Analyst II, Quality Control (Weekend Shift)

Resilience•West Chester, OH

7d•$60,000 - $86,250•Onsite

About The Position

The Analyst II, Quality Control performs analytical testing and environmental monitoring activities to support product quality, regulatory compliance, and sterile manufacturing operations. Collaborates with cross-functional teams to conduct testing, review data, maintain laboratory equipment, and support continuous improvement initiatives.

Requirements

Working knowledge of cGXP requirements and a strong familiarity with production operations.
Good problem-solving skills.
Proficient in math, laboratory and computer skills.
Understand basic statistics and quality control terminology.

Nice To Haves

Bachelor’s degree in Chemistry, biology or related field.
QC chemistry laboratory experience in Pharmaceutical industry.
Working knowledge of laboratory equipment (including HPLC), operations, and safety.

Responsibilities

Performs testing on a range of samples including finished products, raw materials, stability, in-process and water samples.
Maintains and troubleshoots testing equipment.
Supports laboratory investigations, QC method and SOP updates.
Execute laboratory test protocols to support development and validation activities.
Responsible for QC Data review.
Provides and follows up on ideas for continuous improvements in laboratory processes.
Able to take direction and correction when learning procedures and performing analysis.
Participate and contribute to the team atmosphere.
Self-motivated: able to complete all tasks assigned and able to self-assign work without immediate supervision, when appropriate.
Able to knowledgeably and safely handle hazardous materials.
Good verbal, written and interpersonal communication and organizational skills.
The ability to learn and adapt quickly to new priorities and or situations.
This position may require operating equipment in various classified/non-classified areas up to a Class 100 aseptic environment and in a laboratory setting.
This role may require collaboration and communication within the team and with operations groups/QA.
The role may require individuals to autonomously perform tasks related to environmental monitoring to support regulatory requirements of a sterile manufacturing site, including data review and on-the-floor sampling.