Job Alert: Microbiology Applications Engineer

ACORN CONSULTING

Job Title: AA Microbiology Applications Engineer Job Status: exempt Full Time / Exempt
 
General Description:  Work based in Tucson, AZ
To serve as a bridge between product development and sales by developing, supporting and representing the Company’s technology in an industrial environment, through use of knowledge of engineering and programming as well as sophisticated instruments and computers.

To identify customer best fit with Company’s product & assist in development of technical documents and training programs, maintaining customer cGMP compliance.       To work independently and as a team player on simultaneous projects with compressed timelines; traveling up to 50% of the time interfacing with customers and attending or exhibiting at conferences and trade shows.

 

Responsibilities:
Product development engineering support for both hardware and software technologies to support real time microbial detection and analysis.

  • Develop and support lab activities and practices for development validation, manufacturing and field demonstration/installation
  • Plan, design, collect and report test goals, technology, information and data
  • Applies commonly-used concepts, practices and procedures within the biological laboratory to company activities.
  • Assist in the design, development and validation of company technology including hardware and software.
  • Prepare and present notes, reports & literature as required
  • Works within and ensures all team members follow safety, FDA, IS0 9001 requirements
  • Consistency with customer cGMP/cGLP compliance as required
  • Provide demonstrations and training of technology and functionality to potential customers and collaborators.

Customer relations

  • Support instrument and technology functionality and capability to both customers and sales force.
  • Act as the primary technical support contact for customers both pre and post installation or demonstration.
  • Provide feedback to the organization relating insights, requests and opportunities from sales, marketing, and customer interactions.
  • Prepare and present technical presentations and applications notes.
  • Professional representation of the company in various field activities including conferences, trade shows, customer site visits and investor visits.

 

Preferred Qualifications:
BA/BS or MS in biological discipline with at least two years work-related experience. Practical experience in industrial/R&D lab environment with focus toward microbiology. Experience with laboratory instrumentation, technology and tools. Self-motivated with a strong work ethic; independently or as part of a team. Strong written and oral communication skills. Good computer skills; minimum of Word, Excel, Power Point with NI LabView experience preferred. Knowledge of or experience with cGLP or cGMP environment. Competitive salary and benefits commensurate with experience.

To Apply:

Send your cover letter and resume to davidbrownwilson@gmail.com. No calls please.

Job Alert: Supervisor, Environmental Control at Celgene

celgene logo 2012Posting Title:  Supervisor, Environmental Control- 3rd Shift- Phoenix, AZ

 

Celgene Corporation, recently declared “The #1 Employer in America” by Business Insider, continues to grow!  We are 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.

 

Our Phoenix manufacturing site has a need for an experienced Supervisor, Environmental Control for our 3rd shift.  supervises and oversees the activities and personnel in the QC Microbiology Environmental control group as they perform routine and non routine Environmental Monitoring of Classified areas, Aseptic Area personnel, and Critical Utilities.

 

EDUCATION/EXPERIENCE REQUIREMENTS

 

  • Requires a Bachelors degree in Microbiology or related science from an accredited college or university with a minimum of 5 years related experience in a regulated  laboratory, preferably in a pharmaceutical laboratory environment with at least 5 years direct experience in Aseptic Processing Environmental monitoring.

 

  • An equivalent combination of education, experience and training may substitute.

 

Celgene Corporation offers an outstanding total rewards package, including base salary/annual bonus/equity (company stock) and a competitive benefit plan (401k match, etc.).

 

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

 

 

Please see the full details for this opportunity at:   

 

http://bit.ly/ZPgVtb

 

 

Job Alert: Analyst, Quality Control-Microbiology (Enviro) at Celgene

celgene logo 2012

Posting Title: Analyst, Quality Control-Microbiology (Enviro) 3rd Shift


– Phoenix, AZ

 

Celgene Corporation, recently declared “The #1 Employer in America” by Business Insider, continues to grow!  We are 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.

 

Our Phoenix manufacturing site has a need for an experienced Analyst, QC- Environmental Microbiology for our 3rd Shift. This position works both independently and with the team to perform routine and non-routine microbiological testing and Microbiology laboratory maintenance functions.

 

EDUCATION/EXPERIENCE REQUIREMENTS

 

  • Requires a Bachelors degree in Microbiology or related science from an accredited college or university with a minimum of 4 years related experience in a regulated   laboratory, preferably in a pharmaceutical laboratory environment.

 

  • An equivalent combination of education, experience and training may substitute.

 

Celgene Corporation offers an outstanding total rewards package, including base salary/annual bonus/equity (company stock) and a competitive benefit plan (401k match, etc.).

 

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

 

 

Please see the full details for this opportunity at:   

 

http://bit.ly/ZPgFKI

 

 

Job Alert: Senior Scientist- Validation at Celgene

celgene logo 2012

Title: Senior Scientist- Validation (Technical Services)- Phoenix, AZ

Celgene Corporation, recently declared “The #1 Employer in America” by Business Insider, continues to grow! We are 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.

Our Phoenix manufacturing site has a need for Senior Scientist- Validation (Technical Services). This position develops all qualification/validation approaches (risk/science based) and provides the scientific rationale documented in protocols and summary reports (including conducting research into industry standards/FDA guidelines), prepares project schedules, heads up project teams, executes validation studies, and performs data analysis. Primary responsibilities include the following: Process Validation (Process Performance Qualification), Equipment PQ, Continual Improvement Projects, Cleaning Validation and Validation of Single Use Systems.

EDUCATION/EXPERIENCE REQUIREMENTS

• Requires a Bachelor’s degree in Science or Engineering from an accredited college or university with a minimum of 6 years related experience, with at least 2 years validation experience in a pharmaceutical or related industry.

• An equivalent combination of education, experience and training may substitute.

Celgene Corporation offers an outstanding total rewards package, including base salary/annual bonus/equity (company stock) and a competitive benefit plan (401k match, etc.).

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

Please see the full details for this opportunity at:

http://bit.ly/ZPgj6G

Job Alert: Anayst I, QC Chemistry at Celgene

Title:  Analyst I, QC Chemistry-3rd Shift- Phoenix, AZ

celgene logo 2012

Celgene Corporation, recently declared “The #1 Employer in America” by Business Insider, continues to grow!  We are 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.

 

Our Phoenix manufacturing site has a need for an experienced QC Chemist for our 3rd shift.  This position performs and documents testing to support routine analysis of utility, raw material, in-process, finished product and stability samples.  This is an FDA Compliant position and performs shift work as assigned.  Approximate shift hours – 3rd Shift 9:00 pm – 7:30 am (M-Th).  Daily work hours may occasionally extend to up to 12 hours. on an as-needed basis.

 

EDUCATION/EXPERIENCE REQUIREMENTS

 

  • Must possess an Associate’s Degree in Science and four years of experience in a regulated, manufacturing environment- cGMP; or Bachelor’s Degree in Science with two years of experience. (Equivalent combination of experience/education is acceptable)
  • Must be experienced in operating general analytical instruments during testing (e.g. TOC, Conductivity, PSA)
  • Must have a strong ability to operate more advanced instrumentation during testing (e.g. HPLC, GC, ICP)
  • Must live in or be willing to relocate to Phoenix, AZ.

 

Celgene Corporation offers an outstanding total rewards package, including base salary/annual bonus/equity (company stock) and a competitive benefit plan (401k match, etc.).

 

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.

 

Please apply on-line to the posting at:    http://bit.ly/1ua5qbf

 

Celgene’s future has never been brighter. We invite you to explore  “The Promise of Celgene” at  http://www.celgene.com/PromiseofCelgene.pdf

 

Opportunity Alert: Join the Team at SenesTech

SenesTech is seeking dynamic, self-starters to support our research development efforts. SenesTech, Inc. (SenesTech) is a platform biotechnology company specializing in reproductive physiology. Our mission is to complete the development of non-surgical reproduction management technology that could profoundly change the world via wildlife and companion animal population management. We are currently applying our revolutionary technology to the control of rats and mice in both agricultural and urban settings.Continue reading

Opportunity Alert: Director of Genomics Research at Phoenix Children’s Hospital

PCH-Logo-Text-Right

Position Title: Dir, Genomics Research

For more information or to apply for this position, click here.

Position Details
Department: Molecular Medicine Posting #: 44371
Category: Any Date Posted: 6/19/2014
Schedule: Mon – Fri; Days Employee Type: Full Time
Location: Phoenix
Position Summary

The Institutes of Molecular Medicine Genomics Research Director leads the Sequencing group, which provides established services to the research community at Phoenix Children’s Institute, affiliated institutions as well as other academic and non-academic groups. A main goal is to improve existing and evaluate new technologies with a focus on clinical translation. The Director interacts closely with the Director of Clinical Sequencing to evaluate novel technologies, provide technical expertise on existing platforms and help PCH clinical investigators formulate/design research questions in genomics in the field of cancer and inherited disease. Therefore, the research director has abundant opportunity for publishing high quality research data. The director is also responsible for growing and managing the quality of the variant database within the Genomics Core and for stimulating and growing genomics research within the Phoenix Children’s Research Institute.

 

For more information or to apply for this position, click here.

Job Alert: HR Generalist at Ulthera

ulthera-logo

Company: Ulthera, Inc.

Position: Human Resources Generalist

Job Description:

Ulthera is continuing to grow and has an immediate need for a Generalist with experience in Recruiting.

We would strongly prefer someone who has worked in the healthcare segment and/or someone who has worked in an environment with very little direction/process (we are in late stage start-up so people have to be able to find their own answers and just “make it work”).

The pace at Ulthera is incredibly fast with project prioritization being a required skill based on too much to do and not enough time being a standard scenario.  Our purpose-driven culture dictates the need for someone who is kind, ethical and very sharp.

This should be someone who people easily connect with and confide in while still being process oriented enough to get every spreadsheet and task completed meticulously.

It’s a tall order, it always is when you are looking for the best!

Contact Ulthera if you know of anyone who might be a fit and feel free to pay this forward and pass it on!

Who to contact: Stacie Mallen s.mallen@ulthera.com OR  Leticia Gastelum l.gastelum@ulthera.com

Career site: careers.ultherapy.com/