Associate - GMP Training

Role overview

Associate - GMP Training at Pfizer

In this role, you will:

Responsibilities

• Perform assignment of Alternate/Primary Job Codes (AJC) and direct assignment of Curricula upon request
• Work Location Assignment: On Premise

Employment details

• Location: India - Vizag

Application details

• To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .

About the employer

• We rely on agile members who understand the critical impact of their role in Pfizer’s mission.

Additional role details

• Use Your Power for Purpose
• Our breakthroughs would not reach the hands of patients without our dedicated pharmaceutical manufacturing team.
• You will play a crucial role in improving patients' lives by ensuring that our team is well-trained and compliant with Good Manufacturing Practices (GMP).
• Your efforts ensure that patients and physicians have timely access to the medicines they need.
• What You Will Achieve
• Maintains and controls item/ curriculum management and training assignment in the LMS.
• Executes Record Learning in the LMS.
• Manages the archiving of training records and the training record retention.
• Assigns Site curricula, Induction curricula and other required training for new hire orientation (Colleagues Contingent workers and service providers ) and tracks new hires orientation trainings completion timelines
• Processes Curricula requests (Curricula Modification / Learning Plan modification) based on the filled in Curricula requests (adding or removing items, editing metadata, changing ownership, inactivation).
• Initiate curriculum content review: Prepares curriculum review list per ownership and deliver it to the curriculum owner.
• Ensures adherence to good documentation/data integrity (DI) for hand-written training records before the entry into PLA-MEL
• Acts as a Learning Plan Manager and manages profiles and libraries.
• Provide or coordinate training for new LMS users, people managers, training schedulers, report generators and training record administrators.
• Runs reports and collect data for monitoring site training metrics.
• Publishes Knowledge assessment (KA) in PLA-MEL and Uploads the signed KA in GMP shared folder
• For manually created items:
• Creates/Updates/Inactivates the item (and, if necessary, the related Content
• Object) manually.
• Configures metadata and settings of an item after creation (via PPI/QPI or
• manually).
• Adjusts due dates for revised items.
• Here Is What You Need (Minimum Requirements):
• B.
• Pharm, M.Pharma or MSc with 4-8 years of experience in pharmaceutical industry.
• Sterile injectables experience
• Excellent communication skills, both oral and written
• Solid understanding of GMP and Regulatory Training compliance
• Experience in Technical Training Skills
• Proficiency in MS Office, especially Word and PowerPoint
• Strong organizational and time management skills
• Bonus Points If You Have (Preferred Requirements):
• A solid understanding of manufacturing processes and regulatory compliance
• Strong problem-solving skills and attention to detail
• Ability to adapt to changing priorities and manage multiple tasks
• Experience in developing and delivering training programs
• Strong interpersonal skills and the ability to work effectively with diverse teams
• Quick learner and ability to multitask.
• Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity.
• Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
• Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
• Manufacturing