Quality Assurance Specialist (Pharma) # Not IT QA

Net2Source Inc.; Elkton (VA); On-site; USD 50,000 - 80,000; Full time

Job summary

An established industry player in the pharmaceutical sector is seeking a Quality Assurance Specialist to join their dynamic team. This role involves performing analytical testing on a variety of samples, ensuring compliance with cGMP standards, and maintaining the highest quality of work. The ideal candidate will have a strong background in chemical analysis, particularly using techniques such as HPLC and qPCR. This position offers a unique opportunity to contribute to crucial laboratory activities while working in a fast-paced environment that values precision and accuracy. If you are passionate about quality assurance in the pharmaceutical field, this role is perfect for you.

Qualifications

• 1+ years of experience in a GMP laboratory performing chemical analysis.
• Familiarity with HPLC, qPCR, and gel electrophoresis techniques.

Responsibilities

• Conduct analytical testing on various samples in the Quality Control lab.
• Ensure accuracy of test data and maintain cGMP compliance.

Skills

Analytical Testing

HPLC

qPCR

Gel Electrophoresis

Dynamic Light Scattering

cGMP Compliance

Instrument Calibration

Education

Bachelor's Degree

Master's Degree

Tools

Data Acquisition Software

Job description

Quality Assurance Specialist (Pharma) # Not IT QA

Our direct client is looking to hire a Quality Specialist - I (Assistant) in their growing team.

Title: QC Specialist - Analytical Testing

Duration: 12 months

Note:

1. Ability to work a 12hr rotating shift with 2 week cadence
2. Rotating shift will look like the following: (Week 1 - Mon, Thurs, Fri - 12hr days) / (Week 2 - Tues, Wed, Sat - 12hr days, + Sun - 8hr day), then rotation starts over again.
3. Start times are roughly between 7am-8am

Description

1. Perform analytical testing in the Quality Control laboratory on a variety of samples/products
2. Conduct testing such as plate reader based assays, gel electrophoresis, dynamic light scattering, qPCR, ICP and HPLC.
3. Ensure test data is accurate and that all work is Right-First Time
4. Work with team members to ensure the highest levels of cGMP compliance and inspection readiness
5. Assist in laboratory related activities such as second person review, instrument calibration and troubleshooting, deviation investigations
6. Interact and understand various data acquisition/management software

Qualifications

1. Education: Bachelors degree preferred, will consider Master’s degree if applicable to role.
2. Ability to perform a variety of chemical analysis on drug substances which include: instrumental analysis using HPLC and ICP.
3. Familiarity performing plate reader based assays, qPCR, Dynamic Light Scattering and gel electrophoresis.
4. Minimum 1+ years of experience utilizing the listed methods and working within a GMP laboratory.

Seniority level

Associate

Employment type

Contract

Job function

Quality Assurance, Analyst, and Research

Industries

Pharmaceutical Manufacturing, Biotechnology Research, and Food and Beverage Manufacturing