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Posted : Wednesday, September 04, 2024 07:19 PM
Why Patients Need You
Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients.
Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented.
Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.
What You Will Achieve You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team.
You will be responsible for analyzing chemical, biological or microbiological products to support our quality programs.
Your contribution to environmental testing, utility monitoring, analytical testing, microbial identification and sterility testing will help Pfizer provide safe drugs to patients.
Your understanding of Quality Control instruments will help us meet their accuracy specifications against established standards.
You will also be relied on for setting requirements for the transfer of methodology from R&D.
As a Senior Associate scientist, your strong foundation in general scientific practice and in the principles and concepts of the discipline will help us achieve our goals.
You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge.
It is your dedication and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It Perform tasks associated with maintaining Good Manufacturing Practices {also cGMP} compliant Quality Control and Stability laboratories.
Support Quality Control (QC) Bioanalytical testing primarily in the 2nd shift (3:00 - 11:30 pm Monday through Friday).
Act safely and follow Environment, Health and Safety requirements for site and QC laboratories.
Apply existing techniques and procedures, with recommendations, and implement modifications for improved efficiency.
Support product transfers/new product development, regulatory queries, cost improvement projects or Drug Product plant support for Cleaning Validation.
Operate within established HR policies and basic colleague relations guidelines.
Write Standard Operating Procedures (SOPs), technical reports, project plans etc.
independently.
Contribute to the completion of team objectives and assigned project milestones.
Exercise and build basic team effectiveness skills, such as commitment, feedback and consensus management, within the work group.
Qualifications Must-Have Applicant must have a High School Diploma (or Equivalent) and 8 years of relevant experience OR an Associate’s degree with 6 years of experience OR a Bachelors with at least 3 years of experience OR Masters with more than 1 year of experience.
Demonstrated experience in manufacturing, quality or engineering experience in the biotech or pharmaceutical industry Fundamental understanding of laboratory instrumentation function and analytical method troubleshooting Ability to receive feedback and takes accountability for actions and personal development Aptitude for good decision making based on procedures, guidance, and experience Excellent oral, written and interpersonal communication skills Knowledge of Microsoft Office applications, specifically Word and Excel Nice-to-Have Experience with and in depth understanding of QC Bioanalytical testing Experience defending laboratory practices in regulatory audits Knowledge in GMP, LIMS, etc.
Laboratory experience, including PCR, Endotoxin, and ELISA PHYSICAL/MENTAL REQUIREMENTS Ability to lift 30 lbs, stand for 2 to 3 hours at a time, sit for 2 to 3 hours at a time, walk long distances and bend to obtain items from lower shelving/cabinets.
Intellectual capability to perform complex mathematical problems and perform complex data analysis.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Work schedule is primarily 2nd shift (3:00 - 11:30 pm Monday through Friday) and may include weekdays and/or weekend days with first, second, and/or third shift hours as appropriate for assigned tasks/activities.
Relocation support available: No Work Location Assignment: On Premise Last date to apply:09/20/2023 The annual base salary for this position ranges from $62,800.
00 to $104,500.
00.
In addition, this position is eligible for participation in Pfizer’s 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 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.
Quality Assurance and Control
Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented.
Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.
What You Will Achieve You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team.
You will be responsible for analyzing chemical, biological or microbiological products to support our quality programs.
Your contribution to environmental testing, utility monitoring, analytical testing, microbial identification and sterility testing will help Pfizer provide safe drugs to patients.
Your understanding of Quality Control instruments will help us meet their accuracy specifications against established standards.
You will also be relied on for setting requirements for the transfer of methodology from R&D.
As a Senior Associate scientist, your strong foundation in general scientific practice and in the principles and concepts of the discipline will help us achieve our goals.
You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge.
It is your dedication and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It Perform tasks associated with maintaining Good Manufacturing Practices {also cGMP} compliant Quality Control and Stability laboratories.
Support Quality Control (QC) Bioanalytical testing primarily in the 2nd shift (3:00 - 11:30 pm Monday through Friday).
Act safely and follow Environment, Health and Safety requirements for site and QC laboratories.
Apply existing techniques and procedures, with recommendations, and implement modifications for improved efficiency.
Support product transfers/new product development, regulatory queries, cost improvement projects or Drug Product plant support for Cleaning Validation.
Operate within established HR policies and basic colleague relations guidelines.
Write Standard Operating Procedures (SOPs), technical reports, project plans etc.
independently.
Contribute to the completion of team objectives and assigned project milestones.
Exercise and build basic team effectiveness skills, such as commitment, feedback and consensus management, within the work group.
Qualifications Must-Have Applicant must have a High School Diploma (or Equivalent) and 8 years of relevant experience OR an Associate’s degree with 6 years of experience OR a Bachelors with at least 3 years of experience OR Masters with more than 1 year of experience.
Demonstrated experience in manufacturing, quality or engineering experience in the biotech or pharmaceutical industry Fundamental understanding of laboratory instrumentation function and analytical method troubleshooting Ability to receive feedback and takes accountability for actions and personal development Aptitude for good decision making based on procedures, guidance, and experience Excellent oral, written and interpersonal communication skills Knowledge of Microsoft Office applications, specifically Word and Excel Nice-to-Have Experience with and in depth understanding of QC Bioanalytical testing Experience defending laboratory practices in regulatory audits Knowledge in GMP, LIMS, etc.
Laboratory experience, including PCR, Endotoxin, and ELISA PHYSICAL/MENTAL REQUIREMENTS Ability to lift 30 lbs, stand for 2 to 3 hours at a time, sit for 2 to 3 hours at a time, walk long distances and bend to obtain items from lower shelving/cabinets.
Intellectual capability to perform complex mathematical problems and perform complex data analysis.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Work schedule is primarily 2nd shift (3:00 - 11:30 pm Monday through Friday) and may include weekdays and/or weekend days with first, second, and/or third shift hours as appropriate for assigned tasks/activities.
Relocation support available: No Work Location Assignment: On Premise Last date to apply:09/20/2023 The annual base salary for this position ranges from $62,800.
00 to $104,500.
00.
In addition, this position is eligible for participation in Pfizer’s 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 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.
Quality Assurance and Control
• Phone : NA
• Location : Sanford, NC
• Post ID: 9002004769
