QC Specialist II
Company: Tailored Management
Location: Portsmouth
Posted on: March 16, 2026
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Job Description:
Title: QC Specialist II Location: 101 International Drive,
Portsmouth, NH - 03801 Contract: 12 Months - possibility for
extension or FTE conversion Pay Rate:: $18.53 - $30.89/Hour
Benefits Job Description: The Quality Control Technical Transfer
Analyst 3 will act as a team member of the Quality Control
department to support production by contributing to the completion
of the technical transfer activities. Also participate in quality
testing for customer in-process, final product testing and
stability studies when needed. Applies job skills and companys
policies and procedures to complete a variety of tasks of increased
scope. Works on assignments that are semi-routine in nature where
ability to recognize deviation from accepted practice is required.
Works on problems of moderate scope in which analysis of situation
or data requires a review of identifiable factors. Applies job
skills and companys policies and procedures to complete a variety
of tasks. Running test samples for In-Process, Lot Release and
Stability studies. Running test samples for (but not limited to)
investigations, transfers and validations. Reviewing assays
Training others Has experience with: Change Control, Deviations,
CAPAs, Tasks, EICRs, Investigations. Writing- Quality Records
(Deviations, CAPA, Change Control) and Test Methods Projects such
as method transfers, new instruments, method qualifications Use of
Microsoft Suites (Word, Excel, PowerPoint) Use of Laboratory
computer systems Potential previous use of GMP Quality Systems such
as: TrackWise, LIMS Works on assignments that are semi-routine in
nature where ability to recognize deviation from accepted practice
is required. Works on problems of moderate scope in which analysis
of situation or data requires a review of identifiable factors.
Apply Data Integrity principles in all aspects of work, in
compliance with DI policies, guidelines and procedures. Perform
other duties as assigned. Strong ability to speak publicly. Strong
ability to interpret data both alone and with guidance. Perform
assigned, complex and/or varied tasks. Prioritization and problem
solving. Comprehend and follow instructions. Direct, control and
plan tasks/projects. Brainstorming Strong ability to communicate in
both written and verbal format . Exercises judgment within defined
procedures and practices to determine appropriate action.
Self-motivated team player Completes assignments on-time and
accurately Displays commitment to quality and performs job
functions to the best of his/her ability Relate to others in a team
setting. Maintain positive attitude in a team environment.
Timeliness in completing assigned tasks. Works entire assigned
shift, including arriving on time Has experience with or currently
uses the following software: SoftmaxPro, Empower, SoloVPE Has
experience with software validations including but not limited to:
writing GMP procedures and validation documents and executing test
scripts. Acts as a SME for at least one software system
Communicates with cross functional teams to interpret needs and
priorities. Has GMP experience within the pharmaceutical industry
Can perform technical, root-cause analysis for some software errors
Applies Data Integrity principles in all aspects of work, in
compliance with DI policies, guidelines and procedures. Remains up
to date on all assigned training activities. Performs other duties
as assigned. Education: Associates Degree Microbiology,
Biochemistry or Related Science Fields. TMN
Keywords: Tailored Management, Boston , QC Specialist II, Science, Research & Development , Portsmouth, Massachusetts
