Celgene Analyst II, QC Microbiology (2nd shift) in Phoenix, Arizona
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries, and growing - we look for talented people to grow our business, advance our science and contribute to our unique culture.
ANALYST II, QC MICROBIOLOGY
Purpose and Scope of Position
QC Environmental Control Analyst II works both independently and with the team to collects, analyzes and trends environmental monitoring results for the Controlled non-aseptic area, aseptic area, compressed gases, and aseptic personnel. This position requires personnel to analyze and trend results within a lab environmental.
Required Competencies: Knowledge, Skills, and Abilities
Requires the ability to deal appropriately with regulatory agencies.
Ability to multi-task and work flexible work schedule.
Intermediate written and verbal communication skill.
Basic Ability to Interpret and write general business documents.
Basic ability to Interpret and write technical documents.
Intermediate Problem solving skills.
Ability to follow direction well, work cooperatively as an individual contributor and as a team member.
Ability to gown and maintain a sterile work environment.
Ability to work independently for extended periods of time.
Basic proficiency in Microsoft Word, Outlook, and Excel.
Basic knowledge of cGMP, OSHA, DEA, USP, and EP.
Ability to pass an initial full physical with annual monitoring.
Duties and Responsibilities
Collect environmental monitoring samples:
Collect viable and non-viable samples within controlled environments.
Collect viable and non-viable samples for compressed gases.
Collect personnel glove and gown samples.
Participates in aseptic process qualifications:
Documents, Tracks, and Trends test results:
Record daily data results.
Prepares spreadsheets of data.
Trends site specific data.
- Assist in the creation, maintenance, and delivery of controlled and aseptic area training modules.
Performs other tasks as assigned.
Education and Experience
Bachelor’s degree preferred, preferably in science or related field.
2 years’ relevant work experience required, preferably in a regulated manufacturing environment with cGMP requirements.
An equivalent combination of education, experience and training may substitute.
This position involves being fully gowned for extended periods of time within a restrictive movement environment. This may include standing, bending, reaching, kneeling, balancing, pushing, pulling, lifting (NMT 25lb), or carrying (NMT 25lb).
This may also include concentrating, remembering names, effective verbal and/or written communication, analytical thinking, decision making, and adapting to change.
This position involves working conditions with constricted personnel movements for up to 6 hours a day.
This position works within controlled environments with strict gown and gloves requirements.
Requires <10% of the time travel for growth improvements.
Definitions and Abbreviations
United States Pharmacopeia (USP)
European Union (EU)
Japanese Pharmacopeia (JP)
British Pharmacopeia (BP)
Occupational Safety and Health Administration (OSHA)
US Drug Enforcement Administration (DEA)
Personnel Protective Equipment (PPE)
This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.
This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.
Celgene is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Celgene complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Celgene in the U.S.COMMITTED TO IMPROVING THE LIVES OF PATIENTS WORLDWIDE
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.