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Penumbra
Actively Hiring
A global healthcare company focused on innovative therapies
  • B2B
  • Public Stage
    Publicly traded company

QA Manager - DHR Review

Posted: 1 month ago
Visa Sponsorship

Not Available

RelocationAllowed

About the job

As a QA Manager of DHR Review, you will play a pivotal role in overseeing the team of Quality Specialists that performs Device History Record (DHR) review. The QA Manager – DHR Review drives improvements and efficiencies in the area and ensures compliance with Penumbra procedures and regulatory requirements. What You’ll Work On• Select, manage, train, and develop staff. Establish objectives and assignments and provide ongoing feedback through performance reviews and development plans. • Lead, manage, and motivate a team performing DHR review activities while providing guidance, training, and support to ensure high performance and continuous development.• Oversee the DHR review process to ensure compliance with applicable regulations and standards and internal quality policies. • Communicate effectively both within area of responsibility and cross-functionally to ensure daily priorities are in alignment. • Develop and maintain quality metrics for area of responsibility. • Formulate and carry out company directives based on knowledge of the company’s Quality Management System (QMS).• Evaluate procedures for processing improvements, recommend changes to procedures and implement changes, as necessary. • Participate in internal and external audits, including the retrieval of quality records and any other documentation requested, and represent DHR review processes.• Provide additional analysis of situations reviewing various factors to solve problems and proactively seek and implement improvements.

What You Contribute• A Bachelor's degree with 4+ years of experience in Quality Assurance, Quality Control, biotechnology, document control, or a related field, or equivalent combination of education and demonstrated experience• Proficiency with Microsoft Office (e.g., Word, Excel, PowerPoint, etc.)• Knowledge of global medical device regulations and standards including FDA and ISO 13485• Demonstrated experience in managing and leading a team• Strong analytical, problem solving, decision-making, and leadership skills are required• High degree of accuracy and attention to detail• Strong oral, written and interpersonal communication skills

Working ConditionsGeneral office environment. Willingness and ability to work on site. Ability to travel up 25% of the time to other company sites as needed Requires some lifting and moving of up to 25 pounds. Must be able to move between buildings and floors. Must be able to remain stationary and use a computer or other standard office equipment, such as a printer or copy machine, for an extensive period of time each day. Must be able to read, prepare emails, and produce documents and spreadsheets. Must be able to move within the office and access file cabinets or supplies, as needed.

Annual Base Salary Range: $105,000 - $165,000 / yearWe offer a competitive compensation package plus a benefits and equity program, when applicable. Individual total compensation will vary based on factors such as qualifications, skill level, competencies, and work location.

About the company

Penumbra company logo

Penumbra

Actively Hiring
A global healthcare company focused on innovative therapies
Company Industries
Development Platforms
Company Industries
Medical Device
  • B2B
  • Public Stage
    Publicly traded company
Learn more about Penumbra image

Funding

AMOUNT RAISED
$121K
FUNDED OVER
1 round
Round
U
$121,200
Unknown - Nov 2012

Perks

Well-being
Yoga – and other exercise classes – regularly offered on site Discounted gym membership Open and collaborative work spaces Sit/stand desks
Community
Organized events that support local charities Annual donation drive Colleagues who are giving back Recreational sports leagues

Founders

Charul Pant
Founding Member and Editor • 3 years • 12 years
India
image
View the team image

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