**Immediate Opening** Quality Assurance Associate Interested in this role? Reach out directly to apply TODAY to Grace Williams at grawilliams@actalentservices .com (grawilliams@actalentservices.com) Job Description An exciting opportunity to join one of the largest American pharmaceutical company in the world. In which that is dedicated to animal health producing medicines and vaccinations for pets and livestock! If you are interested in jump starting your career for the opportunity to gain hands-on experience, skill development, and career advancement with a global leading company, please reach out to me as I would love to connect with you further! As a QA Associate, you are responsible for the review and analysis of data supporting the quality of products/packaging, and ensures compliance with applicable procedures, cGMP's/standards and regulations. Responsibilities + Provide support to Quality systems. + Organize, critically review, and present information in accordance with written procedures. + Provide support for the production area. + Apply and obtain statistical analysis. + Write, review, and revise GMP standard operating procedures. + Track, maintain, critically review, and correct manufacturing records. + Print additional documentation for manufacturing records disposition. + Maintain communication with QC lab regarding test results pertinent to batch release. + Maintain communication with Supply Chain Representatives to ensure timely batch manufacturing record release. + Approve raw materials for production use by evaluating vendor COA’s, printing permits, and approving materials on site. + Block and unblock material and track vendor information on a shared site. + Maintain communication with MCO’s regarding materials received on site and those urgently needed in production areas. + Print and prepare batch manufacturing records as requested by Supply Chain. + Manually print product shipping labels and verify count and variable data information. + Track and create additional labels as needed. + Maintain communication with area ICO’s to ensure timely pick-up and drop-off of records and labels. + Create or prepare Certificates of Analysis as requested by Customer Service Representatives. + Update Health and Non-Radiation Certifications. + Create Certificates of Manufacturing and Certificates of Conformity. + Track COA requests and create irregular COA’s and COA templates. + Mail documents to Customer Service Representatives. + Maintain communication with Customer Service Representatives to ensure timely delivery of Certificates of Analysis. + Perform inbound Quality Analysis and receipt for printed packaging materials. + Approve printed packaging materials for production use. + Monitor temperature records of bulk material received for Companion Animal Products. + Approve bulk material received for Companion Animal Products. + Own, track, and route documents in Veeva Vault for edit, review, and approval as needed for Quality Assurance Representatives and Technical Service/Manufacturing Science Representatives. Essential Skills + Quality Assurance + GMP, pharmaceutical, Life Science + Batch Record Review + Quality Inspection + Titration + Quality Documentation + pH Test + Analytical skills + Biology and Chemistry knowledge + QA Testing and QA Documentation + SOP Review Additional Skills & Qualifications + B.S/A.S Degree in related field OR 12+ months of QA/GMP experience without a degree + Strong communication, documentation, and math skills + Proficiency with computers + Attention to detail for working in a highly regulated environment + Batch Record Review experience is a plus INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION: *Interview availability this week* + I am scheduling interviews for this position and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to Grace Williams. + HOW TO APPLY DIRECTLY: Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to grawilliams@actalentservices. com or call me directly at (317-567 -6610) Pay and Benefits The pay range for this position is $20.00 - $25.00/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 Clinton,IN. Application Deadline This position is anticipated to close on Jul 28, 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.