LIMS and Quality Candidates looking for a New Job

These are the latest LIMS and Quality Systems experts actively looking for a new job opportunity. If you do not see the skills you need please contact me immediately so we can discuss your job needs in detail.

?

The Laboratory & Quality Systems department at Planet Technology solely focuses on helping our clients find IT resources with in the Laboratory Systems space across all industries. These expertise's include: LIMS, ELN, LES, QMS, GxP, CDS, SDMS, MES, EDMS, VEEVA, Etc.

?

Candidate A: LIMS Business Analyst (Fulltime) - CA:

18 years in laboratories with 8 years as analyst within LIMS, performing hands-on technical configurations as well. 4 years in LabVantage; 2 years in CoreLIMS. LabWare overview through vendor selection process, but not utilization.Serving as sole business analyst to lead 1 full SDLC LabVantage Implementation of ‘Clinical’ non-existent LIMS, into LabVantage, along with an electronic Benchling LIMS for R&D, both into one instance of LabVantage v8.4.6. Also served as sole BA on the requirements gathering phase of 2 other LIMS implementations.?

Resides in CA and seeks a Fulltime opportunity.

Candidate B: LIMS Specialist (Fulltime Or Contract) - IL:

16 years Life Sciences/Quality/cGMP environment, and Lab Systems including SampleManager LIMS and LabWare, as well as Empower, SAP/QM, Lab Tracker 5, Trackwise, IDBS E-Workbook and more. Gathering user requirements for LIMS enhancements; writing technical, validation, IQs, PQs, and migration scripts to determine validation testing; developing support model for new LIMS. SM LIMS migration from custom VGL and database objects, configuring SM12.2 objects/modules, and performing custom reports and labels. Also ensuring correctness for audit transfers for 21CFR Part 11 requirements.

Resides in IL and seeks Full-Time or Contract opportunities. ?

?Candidate C: Director, Computer Systems Validation & Lab IT (FullTime) PA:

?25+ years in GxP Systems including Lab, Quality and Manufacturing, and the same number of years with Astra first then AstraZeneca, within roles varying from user, systems quality, administration and architecture SME.? Supporting systems including LIMS (LabWare), ELNs (SmartLab), CDS (Empower/TotalChrom), QMS (Trackwise), and custom SDMS. Sr. level in analytical instrumentation (HPLC, GC, FTIR, UV-Vis).? Validation Training and Certifications including: “Computer Validation” (AstraZeneca) and “Software Validation Principals” (PDA); authoring validation documentation to include plans, protocols and reports (includes IQ, OQ and PQ protocols); serving as SME/Administrator on regional CDS solution to include performing build, integration, validation, training and maintenance within validated state for 4 labs and 2 sites.

Resides in PA and seeks a Fulltime Opportunity

?

Candidate D: Quality Assurance / Validation Consultant (Hybrid or Fulltime) - PA:

25+ years in implementations, testing, validation, and support of LIMS. Authoring documentation and QA/QC requirements. Worked within highly regulated environments to include GAMP5, GMP and more. Writing IQ, OQ, and PQ protocol test scripts, gap analysis, audits, risk assessments, deviation resolution reporting, and more. Additionally, has liaised with IT Teams to build roadmap, strategies, and processes, while providing communication to IT Risk and Compliance Directors regarding key indicators and milestones related to Data Integrity and Access Management.?

Resides in PA and seeks Full-time or Contract opportunities

?Candidate E: LIMS Administrator (Fulltime or Contract) - PA:

?10 years software experience within BI Tools, Databases and Reporting; 7 years in LIMS to include LabVantage, STARLIMS and iLIMS, as well performing business analysis, systems administration and software development. Worked within LabVantage v 6.2 and 8.1 on developing new screens, custom coding using Java and JavaScript for configurations,? ETL database optimization, Python, R, Machine Learning C++, and more. Also assisting in STARLIMS management and Business Objects servers, created custom LIMS screens and investigating application code within Oracle SQL, and PL/SQL, JScript .NET and SSL.? Extensive documentation. Managed 4 people for about 4 years as team lead too.

Resides in PA and seeks a new Fulltime or Contract Opportunity.

Candidate F: LIMS Specialist (Fulltime) - NY:

?10+years of LIMS in STARLIMS, SQL*LIMS, and Labware. Also a history in GmP and Quality. Responsibilities include serving lab and quality users as LIMS Business Analyst to gather requirements, document these, create workflows, training users on these new solutions and much more. Also served as LIMS Administrator with hands-on systems expertise in the provision of troubleshooting LIMS, providing solutions, master data changes, performing security for user parameters, views, etc., and much more.?

Resides in NY and Seeks a new Fulltime Opportunity

Candidate G: LIMS Technical Business Analyst (Fulltime) - NC:

20+ years in pharma, 13+ years in LIMS to include 6 in LabVantage v8 and 5+ in LabWare v6 as well as a bit of SQL*LIMS. Worked within various areas to include stability, Active Pharma Ingredients, Finished Products, Environmental Monitoring and Quality Control. Has done extensive LIMS Business Analysis to include authoring and editing all documentation in addition to hands-on technical? and systems administration. Served as technical lead supporting up to 50 users in a full SDLC implementation from SQL*LIMS to LabWare to include over 300 stability studies. Assisted in implementation for Mettler LabX and Service Now also used TrackWise. Also worked on LabVantage implementation from paper to electronic and then also an upgrade from v6 to v8, both start to finish.

Resides in NC and Seeks new Fulltime Opportunity.

Candidate H: Sr. Quality Assurance Specialist (Fulltime or Contract) - MA:

20+ years in labs and quality including GMP. Experience overseeing Quality Assurance within small molecule environment, ensuring licensed pharma products are manufactured, tested, stored and distributed according to regulatory standards. On the floor experience in QA includes change control, incident reports, OOS root cause analysis, writing, reviewing, updating and releasing SOPs, supporting manufacturing in both upstream/downstream operations, monitoring and establishing quality system KPIs and more. Creating and editing documentation to include method validation (Test Methods, Protocols, Final Reports and Instruments), QCRM (Material Specifications and SOPs), procedures, workflows, and more.?

Resides in MA and seeks Full-Time or Contract opportunities.

Candidate I: LIMS Engineer (Fulltime or Contract) - IN:

20 years in the sciences starting as an assistant professor; and of development working as software engineer for? of those and having 6 years in Clarity LIMS to include v4.3 and 6. Extensive expertise in Python development with additional in C and C++ and some Java as well as fortran 90/95. Expertise in developing, maintaining and supporting custom LIMS software supporting DNA sequencing laboratories. Working within a small team of 4 developers to support hundreds of users, as well as sole developer for 3 years in support of Clarity LIMS for up to 5O users prior. Serving as POC with Illumina to troubleshoot Clarity LIMS issue; overseeing system upgrades, providing Clarity end-user support and ensuring solutions are properly trained and rolled out, working with internal architecture team int he deployment of software products and data migrations tools to AWS Cloud; developing and maintaining object-oriented Python library for custom enhancements within Clarity to include workflows via RESTful API and PostgresSQL database and much more. Through various upgrades to include on Clarity LIMS upgrade from version 4.3 to v6.?

Resides in Indiana and seeks Remote Fulltime or Contract Opportunity.?

?

Candidate J: Quality Manager (Fulltime) - MN:

9 years’ experience with a focus on Quality, Compliance and some Project management with systems to include LabVantage, Veeva and Trackwise. 4+ years on the systems side having worked as quality systems engineer, performing analysis and administration with hands-on expertise in systems configurations, enhancements and maintenance. Creating databases, new product integrations, deviations and more. Authoring site product quality reviews for commercial products and creating quality management review processes. Also assisted in the creation of a real time dashboard to monitor quality record completion.?

Resides in MN and seeks Full-Time opportunities. ?

Please keep in mind that these LIMS candidates do not showcase our entire network that is currently available. If you have any questions regarding any candidates, needs, rates, or industry insights, please contact me via phone or email.

Best Regards,?

Kevin O'Connor

Director, Laboratory IT & Quality Systems Staffing Division

Direct: 470.509.3569 | Cell: 706-814-4089 | planet-technology.com

Connect with me