Manager Engineering Verification
Manager Engineering Verification
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$ 96300 - 160500
1 Vacancy
Job Description
Use Your Power for Purpose
Whether 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 contribute to delivering medicines to the world at an accelerated pace by envisioning new possibilities and taking decisive action. Your role in the design and development of manufacturing processes as well as in maintenance and reliability support is essential for providing timely access to necessary medications. Working alongside our innovative team you will help expedite the delivery of medicines globally by imagining what can be achieved and making it happen.
What You Will Achieve
In this role you will:
Perform or manage Verification of a variety of systems such as: process equipment process control systems laboratory systems utilities and facilities for large capital projects.
Evaluate develop and manage Commissioning Qualification and Verification life cycle documentation to align with industry standards and company policies.
Evaluate and support system audit trails data integrity and alarm management requirements.
Actively share technical knowledge with others within the team through existing knowledge sharing processes and systems.
Provide recommendations for improvements with a focus on compliance.
Estimate and manage capital project verification resources for automation and equipment to approved project schedules.
Participate generate and/or review/approve standard operating procedures job aids risk assessments commissioning activities FATs and other capital project documentation.
Execute and manage multiple projects at the same time.
Apply good communication skills to keep customers peers and area management up to date with progress of all projects.
Comply with site SOPs change control actions commitments CAPAs and other GMP requirements to deliver a verified GMP system to end users.
Support routine periodic review activitiesand requalifications as needed.
Support regulatory audits as requested.
Provide expertise for troubleshooting and resolution of issues related to verification and compliance
Assess potential impact of changes to qualified/verified systems(automation and equipment)
Here Is What You Need (Minimum Requirements)
Bachelors with at least 4 years of experience
OR Masters degree with more than 3 years of experience
OR an Associates degree with 8 years of experience
OR a High School diploma with 10 years of experience
OR a PhD with 0 years of experience.
Thorough knowledge of cGMP (current Good Manufacturing Practices) combination device regulations and design control
Strong verbal and written presentation communication skills
Bonus Points If You Have (Preferred Requirements):
Relevant experience in the pharmaceutical industry
Proven ability to work collaboratively in a crossfunctional team environment
Strategic planning and forecasting skills
Ability to facilitate agreements between various teams
Other job details
Last day to apply: April 21st 2025
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:
Manager
Employment Type
Full-Time
