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Feb 21, 2023

Conshohocken, PA

|

Drafter

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Contract-to-perm

{"JobID":266259,"JobType":["Contract-to-perm"],"EmployerID":null,"Location":{"Latitude":-75.282,"Longitude":40.0701818181818,"Distance":null},"State":"Pennsylvania","Zip":"19428","ReferenceID":"PHL-604844","PostedDate":"\/Date(1676999640000)\/","Description":"Our large engineering and construction client is currently hiring for 3 CAD/ Revit drafters to join their team across three different locations. These designers/drafters will be working onsite at pharmaceutical clients 4 days a week (remote one day a week). Specifically these individuals will be responsible for working in both AutoCAD and Revit handling mechanical and piping design , as well as handling document control and working closely with the client. These individuals should have the ability to client face, run meetings, and manage document flow as well as the specific designs for the project. Any architectural background as well as a background working on design for pharmaceutical construction is highly preferred.","Title":"CAD Designer","City":"Conshohocken","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- 5-15 years of experience working with AutoCAD and Revit - Mechanical, piping, or architectural design background - Ability to client face","Skills":"Pharmaceutical industry background","Industry":"Drafter","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":54.6000,"SalaryLow":36.4000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Our large engineering and construction client is currently hiring for 3 CAD/ Revit drafters to join their team across three different locations. These designers/drafters will be working onsite at... More pharmaceutical clients 4 days a week (remote one day a week). Specifically these individuals will be responsible for working in both AutoCAD and Revit handling mechanical and piping design , as well as handling document control and working closely with the client. These individuals should have the ability to client face, run meetings, and manage document flow as well as the specific designs for the project. Any architectural background as well as a background working on design for pharmaceutical construction is highly preferred.Less

Mar 21, 2023

Rahway, NJ

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Software Engineering

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Contract

{"JobID":273315,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-74.2744,"Longitude":40.6267909090909,"Distance":null},"State":"New Jersey","Zip":"07065","ReferenceID":"NNJ-611439","PostedDate":"\/Date(1679390054000)\/","Description":"Insight Global is seeking a software engineer to work with the scientists in the Process Research and Development department of a pharmaceutical client to solve key challenges in the processing and analysis of data from scientific instruments. The successful applicant will analyze stored binary data from state-of-the-art analytical instrumentation, write efficient code to expose the underlying raw data to Python applications, and work with our IT partners to connect these data to our cloud infrastructure. This position is a unique opportunity to learn and apply skills at the interface of software engineering, data science, and the physical sciences while developing tools and infrastructure that will have significant impacts pharmaceutical research.Day-to-day work will focus on working with binary file formats, constructing APIs for providing raw data to end users, creating data analysis pipelines, writing documentation and tests, and integrating code with our cloud platforms. There will be considerable flexibility in work arrangements. The successful candidate will have the opportunity to work remotely.","Title":"Software Engineer (Remote)","City":"Rahway","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Strong Python programming skills and a solid grasp of the fundamentals of computer science.Familiarity with documentation, version control, continuous integration, and testing tools.Ability to pass a technical assessment. Candidates will be provided with three binary files in which data are stored with a low, medium, and high degree of complexity, as well as their human-readable counterparts, and asked to provide Python functions to convert from the former to the latter.","Skills":"Pharmaceutical Industry ExperienceFamiliarity with AWS The ability to write C-based extensions or other numerically optimized code","Industry":"Software Engineering","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":60.0000,"SalaryLow":40.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Insight Global is seeking a software engineer to work with the scientists in the Process Research and Development department of a pharmaceutical client to solve key challenges in the processing and... More analysis of data from scientific instruments. The successful applicant will analyze stored binary data from state-of-the-art analytical instrumentation, write efficient code to expose the underlying raw data to Python applications, and work with our IT partners to connect these data to our cloud infrastructure. This position is a unique opportunity to learn and apply skills at the interface of software engineering, data science, and the physical sciences while developing tools and infrastructure that will have significant impacts pharmaceutical research.Day-to-day work will focus on working with binary file formats, constructing APIs for providing raw data to end users, creating data analysis pipelines, writing documentation and tests, and integrating code with our cloud platforms. There will be considerable flexibility in work arrangements. The successful candidate will have the opportunity to work remotely.Less

Mar 22, 2023

Newark, NJ

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QA

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Contract

{"JobID":273799,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-74.1549545454545,"Longitude":40.7416727272727,"Distance":null},"State":"New Jersey","Zip":"07102","ReferenceID":"PHL-612034","PostedDate":"\/Date(1679505236000)\/","Description":"One of our large pharmaceutical clients is looking to hire a QA Associate to join their growing External Quality team within Advanced Therapeutics. This individual will be providing Quality support for site and process qualification activities, engineering runs, and commercial product manufacturing. Main responsibilities will include: -Remote quality support for production activities, including deviation and CPA review, escalation of critical issues, batch review and release and change control. -Support monitoring of EM quality performance and proactively identify risks. -Influence and build relationship with internal and external partners to continuously enhance quality performance. -Interface with other functions i.e. Operations, Planning, Technical Operations, etc. as well as the external manufacturer-Apply cGMP regulations and other FDA and international requirements to all aspects of the position. -Provide on-site support as needed on request of the Janssen team lead","Title":"Sr. QA Associate","City":"Newark","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-Bachelor\u0027s degree with a concentration in engineering, science, or an equivalent technical discipline-Minimum of 10 years working in pharmaceutical aseptic manufacturing operations and quality assurance-Experience with facility and equipment qualification and validation-Previous tech transfer experience-Detailed knowledge of cGMPs related to pharmaceutical production -Strong interpersonal and written/oral communication skills -Ability to quickly process complex information and make critical decisions with limited information in a complex and time-sensitive environment","Skills":"-Experience in Good Tissue Practices-Experience in biologic or vaccine or cell culture products","Industry":"QA","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":66.0000,"SalaryLow":44.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

One of our large pharmaceutical clients is looking to hire a QA Associate to join their growing External Quality team within Advanced Therapeutics. This individual will be providing Quality support... More for site and process qualification activities, engineering runs, and commercial product manufacturing. Main responsibilities will include: -Remote quality support for production activities, including deviation and CPA review, escalation of critical issues, batch review and release and change control. -Support monitoring of EM quality performance and proactively identify risks. -Influence and build relationship with internal and external partners to continuously enhance quality performance. -Interface with other functions i.e. Operations, Planning, Technical Operations, etc. as well as the external manufacturer-Apply cGMP regulations and other FDA and international requirements to all aspects of the position. -Provide on-site support as needed on request of the Janssen team leadLess

Mar 15, 2023

Collegeville, PA

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Project Manager

|

Contract

{"JobID":272382,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.4352727272727,"Longitude":40.2060909090909,"Distance":null},"State":"Pennsylvania","Zip":"19426","ReferenceID":"KPD-610279","PostedDate":"\/Date(1678896969000)\/","Description":"A global pharmaceutical client is looking for a Project Manager to join their team. This position is for an SAP Packaging Solution S4 upgrade and deployment project management role providing support for managing implementation and enhancement related activities. The focus of the position will be to track, report out, and communicate project management deliverables for a multi-year SAP packaging solution upgrade and deployment program.Position Responsibilities: *Responsible for regularly managing the upgrade and deployment projects including integration points with other enterprise efforts. Additionally, responsible for status report, issue tracking, and project communications. *Prepares a schedule within MS application and manages timelines within tool *Monitors plan and highlights anticipated issues or slippage. *Formulates recovery plans or assessing impact if not recoverable and escalates as appropriate. *Records and monitors project actual costs vs. project budget. *Responsible for proactively identifying variances to plan and developing appropriate mitigation plans. *Formulates corrective actions when project deliverables deviate from the work plan with the assistance of team members. *Understands how project decisions impact key business metrics and the enterprise strategy. *Provides clear and reliable communications to internal teams, project stakeholders, external vendors, and customers. *Able to use communication features such as Timeline, Gantt charts, etc. for stakeholder updates when needed.","Title":"Remote SAP Project Manager","City":"Collegeville","ExpirationDate":null,"PriorityOrder":0,"Requirements":"*BA/BS in IT, Supply Chain, Business, or related fields *Excellent writing and communication skills. *Global Pharmaceutical industry SAP implementation experience. *Familiar with software development lifecycle.","Skills":"*Knowledge of SAP or ERP deployment activities *General knowledge of SAP modules; MM, PP, and EHS *General knowledge on Fiori applications deployment","Industry":"Project Manager","Country":"US","Division":"IT","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":117.0000,"SalaryLow":78.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

A global pharmaceutical client is looking for a Project Manager to join their team. This position is for an SAP Packaging Solution S4 upgrade and deployment project management role providing support... More for managing implementation and enhancement related activities. The focus of the position will be to track, report out, and communicate project management deliverables for a multi-year SAP packaging solution upgrade and deployment program.Position Responsibilities: *Responsible for regularly managing the upgrade and deployment projects including integration points with other enterprise efforts. Additionally, responsible for status report, issue tracking, and project communications. *Prepares a schedule within MS application and manages timelines within tool *Monitors plan and highlights anticipated issues or slippage. *Formulates recovery plans or assessing impact if not recoverable and escalates as appropriate. *Records and monitors project actual costs vs. project budget. *Responsible for proactively identifying variances to plan and developing appropriate mitigation plans. *Formulates corrective actions when project deliverables deviate from the work plan with the assistance of team members. *Understands how project decisions impact key business metrics and the enterprise strategy. *Provides clear and reliable communications to internal teams, project stakeholders, external vendors, and customers. *Able to use communication features such as Timeline, Gantt charts, etc. for stakeholder updates when needed.Less

Jan 25, 2023

Eden Prairie, MN

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Case/Care Manager (Healthcare)

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Contract

{"JobID":259320,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-93.4454545454546,"Longitude":44.857,"Distance":null},"State":"Minnesota","Zip":"55344","ReferenceID":"MIA-598418","PostedDate":"\/Date(1674645379000)\/","Description":"The Clinical Research Coordinator (CRC) supports both Site and Sponsor on a variety of Clinical Trials involving pharmaceutical and/or biomedical therapies/treatments. Study support includes a 2 week remote training period \u0026 Patient Recruitment and/or Retention duties. Duties can include any of the following tasks depending on the specific assignment. Tasks: Chart review, phone screening, medical record retrieval, appointment scheduling/follow up, data entry, source document uploading, informed consent procedures and more.","Title":"Clinical Research Coordinator","City":"Eden Prairie","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Research or Clinical Research Experience PreferredClinical/Medical Setting ExperienceEMR/EDC experienceStrong administrative skills using computer systems/applicationsAble to multiple task and handle challenges with ease","Skills":"","Industry":"Case/Care Manager (Healthcare)","Country":"US","Division":"IT","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":43.6800,"SalaryLow":29.1200,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

The Clinical Research Coordinator (CRC) supports both Site and Sponsor on a variety of Clinical Trials involving pharmaceutical and/or biomedical therapies/treatments. Study support includes a 2 week... More remote training period & Patient Recruitment and/or Retention duties. Duties can include any of the following tasks depending on the specific assignment. Tasks: Chart review, phone screening, medical record retrieval, appointment scheduling/follow up, data entry, source document uploading, informed consent procedures and more.Less

Mar 06, 2023

Tarrytown, NY

|

Project Manager

|

Contract

|

$62 - $94 (hourly estimate)

{"JobID":268635,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-73.8429090909091,"Longitude":41.0775454545455,"Distance":null},"State":"New York","Zip":"10591","ReferenceID":"HAR-607783","PostedDate":"\/Date(1678094169000)\/","Description":"Insight Global is looking for a Technical Product Owner / Business Analyst for a consent management system. This will be a fully remote role with one of our largest pharmaceutical clients . The Product Owner/BA will be joining the Commercial IT team within the Marketing technology space. This role will be responsible for build and run operations associated with the OneTrust Consent Management platform and will also be responsible for IT service delivery for omni channel projects. This role will be very hands on with 30% of this person\u0027s time working on administration, configuration, development, and ongoing support of the platform. The other 30% will be spent on the execution and roll out to all brands (in the summer they will be expanding to Global Markets), and the remainder working with the business stakeholders and help define the portfolio, as well as understand the demand.","Title":"Technical Product Owner/ BA One Trust","City":"Tarrytown","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-5+ years\u0027 experience as a Technical Product Owner/ BA for One Trust Consent Management Platform-Experience working with IT team to help develop digital technology solutions for consent management supporting email, SMS, web, and mobile channel-Strong recent experience with application maintenance and support/ configurations (hands on)-Strong recent experience with creating business process flows, application workflows and architectural diagrams-Deep knowledge in data privacy laws including but not limited to GDPR, CCPA, LGPD, LPPD","Skills":"-BOTH OneTrust and Salesforce Cxperience Cloud experience-Experience with integration with web platforms such as Salesforce and Adobe Experience Manager \u0026 CRM platforms like Veeva-Pharma background","Industry":"Project Manager","Country":"US","Division":"IT","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":93.6000,"SalaryLow":62.4000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Insight Global is looking for a Technical Product Owner / Business Analyst for a consent management system. This will be a fully remote role with one of our largest pharmaceutical clients . The... More Product Owner/BA will be joining the Commercial IT team within the Marketing technology space. This role will be responsible for build and run operations associated with the OneTrust Consent Management platform and will also be responsible for IT service delivery for omni channel projects. This role will be very hands on with 30% of this person's time working on administration, configuration, development, and ongoing support of the platform. The other 30% will be spent on the execution and roll out to all brands (in the summer they will be expanding to Global Markets), and the remainder working with the business stakeholders and help define the portfolio, as well as understand the demand.Less

Mar 15, 2023

Temecula, CA

|

Data Warehousing

|

Perm

|

$120k - $165k (estimate)

{"JobID":272334,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-117.213636363636,"Longitude":33.5001818181818,"Distance":null},"State":"California","Zip":"92590","ReferenceID":"OCC-610237","PostedDate":"\/Date(1678889778000)\/","Description":"A client in the pharmaceutical wholesale distribution industry is seeking a Data Engineer to join a BI team of 5 onshore/4 offshore team members. We are looking for someone strong with SQL, Informatica, IICS, and GCP (specifically BigQuery). You will help build reports and views in google BigQuery. We are looking for someone with a strong understanding of GCP and IICS. While this role is 100% remote, we are looking for someone to ideally be flexible and work 8am-5pm PST typically. This will be a direct hire full time role.","Title":"REMOTE - Data Engineer (GCP)","City":"Temecula","ExpirationDate":null,"PriorityOrder":0,"Requirements":"5 years of expeirence in a Data Engineer/BI Engiener role 5 years of experience with Informatica 5 years of SQL experience 2 years of experience with IICS1 year GCP (BIgQuery)Bachelors DegreeFlexibility to work hours with international teams offshore (able to work PST hours majority of the time)","Skills":"Located in PST time zoneSAP (main database is in S/4 HANA)","Industry":"Data Warehousing","Country":"US","Division":"IT","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":165000.0000,"SalaryLow":120000.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

A client in the pharmaceutical wholesale distribution industry is seeking a Data Engineer to join a BI team of 5 onshore/4 offshore team members. We are looking for someone strong with SQL,... More Informatica, IICS, and GCP (specifically BigQuery). You will help build reports and views in google BigQuery. We are looking for someone with a strong understanding of GCP and IICS. While this role is 100% remote, we are looking for someone to ideally be flexible and work 8am-5pm PST typically. This will be a direct hire full time role.Less

Feb 17, 2023

Blue Springs, MO

|

Electrical Engineering

|

Perm

{"JobID":263961,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-94.258,"Longitude":39.0190909090909,"Distance":null},"State":"Missouri","Zip":"64015","ReferenceID":"KCM-604179","PostedDate":"\/Date(1676636036000)\/","Description":"A client in the Kansas City Metro Area is seeking to backfill an Electrical Engineering Manager to their embedded-c and firmware side of the business. The Manager will be responsible for 30% managing a team of 5 Engineers and 70% electrical work. The primary function of this team is to develop control systems for large facilities such as data centers, chemical and pharmaceutical plants for life safety explosion/fire suppression and detection systems. This team works 90% in Embedded-C and 5% in hardware. The right candidate will be interested in doing meaningful work that can be life saving and take pride in doing this kind of work. To start, the manager will work primarily onsite but then will move to a 1-2 in office, 3-4 day remote schedule. Experience with Embedded-C, circuit design and programming is required.","Title":"Electrical Engineering Manager","City":"Blue Springs","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-BS, Electrical Engineering (ABET Accredited or equivalent)-8+ years of advanced knowledge in electrical engineering including circuit design, programming, manufacturing and/or project management -1+ year of experience in a supervisory, leadership or management role (personnel management)-Highly proficient with Embedded-C","Skills":"-MSEE-Background in the manufacturing industry and related system software","Industry":"Electrical Engineering","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":140000.0000,"SalaryLow":125000.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

A client in the Kansas City Metro Area is seeking to backfill an Electrical Engineering Manager to their embedded-c and firmware side of the business. The Manager will be responsible for 30% managing... More a team of 5 Engineers and 70% electrical work. The primary function of this team is to develop control systems for large facilities such as data centers, chemical and pharmaceutical plants for life safety explosion/fire suppression and detection systems. This team works 90% in Embedded-C and 5% in hardware. The right candidate will be interested in doing meaningful work that can be life saving and take pride in doing this kind of work. To start, the manager will work primarily onsite but then will move to a 1-2 in office, 3-4 day remote schedule. Experience with Embedded-C, circuit design and programming is required.Less

Mar 24, 2023

Madison, NJ

|

Project Manager

|

Contract

{"JobID":276173,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-74.4144909090909,"Longitude":40.7735818181818,"Distance":null},"State":"New Jersey","Zip":"07940","ReferenceID":"NNJ-612686","PostedDate":"\/Date(1679674579000)\/","Description":"Our pharmaceutical client is looking for a TIBCO EBX project manager to join their Master Data Management team within their Manufacturing IT department. The company is focused on reducing dependency on legacy systems such as Product Master Application (PMA). To streamline material master process, a detailed analysis and planning for decommissioning of PMA, and implementation is required. This will enable the company in: * Reducing our infrastructure maintenance cost for legacy systems * Reducing our software maintenance cost (OS/DB patches and upgrades) for legacy systems * Streamlined material master creation \u0026 maintenance process with Feather * Enhanced security with lesser legacy systems * Improved audit process with single source of truth. They will support with pending activities for PMA decommissioning. Develop and support requirements coordination and project plan for reference data management buildout. They will also support system validation process and coordinate GxP validation activities.","Title":"Remote TIBO EBX PM","City":"Madison","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-Experience technically with TIBCO EBX-Professional experience 4+ years as a project manager handling TIBCO EBX-Ability to be flexible with working global time zones specifically Europe","Skills":"","Industry":"Project Manager","Country":"US","Division":"IT","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":117.0000,"SalaryLow":78.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Our pharmaceutical client is looking for a TIBCO EBX project manager to join their Master Data Management team within their Manufacturing IT department. The company is focused on reducing dependency... More on legacy systems such as Product Master Application (PMA). To streamline material master process, a detailed analysis and planning for decommissioning of PMA, and implementation is required. This will enable the company in: * Reducing our infrastructure maintenance cost for legacy systems * Reducing our software maintenance cost (OS/DB patches and upgrades) for legacy systems * Streamlined material master creation & maintenance process with Feather * Enhanced security with lesser legacy systems * Improved audit process with single source of truth. They will support with pending activities for PMA decommissioning. Develop and support requirements coordination and project plan for reference data management buildout. They will also support system validation process and coordinate GxP validation activities.Less

Mar 10, 2023

Framingham, MA

|

Information Technology

|

Contract

{"JobID":275699,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-71.485757,"Longitude":42.299744,"Distance":null},"State":"Massachusetts","Zip":"01701","ReferenceID":"VMS-SAN-SNFIJP00007556","PostedDate":"\/Date(1678406400000)\/","Description":"USA-Systems Engineer III IT Position is fully onsite Description: Job Description: bull Installation configuration and testing of Windows operating systems and related applications bull Migration of software and data from legacy systems in use before the OS upgrade bull Interface implementation based on pre-defined standards of laboratory equipment bull Scripting file transfer from laboratory equipment to file server including document parsing where needed bull Analytical and problem-solving skill bull Collaborating and communicate with corporate colleagues as well as frequent contacts and meetings with site SMEs and vendors bull Experience with enterprise endpoint protection and firewall rule configuration bull Setting up of computer hardware systems Expertise: bull 6-9 Years Experience Microsoft operating systems knowledge XP W7 W10 and server 2008 2012 2016 bull Networking essentials TCP/IP DNS VLAN concept firewall remote administration Active Directory use bull Scripting knowledge DOS command line VBScript PowerShell bull Knowledge of lab instrumentation such as balances pH meters HPLCs etc. more specifically experience with network connectivity bull Documentation skills: Technical documentation and SOP creation GXP documentation bull Flexible service-oriented strong communication skills in English bull Be able to work independently and well organized bull Attention to detail and ability to follow directions bull Having worked previously in or for a pharmaceutical company within a lab environment is a plus bull Prior experience with GxP GMP GAMP5 and CFR21Part11 bull Minimum Education Required: HS Diploma or GED","Title":"USA-Systems Engineer III (IT)","City":"Framingham","ExpirationDate":null,"PriorityOrder":0,"Requirements":null,"Skills":null,"Industry":"Information Technology","Country":"US","Division":"Laboratory","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":88.4100,"SalaryLow":72.8100,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

USA-Systems Engineer III IT Position is fully onsite Description: Job Description: bull Installation configuration and testing of Windows operating systems and related applications bull... More Migration of software and data from legacy systems in use before the OS upgrade bull Interface implementation based on pre-defined standards of laboratory equipment bull Scripting file transfer from laboratory equipment to file server including document parsing where needed bull Analytical and problem-solving skill bull Collaborating and communicate with corporate colleagues as well as frequent contacts and meetings with site SMEs and vendors bull Experience with enterprise endpoint protection and firewall rule configuration bull Setting up of computer hardware systems Expertise: bull 6-9 Years Experience Microsoft operating systems knowledge XP W7 W10 and server 2008 2012 2016 bull Networking essentials TCP/IP DNS VLAN concept firewall remote administration Active Directory use bull Scripting knowledge DOS command line VBScript PowerShell bull Knowledge of lab instrumentation such as balances pH meters HPLCs etc. more specifically experience with network connectivity bull Documentation skills: Technical documentation and SOP creation GXP documentation bull Flexible service-oriented strong communication skills in English bull Be able to work independently and well organized bull Attention to detail and ability to follow directions bull Having worked previously in or for a pharmaceutical company within a lab environment is a plus bull Prior experience with GxP GMP GAMP5 and CFR21Part11 bull Minimum Education Required: HS Diploma or GEDLess

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