Associate Manufacturing

Associate ManufacturingJoin Amgen's Mission of Serving PatientsAt Amgen, if you feel like you're part of something bigger, it's because you are. Our shared missionto serve patients living with serious illnessesdrives 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.The Manufacturing 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 Associate position will be focused on:Performing 100% manual inspectionPost inspection packaging operationCharacterization and equipment managementProcess improvement projects/assignments within operationsQuality systems (LIMS/MES/SAP/MAXIMO) supportSupport new product introduction activitiesSupport clinical and commercial productionMaintain open communication between operations teamsThis Associate position will be focused on manual visual inspection in manufacturing operations.Job Scope and Responsibilities:Perform 100% manual inspectionPerform post manual inspection packaging operationsUnder minimal supervision, performs manufacturing unit operations according to Standard Operating ProceduresUnderstand process parameters and can identify process anomaliesOperate critical processing equipmentAssist and implement continuous improvement solutions related to routine functionsAssist in ensuring operations are completed per manufacturing scheduleResource related to processing operations on the mfg. floorIdentify and propose solutions to complex problemsResponsible for identifying and communicating 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 hands-on training to othersProvide suggestions/ideas for corrective actions and preventative actions for deviations/safety incidentsApplies research, information gathering, analytical and interpretation skills to problems of diverse scopesUtilizes basic 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 off-shift and weekends)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 regulationsAbility to understand processing methods for manufacturing areaWhat we expect of youWe are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek will possess these qualifications.Basic Qualifications:High school/GED + 2 years biotech/pharma manufacturing/laboratory or manufacturing support (i.e. laboratories, engineering, facilities, quality) work experience ORAssociate's + 6 months biotech/pharma manufacturing/laboratory or manufacturing support (i.e. laboratories, engineering, facilities, quality) work experience ORBachelor'sPreferred Qualifications:Experience with manual visual inspection in a GMP regulated environment.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 capabilityKnowledgeable of manual visual inspection background 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.