ACAD
39.13
+1.06
+2.78%
AEMD
7.73
-0.12
-1.53%
APRI
1.61
-0.08
-4.73%
ARNA
2.75
+0.05
+1.85%
ATEC
0.59
+0.02
+3.51%
CNAT
3.85
-0.12
-3.02%
CRXM
0.34
-0.01
-2.86%
CYTX
0.37
+0.02
+4.73%
DXCM
88.01
-1.36
-1.52%
GNMK
9.51
-0.3
-3.06%
HALO
16.85
-0.69
-3.93%
ILMN
195.45
-2.66
-1.34%
INNV
0.101
-0.009
-8.098%
INO
7.09
-0.14
-1.94%
ISCO
3.58
-0.12
-3.24%
ISIS
51.57
-0.18
-0.35%
LGND
88.94
-3.48
-3.77%
LPTN
0.25
+0.01
+3.52%
MBVX
1.65
-0.04
-2.08%
MEIP
1.91
+0.05
+2.69%
MNOV
3.16
+0.02
+0.64%
MRTX
25.98
-1.86
-6.68%
MSTX
0.47
-0.01
-1.28%
NBIX
48.09
-1.54
-3.10%
NUVA
51.69
-0.46
-0.88%
ONCS
5.81
+0.05
+0.87%
ONVO
2.5
-0.14
-5.30%
OREX
2.75
+0.01
+0.18%
OTIC
21.56
-0.83
-3.71%
QDEL
20.76
-0.69
-3.22%
RCPT
231.96
0.00
0.00%
RGLS
8.45
-0.79
-8.55%
RMD
51.63
-0.28
-0.54%
SCIE
0.014
0.00
0.00%
SPHS
0.84
-0.01
-1.18%
SRNE
12.71
-0.61
-4.58%
TROV
5.94
-0.39
-6.16%
VICL
0.605
+0.004
+0.7327%
VOLC
18
0.00
0.00%
ZGNX
19.63
-0.87
-4.24%
ACAD
39.13
+1.06
+2.78%
AEMD
7.73
-0.12
-1.53%
APRI
1.61
-0.08
-4.73%
ARNA
2.75
+0.05
+1.85%
ATEC
0.59
+0.02
+3.51%
CNAT
3.85
-0.12
-3.02%
CRXM
0.34
-0.01
-2.86%
CYTX
0.37
+0.02
+4.73%
DXCM
88.01
-1.36
-1.52%
GNMK
9.51
-0.3
-3.06%
HALO
16.85
-0.69
-3.93%
ILMN
195.45
-2.66
-1.34%
INNV
0.101
-0.009
-8.098%
INO
7.09
-0.14
-1.94%
ISCO
3.58
-0.12
-3.24%
ISIS
51.57
-0.18
-0.35%
LGND
88.94
-3.48
-3.77%
LPTN
0.25
+0.01
+3.52%
MBVX
1.65
-0.04
-2.08%
MEIP
1.91
+0.05
+2.69%
MNOV
3.16
+0.02
+0.64%
MRTX
25.98
-1.86
-6.68%
MSTX
0.47
-0.01
-1.28%
NBIX
48.09
-1.54
-3.10%
NUVA
51.69
-0.46
-0.88%
ONCS
5.81
+0.05
+0.87%
ONVO
2.5
-0.14
-5.30%
OREX
2.75
+0.01
+0.18%
OTIC
21.56
-0.83
-3.71%
QDEL
20.76
-0.69
-3.22%
RCPT
231.96
0.00
0.00%
RGLS
8.45
-0.79
-8.55%
RMD
51.63
-0.28
-0.54%
SCIE
0.014
0.00
0.00%
SPHS
0.84
-0.01
-1.18%
SRNE
12.71
-0.61
-4.58%
TROV
5.94
-0.39
-6.16%
VICL
0.605
+0.004
+0.7327%
VOLC
18
0.00
0.00%
ZGNX
19.63
-0.87
-4.24%
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San Diego Biotech Jobs

San Diego, La Jolla, and Carlsbad biotechnology and life science jobs, updated with at least 5 new positions per day. Browse jobs, submit, get email updates.

Maintenance Data Specialist

August 20, 2015 – 9:00 pm

Details: This position is responsible for administering the technical elements of material, equipment, and location master data in SAP for the maintenance function. This is accomplished through collaboration with Engineering, MRO, System Support, and e…

Maintenance Data Specialist

August 20, 2015 – 9:00 pm

Details: This position is responsible for administering the technical elements of material, equipment, and location master data in SAP for the maintenance function. This is accomplished through collaboration with Engineering, MRO, System Support, and e…

Manager of Clinical Operations – Remote

August 20, 2015 – 9:00 pm

Details: Covance’s Early Clinical Development business is seeking an experienced Manager of Clinical Operations to support and lead a team of Clinical Research Associates that focus in Phase I-IIa clinical trials. Manager of Clinical Operations Responsibilities Include: •Responsible for the supervision and performance review process of assigned direct reports •Measure performance indicators for assigned staff within Clinical Operations •Identify individual training needs and assist in the conduct of training and development efforts, regionally •Effectively communicate management strategies, policies and procedures in conjunction with leadership teams •Develop and maintain effective relationships with management team to manage Clinical Operations staff in a matrix environment •Maintain good working relationships with internal and external clients to ensure opportunity for acquiring additional new business •Manages the conduct of on-site Clinical Quality Control Visits for Clinical Operations staff •Has GCP oversight of direct reports by ensuring GCP training is executed, understood and implemented •Identify and escalate GCP issues identified through regular interactions with direct reports and conduct or review of reports from Clinical Quality Control (CQC) Visits •Hold Clinical Operations staff accountable for quality and compliance with project plan and adherence to contract obligations in Source Data Verification, Monitoring Visit cycles, Trip Report quality and on time deliverables •Communicate status of assigned workload of direct reports for metric reporting – via the Resource Forecast Tool •Perform review of direct report billable hours (via Time & Labor) and monthly review of associated utilization, and escalation of outliers to management team for mitigation •Escalates available workload hours, in context of project allocation, supply and demand, to management team •Assist with staff recruitment through screening and interviewing •Accountable for expense management, expense report approval and compliance with Travel Policy of direct reports •Liaise with internal and external customers in relevant process improvement initiatives, including Six Sigma •Encourages use of standardized processes and tools in alignment with associated policies to ensure efficiency and productivity •Ensure Clinical Quality Control visits are conducted for newly hired or promoted CRAs in compliance with the program

Engineer II – pharmaceutical, process, validation, C&Q

August 20, 2015 – 9:00 pm

Details: Since 1993, Hyde E+C has worked as an integral part of project teams for clients and equipment vendors in the pharmaceutical and biopharmaceutical industries, resulting in the successful construction, commissioning and validation of facilities and equipment. As a member of the Hyde team, you will be responsible for providing state-of-the-art custom solutions to leaders in our industry. As we continue to grow our operations globally, we strive to hire the best talent—men and women dedicated to quality and innovation. We offer a collaborative culture, challenging projects, and excellent compensation and benefits. You will find the following values reflected in our company: Family Integrity Respect Wisdom Adventure Engineer II / Commissioning & Qualification Validation Engineer Reporting to the Regional Manager, Southern California, the Engineer II will work with our client in the areas of validation of downstream biopharmaceutical manufacturing equipment and processes. Responsibilities also include performing commissioning and qualification activities in biotech manufacturing facilities. Responsibilities Develop risk assessment, system impact assessments, validation plans, protocols and reports that support the qualification and validation of systems. Commissioning and validation of processes/process equipment, including, but not exclusive to: Sterile Filling, , Buffer Preparation / Hold, Pool Tanks, , Chromatography Columns, UF/DF, Sterile Filtration, Freeze-Thaw Systems, Formulation, Sterile Filling and Freeze Drying. Develop moderate to highly complex protocols for validation projects using a risk based approach that meets regulatory requirements and industry practices Review analyze and interpret system performance data for completed validation and prepare final report packages by summarizing the data Investigate deviations, write investigation reports and create summary reports. Promote cGMP and regulatory compliance into assigned projects Exercise judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions

Materials Handler

August 20, 2015 – 9:00 pm

Details: EdwardsLifesciences, the global leader in the design,manufacturing and marketing of tissue heart valves and related repair products,is growing. We offer anexcellent working environment including: Broad first day benefits, including medical, dental, vision, & more Paid time off – including 3 weeks of vacation and paid holidays Onsite gym & cafeteria Events including fun runs, hiking clubs, cooking clubs, and community outreach 401K and Tuition reimbursement Career growth Opportunity to be a part of a high performing team Impacting the lives of patients throughout the world Materials Handlersensures the transfer of materials as needed for manufacturing to ensurecontinuous production, in compliance with local EH&S guidelines, Edwardsprocedures, and other applicable regulations. Multipledepartments, schedules, and shifts are available. Starting hourly rate of$10.25 Join the EdwardsTeam. Call 801-565-5255, apply at www.edwards.com/careers or in person at 12050 Lone Peak Parkway, DraperUT. Edwards is an EqualOpportunity/Affirmative Action employer including Minorities, Females,Protected Veterans, and Individuals with Disabilities.

Quality Assurance(Pharma and Biotech experience a must) at Key Business Solutions (Lexington, MA)

August 20, 2015 – 8:46 pm

Quality Assurance(Pharma and Biotech experience a must) Lexington, MA Duration: 6months Candidate must be local … well as presenting to high level management. Pharma and Biotech experience a must Responsibilities: • This is a Senior…

Deloitte Digital salesforce.com Senior Manager – (Retail) East – Deloitte (San Diego, CA 92121)

August 20, 2015 – 8:23 pm

…and eight+ years implementation experience in the Life Sciences industry (Pharma, Biotech , Medical Devices, CRO) Experience managing at least four large-scale full-life

Purchasing Agent ( San Diego) – On Call Employee Solutions – San Diego, CA

August 20, 2015 – 7:29 pm

Prior experience in life science, biotechnology or pharmaceutical with lab supplies procurement strongly preferred….
From On Call Employee Solutions – 21 Aug 2015 02:29:37 GMT
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Associate Director – Respiratory, Thought Leader Services – Roche – United States

August 20, 2015 – 7:09 pm

A minimum of 2 years’ previous field management experience in the pharmaceutical, biotech, or related industry….
From Roche – 21 Aug 2015 02:09:12 GMT
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Manager, Facilities – Organogenesis Inc – La Jolla, CA

August 20, 2015 – 6:57 pm

Previous experience in a pharmaceutical, biotechnology or industrial setting is preferred. This position is responsible for the maintenance of all equipment and…
From DeviceSpace.com – 21 Aug 2015 01:57:04 GMT
– View all La J…