Quality Assurance Analyst
Posted on Sep 25, 2024 by Zifo
Lexington, MA
Research
Immediate Start
Annual Salary
Full-Time
Location: Lexington, MA – ON SITE
This role will require the successful candidate to be on-site in Lexington, MA
This role is not eligible for relocation assistance
Description: Zifo is searching for an experience Quality Assurance Analyst with experience in the pharmaceutical domain. The ideal candidate will have extensive experience with lab instrument qualification. This role will require a 100% on-site presence in Lexington, MA.
Requirements
Responsibilities:
Manage change controls necessary for project life cycle through process compliance and interface with Quality Assurance change control area
Author change control documents for client review and approval
Support life cycle documents and execution
Support Instrument Qualification
Author validation life cycle documents for client review and approval
Route drafted documents for review
Request approval workflows to Doc Control
Route reviewed documents for workflow approval
Request performance copies for protocols
Execute approved protocols
Qualifications:
Bachelor’s/ Master’s degree or equivalent in a scientific or health care field.
5 + years experience as a Validation Analyst preferably in the pharmaceutical /Life sciences industry preferred.
A successful Zifo-ite is:
Independent, Self-Motivated & Results driven
Willing & able to quickly acquire new Technical Skills & Business Principles
A critical thinker who possesses logical reasoning
Curious and always looking for creative solutions to complex problems
Benefits
CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we debate, challenge ourselves, and interact with all alike. We are a curious bunch, characterized by our passion to learn and spirit of teamwork. Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team’s knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 7 of the Top 10 Biopharma companies.
We look for Science – Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We possess scientific and technical knowledge and bear professional and personal goals. While we have a “no doors” policy to promote free access within, we do have a tough door to walk in. We search with a two-point agenda – technical competency and cultural adaptability.
We offer a competitive compensation package including accrued vacation, medical, dental, vision, 401k with company matching, life insurance, and flexible spending accounts.
If you share these sentiments and are prepared for the atypical, then Zifo is your calling!
Zifo is an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
This role will require the successful candidate to be on-site in Lexington, MA
This role is not eligible for relocation assistance
Description: Zifo is searching for an experience Quality Assurance Analyst with experience in the pharmaceutical domain. The ideal candidate will have extensive experience with lab instrument qualification. This role will require a 100% on-site presence in Lexington, MA.
Requirements
Responsibilities:
Manage change controls necessary for project life cycle through process compliance and interface with Quality Assurance change control area
Author change control documents for client review and approval
Support life cycle documents and execution
Support Instrument Qualification
Author validation life cycle documents for client review and approval
Route drafted documents for review
Request approval workflows to Doc Control
Route reviewed documents for workflow approval
Request performance copies for protocols
Execute approved protocols
Qualifications:
Bachelor’s/ Master’s degree or equivalent in a scientific or health care field.
5 + years experience as a Validation Analyst preferably in the pharmaceutical /Life sciences industry preferred.
A successful Zifo-ite is:
Independent, Self-Motivated & Results driven
Willing & able to quickly acquire new Technical Skills & Business Principles
A critical thinker who possesses logical reasoning
Curious and always looking for creative solutions to complex problems
Benefits
CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we debate, challenge ourselves, and interact with all alike. We are a curious bunch, characterized by our passion to learn and spirit of teamwork. Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team’s knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 7 of the Top 10 Biopharma companies.
We look for Science – Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We possess scientific and technical knowledge and bear professional and personal goals. While we have a “no doors” policy to promote free access within, we do have a tough door to walk in. We search with a two-point agenda – technical competency and cultural adaptability.
We offer a competitive compensation package including accrued vacation, medical, dental, vision, 401k with company matching, life insurance, and flexible spending accounts.
If you share these sentiments and are prepared for the atypical, then Zifo is your calling!
Zifo is an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
Reference: 202387432
https://jobs.careeraddict.com/post/95564104
Quality Assurance Analyst
Posted on Sep 25, 2024 by Zifo
Lexington, MA
Research
Immediate Start
Annual Salary
Full-Time
Location: Lexington, MA – ON SITE
This role will require the successful candidate to be on-site in Lexington, MA
This role is not eligible for relocation assistance
Description: Zifo is searching for an experience Quality Assurance Analyst with experience in the pharmaceutical domain. The ideal candidate will have extensive experience with lab instrument qualification. This role will require a 100% on-site presence in Lexington, MA.
Requirements
Responsibilities:
Manage change controls necessary for project life cycle through process compliance and interface with Quality Assurance change control area
Author change control documents for client review and approval
Support life cycle documents and execution
Support Instrument Qualification
Author validation life cycle documents for client review and approval
Route drafted documents for review
Request approval workflows to Doc Control
Route reviewed documents for workflow approval
Request performance copies for protocols
Execute approved protocols
Qualifications:
Bachelor’s/ Master’s degree or equivalent in a scientific or health care field.
5 + years experience as a Validation Analyst preferably in the pharmaceutical /Life sciences industry preferred.
A successful Zifo-ite is:
Independent, Self-Motivated & Results driven
Willing & able to quickly acquire new Technical Skills & Business Principles
A critical thinker who possesses logical reasoning
Curious and always looking for creative solutions to complex problems
Benefits
CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we debate, challenge ourselves, and interact with all alike. We are a curious bunch, characterized by our passion to learn and spirit of teamwork. Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team’s knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 7 of the Top 10 Biopharma companies.
We look for Science – Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We possess scientific and technical knowledge and bear professional and personal goals. While we have a “no doors” policy to promote free access within, we do have a tough door to walk in. We search with a two-point agenda – technical competency and cultural adaptability.
We offer a competitive compensation package including accrued vacation, medical, dental, vision, 401k with company matching, life insurance, and flexible spending accounts.
If you share these sentiments and are prepared for the atypical, then Zifo is your calling!
Zifo is an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
This role will require the successful candidate to be on-site in Lexington, MA
This role is not eligible for relocation assistance
Description: Zifo is searching for an experience Quality Assurance Analyst with experience in the pharmaceutical domain. The ideal candidate will have extensive experience with lab instrument qualification. This role will require a 100% on-site presence in Lexington, MA.
Requirements
Responsibilities:
Manage change controls necessary for project life cycle through process compliance and interface with Quality Assurance change control area
Author change control documents for client review and approval
Support life cycle documents and execution
Support Instrument Qualification
Author validation life cycle documents for client review and approval
Route drafted documents for review
Request approval workflows to Doc Control
Route reviewed documents for workflow approval
Request performance copies for protocols
Execute approved protocols
Qualifications:
Bachelor’s/ Master’s degree or equivalent in a scientific or health care field.
5 + years experience as a Validation Analyst preferably in the pharmaceutical /Life sciences industry preferred.
A successful Zifo-ite is:
Independent, Self-Motivated & Results driven
Willing & able to quickly acquire new Technical Skills & Business Principles
A critical thinker who possesses logical reasoning
Curious and always looking for creative solutions to complex problems
Benefits
CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we debate, challenge ourselves, and interact with all alike. We are a curious bunch, characterized by our passion to learn and spirit of teamwork. Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team’s knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 7 of the Top 10 Biopharma companies.
We look for Science – Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We possess scientific and technical knowledge and bear professional and personal goals. While we have a “no doors” policy to promote free access within, we do have a tough door to walk in. We search with a two-point agenda – technical competency and cultural adaptability.
We offer a competitive compensation package including accrued vacation, medical, dental, vision, 401k with company matching, life insurance, and flexible spending accounts.
If you share these sentiments and are prepared for the atypical, then Zifo is your calling!
Zifo is an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
Reference: 202387432
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