This job has expired

You will need to login before you can apply for a job.

QA Inspector

Employer
Tris Pharma
Location
Monmouth Junction, NJ
Start date
Sep 17, 2022

View more

Discipline
Quality, Quality Assurance
Required Education
High School or equivalent
Position Type
Full time
Hotbed
Pharm Country
You need to sign in or create an account to save a job.

Job Details

Tris Pharma, Inc. (www.trispharma.com) is a rapidly growing, technology-driven pharmaceutical company engaged in branded and generic product development located in Monmouth Junction, New Jersey.

We have openings for QA Inspectors for multiple shifts.  

These positions are approximately 3 - 4-month potential temporary to hire opportunities based on successful performance.

The Quality Assurance (QA) Inspector is responsible for performing in-coming inspections of all raw material/components, performing in-process inspections, providing clearance for rooms/lines to run and ensuring adherence to company Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs) and batch record specifications. Responsibilities include, but not limited to:

  • Identify any non-conforming material and control status of materials during in-coming inspection.
  • Identify any in-process failures during in-process inspections.
  • Provide support to the stability program by ensuring all rooms/lines meet requirements specified within procedures prior to use.
  • Follow and adhere to all company and Food and Drug Administration (FDA) guidelines, protocols and Standard Operating Procedures (SOPs).
  • The QA Inspector will need to be able to support a flexible schedule and have a willingness to work overtime and on weekends when required.

Requirements

Qualifications

  • High School diploma or equivalent with minimum 1 year QA and/or manufacturing experience in a cGMP environment REQUIRED
  • Experience in a pharmaceutical, biotech or related manufacturing environment PREFERRED
  • Working knowledge of good manufacturing systems and familiarity with regulatory and manufacturing SOPs and cGMPs REQUIRED
  • Demonstrated ability to read and interpret documents such as safety and environmental policies and procedure manuals, etc. REQUIRED
  • Excellent attention to detail and strong record keeping skills REQUIRED
  • Excellent written and verbal communication REQUIRED
  • Basic Microsoft Office proficiency REQUIRED
  • Excellent ability to identify and distinguish colors REQUIRED

Physical requirements

  • This is a Manufacturing based position: 
  • Ability to lift up to 50 lbs REQUIRED
  • Ability to use Personal Protective Equipment (PPE) REQUIRED
  • Ability to stand for extended periods  REQUIRED
  • Excellent ability to identify and distinguish colors REQUIRED
  • Ability to work overtime and weekends as REQUIRED

Tris Pharma, Inc. offers a highly competitive compensation and benefits package.  To build and enhance our diverse workforce, we encourage applications from individuals with disabilities, minorities, veterans, women, LGBTQ, etc.  Tris Pharma, Inc. is an Equal Opportunity Employer. 

#LI-DNI 

Company

Founded in 2000, Tris Pharma, Inc. (www.trispharma.com) is the 3rd largest specialty pharmaceutical company in the United States. With our intense focus on the application of physical chemistry in biological systems, coupled with the requirements of manufacturing and market demands, we have grown our employee base over 250% in the past three years. Specifically, we are engaged in research, development, and manufacturing of both OTC and Rx branded products and specialty generic products. Our mission is to understand the science driving the delivery of drugs into the human body;develop and bring to market products that add value to our customers and patients and provide a benefit to our company, employees and society at large.

Find Us
Website
Phone
(732) 940-2800
Location
US Highway 130
Monmouth Junction
NJ
08852
United States
You need to sign in or create an account to save a job.

Get job alerts

Create a job alert and receive personalized job recommendations straight to your inbox.

Create alert