Job Opportunities

Process Engineer

Job Title: Process Engineer

Summary:  The process engineer is responsible for the installation, qualification, operation, supervision of a biomedical device assembly facility clean room.  The role includes developing standard operating protocols, training materials, scheduling, and reporting activities for manufacturing within a regulatory controlled environment.  This includes operations of the facility, electrical, process equipment , HVAC, high performance air filtering, and cleaning.

The process engineer is responsible for handling multiple projects for the lifecycle of the controlled environment including commissioning  and qualifications activities to decommissioning.  He or she will be responsible for organizing, budgeting, scheduling, carrying out, instruction, and supervision of the project as directed by company leadership.

Company Overview: Hibernicor is an innovative medical device company that manufactures single use disposable containers which will be marketed for sale in the US and Europe.

Key Position Responsibilities:

The process engineer will be responsible for defining the critical quality attributes, and process parameters in the clean room including particulate levels, relative humidity, and temperature parameters in a GMP compliant manner. The engineer should define the clean room requirements in a user requirements document and solicit input from qualified vendors following established ISPE/ASTM methodologies and guidance.

The process engineer will perform and maintain a risk assessment for all the critical process parameters including quality assurance, quality control, commissioning, validation, manufacturing safety, automation, and project management.  This may include researching, developing and acting on plans  using in depth knowledge of ISO and 21 CFR Part 11 and other regulatory guidelines.

The process engineer will prepare commissioning and qualification protocols, standard operating procedures, and work instructions as needed for equipment and facility operations aligning with an overall master validation plan.  The engineer should be able to write the validation master plan, commissioning and validation documents for the clean room, HVAC systems, and equipment; specifically design qualification, installation qualification, operational qualification, and procedure qualification documents (DQ/IQ/OQ/PQ).  The engineer should be able to prepare checklist and complete inspections that includes both static and dynamic exhaustive testing of systems or major system components to support the qualification of equipment or system based upon manufactures acceptance test or user requirements specifications (FAT/SAT).

The process engineer must of have experience and understanding of clean room facility and requirements.  In addition the engineer must have knowledge of computer system validation requirement and preparation and execution of protocol related to computerized systems provided by vendors. The engineer will supervise with the help of contractors on daily basis with follow up and completion of qualifying activities and GMP documentation including: clean room fitment, filter, HVAC and software automation testing and audit trail verifications.

The process engineer will supervise progress of the commissioning and qualifying activities on a periodic basis and hold status meetings with the stakeholders.  The engineer will maintain alignment to the budgetary guidelines, quality and safety standards.  The engineer will need to maintain and update quality control documents in an existing electronic GMP compliant document management system.

The process engineer will need to manage multiple task to coordinate projects timelines and work collaboratively with vendors and stakeholders to mitigate risk, facilitate problem solving, and to reduce  or avoid delays.

Minimum employee qualifications:

Bachelor degree in engineering or science field
US citizen or permanent resident
A minimum of 3 years of professional experience leading, initiating and completing projects.
Experience with statistical data and an ability to effectively perform technical analysis
Experience making risk based decisions
Experience navigating and adhering to structured system requirements (i.e. Quality Management System)
Demonstrated effective communication of technical information, both verbally and in written reports
Ability and willingness to respond beyond normal business hours (including weekends).

Desired position skills in:

Working in a clean room environment and understanding facility infrastructure, as it relates to supporting a clean room.
Working knowledge of environmental standards (FDA 21 CFR Part 11, ISO 14644, ISO 14698, etc.)
Understanding  of bioburden, endotoxins, particulate, etc. and conducting statistical analysis thereof.

Reporting: The packaging engineer reports to the quality manager and company director.

Location: The location of the job is at the company offices either in the US. If travel may be necessary to accomplish the job responsibilities and is anticipated to be no more than 10% of the employment.

Type of Employment: The position is full time.

Salary Range & Benefits: The salary and benefits are commensurate with the applicant’s qualifications and experience.

How to Apply: Please submit a cover letter, resume and 3 references with contact information. We will respond to suitable candidates by email to setup an initial telephone interview.

Contact Information:

HIBERNICOR LLC
253 Ridge Drive
Jackson, MS 39216
Email:

Request for Proposal – Building Master Plan

Section 1.  Overview

1.1    Purpose

Hibernicor intends to develop a master plan for a multi-story multipurpose building designed with the primary objective of medical device manufacturing in a urban area with access to an international airport and multiple commuting options.  The building shall have a total floor area not to exceed 100,000 square feet with an emphasis on providing employees with plenty of natural lighting in all possible areas.

Basic outline of possible floor configuration is as follows:

  • Roof Top: Terrace with Small Garden, Roof top bar, Generators, Water supply
  • Floor : Gym, Mens/Womens Locker Rms & Showers, Hotel rooms, Child care
  • Floor: Kitchen & Dining Room, Terrrace
  • Floor: Offices, Meeting Rms
  • Floor: Offices, Dry and Wet Lab, Operating Rm
  • Floor: Clean Room, IT
  • Floor: Quarantine, Storage, and Production Assembly Areas
  • Ground Floor: Lobby & Conference/Presentation Room, Security, Reception, Coffee Bar
  • Basement: Shipping Receiving, Storage & Parking, and Mechanical

1.2    Business Context

Hibernicor is medical device manufacturing company sponsoring the development of the Asporto device and software.  Hibernicor’s mission is to provide the standard of care for increasing the quality and quantity of donor hearts available for heart transplantation. Asporto software is an integral part of the business operation which will provide: 1) a safe and reliable means to controlling pump operation, organ perfusion, and monitoring during transportation of the donor heart; 2) controlling the usage of the individual heart containers (for sales purposes); and 3) providing clinical data for auditing each donor heart transport.

1.3    Scope

The purpose of creating the building master plan for a non-site-specific building project for capital fundraising. The master plan needs to be adaptable for site-specific requirement in a subsequent project phase.

The project consultant should provide planning services for all the functions for the building allowing for adequate area and layout requirements based upon user input. The layout requirements and technical data should be incorporated into the master plan.

1.4    Limitations

The following services are not requested:

  • Process development or process assessment for laboratory or production functions
  • Site specific planning (site preparation, local regulations, etc.)
  • Project control (estimates, activity breakdown, change control, progress monitoring, reporting, project documentation, or execution).
  • Contract formulation

Section 2.  Building Concept

This section describes the base requirements for the building including:

  • Project organizational chart describing authority and reporting structure
  • Building functionalities
  • Economic boundaries, overall budget estimation, budgeting milestones
  • Project timeframe as an execution plan including: an estimated overall project duration, phasing for different functions, expansion options.
  • Operational boundaries; maximum number of staff, material flow for specific process requirements
  • Establishment of an initial building design with functional areas and fixed points such as structural walls stairs, windows, and installed services.
  • Definition of based personnel and material flow through the building.
  • Contracting strategy based upon optimal resource allocation and risk mitigation.

The consultant should prepare deliverables of 3D CAD drawings, functional layouts, and building sections specifying the building concept.

2.1  Manufacturing Program

Hibernicor will provide the manufacturing program as well as the block flow diagrams including all manufacturing process steps within the clean room area, laboratory, electronic assembly, and the packaging areas.  The block diagrams will function as a basis for further details to be determined for dimensioning of manufacturing, storage, and logistical areas.

2.2    Manufacturing and Lab Equipment

Hibernicor will provide the consultant with a list of all manufacturing equipment.  From this list the consultant will determine the energy, space and media requirement.

2.3    Material Flow and Logistics

A logistics concept will be developed to integrate the following aspects:

  • Storage demands (temperature, quarantine, hazardous substances, etc.)
  • Material flow including staging and zoning concepts
  • Space needs for storage and staging
  • Waste logistics (solid, liquid, and gas)

The logistics concept should serve as the basis for the physical layout.

2.4    Personnel and Material Flow Clean Room Concepts

The consultant should develop and overall concept for personnel and material airlock process for a clean room including a pictographic drawings, and material airlock processes in a tabular format.

2.5    Layout

The total area demands for all functions will be determined and summarized in an area program to form the general building concept. These conceptual interior block architectural layouts (at 1:200 scale) should have a maximum of three different options.

The block layout should include the basic information:

  • Main equipment setup
  • Personnel flow (manufacturing, lab, and common areas)
  • Material and waste flow
  • Hygiene zones
  • Pressure zones

Laboratories should be classified by wet and dry and zoned for 100% outside air supply.

Wet labs require chemical resistant work surfaces and cabinets that are liquid tight to contain spillage. Chemical and glassware storage and fume hoods are significant factors in space planning and furniture selection.

Dry analytical labs typically require a lot of large shelving to support instrumentation. Height-adjustable work surfaces may be required to allow large counter-mounted equipment to be placed at a comfortable operating height or be completely removed to provide instant space for the addition of floor mounted equipment.

Laboratory should be zoned by a designated spaces:

Options for laboratory types should be considered for optimal workflow.

  1. A) A single corridor lab design with labs & offices adjacent to each other
  2. B) A single corridor with office clustered at the end or in the middle.
  3. C) A single corridor with office clusters directly accessing the main labs

2.6    Utilities

The utility concept, written description, and schematic sketches for the new building will be defined to include:

  • Heating, ventilation, cooling, and air conditioning (HVAC)
  • Clean air
  • Pressurized air
  • Technical gases
  • Drinking water, de-ionized water, and wasted water.
  • Electrical utilities, building automation, security, and communication
  • Clean media (WFI, clean steam, clean gases)

The consultant should prepare a media systems description to define the space requirements for the technical and mechanical areas to be integrated into the building layout.

2.7    Key Site Features

The building concept should also encompass multiple functions for a modern medical device manufacturing workplace including:

  • Receiving area
  • Secure quarantine room
  • Electrical component subassembly
  • Information Technology room
  • Device assembly and storage
  • Clean room
  • Packaging area
  • Wet bench lab and dry chemistry lab.
  • Offices and meeting rooms
  • Gym, Day Care, Kitchen and Dining Rooms
  • Lobby or reception area
  • Large multifunction conference room
  • Shipping area
  • Parking

2.7    Building Surface Visualization

The consultant should prepare a minimum of 5 different building concept sketches 3D hand drawings with elevations and sections.  One concept will be finalized as surface rendering in CAD.

2.8    Common Design Mistakes

Several mistakes that are common in laboratory planning occur from a lack of knowledge, insufficient planning or down grading in the wrong areas to reduce costs.  Design mistakes should be avoided by adhering to GMP design guidelines.

Common mistakes are:

  • No allowances made in the structure for adding new drains or fume hood exhausts in the future
  • Lab modules are too shallow; not enough space
  • No way to expand the facility in the future
  • Critical systems and equipment are not connected to a continual power source or an emergency power system
  • Inadequate distribution system for data cables; no cable trays
  • HVAC is not sufficient to maintain adequate temperature levels or supply makeup air for fume hoods
  • Electrical system lacks sufficient power, appropriate distribution or enough outlets
  • Too little space provided for using and servicing equipment
  • Location of fume hoods is too close to primary exits
  • Not all lab areas have adequate access to primary exits

Section 3.  Project Timeline and Methodology

The consultant will compile a conceptual project timeline for planning and realization of the major milestones based upon practical and theoretical experience.  Options based upon budget, schedule, cash flow, project complexity, risk mitigation, team composition, and project goals should be used to determine a rank order for possible project delivery methods.

  • Design-Bid-Build
  • Construction Management
  • Engineer-Procurement-Construct

3.1    Success Criteria and Metrics

The consultant should identify and define metrics to provide priority and goal setting for the project conceptual design based upon external benchmarks and sources of information.  Value engineering concepts should be utilized to design in optimal value for the initial and long term investment.

3.2    GMP Compliance

The building should be of suitable size, constructed, and located to facilitate cleaning, maintenance and operations. The building layout shall be designed to allow production and components to flow through the building to prevent contamination or mix-ups.

The consultant should define which standards comprise GMP compliance for this building plan.  The standards should be provided in tabular list form with title and publication date, they should be appropriately referenced in the plan.

3.3    Validation Planning

Because the processes described in the building master plan are used to create the actual layout of the facility, the design should be consistent with industry standards and regulations that can be validated following construction.  During designing, experts in different disciplines must coordinate efforts so that the individual design elements align to produce a facility the meets GMP.

3.4    Constructability

The design of the building should be constructible and should have be defined by its constructability; that is the ease and efficiency with which the structure should be built. The design documents should be easy to understand and interpret.  Experienced construction knowledge should go into the conceptual planning and design.  Ideally the building master plan would be independently reviewed by an executive with a minimum of 10 years of experience in pharmaceutical and/or hospital project management and construction.

3.5    Construction Logistics

The overall project development plan preliminary schedule should provide a time frame that has milestones that have a clear timeline and tasks which is understandable from an expert in construction; thus having steps which are logically oriented to prevent unnecessary significant delays or cost overruns in the execution of the project.

3.6    Cost Estimate

The cost estimate should be delivered with an accuracy of +/-30%.

Section 4.  Documentation

The project language will be in English. All documents will be prepared and delivered in English language without typos, grammatical, or spelling errors.  All decision making processes and planning results will be documented and structured in a traceable form with dates and a versioning scheme.

4.1    Documentation File Formats

All intermediate documentation will be an electronic format. Final documents will be provide in both soft and color printed hard copy with blue ink signatures.

Soft Copy:

Microsoft Office 2007, compatible with 2003.

Adobe Portable Document Format (unlocked, Version 1.5, Acrobat 6.x)

Computer Aided Design (CAD) vendor neutral vector format (.step)

4.2    Documentation Coordination

The consultant should provide a plan for optimal design coordination including recommendations for:

  • CAD platform and version
  • CAD standards, procedures, and conventions
  • Drawing numbering standards
  • Deliverables: 2D schematics, piping and instrumentation diagrams, isometrics, orthographs, etc.
  • Project closeout requirements – drawing turnover to construction.

4.3    Document List

The consultant should provide a final plan including the documents meet the sections outlined in this document.

Section 5. Project Organization

People complete projects.  The project organization structure and the selection of the right project team members and their activities are the two most important tasks for this building plan.  The formal leader for this project is Hibernicor’s President (Dr. Andrew Rivard).

It is important that all members of the project team understand the overall goals and objectives of the project, the roles and responsibilities of the team members, project milestones, and measurements for success, and approach for project execution.

The consultant should define a roles and responsibilities matrix using a spreadsheet to define the team members contributions.

5.1    Timeline

The final building master plan should be completed in 10-12 weeks.  A kick-off meeting may be used as well as workshops as needed.

5.2    Travel Expenses

The proposal should not include any travel expenses for the consultant team.

5.3    Acceptance of Services

The individual plan should be divided into parts which have clear deliverables and time frame for payment.

Additional work beyond the scope of this request for proposal needs to be agreed upon with a signed written agreement prior to commencement of such activities.  Work completed beyond the scope of the proposal without prior approval will not be reimbursed.

Director of Quality Affairs

Title: Director of Quality Affairs

Summary: The director is responsible for the creation, strategic implementation and maintenance of the quality system and processes, in compliance with international and United States federal laws.  The director will correspond with Food and Drug Administration and European Union notified bodies as a representative of the company during the preparation and submission of applications for regulatory approval for both new medical products and changes to existing products.  This a leadership position reporting directly to the company President for all performance measures for quality improvement and compliance necessary to support the company operations within the regulatory guidelines.

Specifically, the director must ensure company compliance with global regulations for design controls, good manufacturing processes, facility registration, device listing, licenses, safety reporting, complaints, clinical trial requirements, post-market surveillance, product labeling, and permissible marketing communication. The regulatory strategies are expected to improve the scientific or technical direction of product design and/or development in a cost effective manner with minimal administrative burdon.

The director will provide leadership and subject matter expertise in global regulatory affairs to ensure functional excellence and is responsible for both internal and external quality control.  He or she will interact with global health authorities and establish collaborative relationships with other key influencers.   The director should be persuasive and promote a positive working environment conducive to a productive team atmosphere.

Company Overview: Hibernicor, LLC is an innovative company responsible for designing, manufacturing, assembling, packaging, processing and labeling medical devices and software.  Asporto is Hibernicor’s signature product that allows for the improved and prolonged preservation of the donor heart. Asporto will be marketed for initially for sale in the US and Europe.

Key Responsiblities:

The Director of Quality Affairs will work closely with marketing efforts, research and development, and manufacturing, to develop the regulatory strategy to gain market approval for Asporto as well as other new or modified devices/combination products consistent with company objectives.

The director will interpret national and international regulatory requirements and manage resources needed to support and execute proactive strategies needed to further the global growth of the business.   He or she will lead the preparation, submission, and defense of complex regulatory applications including: premarket approvals (PMA), new drug application (NDA), biologic license applications (BLA), pre-market notification (510k), investigative device application (IDA), combination devices, Notified Body/Competent Authority applications, Health Canada licenses, and submissions to other international health authorities.

The director will also review and interpret regulatory rules as they relate to internal company products and processes. Importantly, the directory will develop quality system policies and procedures to ensure compliance with FDA 21 CFR, Part 820, Quality System Regulation and EU requirements as well as any other regulatory markets. Specifically, the director will guide product development teams in developing new products in accordance with design control, define needed quality metrics, and coordinate data collection from various functions with simplified and efficient document control processes. The director will coordinate and consult in a positive and friendly manner with company stakeholders regarding the quality, content, format, and assembly of regulatory documentation. The director will also ensure subcontractors meet regulatory compliance requirements and are approved by regulatory affairs at the initiation stage.

The director will represent Hibernicor as the official correspondent with external organizations including the FDA and other global health authorities, sponsors, and other organizations; serve as a primary regulatory contact and correspondent during all pre-market activities and monitor Hibernicor supplier’s performance to support the regulatory approval and commercialization efforts in global markets.  Specifically, the director will ensure all periodic national and international regulatory registrations or filings, licenses, listing, and other certifications are maintained to established timelines as required for regulatory compliance and company objectives.

The director will perform periodic audits and advise management of any nonconforming material or process related issues and make recommendations for improvements or administrative disposition.  She or he will set-up and oversee inspection and device dossier activities, manage internal audit activities and coordinate corrective actions. Any change notifications will be evaluated and submitted regulatory bodies as needed. The director will manage the safety reporting and complaint handling processes to ensure corrective actions are established and that root-cause elimination are completed for all identified issues.

The director will ensure preclincial and clinical studies are designed and executed in full compliance to Good Laboratory Practice (GLP), Good Clinical Practice (GCP), ICH, and other pertinent global regulations.

The director should possess in-depth understanding and will actively review evolving laws/regulatory requirements to maintain a proficiency in worldwide regulations and will proactively communicates pertinent information to the company leadership in written and oral presentations.   The director will personally conduct ongoing company-wide trainings on FDA and ISO requirements in a clear and concise manner.   The director will ensure all employees within the assigned teams understand and comply with all applicable company policies and procedures as well as local, state and federal laws and regulations. In regards to advertising and promotional literature the director will assist marketing efforts by providing examples for product labeling and promotional materials.

The director may interpret and provide recommendations for change of company-wide policies and practices, as well as developing written policies appropriate for the company operations and goals.  The director will regularly interact with industry executives, senior management, and major customers.  These interactions frequently will require negotiation skills to influencing customers and/or senior level leaders in matters of significance to organizational quality.  The director is an internal expert resource to provide regulatory consultation in respect to company’s strategic goals.  The director may assist with other duties such as hiring, coaching and counseling employees, including performance reviews, disciplinary action and terminations. The director may also provide leadership guidance, and coaching to maintain an engaged and productive workforce.

Qualifications:

Master’s degree in a life sciences or biomedical engineering fields, fluent native command of written and spoken English language,

Minimum of 10 years of quality management, quality assurance and regulatory affairs experience in the medical device, pharmaceutical, biotechnology, contract research, or similarly regulated industry.

Regulatory Affairs Certification (RAC)

Demonstrated ability to write technical documents and persuasive presentations to competent authorities.

Encyclopedic knowledge of FDA, QSR and ISO standards, regulations and requirements.

Reporting: The Director of Quality Affairs reports directly to the company president.

Location: The location of the job is at the company offices either in the US or UK. If travel is necessary to accomplish the job responsibilities it is anticipated to be no more than 10% of the employment time.

Type of Employment: The position is full time.

Salary Range & Benefits: The salary and benefits are commensurate with the applicant’s qualifications and experience.

Direct Inquiries, Cover Letter, References, and Resume to:

Dr. Andrew L. Rivard
President and Founder

HIBERNICOR LLC
253 Ridge Drive
Jackson, MS 39216
Office: 769-257-6146
Email:

Packaging Engineer

Job Title: Packaging Engineer

Summary: This position is for an engineer to develop and design processes and procedures to manufacture and assemble packaging, and labeling for a sterile single use barrier film container for Asporto. This position is primarily research and development, and the engineer is responsible for product design, development, and support activities during pre and post regulatory approval.

Company Overview: Hibernicor is an innovative medical device company that manufactures Asporto; a heart preservation device that allows for the improved and prolonged preservation of the donor heart using a revolutionary pharmaceutical solution. Asporto will be marketed for sale in the US and Europe.

Key Position Responsibilities:

The packaging engineer will perform hands-on work required for the support of development toward commercialized single use products.  The engineer will work together with the company leadership, quality, and sales personnel to develop a successful product line.

The engineer will work closely with the quality manager for package testing (drop test, burst test, distribution simulation, stability studies) using ASTM and ISO test methods in our on-site package testing labs.  Conduct packaging machine evaluations to determine the optimum set-points across multiple equipment platforms focusing on sealing and machine performance, written test results, and conclusions.

He or she will serve as package testing leader for an innovative medical package line and will compose procedures and work instructions for testing laboratory equipment and clean room manufacturing operations, including: test procedures, test schedules, maintenance contracts, and capital spend requirements for new equipment.  This will include any troubleshooting and mechanical knowledge to repair or replace current and new packaging equipment.  An ideal candidate for the position would be able to use Computer Aided Design and Manufacturing (CAD/CAM) to manufacture new packaging equipment and coordinate the part production, assembly, build and testing of the new equipment. It is important the engineer follows standard job safety procedures including completion of regular safety audits, inspections, and safety analyses for new equipment/processes and base equipment/processes.

Minimum employee qualifications: 

Packaging or materials technology experience in the medical device, pharmaceutical, or biotech industry and/or experience with sterile products or aseptic systems.

A bachelor’s degree in a science-related field is required.

Experience working in laboratory environment dealing with packaging materials and machinery

Strong attention to detail and ability to document test plan, procedures, and results.

Possess good mechanical aptitudes, math and basic computer skills including Excel, PowerPoint, and Word.

Candidate must have strong interpersonal skills and work well independently and in a team environment.

US or UK citizen or permanent resident

Desired position skills in:

CAD (Inventor, Autodesk, Revit, AutoCad (2D and 3D), Solidworks or Pro-E solid modeling systems
CAM (5-axis machining, water-jet, laser/plasma cutting)
3D printing (metal)
Project lifecycle management
Electromechanical systems
Compressed air systems
Polymer chemistry
ASTM and ISO standards experience.

 

Reporting: The packaging engineer reports to the company director.

Location: The location of the job is at the company offices either in the US or UK. If travel may be necessary to accomplish the job responsibilities and is anticipated to be no more than 10% of the employment.

Type of Employment: The position is full time.

Salary Range & Benefits: The salary and benefits are commensurate with the applicant’s qualifications and experience.

How to Apply: Please submit a cover letter, resume and 3 references with contact information. We will respond to suitable candidates by email to setup an initial telephone interview.

Contact Information:

Dr. Andrew L. Rivard
President and Founder

HIBERNICOR LLC
253 Ridge Drive
Jackson, MS 39216
Office: 769-257-6146
Email:

Geoportal Website Developer

Job Title: Geoportal Website Developer

Summary:  This position is for a talented early career web developer who has full stack experience with Python and Django to develop a world class web-based software product. We are seeking an applicant capable of producing some front end and most back end architecture for a web portal project to harness the power of spatially enabled data. The applicant should be able to manage several projects or tasks simultaneously with self-motivation and problem solving skills as well as be able to communicate potential solutions clearly to company leadership.

Company Overview: Hibernicor, LLC is a private innovative company responsible for designing, manufacturing Asporto; a heart preservation device that allows for the improved and prolonged preservation of the donor heart.  Hibernicor is also one of the first companies in the United States to develop an electronic record system designed solely for pre-clinical research purposes. The company is expanding at the frontier of medical innovation and globalization of healthcare information technology.

Key Position Responsibilities:  We seek a motivated, accountable, and experienced software developer who will be able to understand: the needs of the users, and the business requirements.  The applicant should have the ability to work unsupervised and be able to deliver testable and documented solutions. Experience with software requirements, design, development and testing of applications is essential.  Primarily duties include web development using an existing GIS dataset, GUI modifications and backend database in a multi-user environment with security and login controls.

The developer will create an easy to use geoportal using GeoDjango, PostGIS and Javascript (Openlayers) to visualize spatial data allowing users to perform easy-to-use spatial analyses. The developer will create the front and most back-end software for a portal project with hypertext transfer protocol (HTTP), cascading style sheets (CSS) and server-side scripting language (PHP).  The developer will utilize source code versioning (Subversion or Git) collaboration systems as needed.

A successful candidate should remain abreast of industry technical trends and new developments to maintain current skills and changing software programming languages.

Software application requirements:

Django, GeoDjango, postgis
Java / J2EE, Javascript (Openlayers)
Cascading Style Sheets, CSS
XML, HTML, TML, FTP, Telnet
PHP
Active Server Pages, ASP.Net
Structured Query Language, MS SQL Server
PostgreSQL
MS Office, Word, Project, and Visio
MS Access,Visual Basic, VB
Visual Basic for Applications, VBA, VB.Net, VBScript
Photoshop, Flash

The applicant should be able to create software with the following characteristicsAdaptabilityAvailability, CorrectnessDiscoverabilityFlexibilityMaintainabilityReliabilityReusability, RobustnessTestabilityUsability

Minimum employee qualifications:
Bachelors degree or equivalent combination of education and experience or
Bachelor’s degree in computer science, mathematics, or related field or
Bachelor’s degree in MIS/IT/Programming and
Experience working with appropriate programming languages, operating systems and software and
Experience with relational databases.
US or UK citizen or permanent resident

Reporting: The database programmer reports to the company director.

Location: The location of the job is flexible and occasional travel will be necessary to meet at the company offices either in the US or UK.

Type of Employment: The position is contractual and full time.

Salary Range & Benefits: The salary and benefits are commensurate with the applicant’s qualifications and experience.

How to Apply: Please submit a cover letter, resume and either a code sample or a link to your personal Git repository. We will respond to suitable candidates by email to setup an initial phone interview.

Contact Information:
Dr. Andrew L. Rivard
President and CEO

HIBERNICOR LLC
253 Ridge Drive
Jackson, MS 39216
Email:

Web Content Editor

Job Title: Web Content Editor

Summary: Do you have a passion for healthcare information which is easy to navigate, easy to search, and easy to read?  We are looking for a news editor to help us organize a novel website devoted to quality heart transplantation news.  The candidate should be well versed with advanced internet curation tools and able to compile complex, varied sources of content into a simple, intuitive presentation for reader engagement.  Are you a medical informationalist?  Do you love healthcare and biomedical science news?  Hibernicor is in search for an editor to retrieve, critically analyze, and synthesize healthcare information in a flexible work setting.

Company Overview: Hibernicor, LLC is an private innovative company responsible for designing, manufacturing Asporto; a heart preservation device that allows for the improved and prolonged preservation of the donor heart.  Hibernicor is also one of the first companies in the United States to develop an electronic record system designed solely for pre-clinical research purposes. The company is at the frontier of medical innovation and globalization of healthcare technology.

Key Position Responsibilities: Hibernicor’s optimal news editor has a medical mindset and desires to be an integral part of providing quality health care information to improve patient care by helping physicians, allied health professionals, researchers, and the general public to stay abreast of new developments with authoritative heart transplant information.  The content editor will provide design input into and manage an internet blog-like website to bridge the information chasm between scientific and lay public information.  A portion of the job responsibilities includes periodically researching source material with  keywords, keyphrases, and nomenclatures specific to topics or audience.  Information should be validated for accuracy or veracity of the sources.

The news editor is also expected to collaborate with the company stakeholders to maintain information relevance and quality by maintaining a contact list of the who’ who in heart transplantation.  The editor may also assist the company with fund raising, marketing, business and other information technology initiatives.  The responsibilities include digital content sourcing, authenticating, organizing, classifying, and synthesizing to maintain editorial cohesion. The news editor will attend the industries’ largest international conferences for special in-depth audio or video recorded interviews for original publications.

Significant advantages of the part-time position include a flexible work environment which is location independent.  The job position is ideal for a medical librarian, pre-medical student, or allied health-care professional with a specific interest in heart transplantation and an unique ability to provide editorial expertise in both written and visual communication.

Requirements:

  • Experience in written content analysis and content management delivery.
  • Editorial-minded; able to select and deliver the best content from across multiple informational sources.
  • Ability to concentrate in a changing agile environment and juggle multiple priorities.
  • Excellent organizational skills, with a strong attention to detail for content presentation.
  • Ability to determine criteria for critical, important and non-essential news information.
  • Collaborate with the webmaster to ensure consistency across content areas and taxonomy for sharing viewpoints, opinion, perspective, commentary, and valuable insight.
  • Great collaboration and communication skills; able to drive cross-functional initiatives and deliverables and build strong networking relationships.
  • Pro-actively analyze data for new insights about key media topics and influencers.
  • Work to customize and configure datasets, deliver custom reporting, and create dashboards.

Minimum Employee Qualifications:

  • Bachelor of Science or Arts degree.
  • Excellent computer skills and natural comfort learning to use advanced analytical software.
  • Tablet or phone with 3G cellular and WiFi internet-browsing capability.
  • Laptop or desktop computer with broadband internet connectivity.
  • US or British citizen or permanent resident.

Location: The location of the job is flexible and occasional travel may necessary to meet at the company offices either in the US or UK.

Type of Employment: The position is a part time contractor with minimum time commitment of 4 hrs a week.

Salary Range & Benefits: The salary is $15/hr payable monthly.  There are no benefits.

Contact Information:

HIBERNICOR LLC
253 Ridge Drive
Jackson, MS 39216
Email:

Embedded Product Design Engineer

Job Title: Embedded Product Design Engineer

Summary: A product design engineer is needed to design, program, prototype, build and test novel medical instruments. The engineer will be responsible for the hardware and embedded firmware of microcomputer controlled products and they will oversee the initial manufacturing.

The engineer will take a key role in researching, developing, and commercializing a life-enhancing and life-saving technology. The product design includes general analog and digital circuit design, interfacing microcontrollers to sensors and actuators, embedded software design, and programming; including software coding for sensor data acquisitions, real time control, motor control and user interfaces. The applicant will need to be as comfortable with hardware debugging and they are with programming embedded systems.

The applicant’s responsibilities include developing and integrating the firmware with hardware, debugging, and project documentation with a regulated medical environment.

Company Overview: Hibernicor, LLC is an innovative company responsible for designing, manufacturing, assembling, packaging, processing and labeling Asporto; a heart preservation device that allows for the improved and prolonged preservation of the donor heart. Asporto uses a mission-critical embedded system with the ultimate outcome to improve heart transplant patient’s lives. The company is part of cutting-edge medical science which is at the frontier of industrial innovation and globalization of healthcare technology.

Key Position Responsibilities: The embedded system developer will design a computer system that controls a peristalic pump with real-time computing constraints. The embedded microcomputer is part of a complete heart preservation device often including a custom designed printed circuit board and thermoelectric (Peltier) cooling module.

The applicant must have hands-on experience in analog and digital circuit design and analysis, electronic test equipment (oscilloscopes, multimeters, logic analyzers), hardware debugging, and microcomputer interfacing. Experience with electrical schematic design and printed circuit board layout is essential, as is general knowledge of embedded processors and digital hardware circuits.

The applicant should also have experience in embedded programming and real-time control systems such as PC based control, motor control or robotics. They will use compilers, assembles, and debuggers to develop embedded firmware. The engineer applicant must be skilled in the real-time programming required of multi-tasking or multi-threading applications and they must have excellent debugging skills in the C-programming language.

The developer will perform mechanical assembly including soldering of PCB (Printed Circuit Board) assemblies, building and routing of cable and harness assemblies, as well as document procedures to perform necessary electro-mechanical assembly. The developer will also assemble prototype systems and components with visual and mechanical inspections of in-process components and assemblies, in addition to performing troubleshooting to determine cause of system failures during assembly.

Desirable applicant characteristics include talents for understanding how to build a reliable, low power, and low cost devices. The design architecture should ensure functioning within a highly secure & reliable environment. As needed for individual productivity, the developer will obtain software licenses by procuring information from vendors; recommending purchases; testing and approving products to maintain company competitiveness while understanding fiscal and budgetary constraints.

Future responsibilities may include working with networking standards and protocols such as TCP/IP and cellular, wireless, and global positioning system telecommunications standards and is expected that the applicant would learn new knowledge to meet the company objectives.

The developer will create embedded software code and hardware in accordance with design for manufacturability requirements in compliance with FDA and CE requirements. As needed, the developer may design and built test stations to assist quality control and manufacturing.

We are looking for someone with an obvious passion for engineering and building new things, as demonstrated by experience in embedded product design, robotics, communications, microcomputer board use, or application design.

Desired position skills in:

AutoCad (2D and 3D), Solidworks or Pro-E solid modeling systems
TCP/IP, GPRS, Cellular, WiFi
Serial Communication Interfaces (SCI): RS-232
Universal Serial Bus (USB)
Multi Media Cards (SD Cards, Compact Flash etc.)
Ethernet and Fieldbuses: CAN-Bus, LIN-Bus, PROFIBUS, etc.
Real time clocks, PLL(s), Capture/Compare and Time Processing Units
General Purpose Input/Output (GPIO)
Analog to Digital/Digital to Analog (ADC/DAC)
JTAG, ISP, ICSP, BDM Port, BITP, and DB9 ports.
Microcontrollers (68HC11, Freescale 68HCS12, Arduino, ST Microelectronics, Microchip, Atmel ARM)
Programing languages (BASIC, Forth, C, C++, Visual Basic, Java, PHP)
PCB layout and schematic design
Microsoft Office (Word, PowerPoint, Excel)
Design for Manufacturability (DFM)
FCC / Safety certification
IEEE Software Requirements Recommendations

The applicant should have the following personal characteristics: In addition to technical skills, the applicant will need strong communications skills (especially in technical writing), interpersonal skills, and the ability to manage priorities and deadlines. They must be inquisitive and open-minded, enjoy learning about new healthcare technologies and demonstrate the ability to see a project through to completion. The individual must also be self-motivated and be able to work independently as well as within small groups to implement technological change.

The applicant should understand how to problem solve and acquire new skills and techniques to succeed as the leader in their field. Examples of this include a desire to continuously learn and improve by attending conferences, maintaining personal networks, participating in professional organizations, and reading relevant publications.

Minimum employee qualifications:

Bachelor of Science Electrical Engineering or Computer Engineering
US or UK citizen or permanent resident

Reporting: The Embedded Product Design Engineer will reports to the project manager.

Location: The location of the job is flexible and occasional travel will be necessary to meet at the company offices either in the US or UK.

Type of Employment: The position is full time.

Salary Range & Benefits: The salary and benefits are commensurate with the applicant’s qualifications and experience.

Contact Information:

Software Developer – Database Analyst

Job Title: Software Developer – Database Analyst

Summary: This position is for a software specialist who has experience with relational database design, graphical user interface development, permissions and security, debugging, maintenance, and installation. The applicant must be capable of understanding federal regulations to develop and work with software requirements, specifications, verification, validation, and deployment.

Company Overview: Hibernicor is one of the first companies in the United States to develop an electronic record system designed solely for pre-clinical research purposes, using a commercially available program. This database incorporates features facilitating compliance with regulatory guidelines and allows for through and expedited quality assurance auditing of GLP compliance. This database also facilitates comparison of data obtained from testing new heart valves and medical devices with historical data, allowing for a risk-based data analysis. This database is modifiable, to meet both changing needs and new regulatory requirements.

Key Position Responsibilities:

We seek a motivated, accountable, and experienced software developer who will be able to understand: the roles within a surgical research laboratory, the needs of the users, and the business requirements. The applicant should have the ability to work unsupervised and be able to deliver testable and documented solutions. Experience with software requirements, design, development and testing of applications is essential. Primarily duties include software development using an existing Microsoft Access database, GUI modifications and backend database in multi user environment with security and login controls. In addition to technical ability, candidates must be analytical, detail-oriented, well-organized and possess strong oral and written communication skills. The candidate must have extensive experience with Excel and MS Access development and proficiency with Visual Basic for Applications programming including the ability to analyze, debug, and enhance existing VBA applications. The applicant should be able to manage several projects or tasks simultaneously with self-motivation and problem solving skills as well as be able to communicate potential solutions clearly. The position responsibilities may include database migration to a MS SQL Server with a web-based front end depending upon customer preferences.

Software application requirements:

  • MS Access,Visual Basic, VB
  • Visual Basic for Applications, VBA, VB.Net, VBScript
  • Visual Studio, VS.Net, Visual C#
  • Java / J2EE, Javascript
  • XML, HTML, TML, FTP, Telnet
  • Active Server Pages, ASP.Net
  • Structured Query Language, MS SQL Server
  • MS Office, Word, Project, and Visio
  • Crystal Reports
  • Photoshop, Flash
  • JavaScript, Java / J2EE
  • Cascading Style Sheets, CSS

The applicant should be able to create software with the following characteristics:

Adaptability – The data entry forms and tables should be adaptable so that new data entry fields can be created and the layout adjusted.

Availability – Information relating to each animal should be available to each user and only the specific record locked for data entry.

Correctness – Data saved to the tables should not change and should be saved into the correct field.

Discoverability – The user should easily navigate and learn the software without excessive training.

Flexibility – The effort needed to modify the operational program.

Maintainability – New forms can be added as needed and old forms retired.

Reliability – Downtime for changes and following crashes should be minimized during working hours.

Reusability – Code developed should be reusable for newer versions of the database or in another application.

Robustness – If incorrect data or steps are done by the user then the system doesn’t crash.

Testability – The system should be able to be tested so that it performs as intended in a typical user scenario as well as maximum database size.

Usability – The effort required to learn, operate, prepare input and interpret output with daily use of the database should not be slower than a paper based system:

Minimum employee qualifications:

Bachelor of Science Computer Engineering or
Bachelor of Science MIS/IT/Programming

US or UK citizen or permanent resident

Reporting: The database programmer reports to the company director.

Location: The location of the job is flexible and occasional travel will be necessary to meet at the company offices either in the US or UK.

Type of Employment: The position is full time.

Salary Range & Benefits: The salary and benefits are commensurate with the applicant’s qualifications and experience. Successful applications will undergo additional training and company support for learning medical procedural terminology (CPT codes), and international disease classification codes (ICD-9 and 10),

Contact Information: