Associate Scientist
- United States - North Carolina - Sanford
Use Your Power for Purpose
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 an 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.
What You Will Achieve
- Perform tasks associated with maintaining Good Manufacturing Practices {also cGMP} compliant Quality Control and Stability laboratories.
- Support environmental monitoring and water collection in the QC (Quality Control) Microbiology laboratory.
- 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.
- Write cleaning validation protocol and reports and perform complex mathematical problems and data analysis.
- 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.
Here Is What You Need (Minimum Requirements)
- Applicant must have an Associates with at least 0+ years of experience
- Demonstrated knowledge of manufacturing, quality or engineering practices in the biotech or pharmaceutical industry
- Aptitude for good decision making based on procedures, guidance, and experience
- Effective communication skills
- Knowledge of Microsoft Office applications, specifically Word and Excel
- Excellent effective written and verbal communication and interpersonal skills
- Ability to work in a team environment
Bonus Points If You Have (Preferred Requirements)
Experience with and in depth understanding of Microbiology testing
Experience defending laboratory practices in regulatory audits
In-depth knowledge of viable and non-viable environmental monitoring during pharmaceutical manufacturing and an understanding of aseptic techniques
PHYSICAL/MENTAL REQUIREMENTS
Ability to lift 30lbs, stand for 2 to 3 hours at a time, site for 2 to 3 hours at a time, walk long distances and bend to obtain items from lower shelving/cabinets.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Work schedule is second shift (12:00 pm to 8:30 pm) but can include weekdays and/or weekend days as appropriate for assigned tasks/activities. Minimal flexibility in work schedule to cover business needs. Minimal off-shift work to ensure business needs are met.
Must be able to wear appropriate PPE (e.g., lab coat, safety glasses, non-porous shoes, gloves, etc.)
Work Location Assignment: On Premise
OTHER JOB DETAILS
- Last Date to Apply for Job: April 15, 2025
- Referral Bonus Eligibility: YES
- Eligible for Relocation Package: NO
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.