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Company

Pfizer
Address , Andover, Ma
Employment type FULL_TIME
Salary
Expires 2023-07-17
Posted at 11 months ago
Job Description
Why Patients Need You
At Pfizer, our mission is to inspire a best-in-class culture of continuous improvement and project management that empowers colleagues and enables simple, effective processes. Whether you are managing projects or liaising with others, your contribution in this team will help in making our work easier and faster so that we can deliver breakthroughs that change patients' lives.
What You Will Achieve
The Quality Control Analytical group is seeking a highly motivated and experienced candidate to support GMP analytical testing activities for Raw Materials at the Andover site. The work includes testing and review of various instrumental techniques including HPLC, GC, IR, UV, as well as wet chemical methods.
The candidate will guide and train junior analysts, review and revise procedures, participate in continuous improvement activities, and utilize a strong scientific knowledge to troubleshoot technical issues and participate in investigations for root cause determination and resolution. The candidate will be expected to
support additional product testing as well as other QC Analytical business activities, as needed. The successful candidate will have experience performing testing on compendial raw materials following USP, EP, and/or JP compendia as well as on non-compendial raw materials following laboratory SOPs in a
pharmaceutical CGMP QC laboratory. The successful candidate will be team oriented, have a passion for excellence, demonstrate equity and inclusivity, seek continuous improvement opportunities, and take pride in his or her contribution to the team.
This position requires working collaboratively with QC Analytical and QC Micro, Quality Assurance, Warehouse personnel, and the Materials Program team. This position is expected to participate in the culture of the raw materials team as well as actively participate in scheduling, visual management, metrics,
and continuous improvement activities.
How You Will Achieve It
The qualified candidate must have QC experience and the ability perform testing and other laboratory activities for the QC Analytical Raw Materials group. Responsibilities include:
  • Plan and prioritize assignments.
  • Actively participate in visual management, standard work, and 5S activities in the QC
  • Identify and independently troubleshoot technical issues, atypical or out-of-specifications test results, instrument malfunctions and methodology problems, and participate in investigations for resolution and correction.
  • Provide guidance and training to junior analysts.
  • Participate in internal and external audits; maintain audit readiness of laboratory.
  • Communicate potential improvements and updates to Raw Materials Manager
  • Support qualification of instrumentation including coordination of vendor maintenance
  • Utilize continuous improvement tools.
  • Record and maintain all related data and records in compliance with cGMP and quality procedures.
  • Perform work in a manner consistent with company safety policies and procedures.
  • Analytical Raw Materials lab
  • Perform laboratory support functions and maintain work area in a neat and orderly manner.
  • Actively participate in continuous improvement culture within laboratories.
  • Participate in company culture-based programs.
  • Perform analytical testing and review of raw material samples; analyze and interpret results.
Qualifications
Must-Have
  • Excellent communication skills both oral and written.
  • Knowledge and experience in cGMP test methods utilizing and applying compendial monographs and procedures such as USP/NF, EP, JP
  • Candidate must be self-motivated and be able to adapt to rapidly changing project priorities.
  • Proficient with computer systems (Microsoft Office) required.
  • Applicant must have a High School Diploma (or Equivalent) and 8 years of relevant experience OR an associates degree with 6 years of experience OR a bachelors with at least 3 years of experience OR Masters with more than 1 year of experience.
  • Scientific understanding and experience with laboratory instrumentation and techniques such as HPLC, pH, titrations, UV, and wet chemical techniques.
Nice-to-have
  • Experience authoring and reviewing QC documentation such as SOPs and test methods.
  • Strong Technical writing skills preferred.
  • Preferred laboratory experience includes FTIR, NIR, GC, and ICP.
  • Experience with quality investigations.
  • Experience with six sigma, lean, and continuous improvement tools desired
  • Experience with electronic document management systems and laboratory information management systems such as LIMS, SAP,and Trackwise strongly preferred.

PHYSICAL/MENTAL REQUIREMENTS
Normal lifting, sitting, standing, and walking requirements to facilitate testing in a laboratory environment.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Position is first shift Monday through Friday. Some off hour (night/weekend/holiday) support may be required to support staff and operations.
Work Location Assignment: On Premise

OTHER JOB DETAILS
  • Eligible for Relocation Package: YES
  • Referral Bonus Eligibility: YES
  • Last Date to Apply for Job: May 25, 2023
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
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