Use Your Power for Purpose

At Pfizer, every day is an opportunity to make a difference in patients' lives. Your contributions will directly impact patient care, as you work within a flexible, innovative, and customer-oriented culture rooted in science and risk-based compliance. By joining our team, you will help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver meets the highest standards of safety and efficacy.

What You Will Achieve

In this role, you will:

Manage time effectively, develop short-term work plans, and work under limited supervision with periodic review

Receive instructions on complex problems and report issues to management, participating in issue resolution

Provide mentoring within the work group/project team, train junior colleagues, develop training plans, and oversee training activities

Perform tasks associated with maintaining Current Good Manufacturing Practices (GxP) compliant Quality Control and Stability laboratories

Represent Quality Control Analytical in cross-functional and site product meetings and provide subject matter expertise for standard operating procedures and quality standards content

Interpret data, make recommendations, reach decisions based on data and management input, and review and approve environmental monitoring data

Apply existing techniques and procedures with recommendations, implement modifications for improved efficiency, and devise and develop new microbiological methods

Support change controls, investigations, and other technical documents, participate in regulatory filing writing, and determine environmental monitoring locations and qualification requirements for aseptic facility modifications and new facilities

Here Is What You Need (Minimum Requirements)

Applicant must have a Bachelor's degree with at least 2 years of experience; OR a Master's degree with 0+ years of experience; OR an Associate's degree with 6 years of experience; OR a high school diploma (or equivalent) and 8 years of relevant experience

Demonstrated Subject Matter Expert level technical expertise on icIEF and CE- SDS techniques.

Proven track record of independently accomplishing complex analytical method development and validation

Proven track record of independently accomplishing complex analytical method validation.

Experience with troubleshooting assays and improving method performance.

Bonus Points If You Have (Preferred Requirements)

Strong background in leading continuous improvement projects

Demonstrated expertise in defending laboratory practices during regulatory audits

Proficient in organic chemistry, particularly in understanding the degradation mechanisms of pharmaceutical active ingredients and products

Experience in environmental testing, utility monitoring, analytical testing, microbial identification, and sterility testing

Expertise in Quality Control instruments and meeting accuracy specifications against established standards.

Ability to set requirements for the transfer of methodology from R&D

Experience with method validation and method transfer skills to manufacturing site.

Experience with bio-process downstream development

  

Physical/Mental Requirements

Resource is expected to be self-motivated and driven and able to manage day to day work activities with minimum direction.

Should have a positive and teamwork mindset.

Should be an analytical thinker and use their skills to troubleshoot the daily challenges faced at the workbenches, in data reviewing and documentation.

Should be able to lift or handle up to 25 lbs containers

Excellent written and verbal communication skills

Strong interpersonal abilities

Non-Standard Work Schedule, Travel, or Environment Requirements

This role is standard day Monday through Friday work shift: 8-5PM Onsite.

Other Job Details:

Last day to Apply: October 27th

Eligible for Relocation Assistance: No

Work Location Assignment: On Premise.

The annual base salary for this position ranges from $80 300,00 to $133 900,00. In addition, this position is eligible for participation in Pfizer’s 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 life’s 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.com). 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 provider’s 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.

Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@pfizer.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.

Quality Assurance and Control