Why Patients Need You
Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative engineering team, you'll help bring medicines to the world even faster by imagining whats possible and taking action.
What You Will Achieve
Develops and modifies process formulations, methods and controls to meet quality standards. Recommends
and implements improvements, modifications or additions which will document work; tests and solves
problems. Review product requirements with product development compatibility of processing methods to
determine costs and schedules.
Working with Pfizers dynamic engineering team, you will play a critical role in developing and modifying process formulations, methods and controls to meet desired quality standards. Your production engineering skills will help in recommending and implementing improvements, modifications or additions that will help in solving problems. You will review product requirements in terms of product development compatibility and help Pfizer determine optimum costs and schedules of production.
As an associate, your focus on the job will contribute in achieving project tasks and goals. It is your domain knowledge, commitment, collaboration and dedication that will help us achieve new milestones and patients across the globe.
How You Will Achieve It
* Serve as Automated Visual Inspection (AVI) equipment Subject Matter Expert (SME) in the
development, evaluation and validation of critical process parameters in support of new, transferred and
existing product lines. Has enough process and technical depth to represent the Company in discussions
around AVI with external customers and / or auditors.
* Develop and coordinate engineering tests, change requests and protocols as required to meet
regulatory and cGMP requirements. Work with Automation Engineers in the development of complex
equipment recipes to optimize product specific parameters and drive improvements as required.
* Trend and analyze performance of the equipment, uptime and process reliability indicators. Report to
Management periodically this analysis and provide actions plans to tackle potential process shifts. Provide
continuous improvement and anticipate issues. Provide feedback to the Line Supervisor providing feedback
on setup, cleaning, operation and training needs / practices.
* Support AVI operations in troubleshooting, training, developing procedures and process
improvements. Activate Troubleshooting or Reliability teams as needed integrating cross-functional teams.
Seek for necessary support internally, within Pfizer Network or Outside as needed in a timely fashion to
support the Operations to comply with the expected Mfg plans.
* Develop long range plans for future AVI processes and systems to accommodate future growth.
* Contribute to the completion of project milestones, organize own work to meet project task deadlines and communicate progress on scheduled projects.
* Lead or support major equipment related investigations and implement equipment corrective or preventative action and performance improvements.
* Organize testing associated with the development of new process technologies and the support of new product introductions and tech transfers.
* Ensure integrity and compliance of data according to Standard Operating Procedures.
* Coordinate all work on scheduled projects (personnel activities, documentation and outside resources).
* Perform other tasks necessary to support site compliance to Center and regulatory requirements.
* Support cleaning program by performing swabbing and visual inspection of equipment.
* Assist in document preparation and training.
Qualifications
Must-Have
* Bachelors degree or Masters degree in Engineering or Science discipline
* A minimum 1 year of experience in the pharmaceutical industry preferably in a process engineering with a general understanding of the production and VI areas
* Demonstrated ability to provide technical solutions for complex problems through equipment and process understanding
* Working knowledge of Food and Drug Administration Regulations, and Good Manufacturing Practices
* Proactive, has experience with high performance teams, strong interpersonal and project management skills
* Strong written and verbal communication skills
* Microsoft Applications skills
Nice-to-Have
* Demonstrated experience in a relevant manufacturing environment
* Three (3) years of experience in the pharmaceutical industry, in a Process Engineering role.
* Five (5)years of experience in any industry, in a Project Engineering role is preferre
* Knowledge and experience with Drug Product processing and equipment
PHYSICAL/MENTAL REQUIREMENTS
Lifting up to 25 lbs, sitting, standing, walking, bending
Wearing gowning and personal protective equipment in specific areas
Ability to perform mathematical calculations and ability to perform complex data analysis.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Position requires regular onsite attendance, and cannot be performed remotely. Must have the ability to work
efficiently/effectively and manage strict production time and performance deadlines. Limited travel required
but may include international destinations. Regular work shift but may require support off hours, weekends or extended shifts.
Other Job Details:
* Last Date to Apply for Job: February 17, 2021
* Additional Location Information: McPherson,KS
* Eligible for Employee Referral Bonus
* Eligible for Relocation Package
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care providers name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.
Engineering
LI-PFE
New York, New York
Pfizer Inc. develops, manufactures, and sells healthcare products worldwide. It offers medicines and vaccines in various therapeutic areas, including internal medicine, vaccines, oncology, inflammation and immunology, and rare diseases under the Lyrica, Chantix/Champix, Eliquis, Ibrance, Sutent, Xalkori, Inlyta, Xtandi, Enbrel, Xeljanz, Eucrisa, BeneFix, Genotropin, and Refacto AF/Xyntha brands. The company also provides consumer healthcare products that comprise over-the-counter medicines, including dietary supplement products under the Centrum, Caltrate, and Emergen-C names; pain management products under the Advil and ThermaCare names; gastrointestinal products under the Nexium 24HR/Nexium Control and Preparation H names; and respiratory and personal care products under the Robitussin, Advil Cold & Sinus, and ChapStick names. In addition, it offers products that would lose or have lost marketing patent protection; branded generic products; generic sterile injectable products; biosimilars; and anti-infectives under the Lipitor, Premarin family, Norvasc, Lyrica, Celebrex, Viagra, Inflectra/Remsima, Zyvox, Vfend, Revatio, Inspra, Medrol, Sulperazon, Fragmin, Tygacil, Nivestim, and Retacrit, Ixifi Infliximab BS names.
Further, the company is also involved in the contract manufacturing business. It serves wholesalers, retailers, hospitals, clinics, government agencies, pharmacies, and individual provider offices, as well as disease control and prevention centers. The company has collaboration and/or co-promotion agreements with Bristol-Myers Squibb Company, Astellas Pharma US, Inc., and Oncolytics Biotech Inc.; licensing agreement with BionTech AG; strategic alliance with Verily Life Sciences LLC; and collaboration agreements with Pfizer, Merck & Co., Inc., and Eli Lilly & Company, as well as with Merck KGaA and Nektar Therapeutics to develop a therapy for treating pancreatic cancer. Pfizer Inc. was founded in 1849 and is headquartered in New York, New York.