Mid-Level
By joining Bio-Techne, you’ll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.
Pay Range: $55,600.00 - $91,450.00
Position Summary: The Advanced Quality Assurance Specialist will work closely with internal colleagues as a key member of the Quality Assurance team working to maintain and grow Asuragen’s Quality Management System in alignment with international quality and regulatory standards.
Key Responsibilities:
Provides support ensuring compliance with all regulatory standards, systems, procedures, and practices. Includes ISO 13485, FDA QSR, MDSAP, IVDR, and other requirements relating to Quality Assurance activities:
Provide QA support to project core teams.
Provide support to or ownership of key quality management system processes.
Conducts internal and external audits, summarizing the results and providing summaries to Quality Management.
Assists in the management of Document Control, Training, NCR, CAPA, Complaints, Internal Audits, and Supplier Management systems. May be responsible for the management of one or more of these systems.
Reviews and approves validation activities.
Reviews and approves quality equipment calibrations and maintenance.
Supports regulatory and client audits.
Supports the overall QA Department goals.
Generates metrics in support of Quality Management Reviews.
Other duties as assigned.
Education and Experience:
Knowledge, Skills, and Abilities:
Skilled in the use of software programs such as Microsoft Office and database management programs.
Detail oriented and skilled at examining documents for accuracy and completeness. Ability to prepare records in accordance with detailed instructions.
Knowledgeable in QA principles and concepts in a dynamic manufacturing facility
Ability to set priorities and meet deadlines on a personal level. Ability to work under tight deadlines.
Capability to effectively train employees on procedures, processes, and QA concepts.
Team oriented individual with the ability to work effectively with multiple skill level employees. Skilled at dispute resolution.
Excellent written and oral communication skills.
Excellent analytical and problem-solving skills with the ability to work independently with minimal supervision.
Familiarity with statistical tools and concepts and their application in a regulated environment.
Knowledge of cGMP, ISO 13485, MDSAP, IVDD/IVDR and FDA QSR preferred.
Why Join Bio-Techne:
Bio-Techne is an E-Verify Employer in the United States.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.
*This position requires work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States (e.g., H1-B visa, F-1 visa (OPT), TN visa or any other non-immigrant work status). If you require a reasonable accommodation to complete an application, participate in an interview, or take part in any other stage of the recruitment process, please contact hr@bio-techne.com for assistance. *
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