MQA Upstream - Sr. Specialist.

Pfizer Inc.

Vizag, India

Job posting number: #7146923 (Ref:pf-4885474)

Posted: May 25, 2023

Application Deadline: Open Until Filled

Job Description

7 - 10 years of experience.

Qualification M Pharma/ MSc

Responsible for ensuring operating state of cGMP compliance in solution/emulsion preparation, vial/ampoule washing, depyrogenation, filling and capping operations.

Maintain regulatory compliance in accordance with cGMP practices.

Ensure manufacturing policies and procedures conform to Pfizer standards.

Knowledge and hands on experience in reviewing eBR and assessing the impact of AMPs exceptions with technical support/inputs from supervisor.

Review of batch reports and equipment audit trails.

Perform EMS alarm impact assessments and monthly trend reports.

Ensure start-up and in-process activities performed as per batch record and SOP compliance.

Monitor and adherence manufacturing practices with respective standards and approved procedures. Perform daily walk throughs and report observations to the supervisors and ensure appropriate closer of those incidents.

Perform equipment breakdown assessments w.r.t to product quality and patient safety independently. Review and approval of equipment alarms and review of alarm trends.

Report any non-compliance to the supervisor.

Responsible for performing manufacturing investigations, implementation of CAPAs and to approve investigation and CAPAs.

Manage investigation and apply relevant and necessary actions/ systems to ensure appropriate closure of those incidents.

Should have trouble shooting abilities in manufacturing area, which helps the organization to develop, implement and achieve its mission, vision and values.

Identify gaps and involve in process and procedure simplification, thereby reduce downtime and increase the efficiency.

Experience in handling regulatory, corporate and internal auditors / inspectors. Responsible for assisting manufacturing investigators w.r.t collection of data, information and technical support and may perform in conducting investigations.

Ensure that reports are aligned with regulatory requirements, site standards procedures an company policies.

May lead a team of MQA colleagues on an interim basis in the absence of the supervisor.

  
 

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

Quality Assurance and Control

#LI-PFE


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.


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More Info

Job posting number:#7146923 (Ref:pf-4885474)
Application Deadline:Open Until Filled
Employer Location:Pfizer Inc.
New York,New York
United States
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