Senior Process Engineer

Use Your Power for

Purpose

Our breakthroughs would

not reach the hands of patients without our dedicated

pharmaceutical manufacturing team. We rely on agile members who

understand the critical impact of their role in Pfizer's mission.

Patients need colleagues like you who take pride in their work and

continuously strive to improve outcomes. Your efforts ensure that

patients and physicians have timely access to the medicines they

need.

What You Will

Achieve

In this role, you

will :

Coordinate the manufacture of

key API (Active Pharmaceutical Ingredients) Intermediate processes

and ensure flawless execution focusing on safety, quality, supply,

and cost.

Provide essential technical support

to process teams to sustain and enhance the processes, including

diagnosing and rectifying faults within the API manufacturing

Control Systems.

Develop and implement Cost

Improvement Projects (CIP) to enhance efficiency and reduce

costs.

Contribute to moderately complex

projects, managing your own time to meet targets and developing

plans for short-term work activities.

Provide

technical support to sustain and improve changeover processes on

site, collaborating closely with Operations, Safety, Engineering,

Quality Operations, and Value Stream Teams.

Coordinate the tech transfer of processes and

technologies to other international API sites, utilizing site

business processes to support and monitor the Change Over process

effectively.

Support the talent development

strategy at Pfizer sites, ensuring continuous improvement and

excellence in all

operations.

Here Is

What You Need (Minimum

Requirements)

High school diploma (or

equivalent) with 8+ years of experience or associate's degree with

6+ years of experience or BA / BS with 2+ years of experience or

MBA / MS with any years of relevant experience

Demonstrated ability to deliver improvements to site

performance using Lean and Six Sigma tools

Understanding of regulatory standards and guidance

documents as well as evolving cGMPS impact pharmaceutical

production

Strong technical, analytical, and

problem-solving skills with the ability to make timely

decisions

Proficiency in using communication

tools and techniques to explain complex issues and establish

consensus among

teams

Bonus Points If

You Have (Preferred

Requirements)

Relevant pharmaceutical

experience

Strong project management

skills

Excellent interpersonal and

communication skills

Ability to mentor and

guide other colleagues

Experience in

diagnosing and rectifying faults within manufacturing control

systems

Knowledge of Good Manufacturing

Practices (cGMP)

Work Location

Assignment : On Premise