• Quality Assurance Specialist

    Actalent (Tamarac, FL)


    Actalent is Hiring a Quality Assurance Specialist!Job Description

     

    As a Quality Assurance Specialist, you will investigate quality control issues related to raw materials, in-process, finished products, and stability samples. You will identify root causes and implement corrective and preventative actions (CAPAs), ensuring the accuracy of investigation reports before approval. Additionally, you will analyze the impact of proposed CAPAs, discuss findings with relevant departments, and ensure the timely completion of investigations.

    Responsibilities

    + Present investigation status and findings in Daily Lean Manufacturing meetings.

    + Audit laboratory procedures, production systems, and operational processes for compliance.

    + Prepare detailed reports and maintain documentation related to quality investigations.

    + Design and conduct training on quality control procedures and compliance standards.

    + Mentor and coach team members on laboratory techniques and problem-solving.

    + Collaborate with cross-functional teams to maintain quality integrity.

    + Stay updated on industry regulations and incorporate changes into training materials.

    + Initiate change controls for CAPAs, Effectiveness Checks, STPs, SOPs, and Specifications.

    + Ensure compliance with company policies, safety rules, and regulations.

    + Operate according to the Code of Conduct and Business Ethics.

    + Support risk assessment for laboratory and product-related changes.

    + Assist in customer complaint investigations.

    + Conduct training for analysts on QMS trending, CAPA, STPs, and SOPs.

    + Perform data trending for annual product reviews and reports.

    + Perform other relevant duties as assigned.

    Essential Skills

    + Investigation and analysis skills

    + cGMP compliance knowledge

    + Experience with Investigations and HPLC

    + Quality assurance expertise

    + CAPA implementation

    + Root cause analysis

    + Strong understanding of chemistry

    + Fishbone analysis

    + FDA compliance knowledge

    + Instrumentation proficiency

    + QMS familiarity

    Additional Skills & Qualifications

    + Bachelor's degree in Science

    + 5 years of QA experience

    + Experience in GMP and FDA environment

    Work Environment

    This position is based on-site in Tamarac, working Monday to Friday from 8 am to 5 pm in a cleanroom environment. The specialist will have their own office space but will also be required to engage on the floor and communicate with SMEs. Joining a pharmaceutical manufacturer in substantial growth mode, there is a clear career path for growth as the company brings a variety of generic pharmaceuticals to the world.

    Pay and Benefits

    The pay range for this position is $30.00 - $33.00/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 May 29, 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 [email protected] (%[email protected]) for other accommodation options.