Associate Analyst, Quality Control Chemistry (2Nd Shift)

Celgene Corporation Phoenix , AZ 85002

Posted 4 months ago

Job Description: Req #: 1902262

Location: Phoenix, Arizona, United States

Job Category: Quality

Work Location: 620 N. 51st Avenue 85043

Organization: Quality Control

Shift: 2nd Shift_USA

Employee Status: Full-time

Job Type: Regular

Purpose and Scope of Position

The Associate Analyst, QC Chemistry, s responsible for routine analysis of utility samples to ensure

that samples meet required specifications. The Associate Analyst is also responsible for support

activities in the laboratory to ensure the laboratory has glassware and solutions available to perform


Required Competencies: Knowledge, Skills, and Abilities

Basic PC skills

Basic math skills

Basic written and verbal communication skills

Basic proficiency in Microsoft Word, Outlook, and Excel

Basic cGMP documentation skills

Strong attention to detail

Basic knowledge of laboratory safety practices

Ability to use basic hand tools

Ability to use basic instrumentation and instrument software, including but not limited to TOC,

Conductivity meter, and PSA

Ability to perform basic wet chemistry tests, including but not limited to titrations, ROI and pH

Ability to use PPE effectively

Ability to collaborate with peers on day-to-day tasks; cooperative and works well with a team

Ability to communicate effectively with peers and department management

Ability to accurately and completely understand and follow SOP, test method, and cGMP

requirements; uses good judgment and follows procedures

Basic knowledge of cGMP, OSHA, DEA, USP, EP, and JP; ability to deal appropriately with

regulatory agencies

Ability to work highly supervised; solicits direction from supervisor

Demonstrates personal organizational skills

Actively seeks opportunities to learn

Ability to pass an initial full physical with annual monitoring

Duties and Responsibilities

Perform testing of utility samples.

Perform various wet chemistry and analytical chemistry methods.

Follow methods and procedures, with strict adherence to cGMP documentation requirements.

Complete all work assigned in a timely manner.

Work and communicate effectively within the team to ensure timelines are met.

Report all identified problems to designated senior personnel.

Prepare various solutions needed to support method performance; for example, mobile phase, needle

wash, etc.

Prepare solutions per appropriate procedures using appropriate techniques.

Document in accordance with cGMP requirements.

Participate in housekeeping performance and audits.

Perform housekeeping on a regular schedule.

Communicate effectively with management and coworkers regarding housekeeping needs.

Review status of supplies and reagents to ensure items are ordered as needed.

Participate in inventory audits to keep the laboratory stocked.

Place orders for reagents, per management approval.

Communicate effectively with management and coworkers regarding supply needs.

Perform peer review of testing data.

Review all data in accordance with applicable procedures and cGMP requirements.

Apply technical knowledge and abilities to ensure all testing is performed in a compliant


Complete all review in accordance with required release timelines.

Communicate effectively with peers, and demonstrate teamwork, with regards to results of

review and corrections required.

Perform other tasks as assigned.

Education and Experience

High school diploma or equivalent required.
1 year of relevant work experience required, preferably in a regulated industry.

An equivalent combination of education and experience may substitute.

Working Conditions

This position requires regular medical surveillance and may require incumbent to wear a

respirator or gown.

The incumbent must be able to distinguish colors and possess correctable vision to 20/20,

annual eye exam is required.

The incumbent must analyze numerical values on a daily basis.

The incumbent will be working a laboratory setting up to 6 hours per day.

The incumbent will occasionally be working around hazardous materials to include chemical

agents up to 6 hours per day.

The incumbent often works for extended periods alone, up to 8 hours per shift.


About Us


At Celgene, we seek to deliver truly innovative and life-changing drugs for our patients. Our vision as a company is to build a major global biopharmaceutical corporation while focusing on the discovery, the development, and the commercialization of products for the treatment of cancer and other severe, immune, inflammatory conditions.

"At Celgene, we seek to deliver truly innovative and life-changing drugs for our patients."

There are more than 300 clinical trials at major medical centers using compounds from Celgene. Investigational compounds are being studied for patients with incurable hematological and solid tumor cancers, including multiple myeloma, myelodysplastic syndromes, chronic lymphocytic leukemia (CLL), non-Hodgkin's lymphoma (NHL), triple-negative breast cancer and pancreatic cancer.

As committed as we are to clinical accomplishment, we are equally committed to patient support, which is a guiding principle at Celgene. We believe all who can benefit from our discoveries should have the opportunity to do so. Celgene puts patients first with industry-leading programs that provide information, support and access to our innovative therapies.

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Associate Analyst, Quality Control Chemistry (2Nd Shift)

Celgene Corporation