Job Description

Why Patients Need You

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 Achieve

You will be part of a multi-disciplinary team responsible for cGMP (current Good Manufacturing Practices) production of Phase I -III clinical drug product in our Drug Product Manufacturing facilities in Groton, CT. Primary responsibility is in performing daily manufacturing activities for oral solid dosage forms. Additionally, you will contribute to the development of batch and continuous manufacturing technology capabilities by supporting novel process development and process understanding studies. The successful candidate must demonstrate strong teamwork dynamics when interfacing with various groups (e.g., Operations, Quality, Tech Support) and a growth mindset. 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 team 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 It

• Responsible for manufacture of clinical and development batches of solid dosage forms using conventional or novel processes. (primary activity)

• Includes equipment setup, manufacturing, equipment tear-down and cleaning

• Perform in-process operational checks associated with clinical manufacturing (examples include Solid Fraction Determination and Disintegration testing).

• Troubleshooting / manufacturing support during operation

• Provide “hands-on” training for Manufacturing Technicians and contribute to department technical/GMP/safety training.

• Assist with Equipment Lifecycle Management activities.

• Support and implement operational improvements throughout the manufacturing workstream (e.g., with regards to safety, quality, and efficiency)

• Ensure all operations are executed according to Pfizer and OSHA safety standards.

• Capture and share detailed post-manufacturing feedback.

• Support creation and control of GMP batch documentation:

• Assist in preparation of development batch records, working batch records, and review of executed batch records.

• Author or revise standard operation procedures (SOPs)

• Present to partner lines during pre and post manufacturing reviews, highlighting critical manufacturing information.

• Identify and support the resolution of quality concerns; may assist with investigation reports in the quality system.

• Utilize Pivision, Spotfire, and other software tools to create relevant dashboards and knowledge management tools

Qualifications

Must-Have

• Bachelor's degree in chemical/bio-medical engineering or equivalent plus 2 years or less of experience in Manufacturing, Tech Transfer, continuous improvement, and engineering design.

• Demonstrated experience in a biotechnology manufacturing or laboratory environment.

• Ability to execute against Standard Operating Procedures and document entries in a compliant manner.

• Strong interpersonal skills and accountability in day-to-day interactions with an operational focus on business goals, customers and process required.

• Maintains a safe work environment.

• Excellent oral and written communication skills.

• Strong analytical and computer skills.

Nice-to-Have

• Prior experience in a solid oral dose manufacturing environment

• Experience with data visualization software (i.e. Spotfire, Pivision, or Tableau)

PHYSICAL/MENTAL REQUIREMENTS

• Role requires a Groton site presence. The job requires the operation of manufacturing equipment in the Groton Drug Product Manufacturing facilities.
• Standing, bending, climbing, reaching and lifting upward of 55 pounds may be required. Personal Protective Equipment such as gloves, a full Tyvek suit and breathable air and/or filtering face piece is often required.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

• Support of off shift and weekend manufactures when necessary.

Additional Job Details:

• Last day to apply: December 6, 2024.
• Work Location Assignment: On Premise.

The annual base salary for this position ranges from $54,700.00 to $91,100.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.

Relocation assistance may be available based on business needs and/or eligibility.

Manufacturing