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 forward-thinking 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 life-saving medicines to those who need them most.
What You Will Achieve
In this role you will:
Serve as the manufacturing areas technical SME providing expertise in fields such as the process equipment automation documentation.
Act as a Point of Contact for operator-support and issue resolution.
Support batch record and SOP revisions commitment ownership project management and investigations as needed.
Coordinate activities with maintenance to schedule routine work and to resolve corrective mechanical issues without impacting production operations.
Expertise in the Standard Work Plan and ability to coordinate batch activities with other Process Centric Teams (e.g. other manufacturing groups Tech Services QC QA) to meet plan of record.
Spend time on the production floor to proactively identify areas for improved efficiencies and ensure that product quality is maintained through all phases of production including operational parameters of manufacturing equipment automation control processing dynamics and integrated utilities to identify and resolve quality and technical risk to manufacturing.
Capable of identifying technical problems and solving them with minimal guidance. Ability to analyze operational process issues and automation challenges to recommend / initiate appropriate corrective and preventative actions.
Acts as a departmental liaison with primary support groups such as engineering technical services quality control quality assurance development and utilities and collaborate with the aforementioned groups to ensure a robust manufacturing operation.
Review and contribute to applicable documentation (i.e. MBRs SOPs etc)
Participates in process operational improvements
Know the processes and procedures including the principles and practices of good data management (ALCOA) and be able to guide advise and coach their teams.
Here Is What You Need (Minimum Requirements)
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 high-performance 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 cross-functional teams
Requires general knowledge of scientific principles technical knowledge of production equipment automation control systems processing requirements and any related procedural requirements with emphasis on assigned production area.
Bonus Points If You Have (Preferred Requirements)
Demonstrated experience in a relevant manufacturing environment
Knowledge and experience with Vaccines processing and equipment
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
PHYSICAL/MENTAL REQUIREMENTS
Lifting sitting standing walking bending ability to perform mathematical calculations and ability to perform complex data analysis.
NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS
n/a
Other Job Details:
Work Location Assignment:On Premise
Last day to apply: October 1sr
The annual base salary for this position ranges from $80300.00 to $133900.00. In addition this position is eligible for participation in Pfizers Global Performance Plan with a bonus target of 10.0% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of lifes moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution paid vacation holiday and personal days paid caregiver/parental and medical leave and health benefits to include medical prescription drug dental and vision coverage. Learn more at Pfizer Candidate Site U.S. Benefits (). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa FL or any location outside of the United States.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 E-Verify employer. This position requires permanent work authorization in the United States.
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Erfahren Sie mehr über uns als forschendes und produzierendes Pharmaunternehmen: Von unserem Beitrag zum medizinischen Fortschritt bis zur nachhaltigen Produktion.