Quality Assurance Manager

Posted Yesterday
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Brilliant, OH, USA
In-Office
60K-60K Annually
Mid level
Digital Media • Software
The Role
Manage and maintain the company Quality System in compliance with FDA medical device and drug regulations. Responsibilities include document control, SOP and Quality Manual maintenance, audits and inspections, CAPA, complaint and non-conformance trending, personnel training, quality investigations, and cross-functional regulatory support. The role may provide technical supervision and requires occasional travel and local driving.
Summary Generated by Built In

SUMMARY

Responsible for the implementation, monitoring and maintenance of the Quality System in accordance with FDA Medical Device and Drug regulations. 


ESSENTIAL DUTIES & RESPONSIBILITIES

  • Ensure the Quality System regulations are understood by all applicable company personnel and is functioning and effective at all times.
  • Draft, review, maintain, distribute and train personnel on facility documentation and procedures, such as the Quality Manual and Quality System Procedures.
  • Ensure compliance with Document Control, Device History Records and Management.
  • Maintain Quality System Manual Standard Operating Procedures (QSM SOPs),  and Documentation Control.
  • Prepare documentation and systems for compliance with the FDA requirements.
  • Conduct and participate directly in quality inspections, internal and external audits, and FDA inspections.
  • Participate in CAPA systems. Prepare reports and corrective actions.
  • Maintain and update the Quality Manual, QA Procedures, and introduce Quality Plan improvements as applicable.
  • Assist in analyzing and evaluating information concerning manufacturing problems, customer complaints, non-conformances, quality system, etc.
  • Trend customer complaints and/or non-conformances.
  • Assist and/or perform training activities in QM system processes and product quality.
  • Confer with Operations about quality assurance and regulatory issues of products to ensure compliance with quality system.
  • Maintain regular and punctual attendance.
  • Perform other duties as assigned.

SUPERVISORY RESPONSIBILITIES

May provide technical guidance and/or supervision to personnel.


Requirements

MINIMUM QUALIFICATIONS

·       Minimum of three (3) to five (5) years in the medical device/drug industry, with a minimum of two (2) years of direct experience in QC/QA or equivalent.

·       Proven understanding of FDA regulations.

·       Proven leadership experience.

·       Must have clean driving record.

·       Must be able to pass drug test.

·       Must obtain and maintain any necessary security access and/or background checks.


DESIRED QUALIFICATIONS & SKILLS

·       Bachelor's Degree preferred.

·       Strong Quality Systems background and knowledge of QA/QC principles and compliance.

·       Superior communication (verbal, written and interpersonal) skills.

·       Good organizational skills.

·       Motivated self-starter, ability to multi-task, work independently.

·       Aptitude for problem solving, decision making, and an effective cross-functional team participant.

·       Computer proficient, Microsoft Excel, Microsoft Word, and PowerPoint.

·       Confident team player with strong interpersonal skills.

·       Ability to work collaboratively across functions.

·       Possess and exhibit professionalism, energy, high integrity, results orientation, and solutions driven.


WORK SCHEDULE 

Full-time, Monday–Friday day shift. No weekends. May be required to work additional hours as needed to complete assignment or project.


TRAVEL

The expected travel time is less than 25%.


DRIVING REQUIREMENT

Must have or be able to attain a valid state driver’s license and be insurable on the company’s automobile insurance policy. Driving, with or without accommodation, may be required when traveling for training and/or short occasional amounts of local driving.  The expected driving time is less than 10%. 


WORK ENVIRONMENT

The majority of work is performed in a professional office setting and in some off-site locations during project transitioning with a wide variety of people in different functions, personalities and abilities.


PHYSICAL DEMANDS

Frequent sitting, using hands/fingers, handling, reaching with hands and arms, talking, hearing; occasional walking or standing, occasional lifting of up to 10 lbs. It is Katmai’s business philosophy and practice to provide reasonable accommodations, according to applicable state and federal laws, to all qualified individuals with physical or mental disabilities.


Benefits

Compensation & Benefits:

  • Pay: $60,000 per year.
  • Eligible Benefits: Medical, Dental, Vision, Life & AD&D Insurance, Long-Term & Short-Term Disability Insurance, 401(k) Savings Plan, Employee Assistance Program (EAP), Vacation & Paid Personal Time, 11 Paid Federal Holidays, and Leave of Absence.

Compliance:

To be considered for this position, all applicants must apply on the company website, https://apply.workable.com/katmai/

We are a VEVRAA Federal Contractor.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity or national origin, disability status, protected veteran status, marital status, familial status or any other characteristic protected by law.

Preference will be given to Ouzinkie Shareholders, Descendants of Shareholders and Spouses of Shareholders in accordance with Title 43 U.S. Code 1626(g) and Title 42 U.S. Code 2000e - 2(i).

Skills Required

  • Three to five years of experience in the medical device or drug industry
  • At least two years of direct QC, QA, or equivalent experience
  • Understanding of FDA regulations
  • Leadership experience
  • Clean driving record
  • Ability to pass a drug test
  • Ability to obtain and maintain necessary security access and background checks
  • Bachelor's degree
  • Quality Systems and QA/QC compliance knowledge
  • Strong verbal, written, and interpersonal communication skills
  • Organizational skills and ability to multitask independently
  • Problem-solving and decision-making skills
  • Computer proficiency, including Microsoft Excel, Word, and PowerPoint
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The Company
HQ: Anchorage, AK
42 Employees
Year Founded: 2020

What We Do

The workplace of the future is here. Katmai offers a breakthrough solution for remote teams. Our immersive virtual office brings people together in a shared digital space that’s accessible with just a browser. No VR headsets needed here. Katmai combines video conferencing with immersive, photo-realistic environments, allowing remote teams to experience the benefits of an IRL office - natural communication, spontaneity, and real-time collaboration - from anywhere. Work, connect, and feel like a team. Get your own virtual office, totally FREE: katmaitech.com

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