McKesson is seeking a Finance Operations Manager to manage the Generics Customer Rebates operations, accounting and analytics for key customer groups within the RNA and Hospital segments, which totals approximately $400 million annually in rebate payments to 40 big customers.
Manage the administration rebate reports, validations, payments and accruals for accuracy. Manage the contract review process, interpretation of customer agreements and set up of rebates in ...
A QA Associate position will conduct internal Good Laboratory Practice (GLP) audits to ensure that nonclinical studies are conducted in accordance with GLP regulations and provide management support of Internal Quality Systems.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Ensure that internal and external nonclinical GLP studies (including BioAnalytical, PK/TK analysis) are performed in accordance with applicable study protocols, and are in compliance with GLP regulations.
• Support the implementation ...
Candidates should be experienced working on PCR and handling human viral pathogens.
Able to have basic molecular biology lab skills and working independently, operate automated sample prep and PCR instruments.
Work in controlled and regulated environment, handle human specimens, detailed date analysis by MC Excel.
After introduction to work process, candidate should begin to organize, conduct and monitor laboratory experiments utilizing established and published procedures ...
Job Title:Technical Editor Writer
• Meet assigned targets and timelines with limited supervision.
• Prioritize assigned tasks within a fast paced environment.
• Receive specific instruction and work independently to complete tasks.
• Full use and application of basic Business Process/GMP theories, principles, techniques, and technical principles to address routine/complex problems.
• Create and edit controlled documents at all levels of complexity ...
Review of calibration records for completeness and compliance
Determination and implementation of corrective action of calibration deficiencies
Evaluation and improvement of calibration/preventive maintenance programs, including calibration software (CalMAN) functionality and capability.
Support for operations and documentation in facilities, quality control and quality assurance areas.
EXPERIENCE AND QUALIFICATIONS:
Work history must be in the FDA regulated industries, i.e. ...
Job Title:Technical Mgr, Ext Quality
- Perform CMO batch record review in support of lot disposition activities; Collaborate with site management teams, Lot Disposition, Planning, and other stakeholders to meet disposition timelines
- Perform the following to drive closure of deviations, change controls, and CAPAs within team:
Generate Trackwise reports for team to monitor status
Develop and generate metrics to drive on-time closure of records (ie, # of open records, # overdue, etc)
Our client is a division of an international pharmaceutical corporation. They have an immediate opening for a motivated, flexible employee. This position will be 8 hours a day, two days a week. The specific days are to be determined. If you qualify, we want to hear from you right away. This is a great opportunity to be a part of a growing corporation with future potential for additional employment
Job Title Lab Assistant
MUST HAVE RELIABLE TRANSPORTATION AND BE FLEXIBLE ON ...
The selected candidate is required to possess the following:
•B.S. in Computer Sciences, Engineering or other applicable B.S. discipline
•Specific training and certificates in Document Management systems
•BS 6+ years
•MS 0 - 4+ years
•Or an equivalent combination of education and experience.
•5-8 years of experience working with and administering Document Management systems.
•4 years working with Autocad software.
•3-5 years working with engineering documents ...
Position: Major Tasks
Provide expert leadership in medical device regulations in an individual contributor role including: the ability to identify issues of significance, communicate complex issues to site leadership, provide multiple alternatives to the solution of complex problems and the ability to provide guidance in their implementation.
Leads relevant medical device project planning and review meetings; communicating to senior leadership regarding program status and supporting final ...
Review and understanding of clinical Research documents such as Protocols, Case report forms, RAVE reports and Statistical Analysis.
Devise and Review data management plan (DMP), and update data management plan throughout life cycle of the study and ensure the DMP complies with the regulatory requirements.
Design and Development of electronic case report forms by thoroughly understanding the protocol requirements and present it to the cross functional teams for the ...
In-house statistical consultant to departments. Provides consulting services, analyses, and statistical reports to clinical areas. Works closely with programmers to provide specifications for report tables and listings.
Provides statistical consulting to clinical teams in design of clinical studies (including sample size estimation, power calculation and study conduct) and in the analysis and interpretation of study data. Works on complex statistical problems in which ...
Specific Responsibilities and skills for Position :
Actively manages Contract Manufacturing Organizations (CMO’s) for their assigned projects. Ensures all regulatory requirements are met in the manufacturing of bulk API. Ensures availability of raw materials at contract manufacturing sites. Manages transfer of new technology from Process Development to contract manufacturing sites. Assists in the coordination and execution of departmental quality, business and technical audits of API and raw ...
JOB PURPOSE: Maintain greenhouse plant materials, including watering feeding, pruning, propagation, testing, and pest management; operate environmental control equipment, maintain greenhouse facility, including installation, maintenance, and repair of special equipment; and assist in research projects. Investigate the growth, structure, development, and other characteristics of plants and documenting other micro-organisms, such as bacteria, algae, or fungi.
DUTIES AND RESPONSIBILITIES NOT LIMITED ...
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:
• In-house statistical consultant to departments. Provides consulting services, analyses, and statistical reports to clinical areas. Works closely with programmers to provide specifications for report tables and listings.
• Provides statistical consulting to clinical teams in design of clinical studies (including sample size estimation, power calculation and study conduct) and in the analysis and interpretation of study data. Works on complex statistical problems in which analysis of data requires ...
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.
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 ...
Mar 6 -
South San Francisco
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