Quality Control Analyst Ii

Overview

If you have laboratory experience in the biotechnology / pharmaceutical industry and want to work in a small team environment with a seasoned, dedicated group, this is an opportunity you’ll want to explore!

In this role you will perform a variety of lab tests, set your own schedule around testing, and learn to use new, state of art equipment. This role can grow into a team lead position.

Responsibilities

• Perform routine projects independently, compile accompanying reports and/or data summaries.
• Perform in-process, release, stability testing on product and raw material release testing according to Product Specifications, Material Specifications, SOPs, stability protocols, and USP/EP regulations.
• Participate in qualification of software and equipment.

Qualifications

• Bachelor’s degree in Life Sciences/Biology/Chemistry or related discipline.
• Self-driven, organized, adaptable to change, and can work independently under minimal supervision.
• Working knowledge of analytical test methods (e.g. raw material testing, microbiological assays, ELISA, FTIR, Capillary Electrophoresis, and cell-based assays), with a strong knowledge of ELISA and HPLC assays preferred.
• A minimum of 2 years of working experience in the biotech / pharmaceuticals industry, including hands-on experience in a cGMP laboratory and familiarity with standard concepts, practices, procedures, instrumentation, and software in a Quality Control organization.
• Knowledge of operation and maintenance of analytical equipment and the associated software.

Job Type: Full-time

Benefits:

• Health insurance
• 401(k) matching
• 401(k)
• Life insurance
• Referral program
• Health savings account
• Paid time off
• Vision insurance
• Flexible schedule
• Dental insurance
• Tuition reimbursement

Schedule:

• 8 hour shift
• Monday to Friday

Work Location: In person