Validation Engineer, Process Validation
Write and review validation (verification, IOQ, PQ, and PV) documents (protocols, reports, risk assessments, etc.), conduct or coordinate performance testing and perform or oversee the validation of facilities, equipment, utilities, laboratories, equipment, and processes. Involved in validation monitoring activities which include audits with the system owner and review of operational documents. Participates in process development and process ...
QC Analyst III
Performs analytical testing to support the release, stability, and in process testing samples, or final products and supports the release of materials for production or products for commercial use.
Accurately follows relevant SOPs, performs all activities in accordance with cGMP requirements reports abnormalities. Initiates and completes laboratory discrepancy events on time.
Documents test results to ensure completeness and accuracy per cGMPs.
We are currently seeking a Quality Engineer for a 3+ month contract in Hayward (likely to extend):
Tasks and Responsibilities:
In this role you will actively participate in new product introduction activities, ensuring conformance to FDA and ISO 13485 standards. This role will serve as a technical resource to manufacturing to improve product quality, reliability, and process capability. You will facilitate teams in identifying, documenting, assessing, correcting and preventing quality ...
Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.
Title: Environmental Health & Safety (EH&S) Associate II
Job ID: 23438
Location: South San Francisco, CA
Duration: 6 Month Contract
Pay Rate Range: Depends on Experience (W-2 all inclusive rate)
Will provide technical support to ...
The Coordinator is responsible for carrying out basic tasks at a customer site or multiple customer sites in a region. All of which can include but not limited to, inventory management, purchasing, shipping, receiving, chemical tracking, storeroom tracking, and even product delivery. The Coordinator position requires knowledge and application of VWR and routine customer systems. Reporting and customer interaction is typically of a routine nature.
Performs inventory ...
The Gerard Group has been asked to locate, qualify and present strong candidates for the Associate Director of Clinical Data Management. Oncology experience is highly desirable.
Oversee Functional Service Provider (FSP) in data validation engagement to ensure clinical data are processed according to the Data Review Guidelines (DRGs) and Standard Operating Procedures (SOPs).
Design and Implement Electronic Case Report Forms.
Develop data management QC plans and quality ...
The associate is responsible for the growth and recovery of microorganisms used in the manufacture and development of biopharmaceuticals.
Manufacture recombinant antigens to ensure commercial product demands are met:
Provides necessary support for all production activities associated with the Antigen Fermentation.
Operates complex fermentation, filtration and centrifugation equipment
Participates in equipment and process qualification and troubleshooting
2-4 years of experience
Job Summary :
Reports to Operations Supervisor, Laboratory Supervisor or Laboratory Manager. Under minimal supervision incumbent(s) will consistently and accurately perform either a greater number or more varied amount of complex or difficult tasks and assignments than the work performed by a Clinical Laboratory Scientist I. This is considered a senior level position and is the highest in a two level job family.
Duties and Responsibilities:
Jan 16 -
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