Agilent Technologies, Inc. Manufacturing Associate (2nd Shift) in Frederick, Colorado
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.
Agilent Technologies Life Sciences Chemical Analysis business is looking to add a Manufacturing Associate to their high-performance manufacturing team working at the new state-of-the-art, contract API manufacturing facility that specializes in Nucleic Acid Chemistries located in Frederick, Colorado.
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 HOURS: 4:00pm-2:30am Monday-Thursday
BS in chemistry, biology, biochemistry, science or equivalent or equivalent combination of education and or experience preferred but not required
2+ 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
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
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.
For more information about equal employment opportunity protections, please view the 'EEO is the Law' poster available here: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf,
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 (US and Canada only) or email firstname.lastname@example.org. EOE AA M/F/Vet/Disability.
Date Posted: 19/Mar/18
Job Title: Manufacturing Associate (2nd Shift)
Business: Diagnostics and Genomics Group
Job Category: Manufacturing
Job Sub-Category: Manufacturing Associate
Country or Area: United States
Shift: Evening Job
Job Type: Experienced
Travel Required: No
Duration (Temp Positions Only): Not applicable
HR Country Location: United States
HR Town/City Location: Frederick