Zoetis is the world's largest Manufacturer and Supplier of Animal Pharmaceuticals.
At Zoetis, we manufacture high quality medicines for dogs, cats, and livestock. Looking for your chance to work for the #1 Animal Health company in the world? Zoetis is looking for the next amazing colleague to join the family.
Benefits Include:
Great Health Benefits from day 1!
4 weeks accrued paid vacation and 13 paid holidays.
401(k) match with company profit sharing
Tuition reimbursement
Student Loan Repayment Program
Position Summary
Provide the first line of response to address and support manufacturing deviations and investigations. All investigations and process changes are documented and managed within Trackwise, Event Tracking System. Take manufacturing lead in implementation of changes and improvement action items as a fall out of investigations. Support process and product transfers developed by Global Manufacturing Technology (GMT) organization such as new product transfers and continuous process improvements. Conduct activities and make decisions that are in accordance with Company policies & SOPs, Zoetis Values, & global regulatory guidelines (including cGMP/cGLP/cGCP), environmental guidelines, as appropriate, etc.
Hours: 1st shift. Some weekend work may be required.
Position Responsibilities
Learn the ABI processes for in-depth evaluation for process/yield improvements while also routinely collaborating with site Leaders/QA/GMT.
Conduct and author process investigations and reports, utilizing Right First Time (RFT) tools and scientific reasoning.
Ensure corrective actions are identified and implemented to eliminate the root cause of the problem, partner with other Zoetis colleagues within the network when needed.
Examine processes and review data, to identify best practices and take action to reduce contamination, increase efficiencies and increase potencies.
Take the manufacturing lead in continuous improvement efforts. Be proficient in leading change, writing change control documents, and managing /coordinating all aspects of project implementation.
Take the manufacturing lead in the introduction of new processes or modifications to existing processes as supported by Global Manufacturing Technology (GMT). Assist in performing technical evaluations and implementation of GMT initiatives to ensure robust process improvements and transfers.
Provide technical and biological expertise to Process Team process improvement discussions (e.g., as part of Tier Boards) to improve process reliability, robustness, cost, and efficiency.
Review production procedures and data to identify opportunities for yield and other process improvements.
Responsible for identifying and implementing delivering Cost Improvement Projects (CIP).
Collaborate with QA and Regulatory to Review manufacturing directions and associated documents (this includes reviewing OOPs, PMs, SOPs, and Change Controls).
Communicate and work with the Equipment Engineer and/or Maintenance on process improvements of equipment and new projects.
Collaborate with area Team Leaders and other Leads to train and lead colleagues in the performance of best practices.
Education and Experience
Specialist Level: BA/BS with 2-4 years of experience OR MBA/MS with 0-2 years of experience OR 8 years relevant experience.
Associate Level: BA/BS with 0-2 years of experience OR 6 years relevant experience.
Degree in Microbiology, Virology, Immunology, Biological Systems Engineering, Mechanical Engineering, Packaging Engineering, Chemical Engineering or related technical field.
Must have strong technical/analytical skills and possess a high degree of personal motivation.
Excellent interpersonal skills and ability to interact across divisional boundaries.
Technical Skills Requirements
Must have strong technical writing skills.
Must possess a high degree of personal motivation.
Must be capable of communicating (both written and verbally) with colleagues at all levels in the business.
Strong technical/analytical/problem solving skills and experience.
Excellent interpersonal skills and ability to interact across divisional boundaries.
Preferred experience in biological production systems, biological product formulations (blend/fill), and/or biological testing.
A working knowledge of vaccine production methods and experimental design and experience in cGMP.
Demonstrated ability to lead investigations by performing technical evaluation followed by implementation of change initiatives to ensure robust process improvements.
Knowledge of APHIS/USDA, EU regulations applicable to the biological industry is preferred.
Preferred experience in Lean/Six Sigma. Green Belt certification if currently does not have Green Belt certification, commitment to obtain green belt certification within 1 year of training, which may require limited travel.
Physical Position Requirements
Must be able to walk, sit, or stand for extended periods of time.
Must be able to reach above shoulder level, bend/stoop, kneel, push/pull, and handle/grip frequently.
Must be able to work scheduled hours with the ability to work weekends as needed.
Frequent lifting and carrying of 5 to 25 lbs.; maximum of 50lbs.
Regular reaching, bending, stooping, and twisting.
Repetitive motion and substantial movement of the wrists, hands, and/or fingers
Able to become qualified to enter clean room environments.
Work Environment: While performing the duties of this job, the employee occasionally works in environments with extreme temperature (hot /cold) & humidity, with limited lighting and in crowded spaces. The noise of these work environments are typical office noises.