Website Sedia Biosciences Corporation

Sedia Biosciences is hiring a QC Manager at our Beaverton, Oregon location. At Sedia, we create diagnostic and disease-monitoring products that provide cost effective solutions for rapid, near patient testing. We are currently seeking responsible individuals motivated to help research and develop our future diagnostic products.

Position Summary
FLSA Status:   Exempt

Reports to:  (Sr) Director/(Sr) VP Operations

Has primary responsibility for and leads quality control activities in testing and qualification of Sedia’s materials and products (from incoming raw material qualification, work-in-process testing and qualification, and finished goods testing and qualification).
Works collaboratively with other departments to meet corporate objectives.
Primary Responsibilities

Manages day to day activities of the Quality Control department at Sedia.
Responsible for the overall organization, development, direction, coordination and evaluation of Quality Control team members. Ensures all staff are trained to perform duties.
Conducts Trend Analysis and Suggests Opportunities for ImprovementAnalyzes QC technical data toward ensuring quality standards
Drives continuous improvement of testing methods.
Performs analysis and suggests potential solutions to correct/prevent issues from recurring.
Identifies possible changes to improve efficiency and consistency.
Establishes and manages to departmental objectives.
Develops and validates quality test methods in collaboration with Research and Development and Manufacturing teams.
Authors and revises QC documentation, and procedures.
May participate on Design Control project team for new products and assist with technical transfer of products and test methods from Research and Development into the production system
Fosters an environment of strong team spirit, timely and effective communications, sense of urgency, high motivation and inspire teams to achieve goals in the immediate and longer term. Be an active and visible change agent, promoting flexible and open mindsets to new opportunities. Responsible for all quality control functions including scheduling through final product testing and release.
Supervisory Responsibilities

Responsible for the overall organization, development, direction, coordination and evaluation of Quality Control team members.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Degree(s)/Fields: B.S., MS, Or PhD in Biochem/Immunol/Microbiol/Biology/Genetics/or similar
Relevant Experience in Industry: B.S. (6-8+ years), MS (2+), PhD (0); years in
Experience in specific Responsibilities: Experience working under a quality system such as ISO 13485 and or CFR 21 part 820 cGMPs or GLP in medical device or pharma arena.
Supervisory Experience: 3+ Years of prior experience supervising a group; department, group, lab techs, junior scientists, senior scientists.
For consideration, please apply with a resume and cover letter.

Submit your resume and cover letter as an attachment in either RTF, Word, or PDF format to

In the Subject Line of your email, enter: “Your last name, your first name, middle initial (middle initial optional), and Job Title (that you are applying for).” For example, “Smith, Mary, Lab Technician.” If you are applying for multiple positions, please submit separate emails for each position.

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