Career CategoryManufacturing
Job DescriptionAssociate ManufacturingWhat you will doLet's do this! Let's change the world! In this dynamic role you will collaborate with multiple functions within the Thousand Oaks site on a routine basis in a dynamic environment (Quality Assurance, Quality Control, Engineering, Facilities, Maintenance, Process Development, Process Engineering, etc.) while developing a deep understanding of the manufacturing operations and planning activities within the facility. Responsibilities of the role include:
- Executing drug product filling activities, respectively
- Performing initial review of manufacturing batch records
- Maintaining a safe and compliant culture by identifying preventative measures
- Creating and/or revising standard operating procedures
- Leading continuous improvement initiatives, which may be cross-functional in nature
- Performing data analysis (e.g., SPC, CPV) of critical process parameters and making recommendations to Engineering and/or Process Development teams
- Developing finite schedule for tasks including, but not limited to unit operations
- Monitoring productivity and identifying countermeasures for issues impacting cycle time adherence
- Elevating critical and impactful events to management
- Applying appropriate systems for job duties (SAP, QMTS, and LIMS etc.)
- Supporting the introduction of new products and technologies into the facility
- Initiating and owning quality records, including but not limited to non-conformances (NC), Corrective/Preventative Actions (CAPA)
What we expect of youWe are all different, yet we all use our unique contributions to serve patients. The Manufacturing professional we seek is a collaborative partner with these qualifications.
Basic Qualifications:Bachelor's degree OR Associate's degree and 6 months of Manufacturing and/or Operations experience OR High school diploma / GED and 2 years of Manufacturing and/or Operations experience
Preferred Qualifications:- B.S. in a life science or related field
- 2 years of work experience in a GMP environment
- Ability to perform computer operations, such as ability to navigate in MS Office and Excel
- Ability to operate specialized equipment and computers as appropriate to the individual area
- Ability to adhere to regulatory requirements, written procedures and safety guidelines
- Ability to evaluate documentation/data according to company and regulatory guidelines
- Ability to interact with inspectors (internal and external)
- Technical writing capabilities
- Ability to organize work, handle multiple priorities and meet deadlines
- Demonstrated written and oral communication skills
- Presentation capabilities
- Detail oriented as well as flexible and adaptable to changing priorities and requirements.
What you can expect of usAs 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, we'll 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 where possible. Refer to the Work Location Type in the job posting to see if this applies.
Apply now and make a lasting impact with the Amgen team.
careers.amgen.comIn 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.
Sponsorship
Sponsorship for this role is not guaranteed.
Salary Range70,985.20USD -96,038.80 USD
