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Design Control Engineer III

Job in Chesterfield, St. Louis city, Missouri, 63005, USA
Listing for: Pfizer
Full Time position
Listed on 2026-01-04
Job specializations:
  • Engineering
    Biomedical Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 77100 USD Yearly USD 77100.00 YEAR
Job Description & How to Apply Below
Location: Chesterfield

** ROLE SUMMARY
** This position will be part of BTx Pharmaceutical Research & Development located in St.Louis, MO or Andover, MA. The incumbent will lead design control projects for biologics modalities developed as prefilled syringe-based combination products throughout the product and design control lifecycle. They will interact with cross functional development teams working with all levels of employees.
** ROLE RESPONSIBILITIES
*** Ensures that combination product development activities are compliant with quality and regulatory standards – both internal and external.
* Lead design control and risk management activities for combination product development programs, ensuring deliverables are appropriately authored, approved, and maintained to support clinical trials and commercial licensures.
* Provide input and support for design validation, including but not limited to human factors engineering assessments.
* Support the generation of all regulatory submission data and content for assigned device projects.
* Support the assessment of external design companies and suppliers for capability of quality systems, facilities, and procedures to support device development and supply.
* Support device design and manufacturing investigations from devices used in clinical trials and commercial manufacture.
* Support internal and external audits of the DPDD Quality System.
** QUALIFICATIONS
* *** Must Have**
* ** BS degree
** in appropriate Science & Engineering discipline (Chemistry, Biochemistry; Biomedical, Mechanical, Materials, Chemical Engineering; or other related discipline) with a minimum of 6 to 8 years of relevant experience in the Pharmaceutical Combination Product and/or Device industries.

OR
* ** MS degree
** in appropriate Science & Engineering discipline (Chemistry, Biochemistry; Biomedical, Mechanical, Materials, Chemical Engineering; or other related discipline) with a minimum of 4 to 6 years of relevant experience in the Pharmaceutical Combination Product and/or Device industries.
* Thorough working knowledge of ISO 9001, ISO 13485, ISO 14971, 21 CFR 820, ISO 11040 and the EU Medical Devices Directive.
* Working knowledge of EN 62366 and EU Medical Devices Regulation.
* Capable of working independently with minimal supervision
* High level of attention to technical details and accuracy.
* Able to prioritize multiple responsibilities and to work on multiple tasks simultaneously.
* Able to work collaboratively in cross functional teams.
* Excellent communication (e.g. oral, written, presentation) and interpersonal relationship skills.
* Proficiency in general computer software such as word processing, spreadsheets, presentations.
* Understand Good Manufacturing Practices (GMP)
** Nice To Have
*** Knowledge of current US and global Regulations, FDA and ICH guidance, ISO standards for syringes/injectors, luer connectors, and quality system regulations (Part
4) for combination products
* Experience in Design Controls for Combinations Products
* Device Risk Management expertise
* Understand statistical sampling plan and statistical analysis of test results.
* Familiar with Human Factors Engineering - Usability Engineering.
* Understand project management methodologies and capable to provide technical leadership for projects.
* Familiar with device assembling manufacturing process
* Ability to perform mathematical calculations and ability to perform complex data analysis.
** Other Job Details
*** Work Location Assignment:
On Premise  The annual base salary for this position ranges from $77,100.00 to $. 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.…
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