ACAD
31.77
-0.8
-2.46%
AEMD
0.26
+0.01
+2.00%
APRI
1.22
-0.02
-1.61%
ARNA
4.52
-0.14
-3.00%
ATEC
1.36
+0.01
+0.74%
CFN
59.75
-0.23
-0.38%
CNAT
5.34
+0.02
+0.38%
CRXM
0.2
+0.02
+11.11%
CYTX
0.47
-0.01
-1.19%
DXCM
57.92
-0.19
-0.33%
GNMK
13.18
+0.09
+0.69%
HALO
13.89
-0.12
-0.86%
ILMN
196.69
+2.8
+1.44%
INNV
0.25
+0.01
+4.17%
INO
8.62
+0.12
+1.41%
ISCO
0.06
0.00
0.00%
ISIS
71.25
+0.27
+0.37%
LGND
54.86
-0.97
-1.74%
LPTN
2.97
0.00
0.00%
MBVX
1.1
-0.15
-12.00%
MEIP
3.69
-0.1
-2.64%
MNOV
3.52
-0.12
-3.17%
MRTX
19.27
-0.15
-0.77%
MSTX
0.48
+0.00
+0.04%
NBIX
31.71
+0.13
+0.41%
NUVA
46.93
-0.26
-0.55%
ONCS
0.4
+0.00
+0.25%
ONVO
6.32
-0.05
-0.78%
OREX
5.4
+0.12
+2.27%
OTIC
32.83
+3.49
+11.90%
QDEL
24.26
-0.04
-0.16%
RCPT
110.23
+3.01
+2.80%
RGLS
18.53
+0.27
+1.48%
RMD
65.44
+3.58
+5.79%
SCIE
0.01
0.00
-7.75%
SPHS
0.45
+0.00
+1.02%
SRNE
9.96
-0.03
-0.30%
TROV
5.82
0.00
-0.06%
VICL
1.04
+0.01
+0.96%
VOLC
17.96
+0.01
+0.06%
ZGNX
1.34
+0.05
+3.88%
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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.

QA Specialist

January 7, 2015 – 10:00 pm | Edit Post

Details: General QA support duties & responsibilities Principal for document and record control functions Create and/or maintain quality system procedures/work instructions and associated forms Participate in quality system change review/approval Participate in the process of controlling nonconforming product Participate in the various CAPA processes of the quality system Participate in product complaint handling/investigation Participate in the collection, analysis and presentation of various performance metrics (product and QS) Review/approve product and associated processing records for release, including incoming and final acceptance Participate in supplier selection, auditing and performance assessment activities Participate in quality system internal audit activities Participate in QS-based personnel training activities Participate in validation activities associated with non-product S/W Product-related duties & responsibilities Principal for process validation activities (including planning, plan review/approval, protocol development, protocol review/approval, protocol execution, reporting and report review/approval) Participate in development and maintenance of product documentation (e.g., DHF and DMR content) Participate in product design review process Participate in product change review/approval process Participate in supplier selection/audit/approval activities Participate in planning and execution of supplier product qualification activities Participate in planning of incoming acceptance activities (including establishing sampling plans) Participate in planning of final acceptance activities (including establishing sampling plans) Participate in other design transfer activities (as necessary) Review of customer test reports Preferred educational background Bachelor’s degree in a relative technical field (e.g., biology, chemistry, biomedical sciences) Alternative: Associate’s degree in technical field with minimum of 5 years relevant experience or, high school diploma with minimum of 10 years relevant experience Preferred experience (general) Minimum of 5 years of experience, in QA role, in the following types of commercial environments:Development and/or manufacturing of bio./chem. based diagnostic medical products (e.g., IVDDs) Clinical laboratory testing service (e.g., CLIA) operations Minimum of 5 years of hands-on experience with the following types of equipment/analytical methods:ELISA (pipette, plate washer, plate reader) Minimum of 5 years of experience with implementation and/or operation/maintenance of quality systems conforming to GMP/QSR and/or ISO 13485 and/or CLIA requirements Application of common statistical techniques (and associated software) to development, verification, validation, and acceptance activities Use of standard PC applications (word processor, spreadsheet, presentation, etc.)

Biostatistician (Senior)

January 7, 2015 – 10:00 pm | Edit Post

Details: Have you heard? Ockham has merged with Chiltern to lead the industry in Oncology, Source, and Biopharmaceutics development. The new Chiltern is a leading, global, mid-sized CRO focused on providing expertise, engagement, and tailored, responsi…

Associate Scientist II – R&D

January 7, 2015 – 10:00 pm | Edit Post

Details: Working with amultidisciplinary technology team for the development of next generationsequencing assays that will be used in clinical laboratories. Responsibilities will include sample preparation, instrument calibration andoperation, and data…

Clinical Data Manager

January 7, 2015 – 10:00 pm | Edit Post

Details: Ascent Pharma is seeking a Clinical Data Manager in San Diego, CA! ***APPLY TODAY OR REFER A FRIEND! We offer a terrific referral bonus! Madelene Marinas/ Sr. Clinical Recruiter 415-653-0105 Please send your resume directly to: WHAT: Clinical …

QA Specialist

January 7, 2015 – 10:00 pm | Edit Post

Details: General QA support duties & responsibilities Principal for document and record control functions Create and/or maintain quality system procedures/work instructions and associated forms Participate in quality system change review/approval Participate in the process of controlling nonconforming product Participate in the various CAPA processes of the quality system Participate in product complaint handling/investigation Participate in the collection, analysis and presentation of various performance metrics (product and QS) Review/approve product and associated processing records for release, including incoming and final acceptance Participate in supplier selection, auditing and performance assessment activities Participate in quality system internal audit activities Participate in QS-based personnel training activities Participate in validation activities associated with non-product S/W Product-related duties & responsibilities Principal for process validation activities (including planning, plan review/approval, protocol development, protocol review/approval, protocol execution, reporting and report review/approval) Participate in development and maintenance of product documentation (e.g., DHF and DMR content) Participate in product design review process Participate in product change review/approval process Participate in supplier selection/audit/approval activities Participate in planning and execution of supplier product qualification activities Participate in planning of incoming acceptance activities (including establishing sampling plans) Participate in planning of final acceptance activities (including establishing sampling plans) Participate in other design transfer activities (as necessary) Review of customer test reports Preferred educational background Bachelor’s degree in a relative technical field (e.g., biology, chemistry, biomedical sciences) Alternative: Associate’s degree in technical field with minimum of 5 years relevant experience or, high school diploma with minimum of 10 years relevant experience Preferred experience (general) Minimum of 5 years of experience, in QA role, in the following types of commercial environments:Development and/or manufacturing of bio./chem. based diagnostic medical products (e.g., IVDDs) Clinical laboratory testing service (e.g., CLIA) operations Minimum of 5 years of hands-on experience with the following types of equipment/analytical methods:ELISA (pipette, plate washer, plate reader) Minimum of 5 years of experience with implementation and/or operation/maintenance of quality systems conforming to GMP/QSR and/or ISO 13485 and/or CLIA requirements Application of common statistical techniques (and associated software) to development, verification, validation, and acceptance activities Use of standard PC applications (word processor, spreadsheet, presentation, etc.)

Administrative Assistant – Biotech Firm – Newton $15/hr, $45K at Beacon Hill Staffing Group (Newton Center, MA)

January 7, 2015 – 6:45 pm | Edit Post

Our client is a growing biotech in Newton seeking a junior administrative candidate in a temp-permanent capacity ASAP!! In this role you would be sitting at the front desk and responsible for answering phones, greeting visitors and…

Director, Business Development, Oncology Drug Development at Cameron Craig Group (San Diego, CA)

January 7, 2015 – 5:55 pm | Edit Post

sell the platform technology Target existing and potential biotech and pharma clients by demonstrating the value and benefits of platform Provide exceptional service to the territory Understand the drug development needs of the clients and…

Sr. Scientist – Diagnostics Development

January 7, 2015 – 5:18 pm | Edit Post

Sequenom Laboratories, a wholly-owned subsidiary of Sequenom, Inc., is a CAP accredited and CLIA-certified molecular diagnostics laboratory, dedicated to the development and commercialization of laboratory-developed tests (LDTs).
As a life sciences […]

Sr QC Reviewer – PPD – Middleton, WI

January 7, 2015 – 5:16 pm | Edit Post

Independently perform complex laboratory analysis of pharmaceuticals and proficiently uses – analytical instrumentation, calculate and analyze data, and record…
From PPD – 08 Jan 2015 00:16:28 GMT
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Project Manager – PPD – Middleton, WI

January 7, 2015 – 5:16 pm | Edit Post

Monitoring/tracking timelines and budget information, and proven ability to keep attention to detail while not loosing sight of the over-all program goals and…
From PPD – 08 Jan 2015 00:16:21 GMT
– View all Middleton jobs