Strategist / Senior Strategist - Regulatory Affairs
Clinchoice INC · 🌍 Bengaluru, Karnataka, India
Sponsorship verdict
No sponsorship evidence yet
No government record and no wording either way. Not a refusal — ask the recruiter.
- No government sponsor record hereNo government sponsor record covers this employer in this country.
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- Can’t check pay against the visa rulesWe don’t have visa salary rules for this country yet.
- Confirmed live todayWhen a source last listed this job as open.
A verdict summarises public evidence; it is not legal advice and never a guarantee — the employer and the immigration authority decide. Sign in to factor in where you can already work.
Or apply yourself on the official page →
Why not apply?
No register record and no sponsorship wording in the posting. Worth asking the employer before investing significant time.
SponsorApply flags time-wasters so your applications go where they can land. These come from the posting's own wording — read the original listing to confirm. See better-fit alternatives →
Sponsor Radar — Clinchoice INC
No government sponsor record covers this employer in this country.
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Clinchoice INC →
About the role
Responsibilities: • Supports UK, Ireland, Malta, Sweden, Finland, Norway, and Denmark products across the product portfolio. • Supports the team with regulatory strategies (local and regional) that are in line with the business plan • Supports the team with regulatory activities for National and/or European procedures (Decentralized, Mutual Recognition) as appropriate. For example, but not limited to: • Prepares and compiles regulatory submissions, response to questions, renewals, post submission/approval activities (including relevant updates to external websites such as emc, medicines.ie and In-Demand) • Supports ad hoc projects (e.g., compliance reviews, audit preparation etc.) • Signs off on packaging material, leaflets, and SmPCs (as appropriate) • Supports the compilation of the Northern Cluster team metrics for the EMEA biannual metrics report • Supports all regulatory activities in Malta • Ensures regulatory compliance within the department to include: • The maintenance of global, regional, and local databases • Adherence to processes, SOPs, work instructions, and job aids • Updates to relevant local and global databases to track current product information • Supports team with Calls for Information (CFI) and assist in any Pharmacovigilance- related activities within the Northern Cluster, which may include: • Receiving and monitoring responses to CFIs through liaison with UK and EAME colleagues • Ensuring responses are submitted in a timely manner and that they are in line with standard procedures and metrics established by the VP Regulatory Affairs in European Regulatory • Provide support and responses to ad hoc requests received from UK PV group or Global Reg Med Mailbox • Supports the team with regulatory activities for National and/or European procedures (Decentralized, Mutual Recognition) as appropriate. • Ensures regulatory compliance within the department Experience/Qualifications: • Bachelor's/Master's degree in Life Science/Pharma • Minimum of 5 ~ 8 years of relevant work experience working within a Regulatory Affairs Department (e.g., pharmaceutical, cosmetic, food supplements, etc.), with direct accountability for deliverables or a combination of direct Regulatory Affairs experience of CMC, Quality, or Regulatory Operations.