hirly

Envista

Head of Quality Assurance

Sweden, Värmland, Karlskoga

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at Envista first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included

Matched against 2.6M live jobs from 190,000+ employers in 200+ countries.

Tailor my resume for this job →

Apply from your AI assistant

Connect hirly to Claude and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending. ChatGPT: manual setup today.

Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.

hirly's read of this role

Role family
Engineering
Seniority
Lead / management
Country
SE
Work mode
On-site / unstated
First seen by hirly
27 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Job Description:

The Head of Quality Assurance is responsible for Quality Assurance and Quality Control at the production site of Nobel Biocare AB, located in Karlskoga, Sweden. This position ensures the manufacturing site complies with applicable international medical device regulations and standards. A key responsibility will be to lead, maintain, and continuously improve the site Quality Management System (QMS) to guarantee product safety and efficacy. This role focuses on ensuring that production processes remain in a state of control, validations are robust, and processes consistently produce medical devices that meet specifications, Regulatory requirements (ISO 13485 / FDA 21 CFR 820), and patient safety standards.

Lead and develop the Quality department consisting of QC and QA

Ensure the awareness of applicable R egulatory & QMS requirements throughout the organization

Ensure process risk assessment files are in accordance to ISO 14971

Ensure validation s are robust , mon i toring activities are performed and analyzed and o versee revalidation cycles

Ensure manuf acturing process changes are properly assessed

Partner with m anufacturing e ngineering to optimize inspection and testing methods

Supervise incoming inspection as well as final product release including Device History Records (DHR)

Ensure timely resolution of Corrective and Preventive Action s ( CAPA )

Oversee the document control and training process es at the site

Act as the primary site contact for internal and external audits

Job Requirements:

Proven expertise in design and implementation of Quality processes into a manufacturing organization in a regulated industry

Experience with the development of an organizational culture that promotes and sustains Quality

Strong proficiency in validation methodologies (process, software, sterilization)

Practical experience with risk management tools ( f.e. PFMEA)

Strong leadership and ability to influence cross-functional teams (f.e Manufacturing , R&D)

Objective problem-solving skills with the ability to make firm, risk-based quality decisions under pressure

High level of attention to detail and scientific rigor

Fluency (oral and written) in English is mandatory, Swedish is welcome

Sound SAP system understanding is a plus

More than 5 years experience in regulated process industry

Professional experience in Quality Management in industries such as medical device, pharmaceutical or food industry

Experience in Management positions

#LI-PG1

Operating Company:

Nobel Biocare Envista and its family of companies (Envista) will not accept unsolicited resumes from any source other than directly from a candidate. Envista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening. Envista will not pay a fee to any Agency that does not have such agreement and written approval in place.

Original posting on Envista's site ↗

Listed on hirly, a job board. hirly is not the employer: Envista is hiring for this role.

Browse similar roles

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job