Quality Control Supervisor, IPC- Day Shift

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