Fresenius Medical Care

Sr CAPA Engineer

Fresenius Medical Care$95K — $115K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree required; advanced degree is a plus.
  • 6-8 years of experience in Quality, Manufacturing, or Engineering.
  • Experience in medical devices, pharmaceuticals, or regulated industries; automotive PPAP is a bonus.
  • Strong engineering background with experience in a GMP environment.
  • Proven teamwork and collaboration skills across multiple functions.
  • In-depth knowledge of FDA and MDD/MDR regulations.
  • Exceptional communication skills to explain complex topics clearly.
  • Bilingual in Spanish is a nice-to-have.

Responsibilities

  • Develop and maintain Global Product Transfer processes for design and manufacturing.
  • Ensure product quality during transfers at receiving sites.
  • Collaborate with quality, R&D, and manufacturing teams on product transfers.
  • Comply with quality and regulatory standards throughout transfer projects.
  • Establish quality metrics for successful product transfers.
  • Oversee implementation of policies for consistent outcomes.
  • Develop quality and validation plans for new product additions.

Benefits

  • Comprehensive medical, dental, and vision insurance.
  • 401(k) plan with company match.
  • Paid time off and parental leave.
  • Potential for performance-based bonuses.
Full Job Description
PURPOSE AND SCOPE:

Lead the harmonization and standardization of the product transfer process including execution and oversight of the product transfer process for assigned regional/global area.

PRINCIPAL DUTIES AND RESPONSIBILITIES:
  • Develop, implement, and maintain Global Product Transfer processes for design and manufacturing product transfer.
  • Ensure product quality is achieved at the receiving manufacturing site level during product transfer projects
  • Partner with CE vertical quality, R&D teams, plant quality and manufacturing teams (as appropriate) in the transfer of new products or site to site transfers between manufacturing sites.
  • Ensure transfer projects comply with all quality and regulatory requirements, have clearly defined quality planning, including site registration, defined pfmea at receiving sites, training requirements established, inspections plans defined, validation plans developed and any other requirements as defined.
  • Transfer reliable quality products into manufacturing through partnership with vertical value streams and manufacturing operations
  • Assist in establishing receiving site quality metrics for a successful product transfer (example; capability, complaint rates, all quality deliverables achieved)
  • Oversee and execute policies and procedures to ensure consistent outcomes
  • Develop and execute quality and validation plans
  • Deliver all required procedural updates associated with the addition of a new product at the receiving manufacturing facility
  • Ensure all transfer activities are in compliance with the quality system, FDA QSRs and ISO 13485.
  • Performs other related duties as assigned.


Additional responsibilities may include focus on one or more departments or locations. See applicable addendum for department or location specific functions.

PHYSICAL DEMANDS AND WORKING CONDITIONS:

The physical demands and work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • This position requires approximately 30% travel.


SUPERVISION:
  • None


EDUCATION AND REQUIRED CREDENTIALS:
  • Bachelor's Degree; Advanced Degree desirable.


EXPERIENCE AND SKILLS:
  • 6 - 8 years' of relevant experience in Quality, Manufacturing and/or Engineering discipline.
  • Medical device, pharma or other regulated industry (automotive PPAP experience a plus)
  • Engineering background
  • Direct experience in design and/or manufacturing of medical devices/pharma in a GMP environment
  • Proven track record in cross-functional collaboration
  • Knowledge of FDA, MDD/MDR regulation in medical device and pharma
  • Excellent communication skills with the ability to present and explain complex topics to multiple levels within the organization
  • Demonstrated practice of continuous improvement and designing efficiency into processes
  • Bilingual in Spanish- nice to have


ACKNOWLEDGEMENT:

I acknowledge that I have read and accepted this job description. I understand what is expected of me in this position, and I am able to perform the essential functions as outlined with or without reasonable accommodation. Furthermore, I understand that the duties and responsibilities listed in this job description are intended only as illustrations of the various types of work that may be performed. The omission of specific statements of duties does not exclude them from the position if the work is similar, related, or a logical assignment to the position. If I have any questions about duties and responsibilities not specified in this job description that I am asked to perform, I should discuss them with my immediate supervisor or my Human Resources representative.

If your location allows for pay/benefit transparency, please click the link below to request further information on this position. Pay Transparency Request Form

Benefit Overview: This position offers a comprehensive benefits package including medical, dental, and vision insurance, a 401(k) with company match, paid time off, parental leave and potential for performance-based bonuses depending on company and individual performance.

About Fresenius Medical Care

Fresenius Medical Care is a German company specializing in the production of medical supplies, primarily to facilitate or aid renal dialysis. The company is a leading provider of products and services for people with chronic kidney failure. Fresenius Medical Care operates in more than 120 countries and has over 120,000 employees. The company's products and services are used to treat approximately 3.4 million patients worldwide. The company is committed to improving the quality of life of patients with kidney disease and to providing innovative products and services that meet the needs of patients and healthcare professionals.
Learn more about Fresenius Medical Care
Size
122,635 employees
Market Cap
$9.2 billion
Industry
Net Income
$1.1 billion
Founded
1996
Revenue
$17.8 billion
NASDAQ

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