Philadelphia, PA, 19133, USA
12 days ago
QA/QC Technician
Job Title: QAOTF PackagingJob Description Responsible for QA On the Floor support to the Packaging Operation. Partners with production to ensure that processes are carried out in compliance with approved standards. Primary responsibilities include AQL Sampling and inspection, line monitoring, and Line Clearance inspections. Responsibilities + AQL Sampling and inspection of final product containers and packaging. + Oversight of Packaging Operations through line monitoring. + Conduct line clearance inspections during the changeover process. + Maintain a high level of understanding of relevant production processes and quality systems. + Collaborate with Packaging personnel and other Quality professionals to ensure consistent application and execution of key quality systems. + Execute QA processes to maintain the flow of products and documents to meet site objectives. + Ensure that training is up to date and all tasks are completed per SOP or other defined standards. + Use lean principles to suggest opportunities to reduce waste and improve processes in Quality Operations. + Report potential issues of non-compliance. + Conduct activities and interactions consistent with company values and in compliance with the Code of Conduct and supporting Policies and Standards relevant to your role. + Complete all required training on the Code of Conduct and supporting Policies and Standards on time. + Other tasks and responsibilities may be assigned as needed. Essential Skills + Experience with inspection, GMP, QA, biology, Quality assurance, Document control, SOP, Quality control, and Batch record. + Professional manner and excellent verbal communication skills. + Good judgment skills. + Knowledge of packaging operations. + Able to work alone for the majority of the shift. + Able to stand/walk around the packaging area for 90% of the shift. Additional Skills & Qualifications + BS degree in biology or microbiology preferred. + Experience with aseptic techniques. + Prefer at least a year or two of GMP experience in a QA role or documentation within a cGMP role such as manufacturing or lab. Work Environment 1st shift Tuesday-Friday 5:45AM-4:15PM. Fun and welcoming environment. Personal protective equipment (PPE) such as lab glasses and boots will be provided. Seasonal workers receive a pay increase each year they return. Several hiring managers were once seasonal workers and were hired full time. The company provides a 2-week notice before the end of the season to assist in finding the next opportunity. Pay and Benefits The pay range for this position is $35.38 - $39.81 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.
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