Medical documentation reviewer - Hyderabad, Telangana

The Senior Analyst role supports the Document Review Services Team Lead on active projects assigned to respective review team. · Analyzes documents and extracts applicable data, · validates information with peers, · assists higher level employees, · & escalates complex issues.Ana ...

The Senior Analyst role supports the Document Review Services Team Lead on active projects assigned to respective review team this role understands client requirements reviews documents extracts applicable data and validates the extracted information with peers.Analyzes documents ...

The Senior Analyst role supports the Document Review Services Team Lead on active projects assigned to respective review team and assists higher level employees. · Analyzes documents and extracts data · Collaborates closely with SMEs to stay updated on project instructions · ...

This position involves ensuring GLP compliance in laboratory operations. · ...

The Role & responsibilities includes Review and approval of equipment/instruments qualification, calibrations and preventive maintenance documents. Also responsible for planning of all analytical Quality Assurance activities like analytical test reports review of Stability sample ...

Company Description · We suggest you enter details here. · Role Description · This is a full-time on-site role for a Reviewer at Aurobindo Pharma Limited, Unit - III, Hyderabad. The Reviewer will be responsible for evaluating and reviewing documents and records to ensure complian ...

Study Audits: Plan and conduct BA/BE study audits (in-process and retrospective) in compliance with the protocol, SOPs, and applicable GxP standards and regulations. · Document Review: Review draft protocols, study ICFs, and study CRFs in line with applicable GxP standards and ...

Site Selection Audits: Plan and conduct investigator site selection audits and clinical trial study audits at investigator sites in accordance with applicable GCP guidelines and regulations. · Document Review: Review subject ICF and medical records. · CRF Design Review: Review ...

Review documents to ensure quality and adherence to company policies. · ...

We have an opening in both Quality Control and Quality Assurance Department.Quality Control: 05 positions, Quality Assurance: 05 positions · This opportunity helps freshers and early stage employees to learn and proficient in shortest period possible provided one must be dedicate ...

The Senior Manager will be responsible for reviewing LCMS method development and validation, as well as planning and monitoring work for team members. · Review of LCMS method development and validation. · Planning and monitoring of work for team members. · ...

The Process Excellence role involves implementing Daily Work Management (DWM) steps, providing awareness training on DWM, · and handling DWM portal issues within Service Level Agreements (SLAs). Additionally, · this role includes creating and documenting comprehensive business pr ...

Role & responsibilities Responsible to preparation & review of standard operating procedures. · ...

Lead the preparation and submission of technical documents for regulatory markets. · Prepare and review technical documents for regulatory submissions. · Execute submission build activities including creating inter-document links and ensuring timely dispatch. · ...

Implement Business Excellence with TQM documentation , DTQMP preparation for Deming Exam document best practices manage consultant reviews Implement Daily work Management handle DWM portal create SOPs ensure alignment of processes with organizational goals. · Document best practi ...

Designing and development of artworks for the filing and commercial products. Development of Primary Secondary & Tertiary Packaging Materials for new products. · ...

Medical writer will be responsible for medical writing tasks including aggregate reports Periodic Safety Update Reports (PSURs), Periodic Adverse Drug Experience Reports (PADERs), RMPs. · ...

Sr. Regulatory Publishing Specialist is responsible for leading the preparation and submission of technical documents and eCTD publishing. · ...

We are looking for Shift In-Charge in Mfg/any Process Industry with 4+ yrs Exp as Shift In-Charge in Mfg/any Process Industry. · ...

· Job Title: Senior Regulatory Publishing Specialist · Responsibilities: · Technical Document Preparation: Lead the preparation, review, and submission of Technical documents/Dossiers (CTD/ACTD) for both Regulatory and Non-Regulatory Markets. · eCTD Publishing: Proficiently hand ...