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
