MNC InsiderMNC Insider
Amgen logo

Senior Associate Manufacturing

Amgen

Senior Associate Manufacturing

full-timePosted: Jul 29, 2026Updated: Aug 28, 2026US - California - Thousand Oaks

Job Description

Career CategoryManufacturingJob DescriptionJoin Amgen’s Mission of Serving PatientsAt Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity-related conditions. As a member of the Amgen team, you’ll 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, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.Senior Associate ManufacturingWhat you will doLet’s do this! Let’s change the world!The Manufacturing Senior Associate position is part of the Amgen, Thousand Oaks, Drug Product Supply organization. This is a manufacturing support role responsible for manual visual inspection team. This Senior Associate position will be focused on:Characterization, data, and equipment managementProcess improvement projects/assignments within operationsQuality systems (Deviations/CAPA/CAPA EV/LIMS/MES/SAP/MAXIMO) supportSupport new product introduction activitiesSupport productionMaintain open communication between operations teamsThis Senior Associate position will be focused on manual visual inspection operations.Job Scope and Responsibilities:Under minimal supervision, performs manufacturing unit operations according to Standard Operating ProceduresMay schedule operations for multiple functional areasUnderstand process parameters and can identify process anomaliesPerform data analysis of critical process parametersOperate complex critical processing equipmentAssist, plan and implement continuous improvement solutions related to routine functionsAssist in ensuring operations are completed per manufacturing schedule which may include delegation of tasksPrimary resource related to processing operations on the mfg. floorIdentify and propose solutions to complex problemsResponsible for resolving problems during operationsPerform initial review of manufacturing procedures/batch recordsReview, revise, and audit documentsAbility to perform computer operations (MES, EBR, MAXIMO, LIMS and SAP Knowledge)Provide process theory expertise and hands-on training to othersOwn deviations/CAPA or provide suggestions/ideas for corrective actions and preventative actions for deviations/safety incidentsApplies research, information gathering, and interpretation skills to problems of diverse scopeUtilizes project management skills to set project timelines and priorities based project objectives and ongoing assignmentsRecognizes and escalates problemsAble to establish working relationships with others outside area of expertiseAbility and willingness to support flexible shift structure in support of operations (may include 24/7 or weekend)Ability to understand, apply, and evaluate basic chemistry, biology, and physical principles as appropriate for the positionOrganizational skills and an ability to perform assignments with a high degree of attention to detailWritten and oral communication skills. Technical writing capabilityGMP knowledge with ability to interpret and apply applicable regulationsWhat we expect of youWe are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is an employee with these qualifications.Basic Qualifications:Master’s degree ORBachelor’s degree and 6 months of experience in biotech/pharma manufacturing/laboratory or manufacturing support (i.e. laboratories, engineering, facilities, quality) ORAssociate’s degree and 2 years of experience in biotech/pharma manufacturing/laboratory or manufacturing support (i.e. laboratories, engineering, facilities, quality) ORHigh School Diploma/GED and 4 years of experience in a biotech/pharma manufacturing/laboratory or manufacturing support (i.e. laboratories, engineering, facilities, quality)Preferred Qualifications:Prior experience with lab equipment, computers, and intermediate mathematical skillsSignificant experience with manual visual inspection in a GMP regulated environment.Significant experience with PAS X Werum software for electronic batch records with some understanding of editing and validationDegree in Engineering, Chemistry, Biochemistry, Biology or Computer Science with experience in biotechnologyDemonstrated technical writing skillsStrong knowledge of manual visual inspection or strong understanding of related disciplinary areas in bioprocessing (Drug Product operations)Demonstrated ability to work in a teamWhat 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 accountsA discretionary annual bonus program, or for field sales representatives, a sales-based incentive planStock-based long-term incentivesAward-winning time-off plansFlexible 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 deadlineAmgen 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.SponsorshipSponsorship 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 Range86,048.05USD -116,417.95 USD

Locations

  • US - California - Thousand Oaks

Skills Required

  • biotech/pharma manufacturing/laboratoryintermediate
  • lab equipmentintermediate
  • manual visual inspection in a GMP regulated environmentintermediate
  • biotechnologyintermediate
  • manual visual inspectionintermediate

Required Qualifications

  • Master’s degree OR (degree)
  • Bachelor’s degree and 6 months of experience in biotech/pharma manufacturing/laboratory or manufacturing support (i.e. laboratories, engineering, facilities, quality) OR (experience)
  • Associate’s degree and 2 years of experience in biotech/pharma manufacturing/laboratory or manufacturing support (i.e. laboratories, engineering, facilities, quality) OR (experience, 2 years)
  • High School Diploma/GED and 4 years of experience in a biotech/pharma manufacturing/laboratory or manufacturing support (i.e. laboratories, engineering, facilities, quality) (experience, 4 years)

Preferred Qualifications

  • Prior experience with lab equipment, computers, and intermediate mathematical skills (experience)
  • Significant experience with manual visual inspection in a GMP regulated environment. (experience)
  • Significant experience with PAS X Werum software for electronic batch records with some understanding of editing and validation (experience)
  • Degree in Engineering, Chemistry, Biochemistry, Biology or Computer Science with experience in biotechnology (experience)
  • Demonstrated technical writing skills (experience)
  • Strong knowledge of manual visual inspection or strong understanding of related disciplinary areas in bioprocessing (Drug Product operations) (experience)
  • Demonstrated ability to work in a team (experience)
  • Prior experience with lab equipment, computers, and intermediate mathematical skills (experience)
  • Significant experience with manual visual inspection in a GMP regulated environment. (experience)
  • Significant experience with PAS X Werum software for electronic batch records with some understanding of editing and validation (experience)
  • Degree in Engineering, Chemistry, Biochemistry, Biology or Computer Science with experience in biotechnology (experience)
  • Demonstrated technical writing skills (experience)
  • Strong knowledge of manual visual inspection or strong understanding of related disciplinary areas in bioprocessing (Drug Product operations) (experience)
  • Demonstrated ability to work in a team (experience)

Responsibilities

  • Let’s do this! Let’s change the world!
  • The Manufacturing Senior Associate position is part of the Amgen, Thousand Oaks, Drug Product Supply organization. This is a manufacturing support role responsible for manual visual inspection team. This Senior Associate position will be focused on:
  • Characterization, data, and equipment management
  • Process improvement projects/assignments within operations
  • Quality systems (Deviations/CAPA/CAPA EV/LIMS/MES/SAP/MAXIMO) support
  • Support new product introduction activities
  • Support production
  • Maintain open communication between operations teams
  • Characterization, data, and equipment management
  • Process improvement projects/assignments within operations
  • Quality systems (Deviations/CAPA/CAPA EV/LIMS/MES/SAP/MAXIMO) support
  • Support new product introduction activities
  • Support production
  • Maintain open communication between operations teams
  • This Senior Associate position will be focused on manual visual inspection operations.
  • Under minimal supervision, performs manufacturing unit operations according to Standard Operating Procedures
  • May schedule operations for multiple functional areas
  • Understand process parameters and can identify process anomalies
  • Perform data analysis of critical process parameters
  • Operate complex critical processing equipment
  • Assist, plan and implement continuous improvement solutions related to routine functions
  • Assist in ensuring operations are completed per manufacturing schedule which may include delegation of tasks
  • Primary resource related to processing operations on the mfg. floor
  • Identify and propose solutions to complex problems
  • Responsible for resolving problems during operations
  • Perform initial review of manufacturing procedures/batch records
  • Review, revise, and audit documents
  • Ability to perform computer operations (MES, EBR, MAXIMO, LIMS and SAP Knowledge)
  • Provide process theory expertise and hands-on training to others
  • Own deviations/CAPA or provide suggestions/ideas for corrective actions and preventative actions for deviations/safety incidents
  • Applies research, information gathering, and interpretation skills to problems of diverse scope
  • Utilizes project management skills to set project timelines and priorities based project objectives and ongoing assignments
  • Recognizes and escalates problems
  • Able to establish working relationships with others outside area of expertise
  • Ability and willingness to support flexible shift structure in support of operations (may include 24/7 or weekend)
  • Ability to understand, apply, and evaluate basic chemistry, biology, and physical principles as appropriate for the position
  • Organizational skills and an ability to perform assignments with a high degree of attention to detail
  • Written and oral communication skills. Technical writing capability
  • GMP knowledge with ability to interpret and apply applicable regulations
  • Under minimal supervision, performs manufacturing unit operations according to Standard Operating Procedures
  • May schedule operations for multiple functional areas
  • Understand process parameters and can identify process anomalies
  • Perform data analysis of critical process parameters
  • Operate complex critical processing equipment
  • Assist, plan and implement continuous improvement solutions related to routine functions
  • Assist in ensuring operations are completed per manufacturing schedule which may include delegation of tasks
  • Primary resource related to processing operations on the mfg. floor
  • Identify and propose solutions to complex problems
  • Responsible for resolving problems during operations
  • Perform initial review of manufacturing procedures/batch records
  • Review, revise, and audit documents
  • Ability to perform computer operations (MES, EBR, MAXIMO, LIMS and SAP Knowledge)
  • Provide process theory expertise and hands-on training to others
  • Own deviations/CAPA or provide suggestions/ideas for corrective actions and preventative actions for deviations/safety incidents
  • Applies research, information gathering, and interpretation skills to problems of diverse scope
  • Utilizes project management skills to set project timelines and priorities based project objectives and ongoing assignments
  • Recognizes and escalates problems
  • Able to establish working relationships with others outside area of expertise
  • Ability and willingness to support flexible shift structure in support of operations (may include 24/7 or weekend)
  • Ability to understand, apply, and evaluate basic chemistry, biology, and physical principles as appropriate for the position
  • Organizational skills and an ability to perform assignments with a high degree of attention to detail
  • Written and oral communication skills. Technical writing capability
  • GMP knowledge with ability to interpret and apply applicable regulations

Target Your Resume for "Senior Associate Manufacturing" , Amgen

Get personalized recommendations to optimize your resume specifically for Senior Associate Manufacturing. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Senior Associate Manufacturing" , Amgen

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

GeneralGeneral

Answer 10 quick questions to check your fit for Senior Associate Manufacturing @ Amgen.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.