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You will be updated with latest job alerts via email$ 66500 - 110900
1 Vacancy
Use Your Power for Purpose
Every day our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible innovative and customeroriented culture is rooted in science and riskbased compliance. Whether you are engaged in development maintenance compliance or research analysis your contributions have a direct impact on patient care. By being part of our team you help uphold a quality culture that adapts and evolves to meet the needs of patients ensuring that every product we deliver is of the highest standard. Your role is crucial in maintaining this commitment and driving forward our mission to improve patient outcomes.
What You Will Achieve
In this role you will:
Evaluate and review clinical and commercial drug batches to ensure quality.
Ensure product and process documents meet established specifications through rigorous sampling and statistical process control.
Identify and address deviations from manufacturing and packaging standards.
Approve investigations and oversee change control activities to maintain compliance with configuration management policies.
Contribute to project tasks and milestones organizing work to meet deadlines.
Learn and apply basic team effectiveness skills within the immediate work team.
Make decisions within limited options to resolve basic problems under supervisors direction.
Ensure manufacturing and packaging records conform to Pfizer policy and cGMP standards.
Maintain inspection readiness support regulatory and customer inspections and improve quality assurance systems.
Assist manufacturing/packaging staff in realtime compliance error detection and resolution and lead or participate in Quality Risk Management assessments.
Here Is What You Need (Minimum Requirements)
Applicant must have a bachelors degree with 0 years of experience; OR
an associates degree with 4 years of experience; OR a high school
diploma (or equivalent) and 6 years of relevant experienc
Experience in the pharmaceutical industry and Quality administered systems
Sound knowledge of current Good Manufacturing Practices (part of GxP)
Ability to work effectively in a team environment both within ones own team and interdepartmental teams
Effective written and oral communication skills
Bonus Points If You Have (Preferred Requirements)
Experience at a manufacturing site.
Managing and writing deviations
Experience in production batch record review Enterprise Resource Planning system investigation of nonconformance root cause analysis and change control management
Strong problemsolving skills
Ability to work independently and as part of a team
Excellent time management and multitasking abilities
PHYSICAL/MENTAL REQUIREMENTS
Expected to spend time between office and shop floor as needed to support manufacturing.
Will require evening work with occasional oncall weekends.
This is a penicillin manufacturing facility. Any candidates applying must NOT be allergic to penicillin.
NONSTANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS
This is a first shift position. The selected candidate will be required to support manufacturing as needed and be oncall for occasional weekend shifts.
Relocation support available
Work Location Assignment:On Premise
Last Day to Apply: April 11 2025
The annual base salary for this position ranges from $66500.00 to $110900.00. In addition this position is eligible for participation in Pfizers Global Performance Plan with a bonus target of 7.5 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 (uscandidates.mypfizerbenefits). 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 EVerify employer. This position requires permanent work authorization in the United States.
Required Experience:
Unclear Seniority
Full-Time