---
title: 'Commercial Quality Control Chemist II at Serán BioScience'
canonical: 'https://feeny.ai/job/commercial-quality-control-chemist-ii-seran-bioscience-bend-q523axeg2wnk'
type: 'job'
last_seen: '2026-10-16'
---

# Commercial Quality Control Chemist II at Serán BioScience

- **Company:** Serán BioScience
- **Location:** Bend, OR
- **Work type:** onsite
- **Posted:** 2026-09-28
- **Last confirmed live:** 2026-10-16
- **Apply:** https://jobs.lever.co/seranbio/d2b2f9da-fc77-4268-be0f-9d8717ce4d86

## Job description

Serán is expanding its Bend, Oregon campus with a new GMP manufacturing facility and is seeking an industry-experienced Commercial Quality Control Chemist to play a critical role in the facility start-up of the new QC laboratory including equipment and facility qualifications. Once the facility is underway, The Commercial QC Chemist II supports the Quality Control laboratory’s ongoing commercial product testing activities in support of cGMP practices, product quality, regulatory compliance, and customer satisfaction. This position performs and provides technical expertise for commercial pharmaceutical testing, including finished facility testing, product release, stability, in-process control, raw material, and other analytical testing as assigned. The Commercial QC Chemist II serves as a technical resource for assigned analytical instrumentation, methods, and laboratory processes. The role supports analytical data integrity, laboratory investigations, method implementation, equipment qualification, and continuous improvement initiatives.

Supervisory Responsibilities

- May supervise QC laboratory staff continually or on a project basis.
- May assist with recruiting, interviewing, hiring, onboarding, and training new staff.
- May oversee the daily workflow, testing priorities, and execution of assigned commercial QC activities.
- May provide technical guidance, coaching, and support to QC Chemists I and other laboratory personnel.
- May assist QC management with workload planning, resource allocation, and meeting commercial testing timelines.

Duties & Responsibilities

- Perform routine and non-routine analytical testing of commercial pharmaceutical products, including facility testing, finished product release, stability, in-process control, raw material, and other QC testing as assigned.
- Demonstrate intermediate expertise with applicable analytical equipment and techniques, including HPLC, GC, dissolution, Karl Fischer, XRPD, mDSC, UV-vis, FTIR, and other laboratory technologies as qualified.
- Execute approved analytical methods, compendial procedures, and laboratory SOPs in accordance with cGMP requirements, specifications, and established testing timelines.
- Ensure analytical data, calculations, laboratory records, and supporting documentation comply with Good Documentation Practices (GDocP), data integrity principles, and applicable regulatory expectations.
- Technical Data Review: Perform technical review of analytical data, calculations, and supporting documentation for commercial testing, as assigned and within established qualification and authorization.
- Serve as a technical resource for laboratory investigations, including OOS, OOT, deviations, incidents, and unexpected analytical results, in collaboration with QC management and Quality Assurance.
- Assist with root cause analysis, corrective and preventive actions, and implementation of improvements resulting from laboratory investigations.
- Support the transfer, implementation, verification, and optimization of analytical methods for commercial products, as assigned.
- Assist QC management with daily laboratory workflow, testing priorities, resource coordination, and timely completion of commercial testing deliverables.
- Interface with clients and internal stakeholders on technical analytical matters, testing status, data inquiries, and laboratory concerns, as requested by QC management.
- Assist with the development, revision, and technical review of SOPs, specifications, protocols, reports, and other controlled documents.
- Support the training, mentoring, and qualification of QC laboratory personnel on analytical methods, instrumentation, procedures, and GMP practices.
- Maintain compliance with cGMP, GDocP, data integrity, laboratory safety, and applicable regulatory requirements while promoting a culture of quality and accountability.
- Identify and support opportunities to improve laboratory efficiency, testing accuracy, turnaround times, equipment utilization, and right-first-time execution.
- Assist with internal and external audits, regulatory inspections, and preparation of supporting laboratory documentation and records.

Required Skills & Abilities

- Demonstrates intermediate expertise with analytical equipment and techniques applicable to commercial pharmaceutical testing, including HPLC, GC, dissolution, Karl Fischer, XRPD, mDSC, UV-vis, FTIR, or other relevant technologies.
- Strong understanding of cGMP laboratory practices, Good Documentation Practices (GDocP), data integrity, and applicable regulatory expectations.
- Demonstrated ability to execute analytical methods and interpret analytical data accurately and effectively.
- Strong analytical, mathematical, troubleshooting, and problem-solving skills.
- Demonstrated ability to support OOS, OOT, deviation, and other laboratory investigations.
- Excellent verbal and written communication skills.
- Excellent interpersonal and customer service skills.
- Demonstrated ability to communicate effectively with coworkers, clients, and other internal and external stakeholders.
- Excellent organizational skills and attention to detail.
- Excellent time management skills with a proven ability to meet deadlines.
- Strong collaboration and cross-functional teamwork skills.
- Strong technical leadership and mentoring skills.
- Ability to prioritize tasks and coordinate laboratory activities as appropriate.
- Ability to function well in a fast-paced and, at times, stressful environment.
- Proficient with Microsoft Office Suite or related software.
- Familiarity with LIMS, electronic laboratory systems, Empower, or other applicable analytical data systems preferred.
- Accepts feedback from a variety of sources and constructively manages conflict.
- Demonstrated commitment to quality, compliance, safety, and continuous improvement.

Education & Experience

- Bachelor’s degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline, with 2 years of hands-on laboratory experience preferred; or
- Master’s degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline, with 1 year of hands-on laboratory experience preferred.
- Requires 1 year of GMP laboratory experience.
- Experience in pharmaceutical commercial QC testing preferred.
- Experience with applicable analytical instrumentation, laboratory investigations, and analytical method execution preferred.

Physical Requirements

- 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.

Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.

Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Benefits Summary: Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.

The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701

## About Serán BioScience

## Company Overview
- **One-liner**: Serán BioScience is a science-driven drug development partner providing integrated formulation, particle engineering, and clinical manufacturing services to pharmaceutical and biotechnology companies.
- **Entity Type**: Private (Privately Held)
- **Headquarters**: Bend, Oregon, United States
- **Founded**: 2016
- **Founders**: Dr. Smithey (President, CEO, and Co-founder)

## Core Business
- **Primary Industry**: Biotechnology / Drug Development (Contract Development and Manufacturing Organization – CDMO)
- **Target Customers**: B2B – Pharmaceutical and biotechnology companies (from preclinical to commercial stage)
- **Mission**: To provide optimized drug development and manufacturing services for clients, from discovery to the clinic, using a science-first approach to accelerate medicines to patients.

## Products & Services
- **Preformulation Services**: Physicochemical characterization and early feasibility studies to guide formulation strategy.
- **Formulation Development**: Design of robust formulations for poorly soluble compounds using spray drying, hot melt extrusion, fluid bed processing, granulation, and solid dosage forms (tablets, capsules, multiparticulates).
- **Particle Engineering**: Custom-built spray dryers capable of producing nano-to-micro particles; expertise in spray-dried dispersions and engineered particles for inhalation.
- **Clinical Manufacturing**: cGMP manufacturing of clinical trial materials (suspensions, capsules, tablets) with on-site ICH stability storage.
- **Commercial Manufacturing**: A 100,000 sq ft commercial manufacturing campus under construction, including large-scale spray drying for late-stage clinical and commercial supply.
- **Quality Control Laboratory**: Full release, stability, and microbial testing capabilities.

## Market Standing
- **Valuation/Market Cap**: Not publicly available
- **Key Metric**: Total Funding – Not disclosed; Headcount of 146 employees (+0.6% YoY as of latest LinkedIn data)
- **Notable Investors/Partners**: Not publicly disclosed
- **Growth Signals**: Constructing a 100,000 sq ft commercial manufacturing facility; expanding team to over 200 members; adding new development facilities and quality control labs; LinkedIn follower growth of +29.1% year-over-year.

## Competitive Advantages
- **Science-First Approach**: Employs predictive design tools, novel chemistry, and advanced analytical methods from the earliest stages to de-risk development.
- **Particle Engineering Leadership**: Decades of experience with poorly soluble compounds; proprietary spray drying and particle engineering technologies (nano-structures to micro-particulates).
- **End-to-End Support**: Integrated services from preformulation through commercial manufacturing, reducing handoffs and timelines.
- **Right From the Start™ Methodology**: Parallel development of drug product intermediates and final dosage forms to accelerate programs.

## Strategic Focus
- **Commercial Scale-Up**: Investing in a dedicated commercial manufacturing campus to support clients’ late-stage and marketed products.
- **Technology Expansion**: Continuously expanding technical capabilities (spray drying, hot melt extrusion, fluid bed processing) and facility footprint.
- **Talent Acquisition**: Growing the team of scientists, engineers, and support staff to serve an increasing pipeline of complex drug molecules.

## Why Work Here
- **Culture**: Collaborative, respectful, and fun environment where every role contributes to delivering novel therapies. Emphasis on mentoring and continuous learning.
- **Work-Life Balance**: Central Oregon lifestyle with outdoor recreation access; standard business hours (with alternative shifts in manufacturing/QC/QA).
- **On-Site Requirement**: All employees are expected to work on the Bend campus; remote flexibility considered on a case-by-case basis.
- **Benefits**: Paid time off, employer retirement contributions (no match or vesting required after 90 days), fully funded medical/dental/vision for employee and household, basic life and long-term disability, Employee Assistance Program.
- **Ideal Applicant**: Scientific background with GLP/GMP knowledge; inquisitive problem-solver who follows SOPs and collaborates toward common goals.

## Sources
1. [seranbio.com](https://www.seranbio.com/about)
2. [linkedin.com](https://linkedin.com/company/seran-bioscience)
3. [seranbio.com](https://www.seranbio.com/careers)
4. [seranbio.com](https://www.seranbio.com/?portfolioCats=34%2C23%2C29%2C35%2C22%2C24%2C30%2C25%2C28%2C31)
5. [jobs.lever.co](https://jobs.lever.co/seranbio)

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