Use Your Power for Purpose

The Associate Manufacturing specialist role is accountable for the design and development of documents for Drug Products Operations. You will be entrusted with responsibility for on-time delivery of documentation enabling the manufacturing process. You will ensure clarity and efficiency in documentation format with a focus on current Good Manufacturing Practices compliance and Pfizer Human Performance standards. The focus on the job will contribute to achieving project tasks and goals. Through your domain knowledge and commitment you will create a collaborative teaming 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. The role supports solutions that comply with Good Manufacturing Practices (GMPs) Pfizer Quality Standards (PQS) Environmental Health & Safety (EHS) and external regulatory agency requirements with the partnership of the DP Units and leaders.

What You Will Achieve

In this role you will:

The colleague is expected to coordinate training requirements for their assigned operations units including the following responsibilities:

• Perform administrative tasks in the Pfizer Learning Academy (PLA) to support the learning plan for their assigned operations unit(s)

• Maintain training roadmaps from assigned operations unit

• Function as a responsible person and performs Impact Assessment for document changes in the Quality Management System (QMS) change management (CM) system

• Create/Revise SOPs OJTs curriculum and other Documents that may be developed in Microsoft Word or other document-authoring applications.

• Facilitate request for change create draft documents confirm consensus and assure required approvals are completed on-time.

• Partner with Operations to complete periodic reviews as required by SOP

• Facilitate Qualified Job Task Trainer (QJTT) program

• Participate and support Environment Health & Safety (EHS) initiatives such as Good Catch program & Incident and Injury Free (IIF) cultural improvements

• Identify opportunities for continuous improvement within DP compliance and participate in resolution activities such as brainstorming piloting and implementation

• Responsible for facilitating Drug Product Orientation (DPO) on a rotating basis as assigned by management. Orientation assignments may require flexing working schedule to accommodate but advanced notice will be given.

• Independently seeks value Added Work

Here is what you need

(Minimum Requirements)

• Applicant must have a bachelors degree with 0 years of experience; OR an associates degree with 4 years of experience; OR a high school diploma (or equivalent) and 6 years of relevant experience

• Demonstrated good oral and written communication skills

• Proficiency in use of computers and Microsoft Office Applications (PowerPoint Word Excel Outlook Visio)

• Ability to manage workload and gather information in a dynamic environment

• Self-motivated and willing to learn new and changing systems

• Ability to interact effectively with all levels of the organization

Bonus Points If You Have

(Preferred Requirements)

• Pharmaceutical experience in operations

• Proficiency in use of Quality Management Systems (Vault Quality Tracking System QTS Trackwise)

• Experience in document change control processes

• Experience with SOPs BRs and EBR

• Experience with EBR record Processing

PHYSICAL/MENTAL REQUIREMENTS

Physical Demands:

• Long periods of sitting in an office environment

• Long periods of standing and traversing hard surfaces

• PPE and gowning requirements in varied production environments

• Must be present at Pfizers Kalamazoo Production Facility 5 days/week to support operations via face-to-face meetings

NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS

This position works a flexible first shift schedule. Core hours are 8:30a-2p Monday-Friday but may require flexibility based on production requirements. This position requires the ability to work in a remote office environment and will require periodic weekend or evening work supporting a 24-hour/7 day operation. Must be able to work irregular hours on occasion

Work Location Assignment:On Premise

The annual base salary for this position ranges from $58500.00 to $97500.00. In addition this position is eligible for participation in Pfizers 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 lifes 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 (). 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