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Featured Employers
Manufacturing Chemist 1 ( 1st Shift )
Company: Agilent
Location: Frederick All Buildings, CO
Employment Type: Full Time
Date Posted: 09/01/2021
Expire Date: 01/30/2022
Job Categories: Biotechnology and Pharmaceutical, Healthcare, Other, Healthcare, Practitioner and Technician, Information Technology, Manufacturing and Production, Military, Science, Quality Control, Research & Development, Medical
Job Description
Manufacturing Chemist 1 ( 1st Shift )


As a healthcare company committed to protecting the health and safety for our employees, contractors, customers and communities, employees in this role are required to be fully vaccinated against COVID-19, unless an accommodation has been granted for a medical reason or sincerely held religious belief.

Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek ---- so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com.

"What's it like to work at Agilent in Manufacturing? Watch the video"

By delivering high-quality, innovative products to customers when and where they need them, Agilent's Manufacturing Team supports our company's mission to inspire scientists and researchers. Join our fast-growing, dynamic organization and be part of this rewarding work.

A Manufacturing Chemist will check and schedule resources to ensure timely delivery. Their scientific knowledge and background will be demonstrated through the review of formulation documents and active ingredient dilution to ensure that products are manufactured to specification. The chemist's proficiency in analytical testing and immunohistochemistry applications will be required to perform in-process quality control on a variety of products.

In this role, they will have an opportunity to become skilled in the use of a wide range of lab instruments, including but not limited to spectrophotometers, conductivity meters and auto-pipettors, all of which are essential to meeting our customers' requirements. Having the ability to learn quickly on the job, anticipate and resolve potential manufacturing and delivery issues and maintaining the highest level of quality are essential. Additionally, they will work on problems of diverse scope in which analysis of data requires evaluation of identifiable factors. The Manufacturing team member will also exercise judgment within generally defined practices and policies in selecting methods and techniques for acquiring solutions.

Key responsibilities include:

* Actively involved in both the manufacturing of oligonucleotide APIs in a GMP environment, and in aspects of technology transfer and scale-up of oligonucleotide manufacturing processes delivered from Manufacturing Technical Services into Manufacturing.
* Write and revise SOP's according to regulatory and procedural guidelines.
* Work with Validation and Engineering personnel to validate new equipment and facilities.
* Work with Manufacturing Management and Quality to resolve manufacturing problems including drafting quality documentation (CAPA, deviation, change control, etc.).
* Maintain, calibrate, and troubleshoot critical process equipment.
* Ability to work in a cleanroom environment as a successful member of a team working to establish priorities, scheduling, and procedures that collectively will meet department goals and project targets.
* Use individual discretion to meet required project objectives in a timely manner.

Scheduling Details:

* Temporary training hours will be 8:00am-4:30pm Monday - Friday until November 1, 2022.
* The schedule will then be 4:30am - 5:00pm working a pitman schedule of 2 days working, 2 days off, 3 days working, 2 days off, 2 days working, then 3 days off.
* The salary range for this position in Boulder, CO is currently $51,040 - $76,560. Benefits included in brief.

*

B.S. in related field or equivalent combination of education/experience
*

2+ years of related manufacturing experience, pharmaceutical manufacturing environment preferred
*

Previous knowledge of oligonucleotide synthesis, HPLC, UF, conjugation, and lyophilization is advantageous
*

Detail-oriented and can perform technical duties following standard operating procedures and general laboratory safety rules
*

Excellent math, documentation, communication and operational troubleshooting skills
*

Mechanically inclined
*

Previous experience in an FDA regulated manufacturing environment highly desired

Agilent Technologies, Inc. is an Equal Employment Opportunity and Affirmative Action employer. We value diversity at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases.

Agilent Technologies, Inc., is committed to diversity in the workplace and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030.

For more information about equal employment opportunity protections, please see all of our notices for EEO below.

Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled
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