ACAD
38.06
+0.15
+0.40%
AEMD
7.37
+0.22
+3.0699%
APRI
1.395
+0.165
+13.415%
ARNA
2.705
+0.055
+2.075%
ATEC
0.56
-0.01
-1.7719%
CNAT
4.13
+0.45
+12.23%
CRXM
0.38
-0.01
-2.56%
CYTX
0.312
+0.013
+4.3435%
DXCM
94.11
+0.37
+0.39%
GNMK
10.01
+0.58
+6.15%
HALO
18.3
+0.26
+1.44%
ILMN
200.43
-1.51
-0.75%
INNV
0.15
+0.01
+3.45%
INO
7.65
+0.67
+9.60%
ISCO
3.95
+0.3
+8.22%
ISIS
50.86
-0.7
-1.36%
LGND
94.79
+0.54
+0.57%
LPTN
0.223
+0.013
+5.9495%
MBVX
1.7
+0.01
+0.59%
MEIP
1.72
+0.03
+1.7811%
MNOV
3.08
+0.11
+3.70%
MRTX
26.67
+1.18
+4.63%
MSTX
0.465
+0.013
+2.9197%
NBIX
46.28
+0.02
+0.04%
NUVA
53.51
+0.76
+1.44%
ONCS
5.2
+0.02
+0.48%
ONVO
2.48
-0.02
-0.80%
OREX
2.9
+0.14
+5.07%
OTIC
23.32
-0.06
-0.26%
QDEL
20.41
-0.29
-1.40%
RCPT
231.96
0.00
0.00%
RGLS
8.06
+0.58
+7.75%
RMD
52.41
+0.76
+1.47%
SCIE
0.015
+0.001
+3.5714%
SPHS
0.877
+0.017
+2.0116%
SRNE
13.57
+0.25
+1.88%
TROV
6.36
+0.58
+10.03%
VICL
0.57
+0.01
+1.8208%
VOLC
18
0.00
0.00%
ZGNX
18.4
+1.34
+7.85%
ACAD
38.06
+0.15
+0.40%
AEMD
7.37
+0.22
+3.0699%
APRI
1.395
+0.165
+13.415%
ARNA
2.705
+0.055
+2.075%
ATEC
0.56
-0.01
-1.7719%
CNAT
4.13
+0.45
+12.23%
CRXM
0.38
-0.01
-2.56%
CYTX
0.312
+0.013
+4.3435%
DXCM
94.11
+0.37
+0.39%
GNMK
10.01
+0.58
+6.15%
HALO
18.3
+0.26
+1.44%
ILMN
200.43
-1.51
-0.75%
INNV
0.15
+0.01
+3.45%
INO
7.65
+0.67
+9.60%
ISCO
3.95
+0.3
+8.22%
ISIS
50.86
-0.7
-1.36%
LGND
94.79
+0.54
+0.57%
LPTN
0.223
+0.013
+5.9495%
MBVX
1.7
+0.01
+0.59%
MEIP
1.72
+0.03
+1.7811%
MNOV
3.08
+0.11
+3.70%
MRTX
26.67
+1.18
+4.63%
MSTX
0.465
+0.013
+2.9197%
NBIX
46.28
+0.02
+0.04%
NUVA
53.51
+0.76
+1.44%
ONCS
5.2
+0.02
+0.48%
ONVO
2.48
-0.02
-0.80%
OREX
2.9
+0.14
+5.07%
OTIC
23.32
-0.06
-0.26%
QDEL
20.41
-0.29
-1.40%
RCPT
231.96
0.00
0.00%
RGLS
8.06
+0.58
+7.75%
RMD
52.41
+0.76
+1.47%
SCIE
0.015
+0.001
+3.5714%
SPHS
0.877
+0.017
+2.0116%
SRNE
13.57
+0.25
+1.88%
TROV
6.36
+0.58
+10.03%
VICL
0.57
+0.01
+1.8208%
VOLC
18
0.00
0.00%
ZGNX
18.4
+1.34
+7.85%
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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.

Principal Scientist, Immunotherapeutics – Pfizer Inc – La Jolla, CA

February 6, 2015 – 3:26 am

The candidate will need to ensure any data generated by the team has been through a rigorous QC process prior to release….
From Pfizer Inc – 06 Feb 2015 10:26:25 GMT
– View all La Jolla jobs

Global Service Operations Manager – Brooks Automation, Inc. – Poway, CA

February 6, 2015 – 12:01 am

With the largest installed base and support network for automated sample management systems, Brooks has more than 180 systems worldwide, including installations…
From Brooks Automation, Inc. – 06 Feb 2015 07:01:04 GMT
– View …

Program Manager – Brooks Automation, Inc. – Poway, CA

February 6, 2015 – 12:01 am

With the largest installed base and support network for automated sample management systems, Brooks has systems worldwide, including installations in all of the…
From Brooks Automation, Inc. – 06 Feb 2015 07:01:04 GMT
– View …

Field Service Engineer – Brooks Automation, Inc. – Poway, CA

February 6, 2015 – 12:01 am

With the largest installed base and support network for automated sample management systems, Brooks has more than 180 systems worldwide, including installations…
From Brooks Automation, Inc. – 06 Feb 2015 07:01:03 GMT
– View …

Corporate Paralegal

February 5, 2015 – 10:00 pm

Details: Eastridge Legal is recruiting for a Corporate Paralegal with contracts management experience. Seeking polished, professional candidates with a minimum of 3 years, ideal 5 years + experience. Apply for immediate consideration.

Director Of Quality

February 5, 2015 – 10:00 pm

Details: Director of Quality Assurance opening at up and coming San Diego Med Device company who is looking to expand its Quality Assurance department and is looking for a new leader to implement and lead a growing team. This is a permanent position with competitive pay, bonus, and benefits and will be a direct report into the CEO and will be in constant communication with the senior management team. The Director will also be an integral member of the new product development team. This position will work closely with counterparts within the Marketing & Sales, Engineering, Operations, and Clinical groups to assure that the products derived are done so in accordance with the Quality System, regulatory requirements and guidelines, and the company milestones. The Director of Quality Assurance will be the authorized Management Representative and will manage all company internal and external audits. The Director of Quality Assurance will ensure overall Quality Management System compliance with applicable regulatory and statutory requirements, including but not limited to 21 CFR 820 (Quality System Requirements), EN ISO 13485:2003, EN 14971:2012 standards, and CGMP. This Director of Quality Assurance will be responsible for: Management Review CAPA NCRB Complaints Product Field Actions Medical Device Reports (MDR, US) Vigilance Reports (CDN, EU) Internal and External Audits Quality Plan, Quality Policy and overall Quality System compliance Support 510(k)’s, PMA’s, IDE’s and international registrations Requirements/Skills Necessary to Apply: Bachelors of Science in Engineering or Biological Sciences 10 years or more of medical device industry experience or similar regulated industry Excellent verbal and written communication skills Applied understanding of ISO 13485, CDN, and FDA QSR experience leading ISO and FDA Audits as Management Representative with a successful track record. Demonstrated experience developing or managing Quality Management Systems Demonstrated expertize on Process and Product Validation and Statistical Methods Demonstrated auditing experience in medical device or other regulated manufacturing environment Demonstrated ability to lead and work effectively in a global, cross-functional team environment Preferred Skills: Six Sigma Green or Black Belt Certification Internal or lead auditor certification (CQA) is preferred

Sr. Clinical Trial Manager/Associate Director, Clinical Operations

February 5, 2015 – 10:00 pm

Details: BioPhase Solutions specializes in recruiting top talented professionals for San Diego’s Scientific community. We are currently looking for a Sr. Clinical Trial Manager/Associate Director, Clinical Operations to work for a leading San Diego bio…

Senior Scientist, Biotech

February 5, 2015 – 10:00 pm

Details: Position is in Columbia, MO. Relocation assistance is provided Since 1968, ABC Laboratories has delivered expert scientific support to companies working to improve human and animal health. As a member of the ABC team, you’ll work alongside respected technical experts dedicated to scientific excellence in a process driven regulatory compliant environment. Our laboratories are modern. Our instrumentation is state of the art. And our business is thriving, creating important career opportunities. More than 400 people are building their careers with ABC Laboratories. See what it’s like to do what you love and love where you live! Visit www.abclabs.com to learn more about our company and our community. The Senior Scientist is Involved in planning own work and supervising day-to-day activities in the laboratory working under prescribed procedures (protocols, standard operating procedures, methods, etc.). Completes complex work for research and development, CGMP and GLP studies and documents and reports data in a timely manner according to regulatory guidelines. Plans the conduct of a study; monitors study procedures to ensure data accuracy and report quality; conducts complex analysis and experimentation on substances, for purposes such as product and process development and application, quantitative and qualitative analysis and improvement of analytical methodologies. Typically serves as technical leader within group and may also be the project leader/study director on complicated projects. Job Duties and Responsibilities: Designs, carries out, and performs simple and complex experiments and procedures in accordance with all applicable regulatory (e.g. DEA, EPA, FDA, FIFRA, OECD, etc.) requirements as defined by protocol, method, and standard operating procedures (SOPs). Routinely develops procedures and methods for the solution of technical problems. Performs progressively more complex procedures and experiments. Is able to utilize equipment, facilities, and personnel to produce sound scientific results in a timely fashion for ABC clients. Serves as an expert for technical issues for staff and external customers. Adheres to schedule according to ABC’s or contracting organization’s timetable and establishes daily or weekly routines necessary to ensure on-time delivery. Designs and conducts most procedures independently using laboratory equipment, computer resources, and institutional libraries. Prepares standards and specifications for processes, facilities, products, and tests. Conducts studies to determine and deliver results involving the composition, structure, properties, relationships, and all critical parameters of the material contracted for testing. Performs complex data evaluations, reviews the work of others, and writes complex technical reports and standard operating procedures. Responsible for the quality and accuracy of the data and reports sent to clients under assigned responsibility. Depending on area of assignment, handles regulated materials (quarantined matrices, DEA-controlled and radiolabeled materials, etc.), potential biohazard materials, and toxic chemicals according to company procedures. Depending on area of assignment, performs ELISA testing for protein expression. Likely to work on several projects concurrently and may monitor and direct activities of other staff performing work in area of expertise. Conducts training of staff on techniques necessary to perform laboratory assignments. May serve as study director, principal investigator, or project leader for GLP and CGMP studies. May assist in planning the conduct of a study. Confers with scientists and colleagues regarding research, and be required to prepare technical papers and reports. Performs other related duties as required and directed.

* Associate Director, Financial Reporting – Biotech *

February 5, 2015 – 10:00 pm

Details: Ref ID: 02100-138058 Classification: Controller Compensation: $120,000.00 to $150,000.00 per year *** High Growth Publicly Traded Biotech – Boston/Cambridge – Assistant Controller *** My client, a publicly traded Biotech, continues to expand i…

MEDICAL DEVICE SALES REPRESENTATIVE – Work for a Biotech Leader!

February 5, 2015 – 10:00 pm

Details: Zimmer is a worldwide leader in joint replacement solutions and orthopaedic surgical products. Our wide range of products and related services help people every day, in more than 100 countries around the globe, live fuller and happier lives. Z…