Full-Time

Technical Writer II/III

Posted on 12/2/2024

Serán BioScience

Serán BioScience

51-200 employees

Contract development and manufacturing for pharmaceuticals

Biotechnology
Healthcare

Mid, Senior

Bend, OR, USA

Category
Technical Writing
Content & Writing

You match the following Serán BioScience's candidate preferences

Employers are more likely to interview you if you match these preferences:

Degree
Experience
Requirements
  • Excellent verbal and written communication skills
  • Excellent interpersonal and leadership skills
  • Excellent organizational skills and attention to detail
  • Excellent time management skills with a proven ability to meet deadlines and motivate teams
  • Demonstrates the ability to collaborate and work in cross-functional teams
  • Follow detailed written and oral instructions
  • Multitasks and adjusts priorities in a fast-paced environment, while maintaining focus and managing disruption and/or unexpected needs
  • Accepts feedback from a variety of sources and constructively manages conflict
  • Proficient with Microsoft Office Suite or related software
  • Requires 3 years of GMP experience
  • At least 2 years of GMP laboratory experience; heavy focus on document authoring and review
Responsibilities
  • Write, revise, review, and approve SOPs, validation protocols, validations reports, and test methods
  • Participate in audits and inspections
  • Assist in forecasting and scheduling analytical validations with Project Management and Quality Control Management teams
  • Conduct scientific/technical reviews of analytical validations, reports, test methods, and SOPs, as needed
  • Authors investigations, CAPA’s Impact Assessments, Risk Assessments, Validation Discrepancy Reports, as required
  • Adheres to consistent and predictable in-person attendance
  • Responsibilities may increase in scope to align with company initiatives
  • All other 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

19%

1 year growth

19%

2 year growth

19%
Simplify Jobs

Simplify's Take

What believers are saying

  • Serán announced a $200 million strategic growth transaction for expansion.
  • The company plans to build a new commercial-scale manufacturing facility.
  • Increased demand for personalized medicine aligns with Serán's formulation expertise.

What critics are saying

  • Emerging CDMOs in Asia offer lower-cost services, impacting Serán's market share.
  • Potential delays in new facility construction could affect expansion plans.
  • Global talent shortage may hinder recruitment for Serán's expansion.

What makes Serán BioScience unique

  • Serán specializes in advanced drug formulation techniques, including spray drying and particle engineering.
  • The company offers cGMP manufacturing and analytical quality control services.
  • Serán's flexibility allows tailored services to meet specific client needs.

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Benefits

Paid Vacation

401(k) Retirement Plan

Health Insurance

Life Insurance

Disability Insurance

Mental Health Support

Pet Insurance

INACTIVE