Job Description
Quality Control Specialist 2nd shift Wed-Sat
General Summary:
The Vertex Cell and Gene Therapy (VCGT) Type 1 Diabetes (T1D) Quality Control (QC) team is responsible for the testing of samples and associated workflows within our stem-cell based T1D program. VCGT T1D QC carries out all activities under Good Manufacturing Practices (GMP) guidelines.
The Quality Control Specialist is responsible for supporting a variety of analytical functions that occur in the Quality Control (QC) department supporting validation testing and reporting of in-process release and stability samples. This role also helps ensure activities occur in an efficient and cGMP compliant manner while fostering the Vertex vision and values.
Key Responsibilities:
- Typical test methods performed include flow cytometry qPCR (MycoTOOL) ELISA cell counts sterility (BACT) Gram stain and endotoxin (LAL) testing.
- Performs technical reviews of raw data.
- Records test results and maintains raw data and accurate laboratory records.
- Performs general lab and equipment maintenance duties.
- Performs other duties as assigned.
- Weekend shift work: Typical workweek is a 4 day week 10 hours a day first shift Wednesday to Saturday.
Knowledge and Skills:
- Performs tasks with strict adherence to cGMP and cGDP principles.
- Has an understanding of basic laboratory equipment and practices.
- Is proficient in the use of spreadsheets and word processing software.
- Is dependable and able to work well within a team.
- Is interested in learning new things. Open to change.
- Is optimistic and displays a positive attitude even during periods of adversity.
- Shows initiative; acts independently with management approval.
- Possesses a high attention to detail.
Requirements:
- A minimum of a Bachelors degree in Sciences is required.
- 2-4 years of experience in the GMP pharmaceutical/biopharmaceutical industry
Pay Range
Requisition Disclaimer
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
By applying for this position you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials which may include your CV/Resume email address or phone number with Vertex. For more information on how Vertex handles your personal data related to your job application please see Vertexs Careers Privacy Notice. Agreeing to the Atrium Terms and Conditions includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings profiles articles news and other employment-related information as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners
(collectively Atrium Alerts). Atrium Alerts may be sent by email phone or text message. Your personal information will be safely stored within the Atrium & Vertex databases. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time please contact Atrium at .
If you do not agree with the Atrium Terms and Conditions you can still complete your application for this position by emailing your resume to our team at Please include the job title in the subject of your email.
No C2C or Third-Party Vendors
Required Experience:
IC
Job DescriptionQuality Control Specialist 2nd shift Wed-SatGeneral Summary:The Vertex Cell and Gene Therapy (VCGT) Type 1 Diabetes (T1D) Quality Control (QC) team is responsible for the testing of samples and associated workflows within our stem-cell based T1D program. VCGT T1D QC carries out all ac...
Job Description
Quality Control Specialist 2nd shift Wed-Sat
General Summary:
The Vertex Cell and Gene Therapy (VCGT) Type 1 Diabetes (T1D) Quality Control (QC) team is responsible for the testing of samples and associated workflows within our stem-cell based T1D program. VCGT T1D QC carries out all activities under Good Manufacturing Practices (GMP) guidelines.
The Quality Control Specialist is responsible for supporting a variety of analytical functions that occur in the Quality Control (QC) department supporting validation testing and reporting of in-process release and stability samples. This role also helps ensure activities occur in an efficient and cGMP compliant manner while fostering the Vertex vision and values.
Key Responsibilities:
- Typical test methods performed include flow cytometry qPCR (MycoTOOL) ELISA cell counts sterility (BACT) Gram stain and endotoxin (LAL) testing.
- Performs technical reviews of raw data.
- Records test results and maintains raw data and accurate laboratory records.
- Performs general lab and equipment maintenance duties.
- Performs other duties as assigned.
- Weekend shift work: Typical workweek is a 4 day week 10 hours a day first shift Wednesday to Saturday.
Knowledge and Skills:
- Performs tasks with strict adherence to cGMP and cGDP principles.
- Has an understanding of basic laboratory equipment and practices.
- Is proficient in the use of spreadsheets and word processing software.
- Is dependable and able to work well within a team.
- Is interested in learning new things. Open to change.
- Is optimistic and displays a positive attitude even during periods of adversity.
- Shows initiative; acts independently with management approval.
- Possesses a high attention to detail.
Requirements:
- A minimum of a Bachelors degree in Sciences is required.
- 2-4 years of experience in the GMP pharmaceutical/biopharmaceutical industry
Pay Range
Requisition Disclaimer
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
By applying for this position you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials which may include your CV/Resume email address or phone number with Vertex. For more information on how Vertex handles your personal data related to your job application please see Vertexs Careers Privacy Notice. Agreeing to the Atrium Terms and Conditions includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings profiles articles news and other employment-related information as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners
(collectively Atrium Alerts). Atrium Alerts may be sent by email phone or text message. Your personal information will be safely stored within the Atrium & Vertex databases. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time please contact Atrium at .
If you do not agree with the Atrium Terms and Conditions you can still complete your application for this position by emailing your resume to our team at Please include the job title in the subject of your email.
No C2C or Third-Party Vendors
Required Experience:
IC
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