*Hi* *,*
*Hope you are doing great* *Please review the following job description:* *Position: Manufacturing Engineer – 47113* *Location: Mystic, CT* *Duration: 12+ Months* *Job Duties :* Design of Experiments (DOE) and Statistical Process Control (SPC),Determines manufacturing operation requirements and process parameters ,Develops plans to evaluate process repeatability and stability ,Develops product and process improvements, Participates in procedure writing and review ,Performs process and equipment validations ,Provides technical support to other engineers ,Reviews product performance data to identify trends, Specifies and implements process lay-outs, Supports manufacturing, development, and implementation processes, Utilizes FMEA within process development ,Ensures compliance with GMP’s, Generates documentation for engineering protocols and reports ,Writes engineering and manufacturing specifications *Note: Max Rate: 34/hr on C2C* *Please share your consultant resumes on asi...@syglo.com <asi...@syglo.com>* *Skill Set:* *Required:* *Education Level: *Undergraduate Degree *Oral Communication: *Excellent *Written Communication: *Excellent *Desired:* *CAD Systems: *AutoCAD *Six Sigma/Lean Sigma Certifications: *Green Belt *MAIN JOB DUTIES/RESPONSIBILITIES *– · Design, construct, and maintain assembly fixtures and test equipment supporting a Lean manufacturing environment. · Write validation protocols and reports including protocol execution and data analysis for manufacturing processes and packaging equipment. · Develop, improve, and maintain new and existing manufacturing processes, including the creation of manufacturing processing documentation, and equipment operating instructions. · Create and maintain component specifications and bill of materials. · Identify, qualify, and implement quality improvement and cost savings initiatives. · Limited travel will be required. List of following duties are required for all employees. · Complies with the Medtronic Site Quality System. · Performs duties in compliance with environmental, health and safety related site rules, policies or governmental regulations. · Required to interact and communicate with peers and co-workers. · Required to spend extended periods of time on computer-based work. · Performs other duties as assigned. *EDUCATION:* · BS degree in Engineering or Natural Science required. *YEARS OF EXPERIENCE:* · Minimum of 2 years of experience in manufacturing or R&D in a FDA regulated environment. *SKILLS AND QUALIFICATIONS*: · Proven communication skills and ability to function within a multi-functional team. · Experience with Microsoft Office, or equivalent software is required. · Experience with Minitab preferred. · Working knowledge of ultrasonic welding, and adhesive bonding preferred. *Request Notes : * MAIN PURPOSE OF JOB – This position has the responsibility and authority to design, development, and implementation of process improvements for various PVA manufacturing processes that meet internal and external customer requirements in a dynamic business environment. *First Name* *Middle Name* *Last Name* *Postal Address* *Contact Phone* *Email Address* *Education* *Expected Rate* *Willing to relocate/ Commute?* *Work Authorization Status* *Availability for Discussion* *Availability for Face-Face* *Availability to Join* *Thanks & Regards* *Aman Singh* *Sr. Technical Recruiter* *Email: asi...@syglo.com <asingh@syglo.comail>* *www.synico.com <http://www.synico.com>* -- You received this message because you are subscribed to the Google Groups "Open Source Erp & Crm" group. To unsubscribe from this group and stop receiving emails from it, send an email to open-source-erp-crm+unsubscr...@googlegroups.com. To post to this group, send email to open-source-erp-crm@googlegroups.com. Visit this group at http://groups.google.com/group/open-source-erp-crm. For more options, visit https://groups.google.com/d/optout.
