Senior Associate Scientist
Pfizer
**Summary:**
The resource will work on-site at the Pfizer, Sanford, North Carolina facility and will be a member of Pfizer's Quality Control Portfolio Management team to support multiple quality programs. The resource will be able to perform chemical, or biological or microbiological analysis on products. The resource should be able to perform the analytical or chemical or microbial and sterility testing in the GMP laboratory setting and should be able to collaborate efficiently with the external teams. Additionally, the candidate should be able to document all the data to in accordance with cGMP and data integrity principles. The resource should be able to review the validation data as a second analyst reviewer.
**Role responsibilities:**
+ Plan and execute laboratory experiments with minimum guidance.
+ 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.
+ Assisting 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.
**Here Is What You Need** (Minimum Requirements)
+ High School Diploma (or Equivalent) and 4 years of relevant industry experience preferably in GMP OR an associate's degree with 2 years of relevant industry experience preferably in GMP OR BS+0 years of industry experience
+ Extensive hands-on experience and strong background in either Chemistry, Microbiology or molecular biology assays.
+ Experience with troubleshooting assays and improving method performance.
+ Ability to establish strong relationships within business lines
+ Excellent written and verbal communication and interpersonal skills
+ Proficiency in laboratory information management systems and data analysis software
+ Strong problem-solving skills and attention to detail
**Bonus Points If You Have** (Preferred Requirements)
+ Experience in Quality Operations
+ Laboratory experience including Cell Culture, Bioassay, Aseptic Technique, and ELISA
+ Familiarity with regulatory requirements and compliance standards
+ Ability to work independently and as part of a team
+ Strong organizational and time management skills
+ Ability to adapt to changing priorities and work in a fast-paced environment
The resource will report to the Manager, QC-Portfolio Management on regular basis for updates of the projects and job duties in addition to the managing point of contact of the resource provider organization.
**PHYSICAL/MENTAL REQUIREMENTS**
+ Resource is expected to be available at minimum M-F, 8-5PM Onsite. OT and weekend work might be expected.
+ 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.
Work Location Assignment: On Premise
The annual base salary for this position ranges from $66 500,00 to $110 900,00. 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. This position requires permanent work authorization in the United States.
Quality Assurance and Control
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