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Hi,
My name is Pavan Kalyan and I work at (link removed)c. I have seen your resume in one of the job portals and we have an immediate opening for Manufacturing Engineer II in Mansfield, MA - 02048 for a duration of 06+ Months. I am listing the job description below. Please let me know if you have any interest in having a discussion. Please feel free to reach me at 732-702-7384 or attach your resume to pavan.t@intellectt.com
Role: Manufacturing Engineer II
Location: Mansfield, MA - 02048
Duration: 06+ Months on W2
Job Description:
Manufacturing Engineer II
On-site - Mansfield MA Plant
M-F business hours
Potential temp to perm but not guaranteed.
Must be ok with potential 1-2 trips to China to visit site
MUST BE ABLE TO SPEAK/READ/WRITE MANDARIN/CHINESE
Responsibilities:
Generation and execution of validation plans, validation protocols (IQ/OQ/PQ), and completion reports, with a major focus on sterilization and microbiology of medical devices.
Provide statistical analysis of the date to support the reports.
Generation and implementation of change controls and engineering notices (ECO).
Develop statistically based sampling plans for in-process and final testing and inspections, and validations.
Troubleshooting equipment/processes that do not perform as intended during validation runs.
Recommend process/quality improvements as part of validation runs.
Evaluate, investigate and document non-conformances incidents and/or protocol deviations.
Complete assigned Non-Conformance and CAPA investigations and prepare investigation reports.
Develops and maintains an effective cross-functional working relationship with plant and corporate Manufacturing, Engineering, Regulatory, and Quality Assurance personnel.
Work on project teams with other internal departments, external vendors, and customers as required.
Assure that existing processes and assigned activities fully comply with regulatory and/or international agencies, such as FDA, ISO, OSHA, EPA, among others.
Participate in the compilation and review of technical documentation for both domestic and international regulatory submissions.
Participate in external audits such as:
FDA, Notified Body (BSI) and Corporate, among others.
Performs other related duties as necessary.
Qualifications:
Knowledge of FDA, OSHA, EPA, and GMP and ISO requirements.
Knowledge in Organizational Excellence and Lean/Six Sigma.
Strong Project Management skills.
Ability to lead teams through complex projects and provide departmental technical leadership.
Must have excellent communication skills and a strong track record of working cross-functionally.
Must have demonstrated the ability to think strategically.
Able to develop technical documentation such as: Change Controls, Validation Plans, Validation Protocols, Technical / investigation reports, SOP, and others. Teamwork oriented and self-starter.
Education and/or experience:
BS in Engineering, preferably Mechanical, Industrial, Electrical, Chemical, or Biomedical (Professional Engineer License.) or sciences related field.
Lean/Six Sigma Green or Black Belt Certification is a plus.
Experience in validations such as: manufacturing equipment, manufacturing processes, stability or aging, required.
Minimum of 4-6 years of experience in the medical device and/or pharmaceutical manufacturing environment.
Intellectt INC
