Scientist, QC-Portfolio Management
Scientist, QC-Portfolio Management
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Job Description
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.
The resource will work on-site at the Pfizer Sanford North Carolina facility and will be a member of Pfizers Quality Control Portfolio Management team to support multiple quality programs. resource will be able to analyze chemical or biological or microbiological products.
What You Will Achieve
In this role you will:
- Demonstrate comprehensive and specialized knowledge and skills in procedures techniques tools materials and/or equipment needed for the position
- Demonstrate a comprehensive understanding of technical skills and operational knowledge
- Contribute to the completion of project/work group/department tasks
- Act as a lead on icIEF and CE-SDS HPLC and UPLC techniques coordinating the work of others but is not a supervisor (SME)
- Develop or adapts new processes and procedures for work area to improve performance and increase efficiency consciously balancing the risk and reward trade-off
- Non-standard work is periodically reviewed with a focus on soundness of technical judgment.
- May be responsible for reviewing the work of others within the work group
- Demonstrate deep knowledge of varied aspects or a specialized aspect of a discipline
- Recognized as a technical expert with growing scientific contributions
- May use or develop novel processes or hypotheses; applies ingenuity; new ideas and knowledge are used frequently
- Make decisions that require choosing or developing new options to solve moderately complex problems
- Use own scientific judgment to apply and adapt standard methods and techniques with increased independence by applying prior work experience
- Work independently on assignments using knowledge and work experience
- Independently plan and execute laboratory experiments.
- Collaborate with trainers colleagues and subject matter experts to perform the assays in the laboratories including the use of computational predictive tools modeling software and data visualization tools as necessary.
- Assist teams in completing the assays required for the validation and transfer of methods.
- Engage with the method development team and participate in both in-process and final product sample analyses.
- Author relevant sections of technical reports to support interdepartmental technology and method validation and transfer processes.
- Prepare technical reports critically review data as second analyst for the validations and evaluate new instrumentation and analytical techniques as required.
- Independently analyze experimental data and provide conclusive insights.
- Mentor associate and senior and associate scientists and offer technical guidance when required.
Here Is What You Need (Minimum Requirements)
Applicant must have a Bachelors degree with at least 2 years of experience; OR a Masters degree with 0 years of experience; OR an Associates 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 validation.
Experience with troubleshooting assays and improving method performance.
Basic computer skills including data entry with a high level of attention to detail
Bonus Points If You Have (Preferred Requirements)
Masters degree with over 4 years of relevant experience
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 Fridaywork shift: 8-5PM Onsite.
- Occasional OT and weekend work might be expected to support continuous business activities.
Other Job Details:
- Last day to Apply: September 2nd 2025
- Eligible for Relocation Assistance: No
- 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 E-Verify employer. This position requires permanent work authorization in the United States.
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Employment Type
Full-Time
