AWS DevOps/Data Center Technical Operations Engineer 2-11 month contractNorth Reading, MA
*Not open to C2C or visa sponsorshipResponsibilities: Develop method to connect lab resources with development environment hosted in AWS. Review existing backup strategy and recommend/implement improvements. Improve method for building custom AMIs, growing and shrinking EC2 instance count in compute farm. Document newly built infrastructure and its ongoing maintenance. Various infrastructure improvements as time permits on the contract.Top requirements: At least 2+ years of experience in Amazon Web Services (AWS) Experience with scripting languages (e.g. Python) Experience with Raspberry PiAdditional requirements: Experience in the following products and technologies: AWS EC2 AWS IAM AWS S3 AWS Directory Services AWS Route53 AWS Systems Manager AWS Cloud Formation ZFSPreferred skills: Bachelors Degree preferred but not required Experience in the following products and technologies: AWS IoT Greengrass Slurm Distributed Computing AWS Certification highly preferred
Experis is an Equal Opportunity Employer
I hope this message finds you well.
My name is Mohd Ataullah Khan (MAK) with Experis a part of Manpower Group. I have an excellent and long-term opportunity with a direct client of ours. This opportunity is urgent and looking to move very quickly, please apply by sending your email or forwarding on to anyone you know who might be a fit. I am looking forward to connecting with you! I apologize in advance if this is out of range in terms of location.
Role: Upcoming Business Analyst Location: 02138 (CAMBRIDGE, Massachusetts)
Job Type: Contract 4 Months (Possible extension)
Industry: Pharmaceutical Direct Clients
Along with this growth comes a number of exciting opportunities to work with our expanding business areas.
Within Research & Development (R&D) IT, there is a need to support the Regulatory organization team as a contract Business Analyst within the TMF team.
S/he will be expected to partner with the Sr.
Job Title: CAD Designer & Drafter
Location: DANVERS, MA, 01923 Duration: 12+ Months (Possible extension)
Position requires strong CAD skills, specifically in SolidWorks with assemblies, exploded views, and detailed drawings.
Must be capable of solving problems of moderate scope and complexity following established policies and procedures.
Must be capable of working on multiple projects, skilled multi-tasker, meet established deadlines, and follow up on requests for action or information.
Must have the ability to learn new skills.
Demonstrate commitment to customer satisfaction both internally and externally.
Demonstrate strong attention to detail.
Demonstrate ability to work semi-independently, with minimal to moderate supervision.
Strong sense of responsibility, urgency, enthusiasm and high energy.
Demonstrate ability to work in a team and cross function departments environment.
Associate's Degree or equivalent in Computer Aided Drafting with 1-3 years' experience.
Bachelor's Degree or equivalent in an Engineering discipline preferred.
Prior work experience/internship with CAD software, preferably Solidworks, required.
1+ years' experience.
Weekend coverage required.
Thanks & Regards
Anil Kumar PandeyTalent Acquisition SpecialistPhone: 414-323-8455 Ext: firstname.lastname@example.org
Experis is an Equal Opportunity Employer
I would like to introduce you to a new position that I am working to fill ASAP. I have listed the details below. If you are not available at this time, please keep my information and feel free to reach out when you are available. Feel free to forward this if you someone else that might be a fit for this opportunity or perhaps point me in the right direction. If you would like to be considered for this role, please reply back with your resume and best time to call with contact info ASAP to email@example.com
Any feedback would be greatly appreciated.
A Major Pharmaceutical Company is looking for a talented Clinical Trial Associate
(position is remote till covid situation) Position Summary Assist the CPLs for the planning, implementation, execution and compliance of operational plans for clinical study/program with multiple clinical vendors in order to maintain inspection readiness. This is a tactical position and involves protocol execution at the site level via established vendor oversight and escalation pathways. Serve as a peer mentor for staff, as needed. Ensure quality of the trial master file through content (QC) review of document packages submitted for entry into the TMF and liaise with project teams to resolve any issues identified with the documents submitted.
Looking for a Compliance Specialist in Framingham, MA!5 Month ContractCompetitive Salary!The Quality Assurance (QA) Operations department is responsible for quality oversight of operations at the Sanofi Framingham manufacturing facilities. QA's main responsibility is to ensure adherence to CGMPs during manufacturing operations through partnership with the site and direct engagement with daily operations activities. Quality Assurance Operations is responsible for providing support and guidance to the Sanofi Operations function in order to protect the safety, quality and efficacy of Sanofi's products, thereby ensuring the availability of compliant and safe products for our patients and assuring the security of the company's business and global markets
Demonstrate strong leadership qualities and embody Sanofi's core leadership principals.
Support the quality oversight of manufacturing operations, product release, and where appropriate quality data analysis and validation of gmp facilities.
Provide input and support of CAPA and Deviation Quality System improvement initiatives.
Participate in policy discussions and represent the Quality Assurance Operations team on issues impacting the direction of quality in the organization.
Perform the Quality Assurance review and approval of complex change controls, deviations, Environmental Monitoring/Critical Utility investigations, laboratory investigations, and CAPAs to ensure that they meet the requirements of Sanofi standards and procedures, and are clearly and appropriately justified.
Perform product complaint investigations.
Work closely with manufacturing, quality and support groups to resolve Quality System requirements within agreed timelines.
Approve management activities in Quality Management systems.
Facilitate department regulatory related CAPAs and audit responses.
Work closely with manufacturing, quality and support groups to develop effective CAPA.
Generate and present assigned metrics at the required frequency which drive accountability and delivery of targets.
Participate in and/or lead formal risk assessments.
Review and provide guidance for proposed and existing changes through the formal change control process as it applies to validated processes, equipment and test methods.
SNFIJP00002649USA-Compliance Specialist III (Manufacturing/Quality)Description:Perform audits necessary to ensure the compliance of manufacturing procedures to in-house specifications and government regulation. Establish auditing requirements, quality standards and test methods in accordance with regulations and relevant quality requirements. Conduct internal audits of manufacturing processes to ensure compliance. Conduct review of testing results. Review document and complete inspection of returned goods. May be involved with establishing compliance requirements for the methodology transfer from Research to Quality Control. Interpret complex, explicit documentation to ensure quality standards and compliance. May provide training to new employees. Work under only very general supervision. Work is reviewed for soundness of judgment and overall adequacy and accuracy.
Job Title: Data Integration ArchitectLocation: Remote, Later Cambridge, MA
Duration: 6 months with possible extension
Summary: The ability to effectively capture, manage and analyze complex data is critical to Biogen's strategy. While the company has extensive capabilities and resources in relevant areas, they are distributed across the organization - both within and outside of IT. The Data Engineering and Analytics (DEA) team operates as the "hub" in a "hub and spoke" federated model where they collaborate with distributed stakeholder groups (the "spokes") to enable their specific priorities while establishing common enterprise-wide capabilities across information management and delivery competencies and platforms. DEA has been established to enable Biogen to move beyond legacy ways of implementing solutions and eliminate siloed thinking & activity as it relates to information management and delivery.
Looking for a Drug Safety Specialist in Waltham, MA!4 Month Contract +extension possible
Work Schedule9 am to 5 pmResponsible for the collection, data entry, routing, follow-up, and timely reporting/submission of safety information (including expedited and aggregate reports) related to drug products from a variety of sources (clinical trial, spontaneous, literature) in compliance with SOPs and regional & international regulations. This position is especially important in light of the approval and marketing of products and the number and diversity of clinical trials. Authorities conduct periodic, detailed audits to ensure integrity of AE processing, thoroughness of documentation, accuracy of results, and timeliness of reports.
Engineer, Electrical Dev QualityJob Description:Provide Development support to hardware/software R&D and manufacturing, helping to ensure delivery of highest quality product to the customer as part of the new product development team. Provide Quality Engineering support to product development teams, helping to ensure development of highest quality new products.1. Develops Process Monitoring Systems by identifying critical process steps applying methods to reduce process variation in order to reduce/eliminate the cause of defects.2. Develops and implements product quality plans, documents and systems by creating product specifications, quality specifications, quality plans, risk analyses, FMEAs in conjunction with other product development team members. Responsible for creating risk analyses and FMEAs..3.
I am reaching out as I've come across your resume profile and I was impressed with your credentials. I would like to share a role I am currently hiring for, a R&D Engineer for a 06-month contract in Forge Village, MA with a with major medical device company. If you are not in the market yourself for a new opportunity, please let me know if you have any contacts in your professional network that might be interested.
Working under general supervision, supports product development efforts by performing clinical-systems and human factors engineering tasks such as investigating, defining, analyzing, documenting and testing activities associated with the development of specific projects.
Performs additional analysis and/or interviews to determine the requirements and constraints on the assigned portion of the system.
Work requires the application of theoretical principles, evaluation, ingenuity and creative/analytical techniques typically acquired in a recognized four-year or more academic course of study.
Has the ability to apply technical, clinical and marketing understanding of issues to bring tasks to resolution within assigned projects.
Applies engineering and scientific principles to the evaluation and solution of technical problems.
The Executive Assistant will be a dynamic and self-motivated individual able to provide administrative support to the VP of Biologics Drug Discovery and coordination of projects for the EA to the head of the division. The right candidate must be proactive, flexible, organized, collaborative, and calm under pressure. Excellent communication, inter-personal and collaboration skills are essential for this role due to interactions with BTMS leaders, others across all levels of the organization. This position also requires a professional demeanor, sense of urgency, the ability to prioritize and in-depth knowledge of project management and project implementation. Competencies/Capabilities Demonstrated ability to work efficiently and to perform tasks simultaneously with minimum supervision in a fast-paced environment.
Job Responsibilities: Boston, MA - Remote roleStart date 9/5/2020Experis is seeking 1-3 years experience as a Financial Analyst to support a client in the Financial Services Industry located in Boston, MA. This is a Remote roleStart date is 9/5/2020-Project to transition all performance and analytics clients to new platform as a critical part of our overall technology enhancement plan. -It's integrating the accounting and information systems to the new generation performance platform. -This role will involve collecting data and calculation of rates of return. -Validating data-Run Excel reports from different regions for comparison and matching. -Product development team leads the conversion and the data reconciliation but recently asked for ops team help-Calculates distributions.
Experis is seeking A Fund Accountant with Money Market experience for a client a global leader organization across banking, markets and investor services.Candidate should have 3+ years' experience in Fund Administration and Knowledge of Money Market funds desired. Contract with potential to convert to Permanent. Location - Boston, MA Key Responsibilities Daily production of accurate and timely Net Asset Values Working closely with global Hubs/Utilities to resolve queries and issues Producing ad hoc reports for clients Creating, maintaining and updating procedures for the funds Ensuring compliance with all controls and procedures outlined in the procedures manual and general company policies Working closely with the new business team and clients through the on-boarding process Ensuring all schedule work is completed by agreed deadlines, checklists are signed and files contain all required Identifying efficiencies and areas for improvement to reduce risk and become more efficient Qualifications 3 years of experience in Operations Strong technical skills including accounting principles and theories Knowledge of 40 ACTs Accounting-Fund Accounting, Financial Reporting and Tax Operations Ability to be effective in a global operating environment and a matrix management organizations Exceptional leadership and staff development skills with prior team management experience Excellent communication, influencing and negotiation skills with the ability to develop and maintain collaborative relationships both internally and with external clients Strong client service skills Analytical skills, problem solving, good critical thinking and decision-making skills Experience working across multiple business areas and/or functions to deliver results Excellent verbal and written communication skills; executive presentation skills Ability to work independently and multitask in a fast paced environment Working knowledge of one or more CIB/FSO product, service or operations areas preferred Relationship building skills - develop internal and external partnerships to drive results Expert use of Microsoft Project, Word, Excel, PowerPoint, Visio and ability to present to senior management.
Please forward updated resume to Ana - firstname.lastname@example.org
Experis is an Equal Opportunity Employer
Securities Services Operations Derivatives Processing Analyst - 601 J.P.Morgan's Corporate & Investment Bank (CIB) is a global leader across banking, markets and investor services. Location is Boston, MA Initially this will be remote during Covid19. Derivative Operations provides operational support across the CIB covering eight key product areas including FX, OTC Derivatives, Collateral Principal, 3rd Party Derivatives, Cleared Derivatives, Agency Collateral, Billing and CASS with ~1,900 employees. Services provided to our Businesses include: Transaction Processing, Confirmation, Settlement and Clearing, Collateral Management, Client Service, Invoicing and CASS Support Typical daily activity includes settling in excess of $217B via FX trading, leading a Markets OTC portfolio of 2.5M trades, servicing >200 3rd party clients, performing 10,000 margin calls, processing 470k cleared and intermediated trades and producing >9,000 invoices Third Party Derivatives Processing (3PDP) supports four main OTC / CFD derivatives services: NAV Support instruction capture and processing client provided valuations / cash flows; reconciliation to the fund manager Independent Valuations instruction capture, generate in-house/ source TPV valuations and cash flows; reconcile to the fund manager/ counterparties; standard reporting Middle Office same service as Independent Valuations plus confirmation/ settlement management Asset Verification As a utility to T&F, produce Independent Asset Verification of OTC/FFX & CFD trades The individual will work within the Boston 3PDP Team and have responsibility for the delivery of these services to a number of clients.
Looking for a Health and Safety Specialist in Meriden, CT!
13 Month Contract
Work Schedule 9-6 Weekend and Night work may be required
As a member of the MTech and Quality teams at PSC, the candidate will provide right level of support to the transfer from sending site in terms of technical, documentation, and training support. Ensure the transferred process and analytical methods perform to expectations and demonstrate good consistency and robustness, and ensure the resulting operation added to the receiving site be sustainable, reliable, cost effective and compliant with HSE standards.
Candidate will accomplish these tasks in a laboratory setting and through collaborations both internal and external.
Title: R&D IT Senior Business Analyst (BA)Timeline/duration: 6 months w/ possible extensionLocation: Remote, then CambridgeInterview process: Phone + VideoOverviewThe R&D IT Senior Business Analyst (BA) will oversee Clinical Development projects supporting compliance remediations and system retirements. The BA plays a key role in the health and success of projects within a matrixed organization. Has direct relationships with various business and IT groups.This role requires the following abilities:High competency in system retirement and compliance remediation projects; leverages BA tools and techniquesDemonstrate traceable business and functional requirements (show work examples)Monitor, manage, and ensure predictable delivery of the project in a deadline-driven environment.Drive delivery and accountability of project peers and vendorsEarly identification and appropriate escalation of risks and issues that require assistance, attention, or executive resolutionEffective communication of all project aspects to team and leadership, verbally or in written formThe key activities for this position include:Develop GxP-compliant SDLC deliverablesPerform risk assessmentsAssist Test Lead validate functional requirements, where neededCo-develop IT Support documentation (System Management SOP; Knowledge Base)Complete other ad hoc tasks, as requestedProvide status reportsQualifications:Strong interpersonal and teamwork skills, with the ability to interact with business users, technical IT groups, project managers, senior management, outsourced service providers, and vendors5-7 years' experience as a Sr.
Summary: The Loan Processor is expected to maintain accurate and current statuses, track loan status during the life cycle, meet key milestone dates, and proactively follow up on all loans to minimize origination cycle times. Responsibilities: Review all loan applications for accuracy, completeness and compliance. Monitor and maintain an application pipeline. Ensure delivery of initial disclosures or re-disclosure within expected time frames. Verify fees disclosed are accurate prior to issuance. Follow up on disclosure documentation issued and received within regulatory time frames through pipeline management practices. Process loans (Portfolio, RI Housing, FHA, VA, Conventional, Consumer, purchase, refinance, construction) under various programs in a quality consistent with all company policies and procedures as well as meeting all regulatory requirements Image / index, review and submit completed files via the loan origination system to the underwriting department.
Inventory Logistics Receiver 1776 Heritage Dr, Quincy MA 02171
2 years minimum Contract
Minimum of 12 months customer service related experience preferred.
Demonstrated knowledge and experience in a related functional area preferred.
Skills and Attributes:
Computer skills a must email, Microsoft Office, instant messaging and multiple inventory software programs will be used on a daily basis.
Able to effectively communicate in writing and verbally with clients and company personnel.
Effective listening, verbal and written communication skills for a challenging and customer focused working environment.
Planning and organization skills.
Customer service, people oriented. Knowledge of customer service principles and practices.
Able to effectively work independently or in a team environment.
Basic mathematical knowledge.
Demonstrate competency in performing required tasks.
Demonstrate proficiency in operation of related equipment.
High level of accuracy is critical, attention to detail.
May be required to work flexible hours.
Receive assets, including:
Handling order delivery and acceptance, including visually inspecting carton for damage and reconciliation of shipment with shipment documentation (bill of lading)
Validating contents against packing slip and order completion
Notification of receipt and corresponding updates
Notification of discrepancies, if any
Assure asset tags, markings and labels are affixed to assets.
Job Title: Manufacturing/Process EngineerLocation: Danvers MADuration: 12 Months (possibilities of extension)
Job Description:This position will be primarily responsible to develop and write validation protocols, execute validations and compose validation reports. In addition, this role will be supporting equipment installation and procedure writing.
Duties and ResponsibilitiesCollaborate with designers and engineering regarding product tooling and design to ensure effectual production methods.Collaborate with designers and engineering to ensure assemblies and components can be manufactured effectively.Develop and write IQ/OQ/PQ protocols for appropriate equipment and systems within the guidelines of cGMP, internal policies and procedures.Perform and/or supervise the execution of protocols.Review executed protocols and write final reports.Work closely with operations to develop, coordinate, and implement technical training for employees.Create standard operating procedures (SOPs) for various validation related use.Support company policies and procedures, goals and objectives, all regulatory and GMP requirements.
Qualifications3+ years experience in similar roles.B.S.
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