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1 job found for warehouse work available call today start tomorrow in rogers, minnesota

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    • minneapolis, minnesota
    • contract
    • $28.64 - $33.67 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Minneapolis, Minnesota job type: Contract salary: $28.64 - 33.67 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Perform Quality Systems activities associated with commercial cGMP biologics drug substance manufactured at Takeda Brooklyn Park.Serve as the primary Business Administrator and Subject Matter Expert (SME) for company's Electronic Quality Management System.Support quality management procedures and provide targeted technical training (e.g., deviation, CAPA, change management).Drive on-time completion of deviations, CAPAs and change requests with metrics reporting and cross-functional interaction.Report metrics on health of the business as it relates to Quality Systems.Provide assistance to site personnel performing deviation investigations, CAPAs, and change controls.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.  qualifications: 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: DMAIC investigation process; Root Cause Analysis; basic statistics; Peer review/approval of documentation; Quality Training; Quality Improvement Tools (Risk Assessments, flowcharts, metrics generation); Technical Writing and Review; Writing/reviewing/approving investigationsAbility to handle tasks concurrently and use productivity tools to meet deadlines.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, including the values of Takeda-ism (honesty, integrity, perseverance, and fairness) that support teamwork and professionalism.Must be experienced in Microsoft Office applications, especially Word, Excel, and PowerPoint.ASQ Certified Quality Auditor (CQA) or other certification, a plus.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 / Travel 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.  skills: Quality control, Quality Assurance, CAPA, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Minneapolis, Minnesota job type: Contract salary: $28.64 - 33.67 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Perform Quality Systems activities associated with commercial cGMP biologics drug substance manufactured at Takeda Brooklyn Park.Serve as the primary Business Administrator and Subject Matter Expert (SME) for company's Electronic Quality Management System.Support quality management procedures and provide targeted technical training (e.g., deviation, CAPA, change management).Drive on-time completion of deviations, CAPAs and change requests with metrics reporting and cross-functional interaction.Report metrics on health of the business as it relates to Quality Systems.Provide assistance to site personnel performing deviation investigations, CAPAs, and change controls.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.  qualifications: 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: DMAIC investigation process; Root Cause Analysis; basic statistics; Peer review/approval of documentation; Quality Training; Quality Improvement Tools (Risk Assessments, flowcharts, metrics generation); Technical Writing and Review; Writing/reviewing/approving investigationsAbility to handle tasks concurrently and use productivity tools to meet deadlines.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, including the values of Takeda-ism (honesty, integrity, perseverance, and fairness) that support teamwork and professionalism.Must be experienced in Microsoft Office applications, especially Word, Excel, and PowerPoint.ASQ Certified Quality Auditor (CQA) or other certification, a plus.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 / Travel 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.  skills: Quality control, Quality Assurance, CAPA, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

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