IT Sr. Project Manager (Northern NJ Pharma Co.)

  • The overall project management framework and portfolio of IT projects tracking, also including direct management of one or more medium to large sized, moderately to highly complex projects working in partnership with IT leads.
  • Project manage the effort(s) end-to-end working with both internal and external resources.
  • Responsible for scoping, planning, executing, and monitoring the project(s).
  • Will need a level of expertise in aspects of the following areas: Project Management, Resource Management, Finance Management, Knowledge Management, Quality Management, and Control Management

Information Management Associate Director / Director (Northern NJ Pharma Co.)

Information Management Associate Director/Director (AD/D) is a cross-functional role in IT who is responsible for the definition and management of end-to-end information flow across SKLSI.   Working with the various SKLSI business department personnel, the Information Management Director will be responsible for data governance, information stewardship, master data management, end-to-end information/data flows, business intelligence and reporting, and serve as the primary owner of the enterprise business intelligence platform.   The Information Management AD/D will also work in partnership with the business and IT to understand business issues and opportunities from an information context and translate those issues and opportunities into information and data requirements, to enable an integrated SKLSI business intelligence platform to meet reporting and analytics needs.


Enterprise & Value Chain Systems Lead - Associate Director / Director (Northern NJ Pharma Co.)

The Enterprise and Value Chain Systems Lead (EVCSL) is the central point of coordination for IT capabilities to enable Corporate Functions (Finance, HR, Legal) and shared business capabilities (e.g. Document Management). The Enterprise and Value Chain Systems Lead will collaborate closely with the Finance, HR and Legal business leaders, and leaders from all functions (as it relates to enterprise capabilities) to understand business strategy, demand, and priorities and help the business propose projects that align with the overall business and technology strategy. The Enterprise and Value Chain Systems lead is primarily responsible for defining, delivering and evolving the technology portfolio for Corporate and the Enterprise. The EVCSL will collaborate closely with the Development, CMC and Commercial business leaders to understand business strategy, demand, and priorities and help the business propose projects that align with the overall business and technology strategy for the supply chain and will ensure alignment of data integration with business operational and reporting needs.


Manager / Sr. Manager, Regulatory Affairs (Northern NJ Pharma Co.)

The Manager/Senior Manager, Regulatory Affairs will be responsible for managing key nonclinical, clinical and CMC regulatory aspects of development programs in the area of CNS. The responsibilities include working closely with functional areas, project teams, and corporate partner to support product development. The individual must possess a thorough knowledge of global rules, regulations, and guidance’s governing drugs and biologics in all phases of development. Strong verbal and written communication and management skills are required. Additional responsibilities will include support of other late stage programs as needed.


QA Manager (Northern NJ Pharma Co.)

  • Ensures GxP work is done in compliance with applicable laws, regulations and guidelines
  • Works closely with internal and external QA and CMC, Clinical and Non-clinical colleagues through all phases of drug development
  • Executes all Quality system elements, which include but are not limited to investigation of product complaints, deviations, OOS investigations, document creation and control, site audits, change control, validation (e.g. process, cleaning, analytical method, etc.), stability, batch record review, and product disposition
  • Participates in the review, evaluation and approval of Contract Manufacturing Organizations, Non Clinical and Clinical CROs for contracted services
  • Reviews and approves GxP related documents as requested and appropriate
  • Supports QMS management and maintenance for GxP activities
  • Participates on project teams and sub-teams as needed and assigned
  • Ensures documents and records are kept in compliance with regulations and SOPs

Quantitative Developer

We are looking for a Quantitative Developer with the following skills: strong C/C++ programming background; experience in network and multithreading real-time applications on Linux/Unix platform; familiar with scripting languages such as Perl, shell script or python; knowledge of simulator/trading system preferred; experience in high frequency trading model a plus.  Candidates should be smart and talented team players.  Position is located in Greenwich, CT. 

Trading System Operator

We are looking for a candidate to join our clients trading system operations team. The candidate must have development background, very strong problem solving ability, excellent communications skills, strong attention to detail, and ability to work independently and in a very fast-paced environment. From a technical perspective, the candidate must be familiar with Unix, have very strong Perl and Sql skills. Position is located in Greenwich, CT.

Software Engineer  

Seasoned Perl developer who is thoroughly familiar with Linux, web applications (Apache, Mod_Perl, HTML::Mason), MySQL, networking, and systems security. Will be responsible for development of web interfaces and automated dynamic reports. HTML/CSS a plus.  Position based in Greenwich, CT. 


Logistics Technician

1+ years of general warehouse experience (Ship/Receive/Asset).  Must be computer literate.

 Consultant expected to be on client site 100%.

Rate is Open.