QC Specialist II, Sample Management

Planet Pharma; Philadelphia (Philadelphia County); On-site; USD 60,000 - 80,000; Full time

Job summary

An established industry player is seeking a Quality Control Specialist II to oversee the logistics of quality control samples in a fast-paced pharmaceutical environment. This role involves managing sample inventory, ensuring compliance with GMP standards, and facilitating the timely distribution of samples. The ideal candidate will possess strong organizational skills, attention to detail, and the ability to collaborate effectively with various stakeholders. Join a dynamic team dedicated to excellence in pharmaceutical manufacturing and contribute to impactful projects that enhance patient care.

Qualifications

• 3+ years of sample management experience in a GMP environment is essential.
• Detail-oriented with strong mathematical and communication skills required.

Responsibilities

• Manage QC sample logistics including storage, inventory, and shipping.
• Ensure compliance with procedures and maintain sample integrity.

Skills

Sample Management Experience

Inventory Management

Logistics in Pharmaceutical Industry

Mathematical Skills

Communication Skills

Collaboration Skills

Problem-Solving Skills

Time Management

Organizational Skills

Laboratory Experience

Education

Associate Degree

3+ years GMP Experience

Tools

LIMS System

Job description

This range is provided by Planet Pharma. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$40.00/hr - $45.00/hr

CONTRACT-TO-HIRE

MUST HAVES:

• 3+ years sample management experience in a GMP environment
• Experience with inventory and/or logistics in the pharmaceutical industry

SCHEDULE: Wednesday-Saturday from 9:00am-7:00pm

Overview

The Quality Control Specialist II – Sample Management will ensure time-sensitive distribution of quality control samples in support of QC-related activities. They will be responsible for sample inventory management as well as internal and external sample distribution, including storage and shipping under appropriate conditions, for all the iCTC cell therapy asset.

Essential Functions and Responsibilities

• Manage all aspects of QC sample logistics for raw material, in-process, and final product samples including sample storage, sample inventory and reconciliation, scheduling, and shipping in LIMS based system.
• Maintain sample integrity by ensuring that all samples are managed (i.e., stored; handled; shipped) in compliance with procedures, specifications, and cGMP.
• Provide timely distribution of samples internally at the iCTC, and externally to testing vendors.
• Ensure that sample inventory records are maintained and accurate.
• Maintain current knowledge base of regulations, corporate policies, and industry best practices, trends, and standards to ensure that the logistics function remains in compliance with applicable requirements.
• Support audits and inspections as needed.
• Packaging of samples using temperature controlled dewars, cold packs, and dry ice.
• Support ramp up of Quality Control and other activities in a newly built facility.

Required Education, Skills, and Knowledge

• Associate degree or 3+ years of relevant GMP experience (sample management).
• Experience with inventory and/or logistics in the pharmaceutical industry.
• Detail-oriented with strong mathematical skills.
• Excellent written and verbal communication skills.
• Strong collaboration, time management, and organizational skills are required.
• Proven ability to effectively collaborate with a wide range of stakeholders.
• Excellent judgment and creative problem-solving skills.
• Ability to work in a fast-paced and dynamic environment.
• Hands-on laboratory experience with sample handling, inventory, and cryo-shipping.

Physical Demands and Activities Required

• Must be able to wear appropriate cleanroom attire and all Personal Protective Equipment (PPE), i.e., scrubs, gowning coveralls, masks, gloves, etc.
• Able to stand and/or walk 90% (and sit 10%) of the scheduled workday, which may include climbing ladders or steps.
• Must be able to use near vision to view samples at close range.
• Able to crouch, bend, twist, reach, and perform activities with repetitive motions.
• Must be able to lift and carry objects weighing 45 pounds.

Mental

• Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to handle work-related stress; ability to handle multiple priorities simultaneously; and ability to meet deadlines.
• This position will work in both an office and a manufacturing setting. When in the lab, you may be exposed to various chemicals/biochemical, including latex and bleach. Additionally, there is potential for variable noise levels, equipment hazards, strong odors, and other detergents/sanitizers.

Seniority level

Associate

Employment type

Full-time

Job function

Quality Assurance, Research, and Science

Industries

Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing