hr generalist salaries in san francisco, california

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Internationally known for creating cutting-edge biopharmaceuticals for patients who live with rare genetic diseases, our partner strives to develop critical therapies for the small population - mostly children - that suffer from near unheard of conditions. If you're looking for an exciting opportunity to make a difference with an established company, this is the position for you!   location: San Rafael, California job type: Contract salary: $87.29 - 102.69 per hour work hours: 9 to 5 education: Masters   responsibilities: Implement observational research studies in-line with a product's Integrated Evidence Plan under the guidance of a Real World Evidence Product Lead. Specific activities include:Protocol and statistical analysis plan development and reporting of disease understanding studies (retrospective and prospective) relevant to the target patient population including, risk factors, natural history, burden of illness, treatment patterns, co-morbidities, co-medications, outcomes measures, and unmet needSupport post marketing activities including design, analysis plans and/or reporting of post marketing safety and effectiveness studies/registries, evaluation of risk mitigation strategiesSupport implementation of research plans with external collaborators in academia or contract research organizations and work effectively to oversee external groups through the research processPerform targeted literature review of epidemiology of disease, including incidence/prevalence and treatment patterns; work with commercial team on product forecasts and write regulatory documents including Orphan Drug Designation applications  qualifications: A combination of academic training and practical experience in Epidemiology is required. This may consist of: Doctoral degree (PhD, ScD, or DrPH) or Master's of Public Health in Epidemiology and at least 2 years of experience leading epidemiologic research in the pharmaceutical settingDoctoral degree (PhD, ScD or DrPH) or Master's degree in a relevant discipline (ie. Health services research, health outcomes research, public health, statistics, or pharmaceutical sciences) with at least 5 years of experience leading epidemiologic research in the pharmaceutical settingDemonstrated experience conducting pharmaco-epidemiologic research within or in support of the pharmaceutical industrySelf-motivated with the ability to develop credibility with colleagues and interact effectively in a matrix team environmentExperience in collaborating with internal and external research partnersAbility to work well in a business-driven environment, balance priorities and handle multiple tasks through careful planning, stakeholder management, project administration, and organizational skillsAbility to individually contribute to activities and projects based on guidance from Real World Evidence Product LeadExcellent oral and written communication skills and demonstrated ability to communicate scientific evidence to peers and at scientific meetingsExperience in the Epidemiology of rare diseases or Genetic Epidemiology a benefit  skills: Epidemiology Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). Applications accepted on ongoing basis until filled. Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!   location: Novato, California job type: Contract salary: $23.96 - 28.00 per hour work hours: 3 to 11 education: Bachelors   responsibilities: Timely facilitation of incoming sample receipt and accessioning flow, decipher batch assignments across all assay types in accordance with agreed upon best practices.Execute plate-based analytical methods to facilitate in-process testing under applicable cGMP guidelines, as well as contribute to the prompt reporting of results to meet the required timetables of internal customers.Evaluate completed assay validity, calculate and summarize results, analyze data per expected or specification ranges.Perform and collaborate with co-workers to appropriately share general housekeeping activity assignments, and ensure systems for laboratory maintenance are adequate for creating a consistent state of inspection readiness.Attend team huddles and department meetings, generate ideas for laboratory infrastructure improvements and method optimization.Perform other responsibilities as deemed necessary.Work assignments will vary by degree of complexity.Employee is expected to follow SOPs, make appropriate decisions in daily activities with minimal needs for intervention, and be able to recognize deviations from routine practices. Incumbent must accurately complete tasks on time to achieve lab goals, meanwhile limiting GMP / procedural errors, and be capable of accepting and incorporating feedback.Must also demonstrate the ability to both manage time and prioritize routine work effectively.Employee must be able to interpret results against defined criteria, begin to apply critical thinking to routine work. He/she should demonstrate an ability to evaluate results against trend reports, serve some degree of troubleshooting, and embrace an active role in following up on atypical results or issues.Communication of relevant information must be made to appropriate audiences, and attendance of necessary team meetings with some participation in discussions is essential.Employee should also be actively engaged in his/her role, exhibit frequent volunteerism as the work schedule flow permits, and maintain a positive attitude.  qualifications: Bachelor of Science or Bachelor of Arts in a science related field with at least 0-2 years of relevant laboratory experience or Associates of Science with at least 4 years of relevant laboratory experience.Experience with quality management systems, current Good Manufacturing Practices, and QC principles.Demonstrated working knowledge with respect to certified functional activities.Good documentation, written and verbal communication skills are essential.Must possess the ability to perform most tasks with minimal supervision.Computer literacy is required, proficiency with Microsoft Word and Excel is essential, experience with Microsoft PowerPoint, Access, or Visio is desired.Must have a quality service attitude and focus, exhibit flexibility and willingness to work additional hours to meet production or laboratory process requirements.  skills: Quality control, SOP, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). Applications accepted on ongoing basis until filled. Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! Immediate needs for a QC Analyst - Microbiology! The QC Microbiology department is responsible for performing environmental monitoring and microbiological test methods on in-process intermediates and varying stages of drug products under minimal supervision and within cGMP guidelines, to support further manufacturing of commercial and clinical therapeutics. Schedule/Shift: 4x10 schedule, 11am-10pm Sunday - Wednesday, swing shift (11:00am - 10:00pm)Wednesday - Saturday, swing shift (11:00am - 10:00pm)   location: Novato, California job type: Contract salary: $23.96 - 28.00 per hour work hours: 11 to 7 education: Bachelors   responsibilities: Perform daily environmental monitoring sampling of GMP facilities cleanrooms (Galli and Leveroni manufacturing areas) and utility systems (RODI/WFI/Steam water systems and CDA/process gases.)Examine microbial plates daily for quantification and characterization.Perform shared general housekeeping activity assignments, including but not limited to, operation of autoclave sterilization of QC testing material, and CTE chart checks.Assist with monitoring and the control of laboratory media supply and critical reagent inventories.Responsible for continuous upkeep and organizing of QC GMP records.Attend team huddles and department meetings, generate ideas for laboratory infrastructure improvements and method optimization.Perform other responsibilities as deemed necessary.  qualifications: Bachelor of Science (BS) or Bachelor of Arts (BA) in a Biological or Biochemical Science with at least 0-2 years of relevant laboratory experience ORAssociates of Science (AS) with at least 4 years of relevant laboratory experience.Experience in quality control practices, current Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP) beneficial, but not required.Must possess ability to take initiative. Able to work in team, as well as, on an individual basis.Ability to perform most tasks with supervision.Computer literacy is required.Must have excellent record keeping, written and verbal skills.   skills: Quality control, GLP (Good Laboratory Practice), Microbiology, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). Applications accepted on ongoing basis until filled. Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.