Full-Time

Training Administrator

Confirmed live in the last 24 hours

Serán BioScience

Serán BioScience

51-200 employees

Contract development and manufacturing for pharmaceuticals

Biotechnology
Healthcare

Mid

Bend, OR, USA

Position requires onsite presence in Bend, Oregon.

Category
Public Health
Biology Lab & Research
Biology & Biotech
Requirements
  • Excellent verbal and written communication skills
  • Strong presentation skills
  • Excellent organizational skills and attention to detail
  • Excellent time management skills with a proven ability to meet deadlines
  • Ability to design and implement effective training
  • Ability to prioritize tasks and to delegate them when appropriate
  • Proficient with Microsoft Office Suite or related software
  • Bachelor’s degree in related area, or equivalent combination of education and/or experience
  • Preference given to those with a minimum of 3 years of experience working in a related field
  • Requires 2 years of GMP experience
Responsibilities
  • Manages the training program, including the training structure and all training records in the Learning Management System (LMS), Veeva
  • Creates and revises training materials, including classroom and On-the-Job Training
  • Develops training metrics for internal distribution and to support the Management Review program
  • Manages the annual GMP Training program and ensures that all staff comply with training requirements
  • Plans, organizes, and effectively conducts employee training on various onboarding, orientation, and skills training for employees
  • Evaluates program effectiveness through assessments, surveys, and feedback
  • Maintains a robust training matrix within the LMS for all GMP related training
  • Participates in Training Impact Assessments to ensure training requirements are updated as necessary to ensure employees are sufficiently trained in their job tasks
  • Provides support during clients, internal, and regulatory audits
  • Performs other related duties as assigned

Serán BioScience specializes in providing drug development and manufacturing services as a Contract Development and Manufacturing Organization (CDMO). They offer a variety of services, including preformulation, formulation development, dosage form development, spray drying, and particle engineering. Their operations adhere to current Good Manufacturing Practice (cGMP) standards, ensuring high quality and safety in their products through rigorous analytical quality control. Serán BioScience serves a wide range of clients, from small biotech startups to large pharmaceutical companies, and is distinguished by its flexibility in tailoring services to meet specific client needs. The company's goal is to enhance the efficiency and effectiveness of drug development processes for their clients.

Company Stage

Growth Equity (Venture Capital)

Total Funding

$194.5M

Headquarters

Bend, Oregon

Founded

2016

Growth & Insights
Headcount

6 month growth

83%

1 year growth

83%

2 year growth

83%
Simplify Jobs

Simplify's Take

What believers are saying

  • Expansion of cGMP manufacturing capacity at the Bend site indicates growth and increased service capabilities.
  • Partnership with Oregon Bioscience Association to establish an apprenticeship program highlights Serán's commitment to workforce development and community engagement.
  • Serán's expertise in advanced drug formulation techniques can attract a diverse range of clients, from small biotech startups to large pharmaceutical corporations.

What critics are saying

  • The highly competitive nature of the pharmaceutical and biotechnology markets requires continuous innovation to stay ahead.
  • Dependence on pharmaceutical companies for revenue means that any downturn in the pharma sector could impact Serán's business.

What makes Serán BioScience unique

  • Serán Bioscience's focus on advanced drug formulation techniques like spray drying and particle engineering sets it apart from other CDMOs.
  • Their flexibility in tailoring services to meet specific client needs ensures successful outcomes, a competitive advantage in the pharmaceutical industry.
  • The company's commitment to cGMP manufacturing and analytical quality control guarantees high standards of quality and safety, which is crucial in the pharmaceutical sector.

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