T
CSV Analyst/Technical Writer
Salary undisclosed
Checking job availability...
Original
Simplified
Seeking a Technical Writer/ CSV Analyst
Position Overview:
Experienced Technical Writer with a focus on system validation, specifically around validating IT systems, to support the large molecule group in documenting validation processes for their Electronic Lab Notebook (ELN) system.
This role emphasizes the importance of Computer System Validation (CSV) experience and requires the candidate to work independently while engaging with multiple stakeholders, including IT, R&D, Quality & Validation, and Product Owners.
Key Responsibilities:
Develop and author validation documentation for the large molecule group, including:
User Requirements Specifications (URS)
Functional Specifications
Validation and Test Plans
IQ/OQ/PQ protocols
Standard Operating Procedures (SOPs)
Ensure validation documentation meets GxP and compliance standards.
Create and execute testing strategies and scripts to support system validation efforts.
Collaborate with IT, R&D, Quality & Validation, and Product Owners to gather requirements and document workflows.
Manage structured document control and version management within a Document Management System (DMS).
Qualifications:
3+ years of experience in technical writing within a regulated industry (Pharma, Biotech, Animal Health).
Strong CSV (Computer System Validation) experience, specifically in validating IT systems.
Experience with system validation, testing protocols, and technical documentation.
Prior experience with electronic Lab Notebooks (ELN) (Benchling preferred, but any ELN experience acceptable).
Strong knowledge of GxP, 21 CFR Part 11, and validation documentation processes.
Ability to work independently while engaging with multiple stakeholders.
Proficiency in MS Office, Visio, and Document Management Systems (DMS).
This manager sits within the R&D group. He definitely wants someone who comes from CSV in a Life Sciences company. If they have work in R&D groups that would be the best scenario but not 100% needed. Someone who knows GxP and regulations would be great. This is true CSV work within IT systems (not lab equipment).
Pay and Benefits
The pay range for this position is $35.00 - $52.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long-term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully remote position.
Application Deadline
This position is anticipated to close on Apr 30, 2025.
About TEKsystems:
We're partners in transformation. We help clients activate ideas and solutions to take advantage of a new world of opportunity. We are a team of 80,000 strong, working with over 6,000 clients, including 80% of the Fortune 500, across North America, Europe and Asia. As an industry leader in Full-Stack Technology Services, Talent Services, and real-world application, we work with progressive leaders to drive change. That's the power of true partnership. TEKsystems is an Allegis Group company.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Position Overview:
Experienced Technical Writer with a focus on system validation, specifically around validating IT systems, to support the large molecule group in documenting validation processes for their Electronic Lab Notebook (ELN) system.
This role emphasizes the importance of Computer System Validation (CSV) experience and requires the candidate to work independently while engaging with multiple stakeholders, including IT, R&D, Quality & Validation, and Product Owners.
Key Responsibilities:
Develop and author validation documentation for the large molecule group, including:
User Requirements Specifications (URS)
Functional Specifications
Validation and Test Plans
IQ/OQ/PQ protocols
Standard Operating Procedures (SOPs)
Ensure validation documentation meets GxP and compliance standards.
Create and execute testing strategies and scripts to support system validation efforts.
Collaborate with IT, R&D, Quality & Validation, and Product Owners to gather requirements and document workflows.
Manage structured document control and version management within a Document Management System (DMS).
Qualifications:
3+ years of experience in technical writing within a regulated industry (Pharma, Biotech, Animal Health).
Strong CSV (Computer System Validation) experience, specifically in validating IT systems.
Experience with system validation, testing protocols, and technical documentation.
Prior experience with electronic Lab Notebooks (ELN) (Benchling preferred, but any ELN experience acceptable).
Strong knowledge of GxP, 21 CFR Part 11, and validation documentation processes.
Ability to work independently while engaging with multiple stakeholders.
Proficiency in MS Office, Visio, and Document Management Systems (DMS).
This manager sits within the R&D group. He definitely wants someone who comes from CSV in a Life Sciences company. If they have work in R&D groups that would be the best scenario but not 100% needed. Someone who knows GxP and regulations would be great. This is true CSV work within IT systems (not lab equipment).
Pay and Benefits
The pay range for this position is $35.00 - $52.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long-term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully remote position.
Application Deadline
This position is anticipated to close on Apr 30, 2025.
About TEKsystems:
We're partners in transformation. We help clients activate ideas and solutions to take advantage of a new world of opportunity. We are a team of 80,000 strong, working with over 6,000 clients, including 80% of the Fortune 500, across North America, Europe and Asia. As an industry leader in Full-Stack Technology Services, Talent Services, and real-world application, we work with progressive leaders to drive change. That's the power of true partnership. TEKsystems is an Allegis Group company.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
Report this job Seeking a Technical Writer/ CSV Analyst
Position Overview:
Experienced Technical Writer with a focus on system validation, specifically around validating IT systems, to support the large molecule group in documenting validation processes for their Electronic Lab Notebook (ELN) system.
This role emphasizes the importance of Computer System Validation (CSV) experience and requires the candidate to work independently while engaging with multiple stakeholders, including IT, R&D, Quality & Validation, and Product Owners.
Key Responsibilities:
Develop and author validation documentation for the large molecule group, including:
User Requirements Specifications (URS)
Functional Specifications
Validation and Test Plans
IQ/OQ/PQ protocols
Standard Operating Procedures (SOPs)
Ensure validation documentation meets GxP and compliance standards.
Create and execute testing strategies and scripts to support system validation efforts.
Collaborate with IT, R&D, Quality & Validation, and Product Owners to gather requirements and document workflows.
Manage structured document control and version management within a Document Management System (DMS).
Qualifications:
3+ years of experience in technical writing within a regulated industry (Pharma, Biotech, Animal Health).
Strong CSV (Computer System Validation) experience, specifically in validating IT systems.
Experience with system validation, testing protocols, and technical documentation.
Prior experience with electronic Lab Notebooks (ELN) (Benchling preferred, but any ELN experience acceptable).
Strong knowledge of GxP, 21 CFR Part 11, and validation documentation processes.
Ability to work independently while engaging with multiple stakeholders.
Proficiency in MS Office, Visio, and Document Management Systems (DMS).
This manager sits within the R&D group. He definitely wants someone who comes from CSV in a Life Sciences company. If they have work in R&D groups that would be the best scenario but not 100% needed. Someone who knows GxP and regulations would be great. This is true CSV work within IT systems (not lab equipment).
Pay and Benefits
The pay range for this position is $35.00 - $52.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long-term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully remote position.
Application Deadline
This position is anticipated to close on Apr 30, 2025.
About TEKsystems:
We're partners in transformation. We help clients activate ideas and solutions to take advantage of a new world of opportunity. We are a team of 80,000 strong, working with over 6,000 clients, including 80% of the Fortune 500, across North America, Europe and Asia. As an industry leader in Full-Stack Technology Services, Talent Services, and real-world application, we work with progressive leaders to drive change. That's the power of true partnership. TEKsystems is an Allegis Group company.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Position Overview:
Experienced Technical Writer with a focus on system validation, specifically around validating IT systems, to support the large molecule group in documenting validation processes for their Electronic Lab Notebook (ELN) system.
This role emphasizes the importance of Computer System Validation (CSV) experience and requires the candidate to work independently while engaging with multiple stakeholders, including IT, R&D, Quality & Validation, and Product Owners.
Key Responsibilities:
Develop and author validation documentation for the large molecule group, including:
User Requirements Specifications (URS)
Functional Specifications
Validation and Test Plans
IQ/OQ/PQ protocols
Standard Operating Procedures (SOPs)
Ensure validation documentation meets GxP and compliance standards.
Create and execute testing strategies and scripts to support system validation efforts.
Collaborate with IT, R&D, Quality & Validation, and Product Owners to gather requirements and document workflows.
Manage structured document control and version management within a Document Management System (DMS).
Qualifications:
3+ years of experience in technical writing within a regulated industry (Pharma, Biotech, Animal Health).
Strong CSV (Computer System Validation) experience, specifically in validating IT systems.
Experience with system validation, testing protocols, and technical documentation.
Prior experience with electronic Lab Notebooks (ELN) (Benchling preferred, but any ELN experience acceptable).
Strong knowledge of GxP, 21 CFR Part 11, and validation documentation processes.
Ability to work independently while engaging with multiple stakeholders.
Proficiency in MS Office, Visio, and Document Management Systems (DMS).
This manager sits within the R&D group. He definitely wants someone who comes from CSV in a Life Sciences company. If they have work in R&D groups that would be the best scenario but not 100% needed. Someone who knows GxP and regulations would be great. This is true CSV work within IT systems (not lab equipment).
Pay and Benefits
The pay range for this position is $35.00 - $52.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long-term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully remote position.
Application Deadline
This position is anticipated to close on Apr 30, 2025.
About TEKsystems:
We're partners in transformation. We help clients activate ideas and solutions to take advantage of a new world of opportunity. We are a team of 80,000 strong, working with over 6,000 clients, including 80% of the Fortune 500, across North America, Europe and Asia. As an industry leader in Full-Stack Technology Services, Talent Services, and real-world application, we work with progressive leaders to drive change. That's the power of true partnership. TEKsystems is an Allegis Group company.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
Report this job