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Validation Associate III

Company: Ajinomoto Bio-Pharma Services
Location: San Diego
Posted on: March 18, 2023

Job Description:

Why join Ajinomoto Bio-Pharma?Our mission is to help improve the health of humankind.We are a fully integrated contract development and manufacturing organization with sites in Belgium, United States, Japan, and India providing comprehensive development, cGMP manufacturing, and aseptic fill finish services. We pride ourselves in offering a unique environment in which the work we do every day plays a crucial role in society.We hope to inspire employees to come to work engaged and ready to give their all. This allows Ajinomoto Bio-Pharma to meet the commitments it makes to partners, patients and employees.Total Rewards package designed to make your life better:We offer health benefits, annual performance bonus, generous paid time off, paid parental leave, matching 401k contributions (immediate vesting), tuition reimbursement, employee discount program and much more!We are currently seeking a Validation Associate III who will work under minimal supervision, responsible for performing complex validation and qualification activities for critical equipment, utilities and processes used in cGMP Fill Finish, Biologics Manufacturing and Quality Control.
Responsibilities:

  • Documentation Preparation (Protocol and Report Generation).
  • Protocol Execution.
  • Training, database entry, and audit support.
  • Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company's policies and practices
  • Embodies Aji Bio-Pharma's cultural values and aligns daily actions with department goals and company culture.
    Requirements :
    • Bachelors degree in Engineering or similar discipline strongly preferred or (4) years equivalent experience
      • Minimum of four (4) years of relevant experience without an Engineering or other relevant degree
      • Minimum of four (4) years experience in GMP without a degree
      • Strong understanding of GMP compliance and regulations
      • Detail oriented with strong written and verbal communication skills
      • Ability to work independently within prescribed guidelines or as a collaborative team member.
      • Experience with Microsoft Office applications
      • Experience with Kaye Validator operation required
        The anticipated hourly range for candidates who will work in California is $29.76 to $41.66.The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the job, type and length of experience within the industry, education, etc. Ajinomoto Bio-Pharma Services is a multi-state employer and this salary range may not reflect positions that work in other states.
        If you meet the requirements above, and would like to apply for this position, please visit our website at www.ajibio-pharma.com and click on the "Careers" section. Please be sure to note where you saw our ad posting.New hires will pass a background check and drug screen as a condition of employment.We are an EOE dedicated to a diverse work force and Drug Free work environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Keywords: Ajinomoto Bio-Pharma Services, San Diego , Validation Associate III, Other , San Diego, California

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