About the Role We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place. To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.

Pfizer General

Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products.

Responsibilities - Comply with the applicable requirements of current GMP and EHS regulations for the tasks to be performed.

- Report any identified deviations and actively participate in investigating them and preventing their recurrence.
- Develop, follow, and enforce the operating procedures that apply to your area. Ensure adherence to Standard Operating Procedures, batch records, Current Good Manufacturing Practices, and plant protocols.
- Actively participate in IMEx initiatives to promote the improvement of production standards in order to achieve budget compliance in accordance with the current budget.
- Actively share knowledge and encourage a culture of continuous learning and improvement.
- Collaborate in the implementation of validation activities.
- Collaborate in activities aimed at creating a positive work environment for all colleagues.
- Ensure that training is assigned to and completed by colleagues.
- Actively participate in the selection and development of colleagues. Manage the performance of direct and indirect reports, providing mentorship and support to achieve the business objectives.
- Identify and develop innovative concepts for process or product improvements, taking calculated risks to achieve results.
- Lead investigations into equipment failures, implement corrective and preventive actions, and maintain clear communication to prevent reoccurrence.

Specific

Responsibilities - Ensure compliance with EHS regulations related to operational work to prevent accidents (LOTO, emergency plan, use of PPE).

- Ensure compliance with GMP regulations to produce a product that meets the required quality standards. Ensure compliance with the Data Integrity policy (ALCOA).




- Assemble and deploy the work teams necessary to meet the schedules for the various production processes.
- Ensure the necessary resources are available to carry out the processes and meet the Production Plan.
- Lead work teams, verifying their efficiency in relation to production standards and compliance with current instructions.
- Issue documentation for the batches to be processed on the packaging lines.
- Review the documentation for processed batches to request their approval.
- Manage the budget for expenses related to the operation and track operational variations in efficiency, usage, and absorption.
- Ensure that output targets for quantities and hours used in each process are met, in accordance with established parameters.
- Actively participate in IMEx committees to promote improvements in production standards and ensure compliance with the current budget.
- Promote the implementation of improvement projects through IMEx, focusing on the development of production efficiencies (CIPs).
- Manage key metrics for the area (EHS, Quality, Supply, Cost, People) and participate in IMEx meetings (Tier 1, TPM, CI, among others).
- Ensure root cause analysis is conducted in the event of significant downtime or recurring problems (using the 5 Whys, fishbone diagram, and DMAIC tools).
- Verify that all personnel involved in the processes receive the required initial and ongoing training, which is tailored to the needs of the sector.
- Report any identified deviations and actively participate in investigating them and preventing their recurrence.
- Collaborate in the implementation of validation activities.
- Actively participate in the selection and development of colleagues.
- Ensure that the department’s GMP documentation is reviewed and updated.
- Monitor and ensure that your sector, its facilities, and equipment are properly maintained, including verifying their qualification and calibration status.




- Develop succession plans for your position and those of your direct reports. Follow best practices for recruitment and selection.
- Collaborate on activities that contribute to creating a positive work environment for all colleagues.

Minimum

Requirements - High school diploma (Chemical or Mechanical Technician) with 5+ years of experience in pharmaceutical manufacturing or a related field.

- Basic level of English.
- Demonstrated application of process improvement tools.
- Effective written and oral communication skills.
- Ability to manage multiple projects and ongoing work activities.

Preferred

Requirements - Bachelor's degree.

- Intermediate or upper intermediate level of English.
- Proficiency with computer software.
- Continuous Improvement Tools (Six Sigma Green Belt certification or higher).
- Proven record of problem‑solving and decision‑making skills.
- Strong leadership capabilities.
- Experience with regulatory compliance and quality assurance.
- Proficiency in project management tools and methodologies.
- Ability to influence and lead cross‑functional teams.
- Ability to mentor and develop direct reports.
- Ability to foster a culture of safety and continuous improvement.
- Excellent ability to interact with staff from other departments.
- Ability to evaluate and identify opportunities for improvement.
- Communication and knowledge‑sharing skills.
- While all Pfizer competencies for Colleagues apply to this position, the following are most relevant:
- Technical/functional skills - Takes ownership - Builds collaborative relationships - Acts decisively - 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.

EEO Statement 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, or disability.

📌 PCT Shift Lead (sólidos) (Buenos Aires)
🏢 Pfizer, S.A. De
📍 Buenos Aires