Engineer I Upstream Bio Process - Thousand Oaks, CA
Engineer I Upstream Bio Process - Thousand Oaks, CA
Posted on :
27-06-2025
Employer Active
1 Vacancy
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Share
Send me jobs like this
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Monthly Salary
$ 107268 - 107268
Vacancy
1 Vacancy
Posted on :
27-06-2025
Job Description
ATTENTION MILITARY AFFILIATED JOB SEEKERS- Our organization works with partner companies to source qualified talent for their open roles. The following position is available toVeterans Transitioning Military National Guard and Reserve Members Military Spouses Wounded Warriors and their Caregivers. If you have the required skill set education requirements and experience please click the submit button and follow the next steps. Unless specifically stated otherwise this role is On-Site at the location detailed in the job post.
At Amgen if you feel like youre part of something bigger its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.
Since 1980 weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology Inflammation General Medicine and Rare Disease we reach millions of patients each year. As a member of the Amgen team youll help make a lasting impact on the lives of patients as we research manufacture and deliver innovative medicines to help people live longer fuller happier lives.
Our award-winning culture is collaborative innovative and science based. If you have a passion for challenges and the opportunities that lay within them youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Engineer I - Upstream Bio-Process
What you will do
Lets do this. Lets change the world. In this vital role you will support technology transfer and process validation for human therapeutic products (biological drug substance) across the clinical and commercial manufacturing space.
Responsibilities:
Transfer cell culture/purification drug substance processes and perform process improvements from the laboratory into the manufacturing facility and between manufacturing sites
Provide process validation support for late stage commercial processes
Provide on-the-floor technical support for successful scale-up and transfer of process technology and for clinical or commercial manufacturing operations
Provide routine process monitoring and troubleshooting
Perform data trending and statistical process analysis
Provide technical contributions for process related deviations (NCs) CAPAs and change controls
Identify and support process related operational excellence opportunities
Represent process development and collaborate with other functions such as Manufacturing Quality and Regulatory
What we expect of you
We are all different yet we all use our unique contributions to serve patients. The dynamic professional we seek is an individual with these qualifications.
At Amgen if you feel like youre part of something bigger its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.
Since 1980 weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology Inflammation General Medicine and Rare Disease we reach millions of patients each year. As a member of the Amgen team youll help make a lasting impact on the lives of patients as we research manufacture and deliver innovative medicines to help people live longer fuller happier lives.
Our award-winning culture is collaborative innovative and science based. If you have a passion for challenges and the opportunities that lay within them youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Engineer I - Upstream Bio-Process
What you will do
Lets do this. Lets change the world. In this vital role you will support technology transfer and process validation for human therapeutic products (biological drug substance) across the clinical and commercial manufacturing space.
Responsibilities:
Transfer cell culture/purification drug substance processes and perform process improvements from the laboratory into the manufacturing facility and between manufacturing sites
Provide process validation support for late stage commercial processes
Provide on-the-floor technical support for successful scale-up and transfer of process technology and for clinical or commercial manufacturing operations
Provide routine process monitoring and troubleshooting
Perform data trending and statistical process analysis
Provide technical contributions for process related deviations (NCs) CAPAs and change controls
Identify and support process related operational excellence opportunities
Represent process development and collaborate with other functions such as Manufacturing Quality and Regulatory
What we expect of you
We are all different yet we all use our unique contributions to serve patients. The dynamic professional we seek is an individual with these qualifications.
Additional Qualifications/Responsibilities
Basic Qualifications:
Masters degree
Or
Bachelors degree and 2 years of Process Development experience
Or
Associates degree and 6 years of Process Development experience
Or
High school diploma / GED and 8 years of Process Development experience
Preferred Qualifications:
Masters degree in Chemical/Biochemical Engineering or related subject area
3 years of experience in Process Engineering related to biochemical engineering and/or protein biochemistry scale-up principles and manufacturing of biologics (cGMP)
Upstream and/or Downstream process knowledge and hands on cell culture and/or purification pilot/clinical/commercial experience with regard to the manufacture of a biological drug substance
Experience working in/supporting a commercial cGMP manufacturing facility
A firm understanding of cell culture process and related equipment; scale-up from bench to commercial scale mass oxygen transfer capabilities metabolism profiling influence of raw material attributes and impact of process deviations to growth and quality attributes
Knowledge of aseptic processing/techniques harvest and clarification processes used in mammalian cell culture processes AND/OR a good understanding of purification process and associated equipment; chromatography ultrafiltration normal flow filtration virus inactivation and virus filtration operations
Process development (PD) experience supporting cGMP manufacturing at large scale
Strong capability in scientific/engineering/laboratory analysis troubleshooting and ability to apply sophisticated problem resolution abilities
Ability to develop and follow detailed protocols
Independently motivated with ability to multi-task and work in teams
Excellent written and verbal communication with experience with technical writing and presentations
What you can expect from us
As we work to develop treatments that take care of others we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture well support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to relevant skills experience and qualifications.
In addition to the base salary Amgen offers a Total Rewards Plan based on eligibility comprising of health and welfare plans for staff and eligible dependents financial plans with opportunities to save towards retirement or other goals work/life balance and career development opportunities that may include:
A comprehensive employee benefits package including a Retirement and Savings Plan with generous company contributions group medical dental and vision coverage life and disability insurance and flexible spending accounts
A discretionary annual bonus program or for field sales representatives a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models including remote and hybrid work arrangements where possible
Apply now and make a lasting impact with the Amgen team.
In any materials you submit you may redact or remove age-identifying information such as age date of birth or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
Application deadline
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
As an organization dedicated to improving the quality of life for people around the world Amgen fosters an inclusive environment of diverse ethical committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together we compete in the fight against serious disease.
.
Salary Range
93344.00 USD - 107268.00 USD
Employment Type
Full Time
Key Skills
Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.
