2nd shift Quality Control Specialist/Sr. Specialist (Contract) 24531
Posted on Feb 12, 2025 by Vertex Pharmaceuticals
Boston, MA
Research
Immediate Start
Annual Salary
Full-Time
Job Description:
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.
Training maybe 1st or 2nd shift - dependent on training schedule and assay
2nd shift – Sun-Wed 12:30pm-11pm
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, Sunday to Wednesday 12:30 PM – 11:00 PM.
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 Bachelor's degree in Sciences is required.
2-4 years (4+ for Sr.) of experience in the GMP pharmaceutical/biopharmaceutical industry
Pay Range:
$45-$55/depending on experience
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 law. In 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 RESUME/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 Vertex’s 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
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.
Training maybe 1st or 2nd shift - dependent on training schedule and assay
2nd shift – Sun-Wed 12:30pm-11pm
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, Sunday to Wednesday 12:30 PM – 11:00 PM.
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 Bachelor's degree in Sciences is required.
2-4 years (4+ for Sr.) of experience in the GMP pharmaceutical/biopharmaceutical industry
Pay Range:
$45-$55/depending on experience
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 law. In 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 RESUME/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 Vertex’s 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
Reference: 211667516
https://jobs.careeraddict.com/post/99756982
2nd shift Quality Control Specialist/Sr. Specialist (Contract) 24531
Posted on Feb 12, 2025 by Vertex Pharmaceuticals
Boston, MA
Research
Immediate Start
Annual Salary
Full-Time
Job Description:
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.
Training maybe 1st or 2nd shift - dependent on training schedule and assay
2nd shift – Sun-Wed 12:30pm-11pm
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, Sunday to Wednesday 12:30 PM – 11:00 PM.
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 Bachelor's degree in Sciences is required.
2-4 years (4+ for Sr.) of experience in the GMP pharmaceutical/biopharmaceutical industry
Pay Range:
$45-$55/depending on experience
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 law. In 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 RESUME/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 Vertex’s 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
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.
Training maybe 1st or 2nd shift - dependent on training schedule and assay
2nd shift – Sun-Wed 12:30pm-11pm
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, Sunday to Wednesday 12:30 PM – 11:00 PM.
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 Bachelor's degree in Sciences is required.
2-4 years (4+ for Sr.) of experience in the GMP pharmaceutical/biopharmaceutical industry
Pay Range:
$45-$55/depending on experience
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 law. In 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 RESUME/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 Vertex’s 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
Reference: 211667516
Alert me to jobs like this:
Amplify your job search:
Expert career advice
Increase interview chances with our downloads and specialist services.
Visit Blog