Senior Quality Assurance Engineer

Posted 23 Days Ago
Be an Early Applicant
Janesville, WI, USA
In-Office
85K-115K
Senior level
Healthtech • Biotech • Pharmaceutical • Energy
The Role
The Senior Quality Assurance Engineer reviews and develops validation protocols for cGMP processes, ensuring compliance with regulatory standards and communicating findings to stakeholders.
Summary Generated by Built In

Description

SHINE Technologies is seeking a Senior Quality Assurance Engineer who will assist the company in the development, review, and execution of Commissioning and Qualification activities for the facility utilities, equipment, and processes used in the manufacture and testing of cGMP products.

  

The base salary range for this position is $85,000 - $115,000 per year plus a comprehensive compensation package. Our salary ranges are determined by role, level, and location.

Duties and Responsibilities:

Specific duties and responsibilities of the Senior Quality Assurance Engineer include, but are not limited to:

  • Review and approval of product specifications.
  • Establish the Master Validation Plan.
  • Develop necessary standard operating procedures for plant processes, equipment Commissioning and Qualification, and re-qualification and revalidation of critical systems and utilities.
  • Develop Process Validation plans and procedures for cGMP-controlled production processes.
  • Develop Cleaning Validation processes and procedures for production processes.
  • Collaborate with the Chemistry team to develop QC Laboratory Method Validations.
  • Coordinate and oversee scheduled validation and qualification activities with internal and external stakeholders.
  • Review and analyze analytical and physical data generated from executed validation/qualification activities and prepare validation/qualification reports presenting conclusions on the validity of the processes based on objective evidence against product specifications.
  • Develop Risk Matrix for production, FMEA/PFMEA, and collaborate with Engineering and Production to ensure mitigations are identified and implemented, including cleaning requirements and environmental monitoring procedures.
  • Develop Software Validation plans and procedures for internal process controls.
  • Establish reagent and product Stability Testing plans and protocols.
  • Establish product packaging and labeling process and implementation.
  • Develop and provide training and mentoring on validation concepts.
  • Perform Supplier Audits and establish an Approved Supplier List.
  • Report status and progress of validation/qualification activities or projects to the Leadership team.
  • Perform other duties as assigned.

Requirements

  • Bachelor’s degree in engineering, radiochemistry, life science, or related field.
  • At least 5 years of quality experience in a cGMP pharmaceutical setting or at least 5 years of validation experience in a cGMP manufacturing setting, with experience in radiopharmaceuticals preferred.
  • Demonstrated knowledge of Title 21 of the Code of Federal Regulations (CFR), with an emphasis on cGMP.
  • Demonstrated knowledge of regulatory guidelines concerning the establishment, validation, and documentation of test procedures, equipment, processes, and facility systems.
  • Demonstrated knowledge of various laboratory techniques/instruments such as spectroscopy (e.g., alpha/beta, gamma, UV/Vis), chromatography (e.g., IC, HPLC, TLC), trace metal analysis (e.g., AA, ICP), and wet chemistry techniques.
  • Ability to communicate effectively with all levels within the organization, as well as interface with regulators, contractors, and suppliers.

Eligibility for employment is conditioned on the applicant’s ability to qualify for access to information subject to U.S. Export Controls. Additionally, applicant’s eligibility may be conditioned based upon meeting the Nuclear Regulatory Commission requirements for access to Safeguards Information, which typically requires a pre-employment drug screen, fingerprinting and criminal background check.

SHINE values diversity in all its forms as a critical component of innovation, which is fundamental to our success. Every member of the SHINE community benefits from the talents and experiences of our peers, from the mutual respect we exercise, and from the responsibility we take for our actions.

SHINE Technologies is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.

Pay Transparency Policy

Employee Rights Under the NLRA 

Equal Opportunity Employment

E-Verify

Skills Required

  • Bachelor's degree in engineering, radiochemistry, life science, or related field
  • At least 5 years of quality experience in a cGMP pharmaceutical setting or validation experience in a cGMP manufacturing setting
  • Demonstrated knowledge of Title 21 of the Code of Federal Regulations (CFR)
  • Demonstrated knowledge of regulatory guidelines for validation and documentation
  • Ability to communicate effectively with all levels within the organization
Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
294 Employees
Year Founded: 2005

What We Do

SHINE Medical Technologies, LLC is a nuclear technology company focused on developing and producing medical isotopes for diagnostic and therapeutic purposes using fusion technology. They also aim to generate carbon-free energy from nuclear fusion.

Similar Jobs

DFIN Logo DFIN

Senior Software Engineer

Fintech • Software
Remote or Hybrid
United States
1750 Employees

Litify Logo Litify

Quality Assurance Automation Engineer

Cloud • Legal Tech • Professional Services • Software
Easy Apply
Remote or Hybrid
USA
160 Employees
110K-120K Annually

Social Discovery Group Logo Social Discovery Group

Quality Assurance Automation Engineer

Artificial Intelligence • Fintech • Machine Learning • Software • App development • Conversational AI • Generative AI
In-Office or Remote
7 Locations
1000 Employees
5K-5K Annually
In-Office
Milwaukee, WI, USA
50 Employees

Similar Companies Hiring

Camber Thumbnail
Fintech • Healthtech • Social Impact
New York, New York
90 Employees
Sailor Health Thumbnail
Healthtech • Social Impact • Telehealth
New York City, NY
20 Employees
Granted Thumbnail
Mobile • Insurance • Healthtech • Financial Services • Artificial Intelligence
New York, New York
23 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account