Biotechnology Specialist Jobs

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Wincorp Solutions in need of a knowledgeable and experienced Quality Control Lead to play a key role in establishment and hands-on operation of a QSR (21 CFR 820) and ISO 13485:2003-compliant Quality Control function. The candidate should be hands-on and comfortable working in a fast-paced and dynamic company. The candidate will work with upper management to develop and implement the required pro...
Company: Yoh Research Associate needed for a one (1) year Contract opportunity with Yoh's client located in Chesterfield, MO. The Big Picture: You will be responsible for the establishment of product evaluation field trials. The Research Associate will be responsible for working within the database interfaces and IT tools to support the management and execution of product evaluation field trial...
Contracts Specialist Requirements: -BS/BA degree -2 years experience in a Biotechnology/Pharmaceutical R&D environment -Certification in Medidata Grants Manager or similar budgeting tool preferred. -Knowledge of contracting terms and conditions, financial negotiations required. -Proficient in Microsoft Excel and Word Responsibilities: -Responsible for creating clinical trial fair market va...
RESPONSIBILITIES: · Create and update medical information letters · Utilize appropriate resources to respond verbally or in writing in a fair and balanced manner to unsolicited requests received through the call center · Staff the medical affairs booth at major scientific meetings · Provide training support, as needed, to the medical science liaison and commercial teams · Provide verbal and w...
Role Summary Responsible for coordination of technology transfer activities, assay qualification and validation design and execution, Quality Control (QC) department representation at routine contract manufacturing client meetings, review of statements of work (SOW) in support of contract manufacturing, and new product assessment and setup activities. Will serve as lead for complex technical inv...
At Joulé, you could say the right match is in our DNA. We're the specialists in Scientific Staffing. Our unmatched industry network and geographic reach enable us to place professionals like you at top firms every day. For more than 20 years, we've been providing temporary, contract and direct staff to pharmaceutical, biotechnology, food, flavor and fragrance, specialty chemical and other scientif...
At Joulé, you could say the right match is in our DNA. We're the specialists in Scientific Staffing. Our unmatched industry network and geographic reach enable us to place professionals like you at top firms every day. For more than 20 years, we've been providing temporary, contract and direct staff to pharmaceutical, biotechnology, food, flavor and fragrance, specialty chemical and other scientif...
Summary: C S Bio is a fast paced growing Peptide CMO founded in 1993. Our initial products were a complete line of automated synthesizers for manufacturing and process development, with a focus on cGMP production. In 1994, we opened our custom peptide facility. Initially opened to support R&D for our instrument line, we soon began producing high quality compounds for research organizations and ph...
Kelly Services Billerica, MA
Description Title: Regulatory Affairs Specialist Type: Direct Hire (Full-time, Permanent Position) Location: North of Boston, MA The candidate will be a key regulatory expert for our client's portfolio, consisting of APIs, excipients, pharmaceutical chemicals and processing materials. The candidate should have an understanding of regulations relevant to sterile drug manufacturing. In addition,...
Kelly Services West Chester, PA
Description Every day, Kelly Scientific Resources connects professionals with opportunities to advance their careers. We currently have an exciting opportunity for a Global Health Care Compliance Specialist in West Chester, PA. Job Scope: Reporting to the Director, Global Health Care Compliance, this position is responsible for supporting all aspects of Company HCC program with a focus on the o...
Syngenta Global Durham, NC, 27701
Division: Biotechnology Function: Technology / Projects City: Durham State/Province: North Carolina [NC] Country: United States [US] Position Title: Technology Evaluation Specialist Summer Internship Job ID: 5030 Role Purpose/Accountabilities: Syngenta is one of the world’s leading companies with 28,000 employees in over 90 countries dedicated to one purpose: bringing plant potential to li...
Company Kelly Services Branch Wilmington DE US Position: Clinical Document Specialist Location: Wilmington, DE 19850 Service bonus plan and holiday pay* â?¢ Online application system â?¢ Never an applicant fee Kelly Services… About Kelly Services ® Kelly Services, Inc. (NASDAQ… position. The CDS will have operational responsibility to set-up the local Trial Master File eTMF and Investigat...
Kelly Services San Jose, CA
Part-time Documentation Specialist Kelly Scientific Resources is seeking candidates for a Part-time Documentation Specialist in San Jose for a small pharmaceutical company. This is a 3 month contract position. Payrate: $12-14/hour DOE Job Description: Our client has an immediate need for a part-time Temporary Word Processor/Documentation Specialist position; the ideal candidate will be fast an...
Kelly Scientific Resources Reading, PA
Job Description Kelly Scientific Resources (KSR) has an exciting opportunity available for you as a Regulatory Labeling Specialist to support our client in the Reading, PA area. Our client is looking for dedicated, eager, and hardworking individuals to support their organization. If you feel your background meets the qualifications indicated below, please follow the instructions to apply directl...
Kelly Services Santa Fe Springs, CA
Every day Kelly Scientific Resources (KSR) connects scientific professionals with opportunities to advance their careers. We have a direct hire opportunity for a dynamic individual with proven capability as a Regulatory Compliance Specialist to work with a leading chemical manufacturer in Whittier, CA. The Senior Regulatory Specialist must be detail-oriented, flexible, and eager to make a positiv...
Kelly Services San Jose, CA
Description Part-time Documentation Specialist Kelly Scientific Resources is seeking candidates for a Part-time Documentation Specialist in San Jose for a small pharmaceutical company. This is a 3 month contract position. Payrate: $12-14/hour DOE Job Description: Our client has an immediate need for a part-time Temporary Word Processor/Documentation Specialist position; the ideal candidate wi...
Kelly Services Mountain View, CA
Description Cellular Therapy Specialist II/Manufacturing Location: Mountain View, CA 6 month Contract (contract-to-hire) Pay Rate: $22.00-26.00/hour DOE Job Functions: Under the direction of the Operations Supervisor, the Cellular Therapy Specialist I processes, cryopreserves, and otherwise manipulates cell products using sterile techniques, according to written Standard Operating Procedures...
Kelly Services Mountain View, CA
Cellular Therapy Specialist I/Manufacturing Location: Mountain View, CA 3-6 month Contract (temp-to-hire) Pay Rate: $18.00/hour DOE Job Functions: Under the direction of the Operations Supervisor, the Cellular Therapy Specialist I processes, cryopreserves, and otherwise manipulates cell products using sterile techniques, according to written Standard Operating Procedures, in accordance to fac...
Kelly Services Portsmouth, NH
The Process / Cleaning Validation Specialist position requires six or more years of industry experience working in Cleaning and Process Specialist roles. A four-year college degree is required, preferably in a science or technical discipline. Process/Cleaning Validation Specialists are part of the Quality organization at our client. Variable work schedule may be required to maintain project timeli...
Kelly Services Wilmington, DE
Description Kelly Clinical Research is seeking candidates for a Clinical Document Specialist position. The CDS will have operational responsibility to set-up the local Trial Master File eTMF and Investigator Site File including tracking of documents. This is a one year contract position based in Wilmington, DE. Job duties: • Maintain and close the local TMF in electronic or paper form depending...

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