Engineer 2, Manufacturing

Antares Pharma
tuition reimbursement, 401(k)
United States, Minnesota, Hopkins
12500 Whitewater Drive (Show on map)
Feb 07, 2025
Save time and apply through your LinkedIn account. Click the Apply with LinkedIn button and your LinkedIn profile will be imported into our site. In order to move forward, you will need to create an account. Your password must be eight characters long, contain at least one special character, one capital letter and a number. We look forward to discovering your talents. Engineer 2, Manufacturing Welcome to an inspired career. At Halozyme, we are reinventing the patient experience and building the future of drug delivery. We are passionate about the important work we do and constantly strive to do more. We embrace transformation and work hard to innovate for the future. We do this together, as One Team - we rise by lifting others up and believe in the power of working together for the collective win. That's why we need you-to help us make a significant impact by taking on increasingly complex challenges, leaping beyond the status quo, advancing our mission and making our One Team culture thrive. Join us as an Engineer 2, Manufacturing, and you'll be part of a culture that welcomes diversity, thinks differently to solve problems, works collaboratively as one team, and delivers meaningful innovations that impact people's lives. How you will make an impact The Engineer 2, Manufacturing designs, develops, and implements manufacturing processes and equipment to support existing commercial products and products in development. These processes and equipment may be located within Halozyme or at a contracted manufacturer site. In this role, you'll have the opportunity to: Collaborate on device designs to ensure manufacturability Translate device design requirements into process and equipment requirements meeting Regulatory and Quality requirements Collaborate on risk management activities including user and design FMEAs and lead the development and documentation of process FMEAs to identify/reduce risk Develop, implement, and document equipment qualifications and process validations, including master validation plans/reports and IQ, OQ, PQ plans/repo1ts. Apply tools including measurement system analysis (MSA), gage repeatability and reproducibility (GRR), design of experiments (DOE), statistical process control (SPC), and capability analysis to develop, improve, and control processes Support test method and inspection method development/validation used during design verification, process validation, and commercial manufacturing Develop, implement, and support production documentation including manufacturing procedures, routers, and bill of materials (BOM) Apply tools including value stream mapping, overall equipment effectiveness (OEE), and SS to understand and improve quality, labor efficiency, throughput, and cycle time Develop project timelines (Gantt Chart), scope of work, and other project documents to ensure collaboration and project success across functions and companies Provide engineering support and project communication to team members, customers, contract manufacturers, and stakeholders Document technical work and results for presentation of data To succeed in this role, you'll need: Bachelor level degree in Engineering or related Science with at least 2 years relevant experience within the medical device, pharmaceutical, or related industry (An equivalent combination of experience and education may be considered) Experience with plastic injection molding processes and high-volume metal forming processes; manual, semi-automated, and fully automated assembly processes; and equipment specifications and manufacturing process instructions Excellent technical writing skills including protocols/reports Ability to communicate and educate internally and externally (product builders, cross-functional team members, suppliers, customers, stakeholders, regulatory agencies) Knowledge of GMP, CPR, ISO, QSR and other regulations, standards, directives and guidance Experience with statistical tools, data analysis, Six Sigma, and computer software (Minitab, Project, Excel/Word) In return, we offer you: Full and comprehensive benefit program, including an Employee Stock Purchase Program and 401(k) matching. Opportunities to grow in a culture that prioritizes learning, development and progression through in-house programs and tuition reimbursement. A collaborative, innovative team that works as one to amplify your impact-on your career, the work you do and patients' lives. The most likely base pay range for this position is $83,000 - $116,000 per year. Several factors, such as experience, tenure, skills, and particular business needs, will determine an individual's exact level of compensation. Base salary is only one element of employee compensation at Halozyme. Total compensation could include bonuses, sales incentives, and equity awards. Halozyme, Inc. is an Equal Employment Opportunity (EEO) employer. It is the policy of the Company to provide equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. AccessibilityandReasonableAccommodations: Halozyme is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans during our application process. If you need assistance or accommodation due to a disability, contact Human Resources at hrbox@halozyme.com. To view all our open positions, please visit our career page. Additionally, our benefit offerings can be found here.