Laboratory Quality Investigator Position Available In Broward, Florida
Tallo's Job Summary: Actalent is hiring a Laboratory Quality Investigator in Tamarac, FL. This temporary position pays $30 - $33 an hour and requires CGMP qualifications, 5 years of GMP analysis experience, and a Bachelor's degree in a related field. Responsibilities include investigating quality control issues, implementing CAPAs, and ensuring compliance with FDA regulations. This role also involves presenting findings, auditing procedures, and maintaining documentation.
Job Description
Laboratory Quality Investigator Actalent – 3.5 Tamarac, FL Job Details Temporary $30 – $33 an hour 1 day ago Benefits Commuter assistance Health savings account AD&D insurance Disability insurance Health insurance Dental insurance 401(k) Paid time off Employee assistance program Vision insurance Life insurance Qualifications CGMP 5 years GMP Analysis skills Quality assurance Bachelor’s degree Root cause analysis Senior level Lean manufacturing FDA regulations Full Job Description Job Description As a Quality Assurance Specialist, you will be responsible for investigating quality control issues related to raw materials, in-process and finished products, and stability samples. You will identify root causes and implement corrective and preventative actions (CAPAs), ensuring timely completion of these investigations. You will review investigation reports for accuracy, analyze the impact of proposed CAPAs, and discuss findings with relevant departments. Additionally, you will present investigation statuses and findings in Daily Lean Manufacturing (DLM) meetings and audit laboratory procedures for compliance. Responsibilities Investigate quality control issues for raw materials, in-process, finished products, and stability samples. Identify root causes and implement corrective and preventative actions (CAPAs). Review investigation reports for accuracy before approval. Analyze the impact of proposed CAPAs and discuss findings with relevant departments. Ensure timely completion of investigations and CAPAs. Present investigation status and findings in Daily Lean Manufacturing (DLM) 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 / Investigations / HPLC expertise Quality assurance experience CAPA and root cause analysis Knowledge of chemistry and fishbone analysis FDA compliance and instrumentation expertise QMS (Quality Management System) understanding 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, with working hours from Monday to Friday, 8 am to 5 pm. The role involves working in a cleanroom environment, with initial training in Miramar for the first two days before transitioning to the Tamarac site. You will have your own office space but will also be required to go out on the floor and communicate with Subject Matter Experts (SMEs). 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 for other accommodation options.