Associate Manufacturing (Swing Shift 2pm-11pm)

Career Category

Manufacturing

Job Description

Join Amgens Mission of Serving Patients

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.

Associate Manufacturing

What you will do

Lets do this! Lets 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 :

Performing drug product manual visual inspection 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 you

We 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 :

Bachelors degree OR Associates degree and 6 months of GMP / GDP experience OR High school diploma / GED and 2 years of GMP / GDP 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 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 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.

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.

Sponsorship

Sponsorship for this role is not guaranteed.

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.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race color religion sex sexual orientation gender identity national origin protected veteran status disability status or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process to perform essential job functions and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range

73359.00 USD - 85625.00 USD

Required Experience :

IC

Key Skills

Lean Manufacturing,Six Sigma,Continuous Improvement,ISO 9001,Lean Six Sigma,Management Experience,Manufacturing & Controls,5S,Manufacturing Management,Kaizen,Chemistry,Manufacturing

Employment Type : Full-Time

Experience : years

Vacancy : 1

Monthly Salary Salary : 85625 - 85625