Healthcare Consultancy Group (HCG) serves the pharmaceutical, biotech, and device industries by providing strategic, scientific communications solutions at all…
From Healthcare Consultancy Group – 25 Jun 2015 06:17:06 GMT
10+ years of product marketing experience, at least 5 years of experience with executive and concierge health clinics….
From Human Longevity, Inc. – 25 Jun 2015 06:04:39 GMT
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Hands-on execution of all aspects of pilot plant purification. Responsible for preparation of buffers, media and other required reagents. Gilead Sciences, Inc….
From Gilead – 25 Jun 2015 05:20:14 GMT
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Hands-on execution of all aspects of pilot plant cell culture. Responsible for preparation of media, buffers and other required reagents. Gilead Sciences, Inc….
From Gilead – 25 Jun 2015 05:18:53 GMT
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Details: Since 1984, Synectics has been committed to aligning talented professionals with jobs they find challenging and fulfilling. Let us leverage our recruiting experience and our long-standing relationships with our clients to help you in your job search. To view a comprehensive list of jobs offered by Synectics, please visit our website at www.synectics.com . We offer a wide variety of positions in cities throughout the United States. Synectics is an Equal Opportunity Employer. Seeking a temporary third shift Process Development Associate for our BioProcess Development team to carry out fermentation and/or recovery experiments, record process data, and maintenance/ housekeeping within the San Diego Plant. The temporary Process Development Associate will assist in troubleshooting activities within the plant. Responsibilities: Preparing various types of media, solutions, and buffers that are prepared according to Standard Operating Procedures. Preparing, cleaning, in situ sterilization and monitoring of fixed vessel systems (40L and 500L tanks). Cleaning and operating downstream process equipment, including filtration systems and mixing tanks. Frequent use of aseptic technique in laboratory operations. Ensuring compliance with cGMP policies and procedures. Keeping equipment and laboratory clean, organized and communicating any maintenance issues. Frequent use of support equipment: pH meters, spectrophotometers, YSI, densitometer, Biosafety Cabinet/Laminar flow hoods, shakers, balances/scales, autoclave, microscopes and mixers. Collaborating with BioProcess Development team members, fermentation scientists, formulation scientists and R&D researchers on development and optimization of fermentation (40L and 500L vessels) and downstream processes (membrane separation, filtration and centrifugation). Performing data analysis and presenting results on process experiments. Revising and executing procedural Standard Operating Procedures. Maintain 100% compliance with EH&S policies and procedures.
Details: QA / Regulatory Affairs Specialist – Direct Hire – San Diego, CA We are working with a rapidly growing biomedical company that is searching for a QA / Regulatory Affairs Specialist on a direct hire basis in the Boston area. This is the ideal position for the professional that is looking to be working with world class technologies in state of the art facilities. There is also a very strong path to professional growth, development and the ability to move up in the company. Job Description: The specialist is responsible for maintaining and ensuring that the company quality system meets FDA requirements for class I medical devices (IVD and ASR). Also, ensures that products and their labeling meet all regulatory requirements (national and international). Essential Functions: – Manage and establish / maintain compliance with FDA QSRs (GMP) (including company registration, new product submissions, establishing FDA communication/channels for compliance on medical device listings/classifications, management of CAPA system) – Documentation Control Process and Documentation Change Control Process – Conduct internal audits and ensure closing of findings – Establish / maintain compliance with the EU market directive and the Canadian MDR (including CE Mark applications or self-declarations via technical files) – Working with R&D and manufacturing to develop validation protocols for production processes, and generating the final report covering the validation results and a recommendation for approval or disapproval for the release of the process to manufacturing – Ensure compliance of labeling and advertising for all products in a regulated class – Monitor and trend key quality objectives and present data to senior management during management review meetings Qualifications: – Minimum Education (or substitute experience) required: Bachelor of Science Degree Minimum Experience Required: – At least 5 years experience in Quality Assurance and Regulatory Affairs for Medical Devices. – Must have experience with scheduling and performing internal audits.
Details: Ref ID: 00400-130393 Classification: Accounts Receivable Clerk Compensation: $17.10 to $19.80 per hour Accounts Receivable A/R Clerk Assignment for a San Diego based Biotech. This temporary Accounts Receivable (A/R) Clerk assignment starts imm…
Details: Help us advance the practice of medicine. At Millennium Health, we believe our ability to attract the best people helps us transform the science of medication monitoring to improve patient safety and health care for those in need. Our vision for Millennium is to continue to respond to evolving health care challenges and provide the superior technology and service our customers deserve. To do that, we need creative, dedicated, collaborative people. Think you might be a fit? Millennium Health, based in San Diego, is a leading health solutions company that delivers timely, accurate, clinically actionable information to inform the right treatment decisions for each patient at the right time. The company shares a unified belief that everyone has the right to safe and effective medicine and aims to deliver on that idea by providing clinicians with effective tools and information to reach that goal. Millennium Health offers a comprehensive suite of services, including The RxAnte System, Millennium PGT SM and Millennium UDT SM , that can be applied together to better address the goal of better tailoring patient care. Revenue Cycle Manager Responsible for managing full Revenue Cycle Operations within National Central Business Office. Provide all management and leadership to Manager’s, Supervisors, Lead and Team Members overseeing Revenue Cycle functional departments. Areas include Data Entry, Error Processing/Eligibility, Data Management, Claims, Cash Posting and Customer Service on a day-to-day basis. Focus on Maximum reimbursement and compliance with department, XIFIN billing system and healthcare governing agencies. Partner with other related ML departments and their various stakeholders effectively. Improve processes by redesign, cost benefit analysis and technical solutions. Manage and support all Revenue Cycle functions and their related management team. Manages and drives tasks and processes to resolution by having a thorough knowledge of the billing revenue cycle through to cash posting and accounting methodologies. Have a working familiarity with the Health Level 7 interface (HL7), XIFIN Billing System, and MLIS Lab Systems. Support the management team in their efforts of recruit, interview, select and train new team members. Mentor existing management team exercising skill path offsite training, Millennium Labs University and Goal setting to improve overall communication; leadership; effective writing; coaching and other characteristics for proper management and mentoring. Design, develop and implement policy and procedures as necessary. Maintain all policy and procedure following document control protocol on a quarterly basis. Ensures the management team and all team members are trained and knowledgeable on new or updated policies and procedures. Provide and support supervisors with staff development activities. Foster a positive work environment and encourages staff development Manages time and attendance for staff as well as implementing disciplinary and corrective actions, approving/denying time off requests, conducting performance reviews, addressing complaints and resolving problems Support the supervisors in their efforts to plan and prepare work schedules and assigns employees to specific duties. Tracks department productivity and quality and prepares management reports Monthly monitoring and reporting of all account receivables for adherence to department standards for metrics. Meet cash goals and manage account receivables within approved levels. Implement system improvements, testing and production protocol. Design, Develop and Implement revenue cycle process improvements. Provides escalation for supervisors and department members and will contact accounts to resolved issues. Prepares monthly statistical reports for the Revenue Cycle Director and Vice President. Benefits We’re committed to supporting our employees every way we can, with generous health benefits, wellness programs, and discount programs. Here are just a few of our offerings: 100% company paid premiums for medical, vision, dental for employees and dependents Health Savings Account Dependent Care Flexible Spending Account 401(k) – Company contributes a percentage of total compensation to employee account on an annual basis, whether the employee contributes or not. We offer 2% match as well. Company paid life & AD&D insurance and buy-up options Company paid long-term disability insurance Paid vacation and sick time plus paid holidays Wellness programs – walking groups, Millennium sports teams, gym discounts, plus many more! Onsite micro-market
Responsible for leading the development and implementation of customer pull-through and push-through initiatives with the field leadership teams and being the…
From Biogen – 25 Jun 2015 03:51:08 GMT
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We are seeking a Development Engineer for a biotechnology company in San Diego, CA. This position is in our clients R&D department and will be responsible for…
From Kelly Services – 25 Jun 2015 03:09:46 GMT
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