benefits associate salaries in boston, massachusetts

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. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now!   location: Framingham, Massachusetts job type: Contract salary: $54.00 - 55.53 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Responsible for the execution and analysis of experiments and analytical procedures.Display an investigative or technological orientation in designing, executing and interpreting experiments and analytical procedures.Investigate basic technical problems and performs routine scientific procedures and experiments under general supervision.Plan and prioritize concurrent experimental procedures. Integrate, compile, and tabulate data and assist supervisor in the analysis and interpretation of the results.May provide oral presentations on results to other department members.Work under active supervision.Follow established procedures.Work is reviewed for soundness of technical judgment and overall adequacy and accuracy. Contribute to the completion of milestones associated with specific projects.Failure to achieve results or erroneous execution may cause delays in program schedules, and may result in the allocation of additional resources.Frequent internal company contacts.Infrequent inter- departmental and outside constituent contacts on routine matters.   qualifications: BA in Biology, Chemistry or similar2-3 years of lab experience academic and post school.Required skills: Assays - CE, liquid and caliper and HPLC.Preferred - Hamilton liquid system, Strong Microsoft skills will be trained on client specific programs. #LI-BM1   skills: Biology, Chemistry, High Pressure Liquid Chromatography (HPLC) 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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

job summary: In this role the QC Bioassay Associate will support in-process and release testing for raw materials, drug substance and mRNA drug products produced at the company's manufacturing facilities and affiliated contract organizations. Additionally, this position will assist management in ensuring the goals and milestones are met for the QC Bioassay Lab as well as day-to-day operations.   location: Norwood, Massachusetts job type: Contract salary: $30 - 37 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Utilize knowledge and investigations skills to identify and resolve issues and drive continuous improvement initiatives in laboratory operationsSupport Testing for Raw Materials, Drug Substance and drug product, including generation of testing data in support of commercially approved products and clinical studiesAssist in development, implementation, and maintenance of general laboratory operational systems in accordance with cGMP requirementsCollaborate with development groups for method transfers and qualifications in support of expanding the QC Bioassay laboratory capabilities, including sequencing and qPCR assays as requiredConduct technical assessments of deviations and investigations ensuring day to day operations are successfulPerform on the job (OJT) training and act as mentor to QC Bioassay staffAssist in equipment qualification/Validation activities, including maintenanceAssist with scheduling and resource allocation including Tier meetings as neededRepresent the QC Bioassay team in the absence of managementWork directly with management to ensure QC Goals and milestones are metLead and organize continuous improvement projectsTroubleshoot issues related to equipment, laboratory procedures and assay performanceWrite/revise SOP's, technical protocols, and reportsAssist with audit preparation and regulatory complianceResponsible for responding to and addressing CTU alarmsFoster a positive and inclusive work culture that promotes collaboration, innovation, and continuous improvementFollow all relevant GxP Regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirementsExecute tasks precisely as defined in internal guiding documents including but not limited to standard operating procedures (SOP's) and work instructionsFollow Good Documentation Practices and Data Integrity requirements to ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspectionsComplete training and assigned required learning plans accordingly to the defined due dates and prescribed requalification cadence.  qualifications: BS in a relevant scientific discipline (Biochemistry)Experience: 2-4 years of experienceDemonstrated aptitude or ability to learn: Able gain a strong understanding of GxP regulations (specify GMP, GLP, GCP, GVP or other applicable standards and guidances  skills: Quality control, GMP (Good Manufacturing Practice), SOP Development 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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

job summary: In this role the QC Bioassay Associate will support in-process and release testing for raw materials, drug substance and mRNA drug products produced at the company's manufacturing facilities and affiliated contract organizations. Additionally, this position will assist management in ensuring the goals and milestones are met for the QC Bioassay Lab as well as day-to-day operations.   location: Norwood, Massachusetts job type: Contract salary: $30 - 37 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Utilize knowledge and investigations skills to identify and resolve issues and drive continuous improvement initiatives in laboratory operationsSupport Testing for Raw Materials, Drug Substance and drug product, including generation of testing data in support of commercially approved products and clinical studiesAssist in development, implementation, and maintenance of general laboratory operational systems in accordance with cGMP requirementsCollaborate with development groups for method transfers and qualifications in support of expanding the QC Bioassay laboratory capabilities, including sequencing and qPCR assays as requiredConduct technical assessments of deviations and investigations ensuring day to day operations are successfulPerform on the job (OJT) training and act as mentor to QC Bioassay staffAssist in equipment qualification/Validation activities, including maintenanceAssist with scheduling and resource allocation including Tier meetings as neededRepresent the QC Bioassay team in the absence of managementWork directly with management to ensure QC Goals and milestones are metLead and organize continuous improvement projectsTroubleshoot issues related to equipment, laboratory procedures and assay performanceWrite/revise SOP's, technical protocols, and reportsAssist with audit preparation and regulatory complianceResponsible for responding to and addressing CTU alarmsFoster a positive and inclusive work culture that promotes collaboration, innovation, and continuous improvementFollow all relevant GxP Regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirementsExecute tasks precisely as defined in internal guiding documents including but not limited to standard operating procedures (SOP's) and work instructionsFollow Good Documentation Practices and Data Integrity requirements to ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspectionsComplete training and assigned required learning plans accordingly to the defined due dates and prescribed requalification cadence.  qualifications: BS in a relevant scientific discipline (Biochemistry)Experience: 2-4 years of experienceDemonstrated aptitude or ability to learn: Able gain a strong understanding of GxP regulations (specify GMP, GLP, GCP, GVP or other applicable standards and guidances #LI-AM1   skills: Quality control, GMP (Good Manufacturing Practice), SOP Development 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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.