Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members, who understand the importance and impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and always look to improve outcomes. You will help to ensure that patients and physicians have the medicines they need, when they need them.
What You Will AchieveYour expertise in the manufacturing domain will help in analyzing and designing a sequence of operations and workflow to improve the company's production facilities within regulations and Good Manufacturing Practices. You will be involved in activities, such as process monitoring, safety and environmental improvements, process reliability improvements, validation, and technology transfers. You will also conduct studies pertaining to cost control and reduction, inventory control, and production record systems. On the basis of these studies, you will develop and implement plans and programs for facility modifications and revisions to operating methods.
As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.
It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve ItDevelop Manufacturing/Operating Instructions and necessary Standard Operating Procedures.Develop, maintain and troubleshoot the process control system recipe/Models.Investigate, report and troubleshoot findings on both quality and EHS related issues observed during manufacturing or during batch record review.Develop, implement and monitor robust preventive measures for processing issues.Play a pro-active role in ensuring the site safety and quality standards are adhered to.Proactively monitor, identify, develop and implement improvements in processes and equipment.Communicate on a regular basis to the plant personnel on process updates.Train the process technicians on the process and procedures as required.Ensure adherence to approved procedures and update the procedures as required, including the principles and practices of good data management (ALCOA).Focus on Safety and GMP Compliance as operational priorities and as performance measures.Accountable for the Good Data Management and Data integrity understanding and performance.Report and investigate actions or behaviors that may negatively impact the desired outcome of the GMP process or activity.Own one or more multiple equipment/GMP systems in production and present the system overview with evidence compliance to internal and external auditors.Develop courses of action and drive implementation of solutions.Play an active and impactful role to deliver flawless execution for respective PCTs (e.g. API, MS, QO, Leadership, Engineering) by updating performance against metrics, highlighting & resolving issues with appropriate escalations.Work with the PCT to identify and drive improvement as per continuous improvement (CI) goals of the PCT.Uphold Pfizer’s code of conduct and values.QualificationsMust-HaveBachelor's Degree, preferably in Chemical Engineering or degree in science with major in Chemistry5 years' experience in pharmaceutical (API), with relevant manufacturing environmentGood organization skills and attention to detailAbility to document clearly and concisely.Effective written and oral communicationFully complete Covid-19 vaccination and could provide official medical certificate
Work Location Assignment: Flexible
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Engineering