Quality Control Supervisor, IPC- Day Shift

Serán BioScience; Bend (OR); On-site; USD 100,000 - 140,000; Full time

Benefits offered by this job

Paid time off

Retirement plan contributions after 90

Health plans with employee cost-share

Life and long-term disability coverage

Employee Assistance Program

Pet insurance

Job summary

Serán BioScience in Bend, Oregon seeks a Quality Control Supervisor for the In-Process Control (IPC) team. You will supervise Laboratory Analysts, ensure GMP-compliant testing, and collaborate with QC Managers to release materials and data on schedule.

The role requires strong leadership, communication, and organizational skills, with experience in GC, HPLC, TOC, and FT-IR analyses. On-site requirements and a focus on clean, compliant labs are essential.

Qualifications

• Bachelor's degree in a scientific field required.
• Minimum 5 years GMP experience.
• At least 3 years leading and developing successful teams.
• Experience with GC, HPLC, TOC, and FT-IR analyses.

Responsibilities

• Supervise Laboratory Analysts and ensure GMP standards.
• Write, revise, and approve SOPs.
• Coordinate audits and inspections; participate in validations and batch records.
• Manage project workflows and performance evaluations; mentor staff.
• Interface with Operations, Supply Chain, vendors, and clients as needed.
• Develop work plans and oversee cleaning verification activities.

Skills

Leadership

Communication

Time management

Team collaboration

Analytical skills

Microsoft Office

Education

Bachelor's degree in chemistry, physics, engineering, or related scientific discipline

5 years GMP experience

3 years leading and developing successful teams

Tools

GC/HPLC/TOC/FT-IR Analysis

Job description

The Quality Control Supervisor for the In-Process Control (IPC) team supervises the Laboratory Analysts to meet testing requirements in support of the manufacturing schedule. This position works closely with QC Managers to ensure that policies and procedures are followed as written, and revised when necessary. The QC Supervisor works closely with Operations and Supply Chain Management to ensure the timely release of Raw Materials, In-Process, Intermediate test data and equipment cleaning verification test data. This position is responsible for maintaining laboratory organization and cleanliness.

Supervisory Responsibilities

• Directly supervises Laboratory Analysts
• Recruits, interviews, hires, and trains new staff
• Oversees the daily workflow of all assigned projects and team
• Provides constructive and timely performance evaluations
• Perform other supervisory related duties as assigned

Duties And Responsibilities

• Adheres to GMP laboratory standards
• Maintain organization, supplies, and cleanliness of laboratory
• Write, revise, and approve SOPs
• Conducts training activities
• Participates in audits and inspections
• Executes validations, qualifications, and batch records
• Conducts scientific/technical reviews
• Interfaces with vendors
• Interfaces with clients on as-needed basis
• Develops work plans
• Manages cleaning verification assessments
• All other duties as assigned

Required Skills And Abilities

• 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
• Strong supervisory and leadership skills
• Demonstrate the ability to collaborate and work in cross-functional teams
• Strong math, analytical, and problem-solving skills
• Ability to prioritize tasks and to delegate them when appropriate
• Ability to function well in a high-paced and at times stressful environment
• Proficient with Microsoft Office Suite or related software

Education And Experience

• Bachelor’s degree in chemistry, physics, engineering, or related scientific discipline
• Experience with GC, HPLC, TOC, and FT-IR Analysis
• Experience with compendial raw material testing
• At least 3 years of experience leading and developing successful teams
• Requires 5 years of GMP experience

Physical Requirements

• Prolonged periods of sitting or standing at a desk and working on a computer
• Must be able to lift to 50 pounds at times
• Must be able to meet in-office attendance requirements

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

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.