• Chemist 1 Jobs in United States Of America

  • Pfizer Inc.
  • United States Of America, Usa
  • Save Job
  • 3 - 6 Years
  • Posted : above 1 month

Job Description:


Independently performs routine and non-routine quality control testing of raw materials, in process, finished product, and stability samples within the framework of site policies, departmental procedures, and current Good Manufacturing Practices (cGMP) regulations Participates in investigations, team projects, and special project studies to accomplish company and departmental objectives Records and reports data accurately and in compliance with current methods/Standard Operating Procedures (SOPs), United States Pharmacopeia (USP/NF), other compendia as applicable, and cGMP Experienced in HPLC, GC, Chromatography Data Software application, titrations, pH, Karl Fisher, and General Wet Chemistry/Compendial Testing Performs additional duties under the guidance of laboratory management or designee


The essential functions of this position may include, but are not limited to

Performs set up, calibration, operation, and maintenance of laboratory test instruments/equipment
Analyzes samples per established departmental/site/corporate policies, specifications, and procedures
Prepares solutions and standardizes test solutions as defined in analytical method or compendia
Performs assigned work in a timely and safe manner conforming to regulatory, company, and compendial requirements
May assist in routine verification of laboratory standards, solutions, and documentation
Practices cGMP, which includes, but is not limited to, proper laboratory documentation and maintenance, archival of documentation/raw data, attention to specification limits for any tests performed, and immediate notification of any out-of-specification (OOS) results
Complies reports/documentation of analytical tests, ensuring reports are accurate and complete with documentation of procedures, equipment/instruments, and reagents used in analytical testing
Demonstrates practical laboratory skills, and a thorough knowledge of chemistry theories, analytical techniques, and quality procedures
Reviews and revises SOPs, analytical methods and related procedures/documents

The colleague will need to be trained in handling of controlled substances


Knowledge of compendia; USP, EP, and others as applicable, cGMP guidelines, FDA regulations; laboratory safety procedures, laboratory instrumentation, and MSDS; knowledge of inorganic and organic chemistry principals

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily The requirements listed below are representative of the minimum knowledge, skill, and/or ability necessary Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions

Education/Experience Bachelor Degree in Chemistry or related science field and a minimum of 3 years experience, or an equivalent combination of educations and experience/training; some laboratory experience in a GMP regulated environment is desirable

Language Ability Ability to read and understand applicable compendial methods, SOPs, general business periodicals, professional journals, technical procedures, and or governmental regulations; author scientific/technical reports, business correspondence and departmental procedures

Math Ability Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals; perform simple statistical functions and graph data

Reasoning Ability Ability to define problems, collect data, establish facts, and draw valid conclusions interpret an extensive variety of technical instruction in mathematical or diagram forma n deal with several abstract and fixed variables

Computer Skills To perform this job successfully, an individual should have knowledge of Windows based software applications such as Word, Excel, and Outlook; knowledge of chromatography data processing software, specifically Empower, is preferred/desirable

The position requires regular onsite attendance this position cannot be performed on a remote or telecommute basis on a temporary, short, or long term basis

Must have the ability to multi-task across multiple capabilities and functions and handle multiple competing priorities and requirements, including performing site and functional responsibilities, responding to frequent e-mail and phone communications and attending meetings and conference calls Note that these activities may not be time bound to core hours or presence at the site

Must have the ability to work effectively under and manage to strict production, time and performance deadlines

Must be willing and able to work beyond the hours typically defined as a regular workday, which may or may not include weekends and holidays


No unique physical / mental requirements


No expected non-standard work schedule, travel or environment requirements

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

The job is open only to Protected Individuals (as defined by 8 USC 1324b(a)(3), namely, Citizens or Nationals of the United States, Lawful Permanent Residents (green card holders), Refugees and Asylees

Last Date to Apply for Job July 5, 2019

N (Other) (United States of America)

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates

Profile Summary:

Employment Type : Full Time
Eligibility : Any Graduate
Industry : Biotechnology/Pharmaceutical/Medicine, Manufacturing/Industrial
Functional Area : Production/Manufacturing/Maintenance/Packaging
Role : Production/Manufacturi ng/Maintenance
Salary : As per Industry Standards
Deadline : 18th Mar 2020

Key Skills:

Company Profile:

Pfizer Incarfix

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