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Technical Writer - Compliance
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Actalent 2 days ago Be among the first 25 applicants Join to apply for the
Technical Writer - Compliance
role at
Actalent Job Description
We are seeking a skilled Technical Writer Compliance professional who will be responsible for writing and completing investigations and deviations from both compliance and operations perspectives. The role involves reviewing investigations and deviations to ensure manufacturing and GMP compliance, conducting root cause analysis, and managing the entire lifecycle of an investigation independently. This position requires excellent technical writing skills and effective communication as you will be interviewing manufacturing personnel and speaking with vendors regarding investigations. Job Title: Technical Writer Compliance
Job Description
We are seeking a skilled Technical Writer Compliance professional who will be responsible for writing and completing investigations and deviations from both compliance and operations perspectives. The role involves reviewing investigations and deviations to ensure manufacturing and GMP compliance, conducting root cause analysis, and managing the entire lifecycle of an investigation independently. This position requires excellent technical writing skills and effective communication as you will be interviewing manufacturing personnel and speaking with vendors regarding investigations.
Responsibilities
Determine the causes and preventative actions for Deviations, Non-Conformances, OOS, OOT, field complaints, and environmental excursion investigations. Drive investigations to true root cause using appropriate tools and benchmark industry standards. Define and implement effective preventative actions to prevent recurrence. Manage multiple investigations in different stages to meet compliance deadlines and product release dates. Collaborate with cross-functional teams to develop and track CAPA plans. Identify and create trending rules that trigger corrective actions. Analyze process data and evaluate trends to identify major improvement opportunities. Utilize change management approaches effectively. Develop training materials for personnel on writing problem statements and using root cause analysis tools. Champion CAPA plans and implementation. Provide communication plans for ongoing deviations and CAPAs. Create and communicate CAPA plans to responsible parties. Oversee timely completion of deviations, CAPAs, and Change Controls as necessary. Abide by quality standards.
Essential Skills
Compliance expertise Aseptic technique knowledge Root cause analysis proficiency Strong technical writing skills Experience in writing deviations and CAPAs 3-5 years of experience in writing and reviewing deviations and investigations 3-5 years of experience in a pharma company supporting manufacturing Previous quality assurance team experience
Additional Skills & Qualifications
Bachelor's degree in a related scientific field Experience in GMP Operations or Quality Assurance in Cell Therapies, Biotechnology, or Bio-Pharma Preferred experience in pharmaceutical or FDA regulated operations Experience using e-Quality Management Systems Proficiency with IT skills, including Visio, Microsoft Project, and Excel CAPA experience Previous experience with cell and gene or biologics
This position is urgently hiring. If interested, please submit your most updated resume and email your availability over for a 5-10 minute call to kvespia @astoncarter.com
Pay and Benefits
The pay range for this position is $50.00 - $55.00/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 onsite position in Parsippany,NJ.
Application Deadline
This position is anticipated to close on Jul 16, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. Seniority level
Seniority level Mid-Senior level Employment type
Employment type Contract Job function
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Technical Writer - Compliance
role at
Actalent 2 days ago Be among the first 25 applicants Join to apply for the
Technical Writer - Compliance
role at
Actalent Job Description
We are seeking a skilled Technical Writer Compliance professional who will be responsible for writing and completing investigations and deviations from both compliance and operations perspectives. The role involves reviewing investigations and deviations to ensure manufacturing and GMP compliance, conducting root cause analysis, and managing the entire lifecycle of an investigation independently. This position requires excellent technical writing skills and effective communication as you will be interviewing manufacturing personnel and speaking with vendors regarding investigations. Job Title: Technical Writer Compliance
Job Description
We are seeking a skilled Technical Writer Compliance professional who will be responsible for writing and completing investigations and deviations from both compliance and operations perspectives. The role involves reviewing investigations and deviations to ensure manufacturing and GMP compliance, conducting root cause analysis, and managing the entire lifecycle of an investigation independently. This position requires excellent technical writing skills and effective communication as you will be interviewing manufacturing personnel and speaking with vendors regarding investigations.
Responsibilities
Determine the causes and preventative actions for Deviations, Non-Conformances, OOS, OOT, field complaints, and environmental excursion investigations. Drive investigations to true root cause using appropriate tools and benchmark industry standards. Define and implement effective preventative actions to prevent recurrence. Manage multiple investigations in different stages to meet compliance deadlines and product release dates. Collaborate with cross-functional teams to develop and track CAPA plans. Identify and create trending rules that trigger corrective actions. Analyze process data and evaluate trends to identify major improvement opportunities. Utilize change management approaches effectively. Develop training materials for personnel on writing problem statements and using root cause analysis tools. Champion CAPA plans and implementation. Provide communication plans for ongoing deviations and CAPAs. Create and communicate CAPA plans to responsible parties. Oversee timely completion of deviations, CAPAs, and Change Controls as necessary. Abide by quality standards.
Essential Skills
Compliance expertise Aseptic technique knowledge Root cause analysis proficiency Strong technical writing skills Experience in writing deviations and CAPAs 3-5 years of experience in writing and reviewing deviations and investigations 3-5 years of experience in a pharma company supporting manufacturing Previous quality assurance team experience
Additional Skills & Qualifications
Bachelor's degree in a related scientific field Experience in GMP Operations or Quality Assurance in Cell Therapies, Biotechnology, or Bio-Pharma Preferred experience in pharmaceutical or FDA regulated operations Experience using e-Quality Management Systems Proficiency with IT skills, including Visio, Microsoft Project, and Excel CAPA experience Previous experience with cell and gene or biologics
This position is urgently hiring. If interested, please submit your most updated resume and email your availability over for a 5-10 minute call to kvespia @astoncarter.com
Pay and Benefits
The pay range for this position is $50.00 - $55.00/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 onsite position in Parsippany,NJ.
Application Deadline
This position is anticipated to close on Jul 16, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. Seniority level
Seniority level Mid-Senior level Employment type
Employment type Contract Job function
Job function Marketing, Public Relations, and Writing/Editing Industries Business Consulting and Services Referrals increase your chances of interviewing at Actalent by 2x Get notified about new Technical Writer jobs in
Parsippany, NJ . Brooklyn, NY $75,000.00-$82,000.00 4 weeks ago New York, NY $60,000.00-$90,000.00 3 weeks ago Technical Author (multiple roles and seniority levels)
New York, NY $150,000.00-$175,000.00 2 months ago New York, NY $88,000.00-$122,000.00 1 year ago New York City Metropolitan Area 1 day ago New York, NY $125,000.00-$145,000.00 4 weeks ago Associate Director, Writer (Branded Content)
New York City Metropolitan Area 1 week ago New York, NY $94,000.00-$105,000.00 1 week ago New York City Metropolitan Area 2 weeks ago Technical Writer [Must Have ISO 13485] - REMOTE
New York City Metropolitan Area $160,000.00-$200,000.00 3 weeks ago Newton, NJ $88,034.00-$100,610.00 1 month ago Technical Writer (Instructional Designer & SAAS)-US
New York, NY $86,681.00-$109,650.00 3 days ago New York, NY $180,000.00-$180,000.00 2 weeks ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr