Quality & Regulatory Affairs (QARA) Manager
Hyderabad · Senior
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Job description
Quality & Regulatory Affairs (QARA) Manager
About Quin
The role
What you'll own
- Own conformity across our target markets: CE marking, EU Declarations of Conformity and technical files, and the directives and regulations that apply to connected, battery-powered devices.
- Maintain the regulatory horizon calendar and keep the portfolio ahead of upcoming obligations and deadlines across markets.
- Own and evolve the QMS, supplier quality, and the product-quality processes behind our zero-defect delivery standard to partners.
- Own technical files, declarations, and labelling data; run certification programs and manage testing, notified-body and laboratory relationships.
- Lead our extended-producer-responsibility and market-registration obligations, working with Operations and our external regulatory partners.
- Produce the compliance data packages and guidance our partners rely on to launch products containing Quin technology.
- Partner with Engineering on design decisions so products are always conformant by architecture.
What good looks like
- Our portfolio stays conformant and audit-ready across EU and US markets, with a clean, current set of technical files and declarations.
- Regulatory deadlines are met ahead of time.
- We maintain complete compliance packages that make integrating Quin frictionless.
What you'll bring
- Proven ownership of product regulatory compliance for connected or electronic hardware — CE marking, Declarations of Conformity, and technical files.
- Working command of the regulatory landscape for battery-powered connected devices: EU Batteries Regulation, e-waste / EPR regimes (e.g. California SB 1215), RED / FCC, RoHS / REACH.
- A strong quality-management background — QMS ownership and supplier quality — in a hardware or product environment.
- Experience coordinating testing, notified bodies and labs, and external regulatory partners.
- The ability to translate regulation into concrete engineering and operational requirements, and to move fast without dropping rigor.
Strong pluses
- Certifications such as ISO 9001 Lead Auditor or recognised regulatory-affairs credentials.
- Experience spanning consumer and industrial / PPE product categories.
- Familiarity with EU authorised-representative structures and multi-market EPR registration.
- Experience in a fast-scaling product company shipping into multiple regulated markets.
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