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Randstad, San Jose, CA
temporary to hire $ 13.00 - $ 13.00 per hour
We are seeking a motivated individuals for a Quality Control Content Reviewer position in the Redwood City area. This is an innovative company that utilizes new technology to help with customization of products and services. Pay Rate = $13.00 Shift = Day Shift 7am - 3:30pm (days we are flexible) Basic responsibilities for these positions are as follows: -Reviewing customer orders to ensure graphic or text placement is suitable for printing -Emailing with customer of any flaws in the order -Utilizing similar programs as Adobe Photoshop to help crop, fix ass design images and text -Using good judgement to approve or decline customer orders Working hours: Day, Swing, Grave Skills needed: -Needs to know POP CULTURE (you will be reviewing images that could be copyrighted, being able to know movies, actors, logos, quotes, government officials is very key) -Can make immediate decisions -Has software experience such as Photoshop -Able to work flex schedules -Able to work OT, Weekends, Holidays -Pass criminal background and drug screens -Degree is preferred but not required Please email your resume if interested to email@example.com Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law. [show more]
- September 14, 2014
Randstad, Rockland, MA
EMD Serono is the biopharmaceutical division of Merck KGaA, Darmstadt, Germany, a global pharmaceutical and chemical group. We strive to create value and benefit patients by transforming medical science into breakthrough solutions in our core therapeutic areas of neurodegenerative diseases, fertility and metabolic endocrinology, as well as oncology and autoimmune/inflammatory diseases as emerging areas of expertise. KEY ACCOUNTABILITIES - Leadership of the development of several molecules grouped into a program in Early Development (Lead Optimization through Proof of Confidence). - To ensure timely delivery of clinical strategy in accordance of ImmunoOncology vision and goals. - Manage the program portfolio to optimize the resources and maximize the probability of success. - Secure approval of the Target Product Profile (TPP) for each molecule ensuring focus on differentiation and patient stratification when applicable. - Together with a global cross-functional project team translate the TPP into different strategic development options and define PoC criteria. Secure agreement by the ROC and other relevant governance bodies aligning all key stakeholders across the organization. - Accountable for all program decisions requiring execution and implementation of approved strategy. Supported by the Project Manager for operational execution and for proactively identifying/mitigating the risks. Working hours: 8:30-5:00 EDUCATION - MD with experience in early development. MD/PhD and experience in the field of ImmunoOncology is highly desirable- Additional MBA desireable. - Publications in peer reviewed scientific or medical journals. - Good scientific knowledge and experience in TA. WORK EXPERIENCE - Expected 5-10 years experience in global drug development managerial positions within academia, biotech, big pharma. - Experience in leading global cross-functional complex projects at international pharmaceutical company(s); recent biotech work experience desirable. - Demonstrated success in positions requiring influence and stakeholder management in a matrix organization. JOB-SPECIFIC COMPETENCIES & SKILLS - Broad working knowledge of pharmaceutical business including regulatory, nonclinical, CMC development /manufacturing, research, clinical development, commercial and market access aspects of drug development. - Strong mature leadership and interpersonal skills. - Pragmatic decision making based on critical path drivers (cost effective while maximizing probability of success). - Capability to devise complex program strategy with cross-functional and long term thinking. - Ability to formulate, evaluate and convincingly present scenarios / options to company management. - Strong results orientation. - Good understanding of finance and accounting principles in industry setting. - Ability to represent the company and to negotiate at all levels both internally and externally. - Fluent in written and spoken English. Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law. [show more]
- August 25, 2014
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