New · posted Oct 15
ConvaTec · Medical Devices
Quality Manager - Fix term Contract
- Remote, US
- Remote
- Contract
- Manager
Open until filled
The role
This is a fixed term contract opportunity that is expected to last approximately one year with the eligibility for extension
Position Overview:
This function is responsible for the management and oversight of the Quality Management System. Responsible for developing, identifying, analyzing, and improving the quality management system. This process will follow the Convatec Quality Management Systems, Unomedical Quality System, and all applicable regulations and standards (e.g. Quality Management System Regulation - QMSR, ISO13485, Japan MO-169, Brazil ANVISA).
The position requires empowerment and proactivity, time management skills, organization, and attention to detail. The role will have interaction and/or communication, when applicable, with employees, customers, suppliers, third parties.
Authority (if applicable)
This role has signatory rights as listed on Quality Management systems records and procedures
Team
Quality applicable personnel.
Languages
· Speaking: Yes English and Spanish Advanced Required
· Writing/Reading: Yes English and Spanish Advanced Required
Working Conditions (Applicable local workplace laws and statutes should be included in the description of working conditions)
· Office Working.
· EH&S requirements are established in local procedures.
· Employee will not be exposed to any chemicals
· Maintain general awareness of the CVT’s EHS policy and supporting standards.
· Understand EHS risks and applicable legal requirements associated with their job responsibilities and the appropriate controls in place to manage those risks and requirements.
· Carry out job responsibilities with due professional care and in compliance with legal requirements and internal standards without compromising their own safety or that of others.
· Be alert to EHS hazards in the workplace, responding to them as appropriate and communicating them to responsible management as they are identified (e.g., spills).
· Participate in training, awareness, and community initiatives as appropriate.
· Help drive continuous EHS performance improvement by suggesting potential improvements to responsible management.
Special Factors
· Working flexibly.
· Willingness to work weekends, if required.
What you need
Qualifications/Education
- Bachelor’s degree in industrial engineer, business administration (desirable) or any other related grade.
- Knowledge of the Quality Assurance standard for medical devices like ISO13485 and QMSR.
- Knowledge of root cause analysis tools.
- Two (2) years in regulated industries
- 1 year experience in management/principal/Sr. Engineering positions (preferred).
- Experience in leading front or back rooms during external regulatory body Audits.
- Experience leading external audits in sister plants (preferable).
- Experience with submitting Local Registrations (preferable).
- Experience leading investigations of Audit finding (preferable).
- Experience in execution training programs (preferable).
- Experience with QMS regulated software.
- Knowledge of change control principles, quality systems, training, standards, and regulations of Medical Device Quality systems.
- Demonstrated proficiency in complaints, non-conformance and CAPA management.
- Skill on root cause, continuous improvement, and statistical tools.
- Strong motivation to achieve good results is essential. Self-directed leadership, requiring minimal supervision and proactive attitude.
- undefined
Travel Requirements
You will be expected to travel an estimated 30% of the time, mainly to different Convatec plants (depending on business requirements).
What you'll do
- Supervise the Quality team and their support to all relevant product categories.
- Assist and Coach the teams in conducting investigations of Trainings, Document activities, complaints, nonconformities and /or corrective preventive actions.
- Oversee the Complaint system, assuring corresponding evaluations and/or investigations are completed in a timely manner, trends are analyzed, and applicable actions are executed (e.g. CAPAs, SS, HHE)
- Report progress of investigations for complaints, nonconformities, preventive/corrective actions, internal/external audits, stop shipments, HHEs and any other applicable Quality System requirement.
- Oversee the CAPA system, assuring corresponding investigations, corrections, containment, and corrective/preventive actions are taken, as well as insuring that their effectiveness is measured; this while also maintaining a system that complies with QMS requirements.
- Oversee the Training and Document Management system, assuring corresponding activities, trainings, evaluations and/or investigations are completed in a timely manner, trends are analyzed, and applicable actions are executed.
- Execute/report/Analyze trend analysis related to the quality management system.
- Participate in local and/or corporate meetings representing the site Quality System and communicating any action/activities that are needed.
- Oversee/prepare corresponding reports and/or meeting (e.g. trend analysis, management reviews) to assure the Quality System is robust and complies with requirements, and, if applicable raise corresponding action to keep in compliance.
- Lead external audits and certification program, if needed.
- Support and participate in company projects.
- Identify, develop, and implement continuous improvement projects for products and processes.
- Carry out, together with your team and if required, CAPA (Corrective and Preventive Actions).
- Follow and enforce the corresponding policies and procedures, implementing solutions aligned to the needs of the business and its products.
- undefined
Principal Contacts & Purpose of Contact
· Internal: Directors, Managers, Engineers, and Supervisors (all departments)
· External: Directors, Managers, Specialists, Engineers, Supervisors (other manufacturing locations). External auditors, Global Complaint Handling Unit, Global CAPA Handling unit (all departments).
From the posting
About ConvaTec
Already a Convatec employee?
If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!
Pioneering trusted medical solutions to improve the lives we touch
Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. With over 10,000 colleagues, we provide products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention, treatment for hard to heal wounds, at-risk skin and ulcerated tissue to supporting debilitating conditions, improved patient outcomes and reduced care costs. Convatec's revenues in 2025 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more please visit: http://www.convatecgroup.com.
Equal opportunity, accessibility and legal noticesConvaTec's statements, word for word
Beware of scams online or from individuals claiming to represent Convatec
A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.
If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at [email protected].
Equal opportunities
Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.
Notice to Agency and Search Firm Representatives
Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Job intelligence
The context around this role
Live data · October 15, 2026
Salary intelligence
How the pay compares
Manager roles in New Jersey6 roles publishing pay
Manager roles in the US105 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| New Jersey (middle half) | $127,125 | $143,750 | $161,875 |
| All US (middle half) | $126,000 | $153,000 | $167,500 |
Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Assurance
The general path across 845 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not ConvaTec's own promotion track.
Career resources on Quality Assurance
Skills DNA
What this role leans on
How many of the posting's 53 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Quality systems and risk13
- Collaboration and leadership13
- Investigations and CAPA11
- GMP and compliance10
- Documentation and SOPs9
- Data and digital systems1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
Company hiring pulse
ConvaTec on Regulatory Jobs
- 1
- Open roles
- 1
- Distinct roles
- 1
- Locations
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Quality Manager - Fix term Contract at ConvaTec
Open until filled.