Sr Inventory Coordinator

at  Thermo Fisher Scientific

Rockville, MD 20850, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate19 Feb, 2025USD 27 Hourly19 Nov, 2024N/AColor,Perspectives,Universal Precautions,Windows,Sample Management,Microsoft Excel,Microsoft Word,Materials,Discrimination,Microsoft AccessNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

JOB DESCRIPTION

This position is responsible for the inventory management, minimal order management, and material handling of biological specimens, samples, clinical agents, and materials from multiple commercial and government clients. These materials are stored at temperatures ranging from ambient (room temperature) to below freezing with potentially hazardous properties. This position uses database applications and standard precautionary procedures to work independently, be self-directed, communicate optimally, and use good judgment when making decisions. Internal or external client interaction occurs under the guidance of experienced professional or technical staff.

EDUCATION/ EXPERIENCE:

  • Requires a High School Diploma or equivalent.
  • Prefer work experience with data entry, shipping/receiving and sample management.
  • Prefer knowledge of methods to handle, process, and store specimens using a computerized storage and retrieval system.
  • Prefer knowledge of Universal Precautions, general laboratory and quality assurance/control.

WORK CONDITIONS/PHYSICAL REQUIREMENTS:

  • Ability to work in a cold environment with exposure to dry ice, liquid nitrogen cryogenics, hazardous and infectious agents, marked changes in temperature.
  • May push/pull 600 lb liquid nitrogen dewars, and work from a platform ladder.
  • Must use personal protective equipment and enforce to safety protocols.
  • Must be able to lift and carry up to 50 lbs, and push up to 70 lbs.
  • Must be able to process and handle materials frozen on dry ice (-78°C) or liquid nitrogen (-196°C) for up to 6 hours per day.
  • Must be able to work in walk-in freezers or refrigerators periodically for up to 5 hours per day.
  • Must be able to use a computer up to 6 hours per day.
    At Thermo Fisher Scientific, we are committed to creating a workplace where diversity and inclusion are valued. We believe that bringing together individuals with different experiences, backgrounds, and perspectives leads to innovative solutions and better outcomes for our customers. As an equal opportunity employer, we strictly prohibit discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.
    We also offer accessibility services for job seekers requiring accommodations in the application process. If you require assistance due to a disability, please contact us at 1-855-471-2255* to request an accommodation.

Basic Minimum Qualifications: The qualifications listed below are representative of knowledge, skill and/or ability. To perform this job successfully, an individual must be able to complete each crucial duty.

  • Requires ability to communicate effectively verbally and in written form.
  • Requires ability to prepare reports using Microsoft Excel.
  • Requires knowledge of Windows and Microsoft Word and possibly Microsoft Access

Responsibilities:

  • Leads all aspects of the material planning of new product launches, packaging changes, and product phase-outs.
  • Works closely with managers to support customer inquiries, discrepancies, inventory maintenance and database updates.
  • Develops the analysis and assistance with BOM changes and updates.
  • Crafts BOMs, routings, and work orders, and implements Planner Standard Work.
  • Reconciles work order labor and material variances.
  • Responsible for using an inventory management system for data entry, sample tracking, and management of samples.
  • Compiles accurate production reports on a periodic basis.
  • Participates in process improvement activities.
  • Assures compliance to cGMP parts 210 and 211 and company quality systems.
  • Follows standard operating procedures (SOPs), facility safety guidelines, and Food & Drug Administration (FDA) requirements which may include compliance with cGMP CFR parts 210 and 211 where applicable.
  • Other duties may be assigned to meet business needs.

Basic Minimum Qualifications: The qualifications listed below are representative of knowledge, skill and/or ability. To perform this job successfully, an individual must be able to complete each crucial duty.

  • Requires ability to communicate effectively verbally and in written form.
  • Requires ability to prepare reports using Microsoft Excel.
  • Requires knowledge of Windows and Microsoft Word and possibly Microsoft Access.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Logistics/Procurement

Pharma / Biotech / Healthcare / Medical / R&D

Logistics

Diploma

Proficient

1

Rockville, MD 20850, USA