Job Title: Manufacturing TechnicianJob Description As a Manufacturing Technician, you will assist in both direct and indirect manufacturing support functions. Your responsibilities will include tasks such as thawing, blending, filling, staging, preparation, environmental monitoring (EM), and equipment preparation. You will perform standard operating procedures to meet current good manufacturing practices (GMP) and accurately complete required documentation to comply with federal regulations. Additionally, you will maintain product-related records and author SOPs and batch records as needed. Ensuring product quality and patient safety, you will be responsible for all aspects of aseptic manufacturing. Responsibilities + Assist in direct manufacturing support functions such as thawing, blending, filling, staging, preparation, environmental monitoring (EM), and equipment preparation. + Assist in indirect manufacturing support functions, such as cleaning and sanitization of the facility. + Perform standard operating procedures to meet current good manufacturing practices (GMP). + Accurately complete required documentation to comply with federal regulations and assist with batch-record close-out. + Maintain product-related records as required. + Author and review SOPs and batch records as needed. + Ensure product quality and patient safety in the aseptic manufacturing of products. + Prepare equipment and manufacturing components to be used in support of or manufacturing of the product. + Operate basic equipment such as scales, balances, autoclaves, pH meters, and environmental monitoring equipment as delineated in standard operating procedures. + Prepare and formulate special cleaners and solutions needed for cleaning or used in the manufacturing processes and support areas as specified by standard operating procedures. + Carry out assignments in a timely, diligent, and safe manner to comply with domestic and international regulatory agencies (e.g., CFR, EMEA). + Accurately complete documentation to comply with FDA and GCP/GLP/GMP regulations. Essential Skills + Knowledge of GMP and manufacturing processes. + Experience in biology, filling, blending, cleaning, and sanitization. + 0-4 years of related experience or training in a pharmaceutical manufacturing environment. + 0-2 years of related experience or training with an associate degree and/or a four-year degree in science or life sciences field. + Ability to perform standard operating procedures and maintain accurate documentation. Additional Skills & Qualifications + Academic coursework in a related science field, applicable certifications, and/or practical relevant work experience. + Clean room work experience, food, medical device, and/or pharmaceutical manufacturing or aseptic processing and/or assembly experience. + Environmental monitoring, pharmaceutical warehousing, and pharmaceutical packaging experience are acceptable. + Pharmaceutical experience is preferred but not required. + Relevant certifications and licenses are acceptable. Work Environment Work shifts are available as follows: 1st shift: Monday-Friday 6 AM-2:30 PM, 2nd shift: Monday-Friday 2 PM-10:30 PM, 3rd shift: Sunday night-Friday morning 10 PM-6:30 AM. Pay and Benefits The pay range for this position is $26.15 - $33.00 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 Philadelphia,PA. Application Deadline This position will be accepting applications until Dec 24, 2024. 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.