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You will be updated with latest job alerts via emailWhether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability engineering is crucial to ensuring that customers and patients receive the medicines they need precisely when they need them. By collaborating with our forwardthinking engineering team you will play a key role in accelerating the delivery of medicines to the world. Your innovative ideas and proactive actions will help us imagine new possibilities and bring them to life ensuring that our solutions are both timely and effective. Your contributions will be essential in ensuring that our manufacturing processes are efficient reliable and of the highest quality ultimately helping us deliver lifesaving medicines to those who need them most.
Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members who understand the importance and impact of their role in Pfizers mission. Patients need colleagues like you who take pride in their work and always look to improve outcomes. You will help to ensure that patients and physicians have the medicines they need when they need them.
TheAssociate Process Engineersupports the execution of Commercial Clinical and/or Development production according to Standard Operating Procedures and Production Schedule formAb products. The Associate Process Engineer will work on interdisciplinary and cross functional teams to own and implement process improvements and lead/participate in process troubleshooting.
Supportsmanufacturing operations on the production floor for buffer/media makeup tanks glass washers autoclaves bioreactors / fermentors drug product filling filtration equipment inoculum preparation chromatography skids and/or UF/DF skids with varying levels of automation.
Point of Contactforthe execution and issue resolution associated with process equipment commissioning qualification and validation.
Ownstroubleshooting technical support/analysis and resolution of equipment automation and process issues on the manufacturing floor.
DeliversRight first time execution and continuous improvement; Monitor Identify and/or Communicate process and compliance trends in real time.
Participate in the authoring rolefor controlled documentation; SOPs Manufacturing Batch/Formulation Records Forms etc.
Collaborates withthe Subject Matter Expert for manufacturing operations in support of QTS investigations and CAPA implementations.
Responsible for remaining current on assigned training.
LeadsLean Manufacturing Sustainability and Operational Excellence initiatives; facilitate the drive towards continuous improvement in all manufacturing areas.
Leadsin the escalation process through various levels of management when operations personnel safety equipment functionality product supply and/or quality compliance are at risk.
Generateswork requestswhen issues arise with facility / manufacturing equipment. Provides support to maintenance to facilitate resolution when needed. Point of contact for emergency work orders.
Skilledin enterprise systems to support manufacturing operations including but not limited to SAP LIMS AMPS PDOCS and/or QTS.
Identifies the need for escalation through various levels of management when there is a risk to operations personal safety equipment functionality product supply and/or to quality/compliance.
Bachelors degree with any years of experience or an Associates degree with 4 years of relevant experience or a high school diploma (or equivalent) and 6 years of relevant experience
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 with experience in highperformance teams strong interpersonal and project management skills
Strong written and verbal communication skills
Proficiency in Microsoft Applications
Ability to work effectively in a team environment and collaborate with crossfunctional teams
Demonstrated experience in a relevant manufacturing environment
Knowledge and experience with Drug Substance processing and equipment
Experience with process validation and equipment qualification
Familiarity with Lean Manufacturing principles and Six Sigma methodologies
Excellent organizational skills and attention to detail
Strong leadership and mentoring abilities
Ability to adapt to changing priorities and work effectively under pressure
Requires the moving of heavy equipment and the ability to lift 40 pounds.
Moderate repetitive standing sitting bending and ladder climbing on a daily basis.
The incumbent needs to take the necessary safety precautions when working with pressurized systems steam and corrosive chemicals.
The incumbent is required to be skilled and knowledgeable of the operational equipment.
The incumbent will be required to solve problems regarding site assessment specific units used in Biopharmaceutical manufacturing.
The incumbent must be able to follow SOPs MBRs and be skilled in a multitude of enterprise systems including SAP DeltaV etc.
Train 5 is a 24/7 facility. Incumbent will be on fixed 12hour night shifts on 223 rotational model from 6pm to 6am
Last day to apply: May 26th 2025
No relocation support available
Work Location Assignment:On Premise
Relocation assistance may be available based on business needs and/or eligibility.
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 EVerify employer. This position requires permanent work authorization in the United States.
Required Experience:
IC
Full-Time