Pharma Document Reviewer: QC & Compliance Specialist

HS Hiring Solutions Inc; Muntinlupa; On-site; PHP 357,000 - 580,000; Full time

Benefits offered by this job

Performance Bonus

HMO

Job Training

Job summary

HS Hiring Solutions Inc in Muntinlupa is seeking a laboratory data reviewer for an on-site role requiring a Bachelor of Science in Chemistry or Microbiology and 1-3 years of experience in a pharmaceutical lab. The position emphasizes GMP, GDP, and SOP adherence with extensive data review in LIMS.

You will follow Training SOPs, perform document review, ensure accurate entry of results into LIMS, and participate in deviation and OOS handling, audits, and continuous improvement initiatives.

Qualifications

• Minimum Bachelor of Science degree in Chemistry or Microbiology or related science discipline is required, M.Sc is preferred.
• Minimum 2 years’ experience working in a pharmaceutical laboratory or company is required.
• Demonstrated understanding of cGMP regulations is required. Knowledge in compendiums such as USP, EP preferred, JP, BP are advantageous.
• Experience with LIMS, TrackWise Digital or any other QMS system is advantageous.
• Proficiency in Microsoft Office Suite (Word, Excel, and Outlook) is required.

Responsibilities

• Performs review and approval of data according to GDP, GMP and SOPs.
• Follows Training SOP for training records.
• Ensures QC records comply with methods and SOPs.
• Verifies all results entered into the LIMS.
• Audits record books and calibration docs.
• Issues deviations when SOPs are not followed.
• Notifies supervisor to initiate out-of-specification actions.
• Maintains training records per SOP and keeps binder current.

Skills

Communication skills

Time management

Attention to detail

Data interpretation

Learning agility

Education

Bachelor of Science in Chemistry or Microbiology

M.Sc preferred

Tools

LIMS

TrackWise Digital

QMS

Job description

HS Hiring Solutions Inc in Muntinlupa is seeking a laboratory data reviewer for an on-site role requiring a Bachelor of Science in Chemistry or Microbiology and 1-3 years of experience in a pharmaceutical lab. The position emphasizes GMP, GDP, and SOP adherence with extensive data review in LIMS.

You will follow Training SOPs, perform document review, ensure accurate entry of results into LIMS, and participate in deviation and OOS handling, audits, and continuous improvement initiatives.