2nd shift - Quality Control Analyst (Contract) 29397
Atrium Works•Boston, MA
•Onsite
About The Position
Within our Analytical Service team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. As a QC Operations Analyst, you will join the Cell and Gene Therapy Department to support QC operations in a fast-paced GMP environment. 2nd shift - Wednesday-Saturday 12:30pm-11:00pm (3:30pm - 2:00am 2x a month)
Requirements
- Bachelor's degree in Chemical Engineering, Scientific Field, or equivalent and relevant formal academic / vocational qualification
- Previous GMP lab experience that provides the knowledge, skills, and abilities to perform the job is preferred (0-2 years industry experience)
- In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience will be considered sufficient for an individual to meet the requirements of the role.
- GMP experience preferred
- Ability to understand and independently apply GMPs and /or GLPs to everyday work with regard to documentation and instrument use
- Proficient in Microsoft Excel and Word (LIMS is a plus)
- Proven problem solving and troubleshooting abilities
- Good written and oral communication skills
- Time management and project management skills
- Ability to work in a collaborative work environment with a team
- Able to lift and move objects up to 25 pounds.
Responsibilities
- Work cross functionally with internal (facility, validation, metrology) and external (CTL, instrument vendors) teams to minimize day to day lab operations interruptions
- Identifying and creating processes that will ensure success within the QC lab
- Sample, reagent and chemical lifecycle management
- Establish, write, and update Standard Operating Procedures (SOPs) in compliance with GMP guidelines as needed in support of quality control operations
- Sets up and maintains instrumentation by working with the cross functional team (QC, QA, facility and vendors)
- Maintain QC equipment and perform regular performance verification/calibration as specified by equipment SOP
- Communicates project status to project leader.
- Performs work assignments accurately, and in a timely and safe manner.
- Shift work applies
- Comfortable with aseptic gowning
Benefits
- full-time benefits
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
