About TSR :
TSR is a relationship-based, customer-focused IT and technical services staffing company.
For over 40 years TSR, Inc. and its wholly owned subsidiary, TSR Consulting Services, have prospered in the Information Technology staffing business, earning the respect of companies both large and small with well refined candidate screening, timely placement, and a real understanding of the right skill sets required by our clients.
Mission & Vision
- We do not believe in building a vision around the company but building a company around our vision, which is simply;
Every employee's voice matters, their effort is appreciated, and their talent is rewarded.
We challenge each employee daily, to raise the bar on how we treat our consultants and candidates. For far too long in this industry, candidates have been ghosted, lied to, or placed at a client and then forgotten about. Each day our staff works tirelessly at qualifying and placing, top talent with our clients, in a compassionate and caring manner.
Not every candidate is a match for the job, but every candidate and consultant will be treated with respect and professionalism.
Sample Management
Job Description
Location : Devens, MassachusettsType : ContractJob #81346Our client, a leading pharmaceutical company, is hiring for Quality Sample Management, on a contract basis.
Job ID # : 81346
Work Location :
Devens, MA - on site role
Work Schedule :
Second Shift 2PM - 10PM, Monday through Friday
Education / Experience :
HS Diploma required OR enrolled in a scientific program
Knowledge / Skills :
Associates primarily work in a cGMP laboratory and follow techniques which require one to be alert, giving high attention to detail, to properly use Personal Protective Equipment (PPE) and to handle hazardous materials.Associates should be observant of their work area and related tools and identify and report any discrepancy from normal practice or procedure.Knowledge of basic electronic systems (email, MS Office, etc.)Knowledge of science generally attained through studies resulting in a AS or certificate program in the physical or life sciences, supply chain, a related discipline, or the equivalent in related experience.Knowledge of basic laboratory techniques such as working in a BSC, pipetting, aseptic technique; basic laboratory safety practices preferred.Familiarity with controlled temperature storage, sample inventory, and sample shipment and receipt.Attention to detail and demonstrated organizational skills.Demonstrated manual dexterity.Responsibilities :
Performs routine processing and data review of raw materials, in-process, batch release, and / or stability samples of Bulk Drug Substance in a cGMP compliant environment.Performs routine inventory and sample management of routine samples, critical reagents and non-routine samples. Main responsibilities include Chain of Custody.Executes routine procedures owned by the Sample Management functional area. Assignments are made in the LMS, by the hiring manager, based on applicable curricula map(s).Will work in teams and have continual interaction with members of his / her team as well as other sub-teams within Quality Control Organization, in order to exchange information regarding sample management as it relates to meeting department goals and objectivesDaily contact with supervisory staff for work assignments. Routine contact with supervisor for coaching and general performance management discussions.Occasional contact with other line management staff relating to specific project responsibilities may be expected.Occasional contact with Manufacturing and Stability organizations for escalation where appropriateOccasional contact with other sites / vendors for tactical logistical purposes .
