Quality Control Analyst at Agilent Technologies - Colombia

, , United States -

Full Time

Start Date

Immediate

Expiry Date

21 Feb, 26

Salary

53.13

Posted On

23 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Control, Good Manufacturing Practices, FDA Regulations, Analytical Equipment, HPLC, UV Analysis, FTIR, Chemstation, Data Analysis, Documentation Practices, Troubleshooting, Inventory Management, Laboratory Testing, Communication Skills, Problem Solving, Team Collaboration

Industry

Biotechnology Research

Description

Job Description 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. Agilent Technologies, Inc. is looking to add a Quality Control Analyst to its high-performance quality team working at the state-of-the-art, contract API manufacturing facility that specializes in Nucleic Acid Chemistries located in Frederick, Colorado. The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in the capacity and expansion of its Colorado operations. Join our team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life-changing, life-saving medicines. This position coordinates and conducts routine and non-routine testing support. Responsibilities include testing to support manufacturing, raw material release, qualification, and validation activities. Understanding and experience with Standard Operating Procedures, current Good Manufacturing Practices (cGMPs) and other regulatory requirements are required. This position will support weekend coverage Friday-Monday (4 x 10 hours, day shift). Position may require QC testing support in both Boulder and Frederick sites. ESSENTIAL DUTIES AND RESPONSIBILITIES: Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results Outstanding communication skills, both written and oral, and the ability to communicate directly with peers and area managers Conducts analysis associated with clinical and non-clinical laboratory studies under current Good Manufacturing Practices (cGMP) regulations and guidance per Food and Drug Administration (FDA) and Organization for Economic Co-Operations and Development (OECD) as well as international regulations Performs analysis on raw materials, in-process materials, APIs (developmental and commercial), final product and other requested testing as per written procedures. Reviews data for compliance to specifications, report results, and troubleshoots abnormalities Ensures equipment is performing well and communicates and takes appropriate action as necessary Troubleshoots, investigates, and resolves laboratory testing failures and drives solutions to improve the quality control laboratory programs through corrective and preventive actions Maintains inventory and ordering of laboratory supplies Performs maintenance activities on laboratory instruments and equipment Ensures good documentation practices are followed Qualifications A Bachelor's degree (B.S.) or equivalent in Chemistry or related life sciences field; or equivalent combination of education and experience 2+ years of relevant experience within the Industry Exposure and knowledge of FDA regulations and guidelines Knowledge of cGMP guidelines or international regulations (i.e., International Committee on Harmonization (ICH) Q7) Knowledge of analytical equipment and instrumentation utilized for the testing of in-process samples, raw materials, and microbiological samples Proficient with Microsoft Word, Excel, and Chemstation Familiarity with the following laboratory disciplines is highly desired: HPLC Density HPLC-MS IC Solution Preparation UV analysis FTIR Shift Differential for Weekend work Weekend Shift, consisting of 4 10-hour shifts; must be open to working Thursday thru Sunday or Friday thru Monday on day shift. 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 contact +1-262-754-5030 email job_posting@agilent.com. EOE AA M/F/Vet/Disability/Sexual Orientation/Gender Identity. For more information about equal employment opportunity protections, please see all of our notices for EEO below. Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least November 29, 2025 or until the job is no longer posted. The full-time equivalent pay range for this position is $34.00 - $53.13/hr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds 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 creating and maintaining an inclusive in the workplace where everyone is welcome, 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 visit www.agilent.com/en/accessibility. Travel Required: No Shift: Swing Duration: No End Date Job Function: Quality/Regulatory Graduate and Student Career Site Visit our career site and learn more about Agilent Watch our video playlist to get a glimpse of life at Agilent! As a global leader in laboratory and clinical technologies, we are passionate about bringing great science to life. Our commitment to quality and innovation supports cutting-edge life science research, patient diagnostics, and ensures the safety of water, food, and pharmaceuticals. As scientists and clinicians pursue small, everyday advances and life-changing discoveries, we provide trusted answers to their most critical questions and challenges. Leveraging more than 50 years of expertise, we create advanced instruments, software, and consumables supported by teams of highly skilled and knowledgeable people. With 18,000 employees around the world, our global reach and comprehensive solutions provide the most reliable and accurate results, as well as optimal scientific, economic, and operational outcomes. We work collaboratively with our customers on their journey to make a real difference in human lives. Our culture is founded on trust, respect, and uncompromising integrity, and we pride ourselves on being a dynamic and inclusive workplace that celebrates diversity and fosters innovation. We can’t wait for you to join us as we continue our mission to improve the world around us. Information about Agilent is available at Agilent.com.

Responsibilities

The Quality Control Analyst coordinates and conducts routine and non-routine testing support for manufacturing and raw material release. They ensure compliance with specifications, troubleshoot testing failures, and maintain laboratory supplies.