharmaceuticals

Description

About Metro Logics, Inc.
Metro Logics, Inc. (Metro) is a privately owned medical logistics service company located in Olive Branch, MS, with additional facilities in Nevada and Utah. We provide temperature-sensitive storage, warehousing and rapid distribution services for perishable foods, pharmaceutical products and medical devices and supplies. Metro manages highly regulated, temperature controlled, and cGMP compliant warehouse space.
About the role
The Quality Associate is responsible for supporting, maintaining, and overseeing the local site’s compliance quality programs in the cGMP-regulated environment. Occasional out-of-town travel is required.
Responsibilities

Supports cGMP systems and operations, as follows:

  • Interacts with regulated departments, inventory, maintenance, and IT, to improve current quality programs.
  • Documents, reviews, and approves incident reports, risk assessments, deviations, change controls, etc.
  • Reviews maintenance and inventory records.
  • Maintains incident reports, deviations, change controls, risk assessments, maintenance records, and inventory records.
  • Maintains good working relationships with Company personnel.
  • Stays current on training and leads instructor-led training as necessary.
  • Aids in the creation of SOPs.
  • Ensures all employees are compliant with cGMP regulations.
  • Performs internal audits.
  • Supports external audits.

Qualifications

  • A minimum of 5 years of progressive experience in quality or auditing reporting to a Quality or Regulatory unit within a cGMP-regulated industry is required.
  • Candidates must have a Bachelor’s degree or at least four years of supervisory or “team lead” experience in the cGMP industry, reporting to a Quality or Regulatory unit. Relevant experience and/or advanced training, or an equivalent combination of education and experience, will be considered.
  • Other industry certification, such as Certified Quality Auditor (CQA) or similar, is preferred.
  • Knowledge of cGMP and other governmental regulations is required.

Skills

  • Leads by example and drives organizational performance and continuous improvement.
  • Comprehensive understanding of quality systems, current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and other governmental regulations.
  • Ability to connect and build strong relationships with others, while fostering a positive work environment.
  • Must be able to work efficiently and effectively and remain self-motivated.
  • Ability to effectively share knowledge with others within the organization.
  • Capability to work independently or collaboratively with various teams across the organization while managing multiple projects simultaneously.
  • Excellent written and verbal communication skills, analytical abilities and interpersonal skills.
  • Attentive to details.

Metro Logics, Inc. (’Metro’) is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender including pregnancy, childbirth and related medical conditions), gender expression or gender identity (including transgender status), sexual orientation, marital status, military or veteran status, physical or mental disability, protected medical condition as defined by applicable state or local law, genetic information or any other characteristic protected by applicable federal, state or local laws (’protected status’)

Responsibilities

Please refer the Job description for details

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