Manufacturing Associate (Shift Timing--Sun - alt Wed, 1100 - 2330)

JOB TITLE: Manufacturing AssociateLocation: Bothell, WA (100% onsite)Duration: 6 months initial (potential extension/potential right to hire)Schedule: Shift Timing--Sun - alt Wed, 1100 - 2330

Apply promptly! A high volume of applicants is expected for the role as detailed below, do not wait to send your CV.
*Position Summary*The primary purpose of the Manufacturing Associate role is to complete production assignments with high quality and timely output in a cellular therapeutic manufacturing environment.
*Duties/Responsibilities*• Works on routine manufacturing assignments per written procedures, where ability to recognize deviation from accepted practice is required.• Adheres to Good Manufacturing Practices and standard operating procedures.• Weighs and checks raw materials. Assembles, cleans and sanitizes process equipment, monitors processes.• Completes work instructions and maintains clean room environment to comply with regulatory requirements.• Trains for proficiency in the operation of primary production equipment within the assigned functional area.• Trains for proficiency in process systems (i.e. Syncade MES and Oracle interfaces) and some supporting business systems (i.e. Oracle, ETQ, BMRAM etc.).• Assist with the revision and or creation of process documents, such as SOPs and electronic work instructions.• Assists in maintaining material and components inventory level.• Supports safe work environment.• Work in teams and have continual interaction with members of his/her team as well as other• manufacturing teams throughout the production process in order to exchange information regarding the batch(s) in process.• Works on assignments that are routine in nature where judgment is required in resolving problems and making routine recommendations.
*Qualifications*• Associate's or Bachelor's degree in life sciences field is preferred. Minimum of high school diploma and/or equivalent combination of education and experience is required.• 0-2 years of cGMP manufacturing experience is desired or equivalent in work experience or education. Proven experience working on teams where combined contribution, collaboration, and results were expected.• Demonstrated proficiency in common computer tools such as word processing, spreadsheet and web-based applications. Experience where attention to detail and personal accountability were critical to success.• Demonstrates good interpersonal skills, is attentive and approachable. xzbcwsv • Maintains a professional and productive relationship with area management and co-working
If hired, you will enjoy the following Eclaro Benefits:401k Retirement Savings Plan administered by Merrill LynchCommuter Check Pretax Commuter BenefitsEligibility to purchase Medical, Dental & Vision Insurance through Eclaro

If you feel you are qualified with the required skills and if you are interested, please free to send your word version most updated resume TAILORED to the job description above to or call (212)804-7476.
Equal Opportunity Employer: ECLARO values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status, in compliance with all applicable laws.