QAスペシャリスト（契約）

Benefits

Parental leave

Not verified

Non-birth-parent leave

Not verified

Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

Not verified

Relocation assistance

Not verified

Childcare support

Not verified

Learning budget

Not verified

Verification

Not verified

Salary

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Market context

U.S. role benchmark (BLS OEWS)

$61,842 U.S. median for this role

Projected growth (BLS Employment Projections)

+1.9% - Slower

Matched to SOC 11-1021 - Operations aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function

Operations From the posting source checked Jun 20, 2026

Seniority

Mid From the posting source checked Jun 20, 2026

Schedule

Shift type

Not verified

Weekend work

Not verified

Company

Company stage

Public-company From the posting source checked Jun 20, 2026

Equity

Offered Verified - SEC 10-K source checked Jun 20, 2026

Application

Cover letter

Not verified

Assessment

Not verified

Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

QAスペシャリスト（契約） Location not specified At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised. Long Description Job Summary： 品質保証部の一員として、マネジャーおよび社員の指示のもとで、国内入荷製品の不適合製品処理、製品標準書の作成および管理、変更通知の管理、監査関係の事務局等の業務を行う。 20%:国内入荷製品の不適合製品の処理（登録、返送）報告書を英語で作成 20%:変更通知の管理（海外より報告された変更通知の登録) 20%:ISO13485サポート業務（計測機器管理、文書管理等） 15%:製品標準書の作成及び管理 15%:添付文書（XMLファイル）の作成および管理 10%:その他のアドミニストレーション業務 Expected Areas of Competence (i.e. KSAs) 英語の読み書きに抵抗がないこと、会話ができれば尚可 PCの基本的なスキル（Word, Excel, PowerPoint等） Education/ Experience Requirements ヘルスケア業界（主に品質保証業務）における品質保証関連業務の3年以上の経験 化学、物理学、工学等の知識があれば尚可 Travel Requirements 勤務地は平塚事業所（神奈川県平塚市） / テレワークの活用可（週2～3回目安） EOE/M/F/Vet/Disability

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