seo analyst salaries in boston, massachusetts

job summary: --------------------------------------------------------------------------------------------------------------------------------------------------------------------- Client is executing a major version upgrade of its Contract Lifecycle Management (CLM) platform Corcentric Determine. The application is embedded within critical business processes across the organization and requires that the upgrade causes no business disruption to existing activities. This role will be accountable for ensuring the successful delivery of the upgraded environment working across all necessary parties to execute deliverables and resolve issues. Engagement would be across various groups within client as well as with the CLM vendor.  location: Cambridge, Massachusetts job type: Contract salary: $70 - 76 per hour work hours: 8am to 4pm education: Bachelors   responsibilities: This individual will need to be able to work within a controlled GxP environment while still being able to drive activities forward in an expedited fashion. JOB DUTIES - Requirements analysis and validation against actual system capabilities - Requirements traceability (URS, FS, DS, SIT, UAT, and Traceability Matrix) review and end to end mapping of any missing requirements - Documentation of user requirements specifications and functional specifications from existing design documents or other relevant documents - Test script (SIT and UAT) review and revision (where necessary) to reflect actual system functionality - Validation package (e.g. Validation Plan, Validation Report, System Management SOP, etc.) review and revision (where appropriate) of content Quality - ensure a high level of quality in solutions is delivered and GxP standards complied with Vendor Coordination - work closely with the vendor on issues to ensure resolution General project management activities (schedule, status tracking, escalation, etc) REQUIRED SKILLS Bachelor's degree or equivalent experience in computer science, Information Technology and/or related discipline. 3+ years of experience working in a GxP environment (MUST) 5+ years of IT related BA experience strong communication skills and a background of working directly with business users Enjoys detailed analysis and making a positive impact ADDITIONAL EXPECTATIONS Experience working on a CLM system (nice to have) Experience working on SaaS applications Experience working on applications that are used globally and have multiple interfaces   qualifications: Experience level: ExperiencedEducation: Bachelors  skills: Business AnalysisGxPPharmaceutical 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. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

We are currently hiring for a QC Analyst II at Takeda Pharmaceuticals, based in Lexington, MA.  This individual will support rhASA D/TAK-611 QC MV as a part of the QC HPLC team. This is a 9-month contract to start with the potential to extend from there.  Please reach out to ashley.cross@randstadusa.com with any questions!salary: $35 - $45 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilitiesRole is responsible for HPLC laboratories performing a broad range of analytical based techniques such as SE-HPLC, RP-HPLC, IEX, CE-SDS, glycan and peptide analyses in order to support in-process, release and stability testing. Support commercial and clinical testing for defined site-based and external programs, as well as method transfer and validation- introduction of new equipment and technology to improve sustainability and compliance is expected Provide support for Quality projects and implementation of operational excellence initiatives Areas of focus on techniques such as HPLC and SDS-PAGE for purity, identity, potency and charged heterogeneity. Perform and troubleshoot HPLC based assays (SE-HPLC, IEX, RP-HPLC, CE-SDS, Peptide Mapping, and Glycan Mapping) of release and stability Execute and lead method qualification and validation assays as needed Perform and lead OOT, OOS, GMP Investigations, data analysis, deviation and data trending Maintain GMP condition of the lab The essential functions of this role include:working in a smoke free environmentSkillsHPLC (2 years of experience is preferred)SDS-PAGE (2 years of experience is preferred)SE-HPLCIEX RP-HPLCCE-SDSPeptide MappingGlycan MappingQuality ControlQualificationsYears of experience: 2 yearsExperience level: ExperiencedRandstad 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. 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. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

Onsite in Billerica, MA. Great entry level Quality Analyst position for someone with a recent Biology degree or GMP experience.   Perform testing on incoming materials, finished products and stability studies in QC Laboratory. Work in both lab and warehouse areas.  Testing also includes visual inspections, dimensional verifications and analytical testing. 1-3 years of previous experience in the pharmaceutical industry, related GMP environment, or equivalent. Previous experience preferred. BA/BS degree in a related scientific discipline (e.g. chemistry, biology) or equivalent combination of education and experience.salary: $26 - $32 per hourshift: Firstwork hours: 8 AM - 4 PMeducation: BachelorResponsibilitiesPerform routine QC testing and Visual Inspection in accordance with SOPs and cGMP guidelines. Some supervision required. ·       Perform verification of data to ensure accuracy.  Perform approval upon discretion of supervisor. ·       Assist with audit readiness of laboratory area and calibration and maintenance of laboratory equipment. ·       Utilize a range of electronic systems such as LIMS and document/equipment management software. ·       Author SOP changes; participate in change controls, CAPAs and other quality systems.SkillsQuality AssuranceQualificationsYears of experience: 0 yearsExperience level: Entry LevelRandstad 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. 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. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.