Quality Control Analyst I

PSG Global Solutions; Swiftwater; On-site; CAD 45,000 - 75,000; Full time

Job summary

An established industry player in pharmaceuticals seeks a meticulous Quality Control Analyst I to join their dynamic team. This role is crucial in maintaining the integrity of laboratory operations by managing inventory, ensuring compliance with Good Manufacturing Practices (GMP), and handling laboratory waste responsibly. You will be part of a dedicated team that values precision and safety in all processes. If you are passionate about quality control and looking to make a significant impact in the pharmaceutical field, this opportunity is perfect for you.

Qualifications

• Experience in a GMP environment is essential for this role.
• Strong attention to detail and inventory management skills are required.

Responsibilities

• Manage inventory and materials for QC laboratories to ensure operations run smoothly.
• Handle laboratory waste and follow GMP and HSE practices diligently.

Skills

Attention to Detail

Inventory Management

Knowledge of GMP

Waste Handling Procedures

Education

Bachelor's Degree in Life Sciences

Certification in Quality Control

Tools

LIMS

SAP

Job description

Description

We're looking for a Quality Control Analyst I, working in the Pharmaceuticals and Medical Products industry at 1 Discovery Drive, Swiftwater, Pennsylvania, 18370, United States.

Responsibilities include:

1. Cycle count/inventory, order, receive, stock, and distribute materials for use in/by QC laboratories on a timely basis to ensure laboratory operations are able to continuously operate.
2. Handling and discarding laboratory waste, including boxing up in biohazard boxes/buckets, autoclaving and delivering the waste to the dock for disposal and initiating transportation requests.
3. Inventory monitoring of product in a GMP environment, including making adjustments in our various systems (LIMS/SAP) as needed.
4. Preparation/Certification of laboratory logbooks.
5. Follow proper GMP and HSE practices for handling of materials, including company products and biohazard, and will also be required to document activities such as autoclave operation, in accordance with good documentation practices.