2nd shift Quality Control Analyst (Contract) 29397

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) ***

Essential Functions:

• 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

Qualifications

Education and Experience:

• Bachelors 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.

Knowledge Skills and Abilities:

• 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.

$33-$37/hr

This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (Vertex). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation medical benefits fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors including skills competencies experience location and/or being pursued and other job-related factors permitted by addition this role will be eligible for overtime pay in accordance with federal and state requirements

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No C2C or Third-Party Vendors