Validation Supervisor

<p><b>Use Your Power for Purpose</b></p><p>Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our innovative, flexible, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care.</p><p></p><p><b>What You Will Achieve</b></p><p>In this role, you will:</p><ul><li><p>Evaluate, review, and approve validation master plans, protocols, and reports, ensuring compliance with company standards and regulatory requirements.</p></li><li><p>Troubleshoot validation issues for equipment and performance processes, providing expertise for resolution.</p></li><li><p>Conduct statistical analysis of testing results and process anomalies and provide high-level data analysis support for Quality Investigations.</p></li><li><p>Guide the writing, review, and approval of validation process documents and technical reports, ensuring adherence to the latest Pfizer Quality Standards.</p></li><li><p>Contribute to moderately complex projects, manage time effectively, and develop plans for short-term work activities.</p></li><li><p>Manage routine quality systems such as Change Control, Documentation, and Investigations, and coordinate testing with functional groups.</p></li><li><p>Maintain the Site Validation Master Plan, support regulatory audits, and represent validation on site or network teams.</p></li><li><p>Support product transfers/new product development, regulatory queries, and cost improvement projects.</p></li><li><p>Ensuring integration of validation schedules in production and participating in deviation investigations.</p></li><li><p><span style="color:#494949">Maintain and manage of Continued process verification (CPV) and Periodic Cleaning Monitoring (PCM)</span></p></li></ul><p></p><p><span style="color:#494949"><b>Here Is What You Need </b>(Minimum Requirements)</span></p><ul><li><p><span style="color:#494949">You hold a degree in pharmacy, pharmaceutical technology or comparable scientific discipline.</span></p></li><li><p><span style="color:#494949">Minimum two years of experience in pharmaceutical industries combined with strong knowledge of regulatory requirements, GMP, and pharmaceutical development processes.</span></p></li><li><p><span style="color:#494949">Strong technical knowledge with validation/qualification of pharmaceutical processes, equipment, utilities, facilities, and/or computer systems</span></p></li><li><p><span style="color:#494949">Excellent verbal and written communication skills</span></p></li><li><p><span style="color:#494949">Ability to work independently and in a team environment</span></p></li><li><p><span style="color:#494949">Ability to work under pressure and adapt to a fast-paced environment</span></p></li><li><p><span style="color:#494949">Strong analytical and problem-solving skills</span></p></li><li><p><span style="color:#494949">Strong organizational and time management skills</span></p></li><li><p><span style="color:#494949">Willing to be placed in Jakarta</span></p></li></ul><p></p><p><span style="color:#494949"><b>Bonus Points If You Have </b></span></p><ul><li><p><span style="color:#494949">Strong working knowledge of various quality systems and processes</span></p></li><li><p><span style="color:#494949">Ability to mentor and guide other colleagues</span></p></li><li><p><span style="color:#494949">Experience with Solid Oral Dosage/Semi-Solid Dosage/Liquids Dosage forms</span></p></li><li><p><span style="color:#494949">Lean Six Sigma Yellow Belt or Green Belt certification</span></p></li></ul>&nbsp;&nbsp;<br>Work Location Assignment:&nbsp;On Premise<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Quality Assurance and Control<p></p><p></p>