Manufacturing Engineer/Project Coordinator Join to apply for the Manufacturing Engineer/Project Coordinator role at MillenniumSoft Inc Manufacturing Engineer/Project Coordinator Join to apply for the Manufacturing Engineer/Project Coordinator role at MillenniumSoft Inc Get AI-powered advice on this job and more exclusive features. Position : Manufacturing Engineer/Project Coordinator

Location : San Diego, CA

Duration : 12 Months contract

Total Hours/week : 40.00

Work hours: Standard 8-hr shift; 8-5 pm (including lunch)

3 Must Haves On The Resume

Six sigma experience cross-functional project management 5+ industry experience (including ISO, GMP, or GLP)

Job Description

The Manufacturing Engineer/Project Coordinator is responsible for managing quality investigation and process improvement projects within the Dye Production Team. Must be comfortable working with subject matter experts in cross-functional teams under defined deadlines. The successful candidate will have experience with project management in a life science industry. Client Biosciences, a segment of Company, is one of the world’s leading businesses focused on bringing innovative tools to life science researchers and clinicians. Product lines include flow cytometers, cell imaging systems, monoclonal antibodies, research reagents, diagnostic assays, and tools to help grow tissue and cells. Client Biosciences is an Equal Opportunity/Affirmative Action Employer. Sirigen, Inc. is a subsidiary of client Biosciences and produces polymeric reagents for use in Flow Cytometry and Cell Imaging systems.

Duties & Responsibilities

Manages and directs all phases of a project from project proposal and initiation through completion. Creates and maintains project data and documents such as project dashboard, plans/schedule, quality records and communications. Acts as the driving force for all projects (including customer complaints), coordinating the interactions between Production, QC, Sustaining, R&D and QA to ensure on time execution to the project, identify and work through barriers that hinder progress. Continuously assesses risk in project plans and seeks to minimize that risk, particularly where timelines and/or budget may be impacted (e.g. resources, regulatory requirements, materials, etc). Obtains and compiles necessary data in response to dye performance related customer complaints, out of trend production materials or product failures and CAPA initiation assessments. May lead or participate in CAPA investigations to manage data and timelines. Conducts routine meetings with subject matter experts to discuss open issues/action items and improvements to processes. Coordinates data, prepares slides and facilitates routine project update meetings to management and key stakeholders. Participates in and may lead change management activities associated with process improvement or CAPA implementation. Engages leadership and stakeholders to obtain support and buy in for changes. Partners with management, project leaders, and process owners to align process improvement initiatives with business objectives. May conduct cost savings analysis or cost impact to process changes. Coordinate and carry out necessary documentation, training, qualification and validation activities to support new or modified process changes or deviations. Utilize Six Sigma principles (DMAIC approach, SIPOC, Process Capability, Root Cause Analysis, Normal and Non-Normal data Statistical Analysis, Failure Modes and Effects Analysis, Design of Experiments) to analyze data. Provide project management and Six Sigma coaching, training and support to team members. Other responsibilities or projects as assigned by reporting manager. Promotes a safe work environment. Provide recommendations on maintaining the safety of the work environment. Participates in Environmental Health and Safety programs. Addresses corrective actions whenever a hazard is identified. Notifies supervisor of all observed hazardous conditions or unsafe work

Education & Experience

Successful candidate will possess a B.S. Degree in Chemistry, Engineering or Life Science in with 5+ years relevant industry experience. Demonstrated experience managing cross-functional projects, minimum 3 years.

Assets

Experience with quality systems and guidelines such as GLP and GMP processes and ISO standards essential Proficiency in MS Office Suite (Word, Excel, Visio and PowerPoint) is required. Experience with Minitab or statistical software preferred Experience with CAPA investigation procedures is preferred PMP certificate is preferred Experience in designing dashboard, metrics, etc. is highly desirable (Quick Base experience a plus). Certification in Six Sigma methodologies and Lean principles is highly desirable. Strong interpersonal communication skills, effective written and oral communications skills. Ability to relate to a variety of people and establish collaborative relationships. Comfortable working in a matrix environment. Strong prioritizing and multi-tasking skills to work within deadlines. Must possess meticulous organizational skills, great attention to detail, and have a high aptitude for technology and financial systems. Strong desire to work within a dynamic, fast-paced environment with the expectations of the role consistently expanding or changing. Be a self-starter, quick learner with the ability to work independently and efficiently.

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