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Manufacturing Associate, Representative (Night Shift)

Agilent Technologies, Inc. -
Frederick, CO

Apply Now

Job Details

Full-time
$31.92 - $49.88 an hour

Qualifications

Quality control corrective actions
Quality records maintenance
Laboratory equipment maintenance
Technical documentation
Pharmaceutical synthesis
Technical writing experience within manufacturing
Production deviation management
Corrective and preventive actions (CAPA)
Mechanical equipment calibration
Chemical scale-up projects
High school diploma or GED
Manufacturing standard operating procedures
Manufacturing facility experience
Schedule management
Math
Quality control documentation
Quality assurance standard operating procedures
Pharmaceutical company experience
Technology transfer (scale-up process)
Laboratory standard operating procedures
Cleanroom experience
Collaboration with manufacturing teams
Handling nucleic acids
Standard operating procedures (SOPs)
Production documentation
Communication skills
Mechanical knowledge
Entry level
FDA regulations
Standard operating procedures drafting

Full Job 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.

The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in 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, lifesaving medicines.

Key responsibilities include:

Actively involved in the manufacturing of oligonucleotide APIs in a GMP environment.
Actively involved in aspects of technology transfer and scale-up of oligonucleotide manufacturing processes delivered from Manufacturing Technical Services into Manufacturing.
Write and revise standard operating procedures 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 trouble shoot critical process equipment.

Shift details:

The schedule will be Night shift (4:30 PM - 5:00 AM) working a Pitman schedule: of 2 days working, 2 days off, 3 days working, 2 days off, 2 days working, then 3 days off.

Qualifications

HSD or higher education
1+ years of related experience in a pharmaceutical manufacturing environment preferred but not required
Previous knowledge of oligonucleotide synthesis, purification, UF, conjugation, and lyophilization is advantageous
Detail oriented and can perform technical duties following standard operating procedures and general laboratory safety rules
Ability to work both independently and in a team setting on a variety of projects and use individual discretion to meet required project objectives and deadlines
Excellent math, documentation, communication and operational trouble shooting skills
Mechanically inclined
Ability to work as a successful member of a team working to establish priorities, scheduling, and procedures that collectively will meet department goals and project deadlines
Ability to work in a clean room environment
Previous experience in a FDA regulated manufacturing environment highly desired

Additional Details

This job has a full time weekly schedule. Applications for this job will be accepted until at least June 18, 2026 or until the job is no longer posted.

The full-time equivalent pay range for this position is $31.92 - $49.88/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 [email protected] or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.

Travel Required:

Shift:

Morning

Duration:

No End Date

Job Function:

Manufacturing

Apply Now

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