Software Engineer III

Medical Engineering Consultants (MEC) support medical device and pharmaceutical companies to be more efficient and productive by providing resources, knowledge, and expertise to augment and supplement to their work. Our vision is to closely align our clients’ needs with the best resources available in the marketplace. We take proactive, preventative, and corrective action and create a roadmap for ongoing future improvement by identifying, integrating, and executing sustainable solutions that validate processes, ensure fully compliant quality systems, and close gaps between current and FDA expected stages.

MEC offers companies short or long-term support – from high-end leaders, managers and consultants to skill-set Engineering staff and SME’s (Subject Matter Experts).

MEC's mission is to inspire positive cultural change from within, and always exceed our clients’ expectations.

This is an onsite position - Valencia CA. Firm. Applicants must be authorized to work in the U.S. without visa sponsorship now or in the future. The Client is unable to consider candidates who require sponsorship. Local qualified candidates will move to top.

Job Title:

Systems Engineer III.

Job Purpose:

Develops software systems applications firmware and/or provides software systems testing and validation in support of RD and/or Manufacturing Process Engineering. Responsible for analyzing designing programming debugging and modification of local network/internet-related computer programs for commercial or end user applications i.e. materials management financial management HRIS or desktop applications products. May interface with users to define system requirements and/or necessary modifications. Responsible for developing applying and maintaining quality standards for software products.

• Designs develops debugs modifies tests software programs by using current programming languages methodologies and technologies.
• Documents software development and/or test development by writing documents reports memos change requests. Methods used are determined by approved procedures and standards.
• Tracks software development effort by creating and maintaining records in the approved tracking management tool.
• Analyzes evaluates verifies requirements software and systems by using software engineering practices.
• Investigates research selects software designs operating systems and/or practices.
• Continuously improves process and work methodologies by interfacing with peers/cross-functional groups and analyzing activities to improve workflow and work processes.

Quality Systems

Duties and Responsibilities:

Build Quality into all aspects of their work by maintaining compliance to all quality requirements.

• Minimum 5 Years experience per below with BS 3 - 5 Years with MS
• Must have:
• -Python experience
• -Test infrastructure verification and validation experience
• - System architecture
• - System verification
• -Excellent statistical analysis
• -Risk assessment experience
• -Excellent collaboration and communications Medical device experience highly preferred Former regulated environment required

• Sponsorship is not available for this position

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

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