Pfizer

Sr. Packaging Engineer

Pfizer$93K — $156K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • BA/BS with 9-11 years experience or MBA/MS with 7-8 years experience
  • PhD with 0-3 years experience
  • Technical proficiency in formulation development and process optimization
  • Strong knowledge of parenteral packaging components and testing equipment
  • Experience in cGMP manufacturing and clinical trial supply chain management
  • Excellent organizational and communication skills

Responsibilities

  • Collaborate with vendors and SMEs to evaluate and implement components for drug delivery systems
  • Support compliance with regulatory requirements for packaging components
  • Author and review engineering documentation like specifications and risk analyses
  • Contribute to design control teams by documenting design verification and functionality assessments
  • Verify device components and delivery systems through testing and analysis
  • Investigate packaging failures and increase reliability through corrective actions
  • Lead documentation efforts including regulatory submissions

Benefits

  • 401(k) plan with matching contributions
  • Paid vacation, holidays, and personal days
  • Comprehensive health benefits including medical, dental, and vision coverage
  • Paid caregiver and parental leave
  • Relocation support may be available
Full Job Description
About the Role

We are seeking an accomplished and forward-thinking engineer to join our Biotherapeutics Pharmaceutical Research & Development - Drug Product Design & Development (DPDD) organization. In this highly visible role, you will support the selection, qualification and implementation of components and container closure systems for early and late stage projects, as well as, participate in applicable design verification activities for design control projects that support the development and use of certain prefilled syringe (PFS), co-packaged and cross labeled combination products, while championing quality, compliance, and continuous improvement.

This role offers the opportunity to influence strategy, drive operational excellence, and play a critical part in advancing products from development through commercialization-ultimately impacting patients' lives worldwide.

What You'll Do
  • Work closely with vendors, research and development SMEs and commercial Site SME's in the evaluation, development, qualification and implementation of new components and container closure systems
  • Support the formulation and process development groups in Andover and St Louis sites to comply with regulatory requirements and guidance documents related to components and container closure systems
  • Author and/or review engineering and development documentation such as component drawings and specifications, assembly drawings, tolerance stack analyses, risk analyses, etc.
  • Participate on design control teams to author and/or review applicable design control documentation, such as design verification supporting documentation, specifications, component/device requirements and related functionality assessments, risk assessments, etc..
  • Facilitate, support and/or execute verification of device components and delivery systems
  • Conduct and/or assist investigations of parenteral packaging and related delivery device failures to determine root causes and work with teams to implement appropriate corrective and preventative actions.
  • Drive testing activities, protocols, work instructions, lab notebooks, and technical reports for medical devices and combination products.
  • Author and support regulatory submission content and respond to packaging-related regulatory inquiries.


Collaborate & Influence
  • Partner closely with Quality, Regulatory, EHS, Facilities, Manufacturing, and Global Workplace Solutions to ensure alignment and proactive issue resolution.
  • Lead cross-functional initiatives to harmonize laboratory and business processes across teams and sites.
  • Support the transfer of new drug products to commercial manufacturing and post-launch support teams.


Innovate & Improve
  • Contribute to continuous improvement initiatives to enhance efficiency, quality, and scalability of lab and design control processes.
  • Identify and implement best practices, tools, and strategies that strengthen DPDD capabilities and future readiness.


Who You Are
  • A confident technical SME with deep expertise in parenteral packaging and medical device/combination product development.
  • Comfortable working independently while influencing across complex, global, matrixed organizations.
  • Known for attention to detail, strong judgment, and ability to balance multiple priorities.
  • A collaborative communicator who can translate complex technical concepts into clear, actionable guidance.


Qualifications

Must Have
  • BA/BS with 9 to 11 years of experience or MBA/MS with 7 to 8 years of experience
  • PhD with 0 to 3 years of experience
  • Strong technical skills in formulation development and process optimization
  • Strong knowledge of parenteral packaging components and testing equipment (e.g., Instron, ZebraSci, MIMAS, Computrac, plunger movement chambers)
  • Proficiency in using analytical instruments and techniques
  • Experience in cGMP manufacturing and clinical trials supply chain management
  • Ability to work independently and proactively within a team
  • Excellent organizational and time management skills
  • Strong communication and critical thinking abilities


Nice to Have
  • Proficiency with analytical instruments such as HPLC/UPLC, SEC, LC-MS, BiaCORE, DSC, and GC
  • Experience with methods to determine formulation content, including drug, polymer, lipid, and in vitro release
  • Experience in authoring and reviewing technical documentation
  • Strong data management skills, including data processing and report writing
  • 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


Technical Expertise
  • Strong knowledge of parenteral packaging components and testing equipment (e.g., Instron, ZebraSci, MIMAS, Computrac, plunger movement chambers)
  • Experience in GMP and/or ISO 13485 environments
  • In-depth understanding of global regulatory and quality standards (FDA, ICH, ISO 13485, 11040, 10993, USP/EP/JP compendia, combination product regulations)
  • Ability to interface with regulatory agencies and provide sound technical justifications


Work Environment & Travel
  • Combination of laboratory and office-based work
  • Occasional travel (approximately 5-10%) to other sites, vendors, and conferences


Other Job details
  • Relocation support available
  • Work Location Assignment: On Premise
The annual base salary for this position ranges from $93,600.00 to $156,000.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 12.5% of the base salary and eligibility to participate in our share based long term incentive program. 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.

Research and Development

About Pfizer

Hospira, Inc. is the provider of injectable drugs and infusion technologies. Through its broad, integrated portfolio, Hospira is uniquely positioned to Advance Wellness™ by improving patient and caregiver safety while reducing healthcare costs. The company is headquartered in Lake Forest, Ill., and has approximately 16,000 employees.

Pfizer Careers

Joining Pfizer’s global team offers more than just job opportunities; it’s a chance to be a part of a company that leads with science and innovates for better health. As a leading biopharmaceutical company, Pfizer is at the forefront of transforming lives through innovation, leadership, and diversity. Work You’ll Do At Pfizer, you will collaborate with some of the brightest minds in the industry, engaging in work that enhances global health and saves lives. Our culture thrives on intellectual curiosity, professional growth, and inclusivity, making every day a learning opportunity. Here, your skills will be honed, your professional acumen will be expanded, and you will be part of a team that values the power of diverse insights to drive success. Pfizer’s Leadership and Growth Lead and innovate with Pfizer, where we value the growth of each employee. Our leadership is committed to providing employees with the training and resources needed to excel in their careers. Pfizer offers a variety of career paths, including roles in research, marketing, finance, technology, and more, each offering a unique blend of challenges and rewards. Internship and Employment Opportunities Start your career with Pfizer through our internship programs or dive straight into a full-time position. We are hiring individuals who are passionate about healthcare and who seek to make a difference in the world. Our internships provide invaluable industry experience, networking opportunities, and a potential pathway to full-time employment. Benefits and Culture Pfizer is dedicated to fostering a workplace where all employees feel valued and can achieve their full potential. We offer competitive benefits packages that support the health, well-being, and financial security of our employees and their families. At Pfizer, you’ll find a culture that encourages collaboration, innovation, and continuous learning. Join Our Team Explore the numerous job opportunities at Pfizer by searching open positions that match your skills and interests. We look for driven, curious, and innovative team players who are ready to advance their careers in a transformative company. Stay Connected Keep up to date with career tips, insider perspectives, and industry-leading insights you can put to use today—all from the people who work here. Personalize your subscription to receive job alerts, latest news, and insider tips tailored to your preferences. Discover the exciting and rewarding career opportunities that await at Pfizer. Interview and Resume Tips Prepare for your future with Pfizer by utilizing our resources for resume building and interview preparation. We provide guidance on how to effectively showcase your skills and experiences to align with the needs of a position at Pfizer. Our goal is to help you succeed in securing a role that suits your professional goals and personal growth aspirations. Pfizer: A Place Where You Can Make a Difference Every position at Pfizer contributes to our mission of making the world a healthier place. Whether through direct patient care, research innovation, or corporate roles that support our operations, your work will have global impact. Join us in our journey to change lives—explore Pfizer careers today.
Learn more about Pfizer
Size
79,000 employees
Market Cap
$285.9 billion
Industry
Net Income
$9.6 billion
Founded
1849
5 Year Trend
+9%
Revenue
$41.9 billion
NASDAQ

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