Actalent
Document Control Specialist
The Specialist - Global Quality & Compliance will create, revise, and manage global quality documentation, including SOPs, policies, the Global Quality Manual, and the Global Quality Policy. This role supports global and site quality initiatives, ensuring compliance with regulatory standards and internal requirements.
Responsibilities
Author and manage SOPs and policies.
Update the Global Quality Manual and Policy.
Collaborate with SMEs for accurate, compliant documentation.
Support quality initiatives with clear, precise documentation.
Ensure timely updates and distribution of documents.
Implement changes in the document management system.
Maintain consistent documentation practices across sites.
Participate in document reviews and approval processes.
Recommend improvements to documentation processes.
Support audits with organized documentation and follow-ups.
Additional Skills & Qualifications
Experience in Regulatory Affairs
Familiarity with FDA regulations
Knowledge of cGMP
Knowledge of Quality Systems
Pay and Benefits
The pay range for this position is $26.00 - $28.00/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 Tamarac,FL.
Application Deadline
This position is anticipated to close on Feb 7, 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.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
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 process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
The Specialist - Global Quality & Compliance will create, revise, and manage global quality documentation, including SOPs, policies, the Global Quality Manual, and the Global Quality Policy. This role supports global and site quality initiatives, ensuring compliance with regulatory standards and internal requirements.
Responsibilities
Author and manage SOPs and policies.
Update the Global Quality Manual and Policy.
Collaborate with SMEs for accurate, compliant documentation.
Support quality initiatives with clear, precise documentation.
Ensure timely updates and distribution of documents.
Implement changes in the document management system.
Maintain consistent documentation practices across sites.
Participate in document reviews and approval processes.
Recommend improvements to documentation processes.
Support audits with organized documentation and follow-ups.
Additional Skills & Qualifications
Experience in Regulatory Affairs
Familiarity with FDA regulations
Knowledge of cGMP
Knowledge of Quality Systems
Pay and Benefits
The pay range for this position is $26.00 - $28.00/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 Tamarac,FL.
Application Deadline
This position is anticipated to close on Feb 7, 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.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
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 process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.