QC Sample Aliquoting Coordinator

Harmans, MD

Posted: 01/19/2021 Industry: Manufacturing Technician Job Number: JN -012021-12421

Job Description

QC Sample Aliquoting Coordinator

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.
  • Title: QC Sample Aliquoting Coordinator
  • Location: Harmans, MD
  • Industry: Pharmaceutical
  • Hours: Friday, Saturday, Sunday, Monday; 7am 5pm
  • Salary: $28.85hr (Paid Weekly - Benefits Available)
  • Employment Type: 6 month Contract
Environment: This client manufactures thousands of pharmaceutical, biologic, consumer health and beauty products utilizing superior and innovative drug delivery technologies to improve their value to patients and consumers. Our customer believes in a Patient First culture putting patients at the center of their work to ensure the safety, reliable supply and optimal performance of our products.

Knowledge/Skills Requirements:
Respond to other department inquiries regarding status of aliquoting requests
Preparation of labels and label vials for samples
Reconstitution and aliquoting of samples
Sample coordination and receipt from other departments for internal and external testing
Ensure that suitable written records and work undertaken are kept in accord with cGMP and company procedures
Receive Batch Records and Test Request forms from other departments
Order and receive supplies for groups as necessary
Execute document revisions
Works closely with Manufacturing for scheduling of samples submission to the QC lab. May also interact with Project Managers on sample coordination.
Ensure adequate stock of aliquoting supplies through forecasting of upcoming sample submission
Assist in preparing of samples for shipment to contract laboratories
Assist with tracking sample receipt and chain of custody for internal and contract laboratory submission
Work under general supervision to meet project goals
Flexibility in following unique campaign requirements that may include off-hour and weekend work
Assist with tracking internal / external testing as necessary
Assist with QC reagent preparation as necessary
Perform laboratory cleaning as part of routine work
Assist with maintaining inventory of QC non-critical and critical reagents as necessary
Perform QC document archival activities (i.e. submission and requests to Document Control department)
Other duties as assigned

Strong pipetting and aseptic technique
Ability to produce results in a fast-paced environment to meet client deadlines under minimal supervision
Able to work in a team setting and independently under minimum supervision
Experience with MS Excel and Word for tracking of testing
Strong organizational skills and attention to detail
Ability to set goals and objectives
Strong ability to understand and implement priorities and work load and to establish strong collaborative relationships with peers

B.S. or A.S. in a Life Sciences discipline preferred and a minimum of 2 years of relevant experience working in a cGMP environment
Experience working in cGMP Quality Control
Strong attention to detail and strong organizational skills
Familiarity with Good Manufacturing Practices (cGMP s)
Strong written and verbal communication skills
Experience working in a Phase III / Commercial Manufacturing setting preferred
Have the knowledge and ability to apply basic scientific and regulatory principles to solve operational and other routine quality tasks.

Positive, professional attitude toward work and willingness to cooperate with co-workers and supervisors and to contribute to a project team
Dependable and can work with minimal supervision on scheduled tasks
Timeliness and accuracy in completion of projects and paperwork (quantity of work)
Contributions to projects beyond general responsibilities (quality of work)
Identification of problem areas affecting operations (knowledge/problem solving)
Exercises good judgment in dealing with operational problems
Demonstrated understanding and adherence to Company policies, safety procedures and the cGMPs
Ability to succeed in a team-oriented environment under very dynamic conditions


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