MSAT Scientist II
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Job Location:
Rocky Mount, NC - USA
Monthly Salary:
$ 66500 - 110900
Posted on:
30+ days ago
Vacancies:
1 Vacancy
Job Summary
Use Your Power for Purpose
The MSAT (Manufacturing Science and Technology) Scientist II is responsible for conducting laboratory operations to support manufacturing excellence across Focus Factories. This role serves as a Center of Excellence ensuring alignment with global manufacturing science standards and driving initiatives that enhance product quality compliance and operational efficiency. The MSAT Scientist II will execute studies such as material compatibility filter validation and compendial testing while also supporting new product introductions technology transfers and complex investigations. The role collaborates cross-functionally to implement PQS/Global Standards within the Focus Factory and site MSAT team.
What You Will Achieve
Provide MSAT Laboratory and strategic support for Focus Factories and Center functions.
Execution of critical testing programs including Material Compatibility Filter Validation and Compendial Testing (e.g. elastomers glass plastics). Ensure these programs meet regulatory and quality standards.
Contribute to New Product Introductions (NPIs) and Technology Transfers by providing laboratory-based technical assessments and qualification support for method transfers.
Assist in complex investigations requiring laboratory input. Apply scientific and data-driven approaches to root cause analysis and corrective/preventive action (CAPA) development.
Drive continuous improvement initiatives to enhance quality and efficiency.
Provide laboratory support to ensure alignment with long-term manufacturing and innovation goals.
Utilize small-scale production processes within the MSAT laboratory to enable process troubleshooting.
Here Is What You Need (Minimum Requirements)
Applicant must have a High School Diploma (or Equivalent) and 6 years of relevant experience OR an Associates degree with 4 years of experience OR a Bachelors degree with 0 years of experience.
Effective communication skills and attention to details
Experience in a GMP-regulated laboratory or manufacturing science and technology (MSAT) environment.
Excellent communication and cross-functional collaboration skills.
Proficiency in data analysis trouble-shooting problem-solving technical documentation and project management.
Self-motivated attitude with the ability to work with minimal direction
Flexibility and adaptability to changing priorities
Ability to meet deadlines and perform well under pressure
Bonus Points If You Have (Preferred Requirements)
2 years of experience in a pharmaceutical manufacturing site
Knowledge of US EU and ROW cGxP; ICH guidelines; analytical chemistry and/or Microbiology techniques
Knowledge of LIMS QTS eQMS PDOCs & GDMS
PHYSICAL/MENTAL REQUIREMENTS
Ability to work in a laboratory environment including standing for extended periods and handling laboratory equipment and materials.
Capability to perform detailed technical reviews and data analysis with a high degree of accuracy.
Ability to manage multiple complex projects simultaneously and make sound decisions under pressure.
Strong problem-solving skills and the ability to think critically and analytically in high-stakes situations.
Occasional lifting of laboratory materials or equipment (up to 25 lbs) may be required.
Visual acuity sufficient to read and interpret technical documents data charts and laboratory results.
NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS
May require occasional off-shift or weekend work to support urgent laboratory investigations or production-related testing needs.
Occasional domestic or international travel may be required to support technology transfers audits or cross-site collaboration.
Must adhere to safe laboratory practices including the use of personal protective equipment (PPE) and aseptic gowning when entering classified areas.
Flexibility to respond to critical issues outside of standard business hours particularly during new product introductions or major investigations.
Work Location Assignment:On Premise
Last Date To Apply: September 30 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 (). 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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Key Skills
- Laboratory Experience
- Immunoassays
- Machine Learning
- Biochemistry
- Assays
- Research Experience
- Spectroscopy
- Research & Development
- cGMP
- Cell Culture
- Molecular Biology
- Data Analysis Skills
About Company
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