Jobs / Colombia / Pfizer INC

Pfizer INC

Data & Conformance Manager, Associate

Colombia - Bogota - Suba Posted today

Apply on employer site ↗ Tailor my CV first Source: Company careers site

Optional: we can tailor a CV and cover letter for this job from your real experience first (the first one is free).

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.
Details and sources

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.

Before you apply

Sponsorship unknown

No register record and no sponsorship wording in the posting. Worth asking the employer before investing significant time.

These come from the posting’s own wording. Read the original listing to confirm. See better-fit alternatives →

About the role

JOB SUMMARY The Data & Conformance Manager focus within Regulatory Data & Conformance Management (RDCM) is to interpret, manage and ensure the quality, accuracy, and proper management of global regulatory data and conformance activities received across different geographies, functions and divisions. Ensuring key activities and regulatory systems updates are completed whilst adhering to all policies, practices and procedures. These activities ensure data integrity to enable the organization to have visibility across all functions within a products lifecycle. It is essential that all systems are clearly and accurately updated within the timelines specified in the Standard Operating Procedures (SOPs) or business process documentation to ensure regulatory compliance. RESPONSIBILITIES - Review and interpret the data provided by GRS to establish the system / tools required to be populated in line with current standard operating procedures or business process documentation, including systems and SOPs associated with the regulatory data scope. - Accountable for maintaining the HA status in corporate change and dossier management system for the allocated Regions / Markets - Responsible for making updates in regulatory systems for all the CMC events upon receipt of notification of Submission and Approval evidence - Perform data entry and quality control tasks associated in all global regulatory systems impacted, including systems associated with the regulatory data scope. - Adhering to quality control procedures and standards related to the systems or tools ensuring Regulatory Compliance - Support global/local team members with data management workload when necessary to provide flexible support for the portfolio. - Contribute to local and regional regulatory initiatives promoting a culture aligned with Pfizer values - Assist in ensuring internal regulatory processes and procedures are well documented - Support the teams in ADHOC activities including assisting presentations / review of metrics - Makes timely decisions on straight cases within guidelines and policies Work Location Assignment: Hybrid EEO (Equal Employment Opportunity) & Employment Eligibility  Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.     To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on  Pfizer Careers .     Regulatory Affairs

Apply on employer site ↗