business analyst salaries in boston, massachusetts

job summary: Randstad Digital is partnering with a leading consumer goods retailer to find a QA Analyst to support their global ticketing application. Familiarity with NiceLabel Loftware for barcode production is essential. Candidates must be local to Marlborough, MA and be willing to come into the office as-needed for testing.    location: Framingham, Massachusetts job type: Contract salary: $43 - 48 per hour work hours: 8am to 5pm education: Bachelors   responsibilities: - Performs testing of medium to high complexity to ensure that the system is implemented and functions as designed - Ensures that testing meets organization standards for compliance - Partners and collaborates with project team members and the business to design/develop testing strategies - Creates medium to high complexity test plans and test cases utilizing business/solution requirements and technical design documentation - Executes medium to high complexity test cases both manually and/or by automation - Performs triage for medium to high complexity defects, which include detection, risk assessment, documentation and retesting. Calls out more complex defects to the appropriate level - Assesses software for stability - Provides input to QA Project Leader on project status - Share knowledge and provide guidance to team members - Performs other duties as assigned - Ensures thorough testing the end-to-end solution meets user requirements - Provides first level testing approval - May assign and monitor tasks to team members and third-party vendor contractors to ensure deliverables align with the project plan   qualifications: 3-5 years of QA testing and NiceLabel experience 6-8 years of QA testing without NiceLabel experience 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 Digital, 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 Digital 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: Step into a critical contract role as a Data Review Specialist - Bioassays in Norwood, MA, offering a competitive rate of $40-$51/hour. This position is ideal for a highly experienced professional with a Bachelor's degree in a scientific field (Biology, Chemistry, or similar) and 5+ years of direct experience in GMP QC labs. The specialist will be responsible for the rigorous data review and release of executed QC Bioassay test records, ensuring strict GDP/GMP compliance, including audit trail review. Core functions also involve managing quality systems by authoring and revising SOPs, procedures, and reports, and supporting the creation of quality records such as deviations, change controls, and CAPAs, while contributing to investigations and troubleshooting efforts.   location: Norwood, Massachusetts job type: Contract salary: $40 - 51 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Review executed QC Bioassay test records for product release.Work with QC group to maintain and update all necessary training documentation including On-The-Job Trainings, Training Materials, Instructor Led Training, and Knowledge Checks.Support authoring and revision of laboratory procedures and reportsSupport authoring quality systems records such as deviations, change controls, CAPAs as requiredSupport team to investigate and resolve issues related to assay failures, system deficiencies, and equipment / assay troubleshooting.Additional duties may be assigned  qualifications: Required: BA or BS degree in Biology, Chemistry, or similar field5+ years of direct experience in GMP QC labs with experience performing Bioassay methods. e.g. DNA Sequencing, Electrophoresis, PCR, Residual Protein Assays, and Cell Culture.Previous experience reviewing data for GDP/GMP compliance as well as audit trail reviewPrevious experience managing quality records such as change controls, deviations, and lab investigationsA desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative. #LI-KH1   skills: Quality control, CAPA, Assay Method, Cell Cultures, 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: 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: The Compliance Specialist will perform critical QA tasks in support of GMP and non-GMP manufacturing programs and Regulatory Submissions at AIRM. The successful candidate will foster data integrity, quality, and compliance across a broad range of Quality Assurance areas and will work closely with talented counterparts at Company to help ensure high quality standards and value delivery for our patients.   location: Westborough, Massachusetts job type: Contract salary: $40.00 - 44.07 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Performs QA review of executed GMP analytical batch records; in-process, release, and stability data to ensure compliance with regulatory requirements, internal quality standards, internal procedures, and contribute to the overall Quality Assurance processes.Performs QA review of executed development studies intended for regulatory submissions, included but not limited to, draft batch records, analytical test records, and calibration records to ensure Developmental studies are conducted and data collected in compliance with approved protocols, appropriate corporate guidelines, internal procedures, domestic and global regulatory guidelines and standards. Identifies and reports documentation errors and deviations from test / data records, protocols, Standard Operating Procedures (SOPs), or specifications in a timely manner.Collaborates with cross-functional stakeholders regarding quality events, ensuring quality records are clearly written and technically sound with supporting evidence.  qualifications: BS/BA in Life Sciences, Engineering, or Chemistry, with 2-3 years of related Quality Assurance experience within GMP-regulated industry, or 1-2 years with Masters degree. In lieu of a Life Sciences degree, consideration will be given to candidates with minimum of 6+ years of industry experience in biotechnological and/or pharmaceutical quality, manufacturing, or other industry requiring high technical aptitude and attention to detail.Working fluency in the Microsoft Office productivity suite (including Excel and PowerPoint). Preferred Qualifications: Demonstrated knowledge of cGMPs for biotechnology, cell therapy, and/or gene therapy and other international regulatory requirements.Ability to interpret regulatory rules, guidance, and normative industry standards to make objective, risk-based decisions, and exercise sound Quality-by-Design principles. #LI-JW1   skills: Quality Assurance, MS-EXCEL, GMP (Good Manufacturing Practice), Good Manufacturing Practices (GMP), Quality Assurance (QA), Batch Record 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.