Salary
≈ $62k – $136k per year (Estimated)
Location
In office (Oregon)
Seniority
Middle · 3+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
At Serán, we use science-first methodology and cutting-edge drug delivery technologies to enable our client's medicines and improve patients' lives.
Serán BioScience is searching for an experienced Quality Control Scientist II to support an extended manufacturing schedule. This role would support all testing functions for Quality Control, primarily focused on in-process control lab methods to ensure manufacturing excellence. The Scientist II needs to exhibit experience and confidence within a cGMP laboratory with proficiency in analytical equipment operations and data record management.
The preferred schedule of this role is 11:00 am - 8:00 pm Monday - Friday. Specific schedule is negotiable in support of manufacturing swing shift operations.
Duties and Responsibilities
- Adheres to Standard Operating Procedures, cGMPs, Quality Manual, and company policies
- Performs routine extractions for dissolution, assay, and impurities testing
- Performs routine testing using analytical equipment including but not limited to KFC, dissolution apparatus, water activity, FTIR, etc.
- Conducts appearance testing, raw materials sampling, solution preparation, and pH measurements
- Drafts stability tables, sets-up stability studies, logs-in samples and standards
- Cleans lab and glassware and disposes of analytical waste appropriately
- Participates in process improvement and other non-routine projects
- Conducts peer review of routine testing at the discretion of management
- Performs hypothesis testing or investigative work for OOS results under management and SME guidance
- Trains and mentors staff on established processes and procedures
- Demonstrates cross-functional support capabilities with other QC teams
- Responsibilities may increase in scope to align with company initiatives
- Performs other related duties as assigned
Required Skills and Abilities
- Proven analytical instrumentation experience (preferably HPLC) with at least 1-2 years in a cGMP pharmaceutical industry laboratory
- Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the Company
- Follow detailed written and oral instructions
- Demonstrated ability to collaborate and work in cross-functional teams
- Strong organizational skills and attention to detail
- Multitasks and adjusts priorities in a fast-paced environment, while maintaining focus and managing disruption and/or unexpected needs
- Strong analytical and problem-solving skills
- Accepts feedback from a variety of sources and constructively manages conflict
- Ability to prioritize tasks and to keep leadership apprised of performance to timelines
- Experience with Empower preferred
- Proficient with Microsoft Office Suite or related software
Education and Experience
- Bachelor’s degree in a scientific discipline or related field
- Minimum of 3 years of dedicated lab experience
- Requires 2 years of GMP experience
Physical Responsibility
- Prolonged periods of sitting or standing at a desk and working on a computer.
- Prolonged periods of standing or sitting while monitoring laboratory equipment.
- Must be able to lift up to 15 pounds at times.
- Adheres to consistent and predictable in-person attendance.
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