Location: Frederick,CO, USA
Job DescriptionAs a Manufacturing Representative, you will check and schedule resources to ensure on-time delivery. Your scientific knowledge and background will be leveraged through your review of formulation documents and active ingredient dilution to ensure that products are manufactured to specification.You 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 critical. Additionally, you will work on problems of diverse scope in which analysis of data requires evaluation of identifiable factors. You will also exercise judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.Key responsibilities include: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:During training, shift will be M-F, 7:00 AM - 3:30 PM. Training will be approximately 3 weeks. Post-training shift will transition to a night shift on Pitman Schedule.The schedule will be Night shift (4:30pm - 5:00am) working a Pitman schedule: of 2 days working, 2 days off, 3 days working, 2 days off, 2 days working, then 3 days off.QualificationsBachelor's or Master's Degree or equivalent in related field or equivalent combination of education/experience strongly preferred1+ years of related manufacturing experience, pharmaceutical manufacturing environment preferredPrevious knowledge of oligonucleotide synthesis, HPLC, UF, conjugation, and lyophilization is helpfulDetail-oriented and can perform technical duties following standard operating procedures and general laboratory safety rulesExcellent math, documentation, communication and operational troubleshooting skillsClean room environment experience desiredExperience working in a FDA regulated manufacturing environment highly desiredAdditional DetailsThis job has a full time weekly schedule. Applications for this job will be accepted until at least October 29, 2024 or until the job is no longer posted.The full-time equivalent pay range for this position is $29.42 - $45.97/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: 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 ...@agilent.com or contact +1-262-###-####. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.Travel Required: NoShift: MorningDuration: No End DateJob Function: Manufacturing