LIMS Specialist
- East Coast
- Contract
- Commissioning, Qualification and Validation
This vacancy has now expired
Our client, a global Pharmaceutical manufacturing organization are looking for a talented LIMS Specialist to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States.
Responsibilities:
- Leverage existing processes, procedures, and documents from other facilities where possible to provide an efficient CQV activities for the project
- Assure suitability and/or cGMP compliance of equipment in quality control
- Create and maintain project document QC approval plans and status updates
Requirements:
- Setup complete LIMS Master Data including Analysis, Product Build and Static data
- System administration and maintenance of LIMS (Labware LIMS v6)
- User access administration, Label printer setup - optional
- Analyze root causes of issues and provide appropriate resolutions based upon troubleshooting
- Understanding of the ER (Entity Relationship) model – data structure of Labware LIMS to troubleshoot data issues
- Experience in major Labware LIMS modules (i.e., Sample management, Inventory, Lot, Stability), and Instrument interfacing
- Experience in Crystal reports development in LIMS (i.e., critical reports such as CofA, Analytical Reports)
- Perform Change management including drafting IQ, OQ scripts along with defect management following GxP guidelines
- Knowledge of the Pharmaceutical or Biotech industries
- Have excellent communication / presentation skills, and be able to articulate complex information to stakeholders and supporting functions such as CQV, QA, Engineering, Automation, and others
- Be a team player who works well with colleagues and cross-functional teams
- Be a self-starter and have a flexible, proactive, and dynamic approach to completion of work objectives and working with colleagues
- Prior project or lab startup experience preferred
If this role is of interest to you, please apply now!
#LI-MC1
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
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