Manufacturing Specialist - 1st shift Monday - Friday 6:00 AM - 2:30 PM

At Argenta, were more than a company were a global team, dedicated to healthier animals. We believe that when their lives are made better, we're all the better for it.

Founded in 2006, we support companies big and small to develop and manufacture health products for pets and livestock. Our trusted, innovative solutions and services cover every stage of the process, from molecule to market.

Were in a unique position. We are the worlds only combined contract research and contract development and manufacturing organization (CRO/CDMO) dedicated to animal health.

Our uniqueness means:

• We are ambitious, growing and building a one team culture, guided by our values.

• We are team players;

• We are doers;

• We are customer-centric;

• We are innovators.

We value diversity, as a global company, we get the richness of working with different people in different places whether it be location, stages of their career, their development, their role. We believe that when everyone works together and puts their best paw forward we will make the lives of the animals we care for, better.

With bases in New Zealand, the US, the UK and Europe, our 900 colleagues are driven by our partnership approach and purpose: Healthy Animals. Lets Make It Happen, Together.

TEAM PLAYERS who want to DO
great work and find INNOVATIVE ways to make animals lives better through our CUSTOMER CENTRIC efforts should apply.

Argenta is currently looking to fill the role Manufacturing Specialist at our Shawnee, KS location

Responsibilities:

• Comply with all workplace standards and safety procedures, including Lockout Tagout, Current Good Manufacturing Practices (cGMPs), Occupational Safety Health Administration requirements (OSHA), Standard Operating Procedures (SOPs), and Company Guidelines.
• Perform equipment setup and changeover activities. Act to safely reduce equipment setup and changeover times.
• Initiate and establish equipment operating parameters to maximize production, while meeting all product specifications. Meet line Operational Asset Effectiveness requirements per area targets. Ensure downtime is escalated properly.
• Perform the daily setup and routine operation of the packaging line, including, but not limited to: bottle in-feed, unscrambler, filler, bottle capper, torquer, labeler, vision systems, weighing systems, bar coding systems, sealers, disassembly/assembly, cleaning, resolving equipment stoppages and jams, and all material handling as trained.
• Perform preventive maintenance tasks as needed and trained.
• roubleshoot Variable Frequency Drives and Servo Drive systems as trained.
• Inspect packaging components, in-process items, and packaged drug products to assure compliance to specifications, identify any non-conforming item and initiate appropriate actions.
• Palletize both finished and unfinished products and operate motorized and non-motorized material handling equipment.
• Complete, maintain, and update production documentation (both electronic and paper) to perform material movements, material take-outs and yield determinations by following SOPs and utilizing systems as required such as Systems/Applications/Products (SAP), Manufacturing Execution Systems (MES), Electronic Batch Records (EBRs), etc.
• Take ownership of training and learning to develop high performance competencies such as technical skills, communication skills, and skills to build a team-oriented culture (i.e., training team members, motivating and supporting team members, sharing knowledge to continuously improve the process, etc.).
• Meet the production schedules outlined by line team and/or Supervision. Review and approve work output for team members by using validated methods.
• Manage area cleaning requirements including facility, equipment, and Operational Excellence initiatives.
• Area Specific Responsibilities:
• Weigh/Dispense
  • Manage Material movement functionalities and dispensing of materials for planned batches.
• Solid Dose Compounding
  • Manage Solids Compounding Operation that includes CIP, EQ Setup, Raw Material Additions, and general process steps.
  • Manage Batch control system recipe operations.
• Liquids Compounding
  • Manage Liquids Compounding Operations that include CIP, SIP, Equipment Setup, Raw Material Additions, and general process steps.
  • Manage Batch Control System Recipe Operations.
• Sterile Filling
  • Perform the functions required for the Bio-Class I clean room.
  • Sterile filling and sterile filtration of all sterile drug solution products from bulk into final containers. This position will also include running the autoclave, terminal sterilizer, preparation of filling equipment and components, and maintaining area logbooks and housekeeping procedures. Includes monitoring, trouble shooting, and training for activities of filtration, and filling preparation which include basic understanding of MMI (Man Machine Interface) Systems, CIP (Clean In Place) Systems and SIP (Steam In Place) processes.
  • Participate in Sterile Media Fill qualifications for Sterile Filling and maintenance activities. This is a critical qualification for duties performed in the sterile core.
  • Disassemble, clean, reassemble, and prepare all sterile filling product contact equipment and supplies for sterilization.
• Filling and Packaging
  • Perform line start-up to ensure the proper drug products, labels, and components are used in the filling/packaging process.
  • Manage filling and packaging operations with the ability to run all equipment in the area including filler, cartoner, labeler, bundler, etc. Must be proficient enough to train other operators.

Requirements:

• 2 yearsmanufacturing experience.
• Previous experience using automated inventory system is required (i.e., SAP, MES, etc.).
• Previous experience using motorized & non-motorized material handling equipment required.
• SAP or other Enterprise Resource Planning (ERP) experience highly desired.
  
• Demonstrated ability to successfully changeover/set up multiple pieces of packaging/manufacturing equipment and strong troubleshooting skills required.
• Good written and verbal communication skills in English required.
• Good PC Skills, including use of e-mail, attaching documents to e-mail required. Previous experience using electronic databases and on-line tools required (i.e., but not limited to, Lotus Notes database, Employee Self-Services on-line tools, etc.).
  

Experience in a government regulated, Good Manufacturing Practices (GMP) or Standard Operating Procedures (SOP) environment preferred.

Argenta has strongly embedded company values which is key to who we are and how we deliver. We offer an opportunity to work for a successful and rapidly expanding global business where your input will be valued.At Argenta we are a hard-working group who really enjoy the people we work with each day. That is why we support our people through strong culture, great benefits, and opportunity for growth.

Argenta is an equal opportunity employer

To find out more about Argenta, click here: www.argentaglobal.com