Work as MQA Upstream Specialist at Pfizer | M.Pharm, MSc, B.Pharm
Founded in 1849, Pfizer is the world’s premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support.
Post :MQA Upstream Specialist
Job Description
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 Sr. Specialist or 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 the manufacturing practices and ensure compliance with respect to standards and approved procedures. Perform daily walk throughs and report observations to the supervisors. Perform equipment breakdown assessments w.r.t to product quality and patient safety with technical support/inputs from Sr. Specialist or Supervisor. Review and approval of equipment alarms and review of alarm trends. Report any non-compliance to the supervisor. 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.
Candidate Profile
B.Pharm / M. Pharm / M.Sc (Any specialization)
02 to 03 Years of experience in Manufacturing Quality Assurance / Quality Assurance/ Production of a pharmaceuticals manufacturing facility (preferred sterile manufacturing facility).
Additional Information
Experience :Â 02 to 03 Years
Qualification :Â B.Pharm / M. Pharm / M.Sc
Location :Â Vizag
Industry Type :Â Pharma/ Healthcare/ Clinical research
Functional Area :Â Manufacturing Quality Assurance / Quality Assurance/ Production
End Date :Â 30th March, 2021
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