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1) Licensed PM Shift Clinical Laboratory Scientist (CLS) Supervisor – Full Time Position (San Francisco Bay Area) J75SP
2) R&D Software Developer Medical Technology – Full Time or Contract Position (San Francisco Bay Area) L74HT
3) Program Manager-Molecular Diagnostics (MDx) – Contract to FTE (San Francisco Bay Area) P73BY
4) Clinical Laboratory Scientists (CLS)/Research Associate (RA) – Full Time Position (San Francisco Bay Area) BD64G
5) Sr./Staff Software Engineer – Full Time Position (San Francisco Bay Area) C64GH
1) Licensed PM Shift Clinical Laboratory Scientist (CLS) Supervisor – Full Time Position (San Francisco Bay Area) J75SP
DESCRIPTION:
The PM Clinical Laboratory Scientist Supervisor is responsible for supervising Clinical Laboratory Scientists and Clinical Lab Assistants, performing high complexity laboratory testing on patient specimens, interpreting and reporting patient results, performing quality control and quality assurance procedures, and complying with all applicable local, state and federal laboratory requirements. The high complexity nature of the work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask, flexibility with tasks and schedules, and the ability to work independently in a team environment.
Principal responsibilities include:
- Performance of laboratory tests, procedures and analyses according to the laboratory’s standard operating procedures.
- Performance, review and documentation of laboratory quality control procedures.
- Operation and maintenance of laboratory equipment.
- Preparation of reagents required for laboratory testing.
- Review, interpretation and reporting of patient results.
- Identifying and remedying problems that adversely affect test performance.
- Reporting all test quality and safety concerns to the Laboratory Director or Safety Officer.
- Preparing performing reviews on testing personnel within specified time-frames.
- Tracking training and competency of testing personnel.
EXPERIENCE AND QUALIFICATIONS:
- A successful track record and comfortable with a start-up environment.
- Must possess a valid California CLS license.
- A minimum of six years of relevant laboratory experience.
- Possess working knowledge of local, state and federal laboratory regulations.
- Strong computer skills, and automation experience preferred.
- Ability to analyze and problem solve basic issues that impact test performance.
- Strong communication skills with the ability to maintain open communication with coworkers, non-laboratory personnel, and managers.
- Previous supervisory skills a plus.
- Work the PM shift (3:30-12:00 or 4:30PM to 1:00AM, still TBD).
To apply for a position send your resume to Jobs@JGBBioPharma.com
2) R&D Software Developer Medical Technology – Full Time or Contract Position (San Francisco Bay Area) L74HT
DESCRIPTION:
- Design, develop and prototype pattern recognition, data collection and data processing algorithms
- Use various software tools for processing and visualization of the experimental data
- Work closely with interdisciplinary development team on acquisition and processing high quality data
- Participate in digital signal processing algorithm development
- Write documentation and white papers on algorithms, data processing and data presentation
- Participate in definition of features, functionality and other software requirements
EXPERIENCE AND QUALIFICATIONS:
- Excellent written and oral communication skills
- Experience in object oriented design and development
- Knowledge of Linux and Windows operating systems
- Experience in Qt and/or .NET frameworks
- Familiarity with source code control tools preferably Mercurial (Hg)
- Experience in grant proposal writing
- MS/PhD in Computer Science, Math or Physics
- Strong knowledge of pattern recognition and signal processing algorithms
- Strong knowledge of statistics and data processing
- Experience in MATLAB and Scilab
- Experience in software development using C++ or other object-oriented language
- Experience in data presentation and visualization
To apply for a position send your resume to Jobs@JGBBioPharma.com
3) Program Manager-Molecular Diagnostics (MDx) – Contract to FTE (San Francisco Bay Area) P73BY
DESCRIPTION:
The Program Manager for the Molecular Diagnostics (MDx) Business Unit manages the development of internally developed diagnostics products or companion diagnostics products co-developed with external partners. This responsibility requires involving departmental or cross-functional teams focused on the delivery of new products. Plans and directs schedules and may monitor budget/spending. Monitors the project from initiation through delivery. Organizes the interdepartmental activities ensuring completion of the project/product on schedule and within budget constraints. Has overall project management responsibility. In this role, direct people management responsibility is not required.
Essential Functions:
- Leads cross functional core team through product launch
- Develops project plan and timeline
- Coordinates with external Assay Partner teams to achieve project / product deliverables
- Be the internal expert in PCP process and IVD project management.
- Act as “mini GM” as leader of cross functional core team.
- Act as communication liaison with Business Unit Management to assure deliverables are met, appropriate resources are applied and team(s) remains focused and engaged
Competencies:
- Facilitative leadership skills, particularly the ability to influence stakeholders in other functions over whom the Project Manager has no direct authority. Must be a highly-motivated driver able to complete tasks by leveraging relationships and established goals.
- Has analytical skills, especially the ability to generate alternative solutions and manage risk by identifying criteria for trade-off decisions and helping to facilitate difficult conversations.
- Willingness to be flexible and adaptable in a complex, matrixed environment. The ability to adapt to changing needs and parameters caused by time, budget, or other constraints
- Discusses and presents factual information to other members of the team. Ability to convey very complex information in both written and oral form. Actively and constructively contributes to core team’s efforts through networking within the organization and effectively communicating to MDx management. Able to influence others and gain acceptance and build consensus.
- Ability to manage moderately complex projects and initiatives.
- Acts as a mentor/role model for team members.
- Demonstrates understanding of company’s external customer needs and how they affect business unit products and services.
- Makes decisions that involve the consideration of complex issues.
- Works autonomously and checks-in as decisions are made.
EXPERIENCE AND QUALIFICATIONS:
- The candidate will have 3-5 years of project management experience in IVD product development
- Working knowledge of design control and FDA QSR requirements
- Microsoft Project Management skills
- The candidate will have proven ability to execute through influence within a matrixed organization
- The candidate will have an undergraduate degree in science or engineering. Additional advanced degrees are preferred but not required
- In their repertoire, the candidate will be self-motivated & a driving force of execution in their current or past organizations
- Experience working with external collaborators; Negotiations skills; Leading through influence
- Strong written and verbal communication skills
- Strong presentation skills
- PMP certification is preferred
To apply for a position send your resume to Jobs@JGBBioPharma.com
4) Clinical Laboratory Scientists (CLS)/Research Associate (RA) – Full Time Position (San Francisco Bay Area) BD64G
DESCRIPTION:
Responsible for performing high complexity laboratory testing on patient specimens, interpreting and reporting patient results, performing quality control and quality assurance procedures and complying with all applicable local, state and federal laboratory requirements. The high complexity nature of the work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules and the ability to work independently in a team environment.
Principal responsibilities include:
- Perform laboratory tests, procedures and analyses according to the laboratory’s standard operating procedures.
- Perform, review and document laboratory quality control procedures.
- Operate, maintain and troubleshoot laboratory equipment.
- Prepare reagents required for laboratory testing.
- Review, interpret and report patient results.
- Independently identify and troubleshoot basic problems that adversely affect test performance.
- Report all concerns of test quality and/or safety to the Supervisor or Safety Officer
- Assist with final development of protocol and processes for a Laboratory Developed Test and perform other duties as assigned.
EXPERIENCE AND QUALIFICATIONS:
- Proven successful track record and comfortable with a start-up environment.
- Must possess a valid California CLS license, generalist preferred.
- Completion of a CLS training program at an accredited institution or clinical laboratory work experience within the last five years.
- Possess working knowledge of local, state and federal laboratory regulations.
- Computer skills a must, automation skills preferred.
- Ability to analyze and problem solve basic issues that impact test performance.
- Strong communicator with ability to maintain open communication with internal employees, managers and customers as needed.
- Must communicate effectively with coworkers and non-laboratory personnel
- Able to integrate and apply feedback in a professional manner.
- Able to manage daily test processing needs with high emphasis on quality.
- Ability to work as part of a team.
- Ability to perform repetitive tasks.
- High volume laboratory experience preferred.
- Training in molecular biology techniques preferred.
To apply for a position send your resume to Jobs@JGBBioPharma.com
5) Sr./Staff Software Engineer – Full Time Position (San Francisco Bay Area) C64GH
DESCRIPTION:
Primarily responsible for R&D and lab software development activities but may also participate in other corporate matters.
Principal responsibilities include:
- Creating and maintaining custom laboratory information management systems (LIMS) software primarily written in Java and C# to track process data and workflow queues.
- Creating/maintaining/tuning database SQL required to support LIMS functionality and other database centric applications used at the Company.
- Developing new software/systems to support delivery of data to customers,
R&D personnel and enterprise resource management systems using a variety of web-based programming tools.
- Mentoring junior software engineers and database developers to teach them coding techniques and good software development practices.
- Supporting end-users in a 24/7 production environment as needed.
EXPERIENCE AND QUALIFICATIONS:
- Proven successful track record and comfortable with a start-up environment.
- Experienced developer with skills in OOP using C, C# and/or Java in a client/server architecture.
- Experience with developing complex custom GUI and visual components.
- Experience database programmer with skills in writing complex SQL queries, optimizing stored procedures and data table performance. MSSQL experience preferred.
- Strong math and logic skills.
- Understanding of laboratory processes and workflow systems is a plus.
- Strong communicator with ability to maintain open communication with internal employees, managers and customers as needed.
- Able to integrate and apply feedback in a professional manner.
- Able to manage daily test processing needs with high emphasis on quality.
- Ability to work as part of a team.
To apply for a position send your resume to Jobs@JGBBioPharma.com
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