Analyst II, Quality Control; Night Shift

Position: Analyst II, Quality Control (Night Shift)
## Analyst II, Quality Control (Night Shift)
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USA - OH - West Chester:
Full time:
Posted Yesterday:
R-107215A career at Resilience is more than just a job – it’s an opportunity to change the future.

Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.

For more information, please visit
** Brief

Job Description
** The position involves on-the-floor sampling, data review, and documentation in compliance with cGMP standards. The individual will conduct testing on a variety of samples, including finished products, raw materials, stability, in-process materials, and water systems. Strong attention to detail, adherence to quality standards, and the ability to work autonomously in a regulated environment are essential.  
** Job Responsibilities*
* ** Core 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.
* Executes 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.
* Participates in and contributes 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.
** Experience & Education*
* ** Minimum Qualifications*
* * Working knowledge of cGXP requirements and a strong familiarity with production operations.
* Good problem-solving skills.
* Proficient in math, laboratory and computer skills. Understands basic statistics and quality control terminology.
** Preferred Qualifications*
* * Bachelor’s degree in chemistry, biology or a related field.
* QC chemistry laboratory experience in the pharmaceutical industry.
* Working knowledge of laboratory equipment (including HPLC), operations, and safety.
** Physical & Work Environment*
* * Work is performed onsite in a cGMP manufacturing and laboratory environment, including clean rooms classified up to Class 100 (ISO
5) aseptic areas.
* Requires gowning and adherence to aseptic behavior requirements for the duration of cleanroom activities.
* Requires standing, walking, bending and reaching for extended periods, and the ability to lift up to 25 pounds.
* Requires the ability to work a rotating 12-hour night shift, including weekends and holidays as scheduled.
*
* Work Schedule:

*
* ** Night Shift - 6pm - 630am with a 12-hour rotation on a 2 nights on, 2 nights off, 3 nights on, 3 nights off with the rotation starting over.
** The work schedule listed reflects the employee’s expected schedule at the time of hire. The Company reserves the…