This job is closed
Applications are no longer available for this announcement. Explore current related opportunities below.
Job description
Job TitleThis position reports to a Supervisor, Manufacturing. The hours of this position are Monday to Friday 7:30a to 4:00p.Position SummaryThis entry-level position involves working with a small team in a GMP environment to manufacture commercial and/or clinical-scale batches.ResponsibilitiesThe essential functions of this position include:Production, bulk packaging, and inspection of pharmaceutical drug formulationsAssisting with facility cleaning and operational maintenanceCleaning all manufacturing equipment and areasAssisting with facility and process validations as requiredAssisting with environmental and water system monitoring as requiredAssisting with RCRA and safety inspections as requiredDocumenting all work as required by cGMPs and GDPs on a timely basisReading and following all Company SOPs and guidelinesAbiding by all safety requirements as defined by the companyCompleting other tasks as assigned by supervisionQualificationsPreferred Qualifications:Basic knowledge of the Scientific MethodBasic math skills including addition, subtraction, multiplication, division, and percentagesBasic knowledge of and adherence to current GMPs and GDPsBasic knowledge of chemistry and biologyBasic knowledge of HAZCOM, RCRA, and other Safety requirementsBasic level of mechanical aptitudeGood documentation skillsAbility to learn how to operate all types of production equipment (i.e. Blenders, HMIs, Tablet presses, Coaters, Wash off lines, Comils, etc.)Ability to read, understand, and accurately follow company SOPs and guidelinesBasic knowledge of computer systems (Microsoft Suite, SAP, Veeva Vault, LMS)Understanding and comprehension of Master Batch RecordsDetail-orientedWillingness to learn new tasks and skillsAbility to work well in a team environmentAbility to respond quickly and execute assignmentsWillingness to readily adapt to changing job dutiesPositive attitudeUnderstanding of and promotion of company and customer objectivesAbility to follow all procedures to ensure a high-quality productEducation and Experience:Manufacturing Associate IHigh School diploma or equivalentPreferred Qualifications:0-1 years of experience in a pharmaceutical manufacturing operation, preferably in OSDA bachelor's degree is preferred; other relevant work experience, education, and training will be considered.Manufacturing Associate IIHigh School diploma or equivalent1-3 years of experience in a pharmaceutical manufacturing operation.Preferred Qualifications:1+ year experience in OSD ManufacturingAssociate degree or higher in a science/technical disciplineOther relative work experience, education, and training will be consideredManufacturing Associate IIIHigh School diploma or equivalent4-5 years of experience in a pharmaceutical manufacturing operation.Preferred Qualifications:2-3 year experience in OSD ManufacturingAssociate degree or higher in a science/technical disciplineOther relative work experience, education, and training will be consideredWorking Conditions:Available for any shift with the possibility for overtime (as necessary)Physical Requirements:Ability to push and/or pull equipment or product using a pallet jackAbility to lift/move 40 lbs. overhead.Ability to properly gown and don PAPR for potent controlled substance formulations for extended periods of timeMust be able to be medically cleared for respirator use (PAPR)Ability to operate different types of production equipment.Ability to gown correctly for clean room manufacturing operations.Ability to stand or sit for extended periods (up to 4 hours at a time).Must be able to work in an office and a manufacturing environment.About UsAlkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts' Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine.Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Alkermes is an E-Verify employer.Job InfoJob Identification 14013Job Category OperationsLocations Wilmington, OH, United States
Worksite address
wilmington, OH, 45177, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.