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Pearl River, New York
Start date
Aug 2, 2022

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Science/R&D, Biotechnology
Required Education
High School or equivalent
Position Type
Full time
Pharm Country, Best Places to Work
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Job Details

Role Summary

Ensures that quality control procedures adequately evaluate an organization's products. Determines if current methods and techniques result in meeting reliability standards or require modification. Devises testing plans, methods and equipment to assure reliability of product in conjunction with product design and specifications.

Accountable for microbiological testing such as final sterility, endotoxin, bioburden, TAMC, growth promotion, and MLT on raw materials, excipients, Active Pharmaceutical Ingredients for in-process and final product, environmental monitoring samples, process & cleaning validation samples using standardized and validated methods per company, compendia and regulatory requirements. Results are compared with specifications and documented.

Incumbent will master most or all fundamental technical and quality concepts. In addition, writes protocols, reports, and investigations associated with the laboratory and to support method validation activities.

Role responsibilities

  • Accountable for the accuracy and validity of testing results. Performs mathematical calculations, interprets results, and records observations.

  • May utilize Laboratory Information Management Systems. Develops problem solving skills.

  • Maintains all related records, prepares and records media, buffers and reagents, etc., and maintains work area in a neat and orderly manner. May assist in coordinating the testing activities of the group.

  • Learns to analyze and interpret project/study/investigation results and findings.

  • Determines next steps under guidance of Manager and in compliance with applicable regulations; carries out technical and administrative duties as assigned.

  • Responsible to ensure timely analyses of biopharmaceutical products during manufacturing, release testing and stability monitoring. This will be achieved by efficiently managing the testing schedule based on laboratory and operational needs.

  • Evaluation of results and resulting trends as needed.

  • Participation in resolving laboratory investigation and in activities related to change control process as needed.

  • Review of relevant documentation within the laboratory.

  • Support the creation of laboratory reports, method procedures, validation protocols and validation reports and instructions.

  • Monitoring and implementation of GMP and other relevant regulatory requirements for biopharmaceutical products as it pertains to the laboratory.

  • Responsible to maintain data integrity principles in everyday laboratory operations.

  • Performing other jobs and tasks as needed in accordance with professional qualifications and experience, such as completing analysis of samples within the laboratory.


Basic qualifications
  • 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+ years of experience.

  • Knowledge of various microbial test methods.

  • A team player with strong interpersonal, organizational, and communications skills are a must. Additionally, the candidate must be self-motivated, engaged and able to perform moderately complex tasks independently.

Preferred qualifications
  • Bachelor's degree in Biology and Microbiology.

  • 5 - 8+ years of laboratory experience.

  • 2+ years of work experience in a regulated industry.

  • Biopharma/pharma industry experience that includes a broad understanding of Biopharmaceutical Sciences processes and Quality Systemspreferred.

  • Experienced practitioner of DMAIC principles.

  • Knowledge of GMP regulations/guidances (21 CFR Parts 11, 210 &211; EC Annex 15; ICH 7) as they pertain to the pharmaceutical/biopharmaceutical industry.

  • Knowledge ofpharmaceutical QC quality systems.

Physical/Mental requirements
  • This position will spend significant time in a laboratory environment and must be able to wear all required PPE.

Non-standard work schedule, travel or environment requirements
  • May require support for site as needed beyond core business hours.

  • Little to no travel required.

Other information
  • Last Date to Apply for Job: August 25, 2022.

  • Eligible for Relocation Package: No.

  • Eligible for Employee Referral Bonus: Yes.


Work Location Assignment:On site.

Pfizer requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, Pfizer will consider requests for Reasonable Accommodations.

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



Join world-class scientists and leaders who are dedicated to bringing therapies that will significantly improve patients' lives.

As one of the world's premier innovative biopharmaceutical companies, we're driven to discover the cure --driven to significantly improve the lives of everyone...everywhere. If you're similarly driven, you'll find there's no better place to begin --and continue --your career than at Pfizer.

Science is the foundation of our company.  This is why it's no surprise that the most driven scientists in the world choose to carry out their life's passion at Pfizer.  We arm them with the resources, technology, and facilities they need to solve some of the world’s most complex health challenges. This combination empowers our scientists with expertise in vaccines, small-molecule medicines, biotherapeutics amongst many others, to collaborate on breakthrough science, including the world's first mRNA-Based Covid19 vaccine.  Our colleagues advance science and technologies into the therapies that matter most.

Join us and you'll partner with colleagues of diverse backgrounds and abilities who contribute to all aspects of what we do. Great things happen when people come together with one shared goal. If you're driven to discover the cure- ensure it has the latest technology to make it a reality or help improve the lives of others- join those who are similarly driven at Pfizer. The future of medicine is happening here.

Visit and connect with us.



Find Us
(212) 733-2323
235 East 42nd Street
New York, NY 10017
United States
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