Unfortunately, this job posting is expired.
Don't worry, we can still help! Below, please find related information to help you with your job search.
Some similar recruitments
Qc Associate Scientist, Em Data Analyst
Recruited by Pfizer 9 months ago Address , Sanford
Qc Scientist Method Transfer And Validation
Recruited by Pfizer 9 months ago Address , Sanford
Qc Supervisor Jobs
Recruited by INX International Ink Co. 9 months ago Address , Lebanon, 45036
Scientist Molecular And Cellular Technology
Recruited by Bristol Myers Squibb 9 months ago Address , Brisbane
Qc Associate Scientist Jobs
Recruited by Pfizer 9 months ago Address , Sanford, Nc
Qc Scientist Iv Jobs
Recruited by Inclusively 9 months ago Address , Andover, Ma
Qc Analyst Ii Jobs
Recruited by Emergent Biosolutions 1 year ago Address , Canton, 02021, Ma
Qc Scientist Ii Jobs
Recruited by Pfizer 1 year ago Address , Andover, Ma
Qc Scientist I Jobs
Recruited by Pfizer 1 year ago Address , Andover, Ma
Qc Technician I - Molecular Diagnostic Products
Recruited by Maine Molecular Quality Controls(MMQC) 1 year ago Address , Saco, 04072, Me
Qc Scientist I Jobs
Recruited by Pfizer 1 year ago Address , Andover, 01810, Ma
Senior Associate Scientist, Qc Bioanalytics
Recruited by Pfizer 1 year ago Address , Sanford, Nc
Qc Scientist Ii Jobs
Recruited by Pfizer 1 year ago Address , Andover, 01810, Ma
Qc Analytical Scientist I
Recruited by Pfizer 1 year ago Address , Andover, 01810, Ma

Qc Sr Associate Scientist - Qc Analytical Chemistry

Company

Pfizer

Address , Sanford, Nc
Employment type FULL_TIME
Salary
Expires 2023-10-03
Posted at 9 months ago
Job Description
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, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams.
It is your hard work and commitment that will make Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It
  • May initiate and develop project plans to ensure projects timely completion.
  • Analyzes and interprets results, makes decisions regarding the accuracy, completeness and compliance.
  • Responsible for knowing, understanding and acting in accordance with Pfizer’s values and our OWNIT culture
  • Responsible for reporting issues to management and participating in issue resolution (such as reporting OOS result and participating in associated laboratory investigation, reporting instrument issues and assisting with troubleshooting, etc.)
  • May perform data trending activities and assist with metrics reporting.
  • Responsible for appropriate creation, review and approval of GMP documentation (test records, and as assigned validation protocols/reports, test methods, equipment records, etc.) and ensuring adherence to Pfizer standards, guidelines and values.
  • May serve on cross functional teams to facilitate communications between Quality Control and other departments.
  • Performs tasks associated with maintaining GMP compliant Quality Control and Stability laboratories.
  • Assessing existing situations and suggesting improvements to increase compliance and innovation.
  • Performs testing including, but not limited to clinical and/or commercial product, raw materials and validation samples.
Qualifications
Must-Have
  • Basic computer skills (data entry and attention to detail) in Microsoft
  • Excellent effective written and verbal communication and interpersonal skills
  • Demonstrated experience in manufacturing, quality or engineering experience in the biotech or pharmaceutical industry.
  • Understanding of laboratory practices and analytical testing and use of analytical equipment: i.e. UV-VIS, HPLC, UPLC, pH, appearance, osmolality, TOC and conductivity, and various other instruments.
  • Applicant must have a High School Diploma (or Equivalent) and 6 years of relevant experience OR an Associate's degree with 4 years of experience OR a Bachelor’s degree with 0-2 years of experience.
Nice-to-Have
  • Experience in biotech or pharmaceutical industry
  • Experience leading continuous improvement projects.
  • Experience in Quality Operations
  • Laboratory experience, including HPLC with Empower
  • Experience with Laboratory Information Management System (LIMS)
  • Degree in Science or related field.
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
  • 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, ect.)
  • Not expected to travel.
Other Job Details:
  • Last day to Apply: August 17th, 2023.
  • Work Location Assignment: On Premise
  • Eligible for Relocation Assistance: 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.
Quality Assurance and Control
#LI-PFE