Student Veterans of America Jobs

Welcome to SVA’s jobs portal, your one-stop shop for finding the most up to date source of employment opportunities. We have partnered with the National Labor Exchange to provide you this information. You may be looking for part-time employment to supplement your income while you are in school. You might be looking for an internship to add experience to your resume. And you may be completing your training ready to start a new career. This site has all of those types of jobs.

Here are a few things you should know:
  • This site is mobile friendly. You do not need a log-in or password to access information.
  • Jobs on this site are original and unduplicated and come from three sources: the Federal government, state workforce agency job banks, and corporate career websites. All jobs are vetted to ensure there are no scams, training schemes, or phishing.
  • The site is refreshed daily to remove out-of-date content.
  • The newest jobs are listed first, so use the search features to match your interests. You can look for jobs in a specific geographical location, by title or keyword, or you can use the military crosswalk. You may want to do something different from your military career, but you undoubtedly have skills from that occupation that match to a civilian job.
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MILLENNIUM PHARMACEUTICALS, INC. Quality Assurance Specialist II-R0023928 in Brooklyn Park, Minnesota

By clicking the Apply button, I understand that my employment application process with Takeda will commence and that I agree with Takedas Privacy Notice, Privacy Policy and Terms of Use.Job DescriptionOBJECTIVES:Perform Quality Assurance activities associated with commercial cGMP biologics drug substance manufactured at the Brooklyn Park site of Takeda.Responsible for review of batch records and associated documentation in support of timely commercial drugsubstance batch disposition.Provides assistance to site personnel performing deviation investigations, CAPAs, and change controls.Focused primarily on providing support and guidance on non-complex and routine quality-related issues.ACCOUNTABILITIES:Performs documentation review thoroughly, with a high attention to detail, using working knowledge of quality concepts and internal procedures and controls.Supports GMP compliance with time spent in the Manufacturing environment on a regular basis.Analyzes and interprets projects, studies, or investigations to determine next steps in consultation with management. Makes basic decisions independently. Reviews more complex decisions with management.Identifies and resolves basic technical issues using problem-solving skills, in consultation with management.Assesses deviations assigned a direct root cause, defined CAPAs, and entry-level change controls.Revises department-specific controlled documents independently.Receives minimal supervision on routine work assignments. Receives specific instruction on new assignments.Identifies and proposes Quality Process and system improvements.Complete mandatory training within required timeframe.Performs additional duties, as assigned, including support of Compliance and Supplier Quality functions.EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS:BA/BS (or Master's) in any Life Science discipline preferred, and/or 3-5 years experience in Regulated (food, medical device, or pharma/biotech) industry.Understands and applies good working knowledge of quality and GMP principles.Familiarity or experience with the following is preferred: Auditing; basic statistics; Internal / External Auditing; Peer review/approval of documentation; Quality Training; Quality Improvement Tools (Risk Assessments, flowcharts, root cause analysis); Supplier Quality; Technical Writing and Review; Writing/reviewing/approving investigationsAbility to handle multiple tasks concurrently and in a timely fashion.Good interpersonal skills and ability to work effectively and efficiently in a team environment to accomplish goals.Excellent verbal and written communication skills and ability to communicate effectively with site personnel, peers, and management.Must be able to read, write and converse in English.Must display eagerness to learn and continuously improve.Positive work attitude that supports teamwork and continuous improvement.Must be experienced in Microsoft Office applications, especially Word, Excel and PowerPoint.LICENSES/CERTIFICATIONS:Certified Quality Auditor (CQA) a plusPHYSICAL DEMANDS:Stand or sit -> Must be able to remain in a stationary or standing position for extended periods of time.Wrist and hand motion (e.g. typing, writing)Must be able to work in controlled or clean room environments requiring special gowning.OTHER REQUIREMENTS:May be required to wear personal protective equipment (PPE) and other clean room garments daily. This may include: safety shoes, safety glasses, aprons, face shields, lab coats, full body gowns, hair nets and gloves and hearing protection.May be required to participate in an on-call rotation for off-shift coverage or occasionally work off-shift hours to help support a 24-7 manufacturing department.Willingness to travel to various meetings or training, this could include overnight trips.Requires approximately 5% travel.LocationsBrooklyn Park, MNWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull timeEqual Opportunity Employer minorities/females/veterans/individuals with disabilities/s

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