QC Compliance Officer at LM Manufacturing LTD
NN4, , United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

12 Nov, 25

Salary

30000.0

Posted On

12 Aug, 25

Experience

7 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Investigation, Interpersonal Skills, Project Management Skills, Root, Control Environment

Industry

Pharmaceuticals

Description

JOB DESCRIPTION FOR LABORATORY – QUALITY CONTROL COMPLIANCE OFFICER

Quality Control Compliance Officer ensures that laboratory operations comply with regulatory standards, internal policies, and quality systems. This position plays a pivotal role in dealing investigations related to non-conformances, maintaining data integrity, preparing for audits, and ensuring that all testing activities meet required guidelines.

QC Compliance officer, eligibility criteria and skills requirement:

  • Degree level qualification in a relevant field.
  • Approximate 7-10 years of experience in Pharmaceutical Quality Control environment.
  • Excellent knowledge of cGMP and Quality Management Systems.
  • Flexible to work between various shifts according to business requirement.
  • Knowledge on root cause analysis techniques.
  • Experienced in investigation report writing preferred.
  • Proficiency in risk-based problem-solving.
  • Strong communication and interpersonal skills.
  • Effective project management skills and computer literature.
Responsibilities
  • Lead or support investigations into out-of-specification (OOS), out-of-trend (OOT), or other non-conformances e.g., laboratory incidents, deviations, complaints, and recalls.
  • Ensure root cause analysis is properly conducted and documented.
  • Implement and track corrective and preventive actions (CAPAs).
  • Monitor laboratory activities to ensure compliance with applicable regulations (e.g., FDA, MHRA, cGMP, GLP).
  • Stay current with changes in regulatory requirements and update procedures accordingly.
  • Support and manage regulatory inspections and internal/external audits.
  • Review and approve laboratory documentation (e.g., SOPs, record of analysis, deviations, change controls).
  • Ensure proper documentation practices (GDP) are followed.
  • Maintain compliance-related documentation and ensure data integrity.
  • Develop, review, and update standard operating procedures (SOPs)
  • Coordinate and deliver training related to compliance topics, SOPs, and regulations.
  • Identify areas for improvement and ensure follow-up actions are taken and implemented on time.
  • Support continuous improvement initiatives and quality risk management.
  • Monitor and report on key quality indicators (e.g., deviations, CAPAs, audit findings).
  • Collect quality metrics data and prepare summaries to deliver to senior management.
    Job Types: Full-time, Temp to perm
    Contract length: 3 months
    Pay: Up to £30,000.00 per year
    Work Location: In perso
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