Job Summary We are hiring a GMP Batch Record Reviewer / MBR Specialist with strong experience in pharmaceutical or biotech manufacturing environments . This role focuses on reviewing, authoring, and maintaining batch records (MBR/BPR) while ensuring full compliance with cGMP, FDA, and data integrity
Position Summary We are seeking a detail-oriented and experienced Batch Record Reviewer to support a six-month on-site project. The selected candidate will be responsible for reviewing manufacturing batch records to ensure compliance with cGMP requirements, internal procedures, and regulatory standa
Our client, a leading organization in the pharmaceutical and medical device industry, is seeking a Documentation Specialist to join their team. As a Documentation Specialist, you will be part of the Site Operations team supporting documentation management and operational readiness *Job Title:** Docu
Operations Batch Review Specialist The Operations Batch Review Specialist is responsible for reviewing batch documentation post execution to ensure that all work completed was carried out in accordance with regulatory requirements, Good Manufacturing Practices (cGMP) and Standard Operating Procedure
Operations Batch Review Specialist The Operations Batch Review Specialist is responsible for reviewing batch documentation post execution to ensure that all work completed was carried out in accordance with regulatory requirements, Good Manufacturing Practices (cGMP) and Standard Operating Procedure
Operations Batch Review Specialist The Operations Batch Review Specialist is responsible for reviewing batch documentation post execution to ensure that all work completed was carried out in accordance with regulatory requirements, Good Manufacturing Practices (cGMP) and Standard Operating Procedure
Operations Batch Review Specialist The Operations Batch Review Specialist is responsible for reviewing batch documentation post execution to ensure that all work completed was carried out in accordance with regulatory requirements, Good Manufacturing Practices (cGMP) and Standard Operating Procedure
Category Nursing Job Family Remote / Work from Home / Virtual / Hybrid Department Clinical Doc Improvmnt Schedule Full-time Facility Castleway / Castleton Office Park Castleway Drive Indianapolis , IN 46250 United States Shift Day Job Hours Flexible shift Monday - Friday, but required to start by 10
At Endress+Hauser, progress happens by working together. As the global leader in measurement instrumentation, our ~17,000 employees shape the future in the field of process automation. Whether developing and realizing new technology as a team, collaborating to build instrumentation, or strengthening
Working closely with the QA Batch Manager, the Senior QA Specialist will be instrumental in supporting major QA programs related to batch review, disposition and continuous improvement. They will also be key in championing and developing the organization’s Quality Mindset, and culture of efficiency,
Full timeOn-site
1 months ago
Estimated salary for Batch Documentation in Indianapolis
$40,000 – $63,000/year
Estimation confidence: Low
Estimate based on market data for Indianapolis. Actual salaries may vary depending on experience, company, and area.