warehouse manager 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. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you!   location: Cambridge, Massachusetts job type: Contract salary: $118.33 - 183.07 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Provides guidance and subject matter expertise on risk management and risk minimization strategy to an assigned therapeutic area to ensure that product risk management strategies are consistent worldwide Provide guidance and subject matter expertise on the structured benefit risk assessment framework and the development of the benefit risk assessment documentEngages with partner global functions (e.g. Clinical Science, Med Affairs, Regulatory Affairs, Biostats) to ensure alignment of global position for pharmacovigilance risk management processes to maximize patient safetyProvide strategic expertise to cross-functional product team members in developing pharmacovigilance risk strategies including benchmarking and scenario planning.Support the development of risk management plans (RMPs) in modular format, review RMPs) and ensure alignment with Good Pharmacovigilance Practices and other applicable regulationsDevelop and review risk minimization documents such as additional risk minimization measures (aRMMs) and Risk Evaluation and Mitigation Strategy (REMS)Provide subject matter expertise and thoughtful contributions to qualitative and quantitative structured benefit risk assessmentsProvide guidance on incorporation of the patient's perspective into benefit risk activities (e.g. patient preference studies)Collaborate with Safety Leads, Clinical Leads, PV scientists and Clinical Research Scientists, and others cross functional teams on benefit risk assessment strategyDevelop and provide recommendations for appropriate risk management interventions such as direct healthcare professional communications, educational materials, controlled access programProvide guidance regarding tracking risk management commitments including utilization of a tracking platform and system improvement assessmentMonitor and report risk management metrics to ensure complianceProvide centralized support, training and leadership for safety and cross-functional members who work on risk management plans and risk minimizations activities.Support inspections and audits activities with regards to risk management processesPerform other duties as defined in standard operation procedures or requested by supervisor.  qualifications: Associate Director: PhD/PharmD/DO/MD + 4 years; OR Masters + 7 years; OR Bachelors + 10 years Minimum 2 years in PV/safety OR clinical development preferredMinimum 3 years of pharmaceutical industry/drug development experiencePharmaceutical industry experience, with exposure to PV risk management, additional risk minimization measures and/or REMS programs preferredStrong track record of scientific and analytical thinkingExperience presenting to technical and lay groups at public meetings is desirableDemonstrate integrity and work productively in a high-pressure environmentGood analytical/judgment capabilities to understand/analyze/synthesize and communicate Project Management abilitiesAbility to identify and understand proactively the interactions necessary for achieving business goals and objectivesAble to manage both time and priority constraints and to manage multiple priorities simultaneouslyAttention to details, computer literacy, knowledge of safety databasesTake initiative and autonomous actionProven ability to work in an international environment and with cross-functional teams, with good interpersonal skills / assertiveness / team spirit / coaching skills  skills: Risk Evaluation and Mitigation Strategies (REMS) 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 company is seeking a highly motivated and detail-oriented Quality Control Specialist to lead our growing QC Sample Management function. This individual will serve as a subject matter expert for cGMP sample lifecycle activities while actively contributing to hands-on lab operations and leading a team of associates.You will work at the intersection of science, digital systems (such as LabVantage LIMS), and continuous improvement. The role includes broad exposure to analytical chemistry, microbiology, bioassay, and raw material testing workflows and offers the opportunity to interface with digital transformation projects, including those involving AI tools in the lab data lifecycle.   location: Norwood, Massachusetts job type: Contract salary: $35 - 41 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Lead a team of QC Sample Management Associates supporting Chemistry, Microbiology, Bioassay, and Raw Materials workflows from CMOs and Development labs.Oversee and coordinate the daily schedule to ensure timely sample processing, compliance documentation, and lab record completion.Create weekly schedules and lead team meetings to align on operational goals and address troubleshooting needs.Partner with Digital teams to expand and optimize the use of LIMS (LabVantage), with a pathway to incorporate next-generation data tools including Generative AI in QC workflows.Act as primary support for audit readiness and participate in both internal and external inspections.Author and revise SOPs, quality records, deviations, CAPAs, and change controls.Oversee hiring, onboarding, development, and performance reviews for Sample Management Associates, including 1:1 coaching.Maintain compliance of training records for the team and assign appropriate training modules.Lead investigations and resolution of compliance issues related to sample handling.Manage controlled temperature unit (CTU) systems, including maintenance and troubleshooting.Foster a culture of safety and compliance in the lab environment.ou will be responsible not only for the execution of sample management activities but also for building and evolving the systems that support them-demonstrating accountability for both people and processes.In this role, you will help drive LIMS optimization and connect with broader initiatives that enable digital QC and data automation, unlocking potential for advanced analytics and AI-enhanced compliance tracking.  qualifications: Required: BA/BS in a relevant scientific discipline with a minimum of 3-5 years of Quality Control experience in a cGMP organization OR MS in a relevant scientific discipline with a minimum of 1-3 years of Quality Control experience in a cGMP organizationDemonstrate ability to effectively and independently prioritize, manage, and complete multiple projects and tasks in a fast-paced environmentDetailed knowledge of LIMS system (LIMS) and quality document system (Veeva)Working knowledge of relevant and current FDA, EU, ICH guidelines and regulationsExperience with gowning, aseptic technique and general lab safety practicesFlexible schedule to support periodic on call, weekend or holiday coverageStrong and effective people management skills #LI-KH1   skills: Chemistry, Laboratory Information Management Systems (LIMS), Aseptic Technique, Veeva Vault, Good Manufacturing Practices (GMP) 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 CMC Synthetics Platform within the company R&D organization, is responsible for the process development of small molecule drug substances undergoing clinical studies. We are seeking a hands-on laboratory manager with excellent organizational skills to support our activities.   location: Cambridge, Massachusetts job type: Contract salary: $55 - 59 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Job Responsibilities The person will provide services to company at the Cambridge Crossing (CX), Cambridge, MA site.Provide on-site service to the Client for both laboratory functions and laboratory equipment and instrumentation maintenance and upkeepPerform experimental protocols to support the Client's technology platformsEnsure compliance with health and safety teams and training as required for company lab operationsSupport inventory management, purchasing, and shipping of chemical compounds and laboratory supplies Laboratories support activities: Maintain equipment and support new equipment installation and material readiness for technology platformsSubmit and track work requests and coordinate with service engineers to ensure timely service in cases of equipment failureWrite and maintain training documentation describing the proper use of equipment and workflowsCoordinate with IT for laboratory computer troubleshootingAssist scientists with shipping of chemical samples and bulk chemicals and intermediates between sites and CROs/CMOs including international shipping logisticsMonitor and maintain HPLC/UPLC diluent and eluent supplies as neededGenerate experimental data by following platform protocols   qualifications: Education & Qualifications B.S. or B.A. in relevant field (Chemistry or related discipline) with at least 3 years of relevant experience, or Master's in ChemistryDemonstrated aptitude for working in the lab and hands-on experience with equipment and instrument maintenanceExcellent communication skills (oral and written) and organization skills are requiredAbility to work independently and set own scheduleMicrosoft Word, Excel, and Outlook. Experience participating in teams and collaborative work environments. Must have experience: Lab Manager, someone who is readily available in lab, basic experience with equipment, chemicals comfort with PPE, collab with vendorsHPLC instrumentation troubleshooting experiencePrevious experience working with vendors, relocating chemicals, solvents liquids, working to support other ScientistsProficient in MS SuitePrevious data generation experienceMinimum of 3 years of relevant laboratory-based experience, must be professional experience; within pharma, biotech or academic labs. Same min # of years applicable to both bachelor's degree and master's degree candidates. Nice to Have/ Preferred Skills: Chemistry Lab Management experience #LI-AM1   skills: Chemistry, Ultra Performance Liquid Chromatography (UPLC), High Pressure Liquid Chromatography (HPLC), Chemistry Manufacturing and Controls (CMC) 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.