- 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 troubleshoot critical process equipment.
- B.S. in related field or equivalent combination of education/experience strongly preferred
- 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
- Clean room environment experience desired
- Experience working in a FDA regulated manufacturing environment highly desired.
Manufactuing Associate - Frederick, United States - Agilent Technologies, Inc.
Description
Job DescriptionAs a Manufacturing Associate, 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 maintain 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:
During training, the shift will be M-F, 7:00 AM - 3:30 PM. Training will be approximately 1 Month. The post-training shift will transition to a night shift on Pitman's Schedule.
The schedule will be Night shift (4:30 pm - 5:00 am) working a Pitman schedule: 2 days working, 2 days off, 3 days working, 2 days off, 2 days working, then 3 days off.
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 or contactFor more information about equal employment opportunity protections, please visit
Pay Range
$61,200.00-$95,625.00
The salary range for this position may differ based on your actual work location.
Eligible for Company Car
No
Benefits in Brief
Travel Required
No
Schedule
Schedule:
Full time
Shift
Morning
Duration
No End Date
Job Function
Manufacturing