The Senior Manufacturing Associate performs all production activities to manufacture biologic medicines in their assigned area, which may including upstream/cell culture, downstream/purification, preparation of media and buffer solutions, and/or aseptic fill finish operations. Teva’s Biologics Manufacturing Facility (BMF) uses state-of-the-art technology including single use bioreactors and isolator filling technology. Associates are initially placed on a production team based on the current business need but are expected to cross-train and support other areas as needed. The BMF is primarily a first shift, Monday-Friday operation; however, occasional split shift, weekend, and holiday work will be required as well as rotating on-call coverage. Senior Manufacturing Associates are essential to the success of our business and are expected to have a quality and continuous improvement mindset.
This position will be assigned to the Media & Buffer Solution Prep manufacturing team. This is a full time on-site manufacturing position.
ESSENTIAL DUTIES
• Perform routine manufacturing operations related to the preparation of GMP solutions such as handling of raw materials (sampling, weighing, dispensing, formulating), pipetting, titration, filtration and filter integrity testing, and cleaning and disinfection of materials and equipment.
• Set up, operate, and maintain complex manufacturing equipment such as mixers, balances, autoclaves, and parts washers.
• Lead and train junior associates in manufacturing processes and activities.
• Perform all work in a compliant manner in alignment with current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).
• Draft, revise, and follow Standard Operating Procedures (SOP’s) and batch records using good documentation practices.
• Identify opportunities for continuous improvement and improved quality compliance.
• Support area management in deviation investigations, change controls, validation protocols, and other activities as needed.
• Collaborate within assigned team and other stakeholders to build a positive and high performing collaborative culture.
MINIMUM REQUIREMENTS
• BS in science or a related field and 3+ years relevant experience in pharmaceutical manufacturing OR 6 + years relevant experience in a pharmaceutical manufacturing environment.
• 1+ years direct experience formulating media and buffer solutions for use in biologics manufacturing.
• Routine use of full face and/or positive air pressure (PAPR) respirators.
PREFERRED REQUIREMENTS
• Experience in upstream, downstream, and/or aseptic fill/finish processing operations
• Experience leading a team or in a supervisory role (formal or informal)
• Experience writing SOP’s, batch records, change controls, and/or deviation investigations.
• Experience or training in Lean Sigma principles and continuous improvement and/or Leadership.
We are strengthening and adding to our critical teams with great talent and capabilities: Teva, a global organization with a brand of evolving success. Be part of it!
We offer a competitive benefits package, including Medical, Dental, Vision, and Prescription coverage starting on the first day. We also offer Disability and Life Insurance, Paid Time Off, Paid Holidays, 6% match on the 401(k), Employee Stock Purchase Plan, and Tuition Assistance.
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.