MedPharm

Topical and transdermal drug delivery CDMO

QA Specialist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours

Full-timeGuildford, UKNo salary listedIn-person

About the Job

Requirements

A Bachelor's or Master's degree in a scientific discipline (for example, Pharmaceutical Sciences, Chemistry, or Biology), or equivalent industry experience; this is desirable but not essential.
At least 2 years of experience in a GMP-regulated pharmaceutical or biotechnology environment, preferably supporting investigational medicinal product manufacturing or clinical trial supply.
Experience working within a Quality Management System, including deviations, CAPAs, change controls, investigations, and audit responses.
Experience reviewing batch manufacturing records, manufacturing documentation, and quality data to support batch release and Qualified Person certification.
Experience supporting regulatory inspections, client audits, and internal audits in a GMP environment.
Working knowledge of GMP, GCP, and GLP regulations, including EU GMP requirements and clinical trial manufacturing expectations.
Understanding of Quality Management Systems, including deviation investigations, CAPA management, change control, and risk management processes.
Experience reviewing manufacturing and quality documentation, including batch records, specifications, protocols, and reports.
Ability to lead or support complex deviation investigations and root cause analysis activities.
Understanding of data integrity principles, including ALCOA+, and regulatory expectations for documentation and electronic systems.
Experience supporting audit readiness and inspection preparation in regulated pharmaceutical environments.
Ability to provide technical QA oversight and guidance to cross-functional teams including Production, Quality Control, and Research and Development.
Familiarity with electronic Quality Management Systems such as MasterControl or similar platforms.
Ability to prioritize multiple quality activities and work effectively in a fast-paced regulated environment.
Ability to mentor and support the development of junior QA personnel.
Ability to communicate quality requirements across departments in writing and verbally.
Project management and change control skills.
Ability to influence and drive adoption of new systems across multidisciplinary teams.
Ability to sit at a desk and use a computer regularly; occasionally stand, walk, bend, reach, and lift items up to 10 kg.
Highly organized.

Responsibilities

Raise, review, and manage Quality Management System records including deviations, change controls, CAPAs, investigations, complaints, and quality risk assessments.
Support timely progression and closure of quality records in accordance with internal procedures.
Ensure quality records are complete, scientifically justified, and compliant with regulatory expectations.
Support continuous improvement of Quality Management System processes.
Review and approve controlled documents, including SOPs, forms, protocols, reports, specifications, and quality records within the electronic Quality Management System.
Ensure documentation complies with Good Documentation Practice and ALCOA+ data integrity principles.
Maintain document control processes, including document issuance, revision, archival, and retention.
Support management of controlled templates and quality documentation.
Perform QA review of Batch Manufacturing Records before manufacture where applicable.
Review completed manufacturing documentation for completeness, accuracy, and compliance prior to Qualified Person certification.
Provide QA support during manufacturing activities as required.
Support review of manufacturing investigations and manufacturing deviations.
Escalate quality concerns where product quality or patient safety may be impacted.
Review Quality Control documentation, including specifications, analytical methods, sampling instructions, and protocols.
Support review of analytical investigations, including out-of-specification, out-of-trend, and atypical results.
Review laboratory documentation to ensure compliance with GMP, GLP, and internal procedures.
Support QA oversight of reference standards, retained samples, and stability documentation where applicable.
Perform QA review and disposition of starting materials, packaging materials, and finished products in accordance with approved procedures and delegated QA authority.
Support supplier qualification activities, including supplier assessments, audits, and technical agreements.
Support ongoing supplier performance monitoring.
Participate in internal self-inspections and supplier audits.
Support preparation for customer audits and regulatory inspections.
Assist with implementation and follow-up of audit observations and CAPAs.
Support inspection readiness activities across the site.
Ensure quality documentation and electronic records comply with applicable data integrity requirements.
Promote Good Documentation Practice throughout the organization.
Identify and escalate potential data integrity concerns.
Support implementation of Quality Assurance procedures across the organization.
Deliver or assist with GMP and Quality training where required.
Support maintenance of QA training records.
Act as GLP Archivist where applicable.
Coordinate archiving activities in accordance with company procedures and regulatory requirements.
Ensure records are retained and retrieved in accordance with approved retention schedules.
Identify opportunities to improve Quality Systems and regulatory compliance.
Participate in quality improvement projects.
Support implementation of new quality processes and systems.
Support quality metric reporting and trend analysis.
Build effective working relationships with internal departments, clients, and external service providers.
Maintain current knowledge of applicable GMP, GCP, GLP, and regulatory requirements.
Perform other duties appropriate to the position as requested by QA Management.

Position Summary
The QA Specialist provides Quality Assurance support for Investigational Medicinal Product (IMP) manufacturing and associated Quality Management Systems at MedPharm.
The role is responsible for supporting compliance with Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP), applicable regulatory requirements and internal quality procedures through the review of quality documentation, management of quality systems and QA oversight of manufacturing and laboratory activities.
The QA Specialist works closely with Production, Quality Control, Pharmaceutical Development and other departments to ensure quality systems remain effective, regulatory expectations are met, and products are manufactured and released in compliance with applicable legislation and client requirements.

Essential Functions

Quality Management System
- Raise, review and manage Quality Management System (QMS) records including deviations, change controls, CAPAs, investigations, complaints and quality risk assessments.
- Support timely progression and closure of quality records in accordance with internal procedures.
- Ensure quality records are complete, scientifically justified and compliant with regulatory expectations.
- Support continuous improvement of Quality Management System processes.
Documentation Control
- Review and approve controlled documents including SOPs, forms, protocols, reports, specifications and quality records within the electronic Quality Management System (eQMS).
- Ensure documentation complies with Good Documentation Practice (GDP) and ALCOA+ data integrity principles.
- Maintain document control processes including document issuance, revision, archival and retention.
- Support management of controlled templates and quality documentation.
Manufacturing QA Oversight
- Perform QA review of Batch Manufacturing Records (BMRs) before manufacture where applicable.
- Review completed manufacturing documentation for completeness, accuracy and compliance prior to QP certification.
- Provide QA support during manufacturing activities as required.
- Support review of manufacturing investigations and manufacturing deviations.
- Escalate quality concerns where product quality or patient safety may be impacted.
Laboratory QA Support
- Review Quality Control documentation including specifications, analytical methods, sampling instructions and protocols.
- Support review of analytical investigations including OOS, OOT and atypical results.
- Review laboratory documentation to ensure compliance with GMP, GLP and internal procedures.
- Support QA oversight of reference standards, retained samples and stability documentation where applicable.
Materials Management
- Perform QA review and disposition of starting materials, packaging materials and finished products in accordance with approved procedures and delegated QA authority.
- Support supplier qualification activities including supplier assessments, audits and technical agreements.
- Support ongoing supplier performance monitoring.
Audits and Inspections
- Participate in internal self-inspections and supplier audits.
- Support preparation for customer audits and regulatory inspections.
- Assist with implementation and follow-up of audit observations and CAPAs.
- Support inspection readiness activities across the site
Data Integrity
- Ensure quality documentation and electronic records comply with applicable data integrity requirements.
- Promote Good Documentation Practice throughout the organisation.
- Identify and escalate potential data integrity concerns.
Training
- Support implementation of Quality Assurance procedures across the organisation.
- Deliver or assist with GMP and Quality training where required.
- Support maintenance of QA training records.
Archiving
- Act as GLP Archivist where applicable.
- Coordinate archiving activities in accordance with company procedures and regulatory requirements.
- Ensure records are retained and retrieved in accordance with approved retention schedules.
Continuous Improvement
- Identify opportunities to improve Quality Systems and regulatory compliance.
- Participate in quality improvement projects.
- Support implementation of new quality processes and systems.
- Support quality metric reporting and trend analysis.
General
- Build effective working relationships with internal departments, clients and external service providers.
- Maintain current knowledge of applicable GMP, GCP, GLP and regulatory requirements.
- Perform other duties appropriate to the position as requested by QA Management

Key Relationships

Heads of Departments
Senior Management
Production
Pharmaceutical Development
Quality Control
External Contractors (including specialists)
Vendors/Suppliers
Qualified Persons
Contract Laboratories

Travel requirements:
None

Education and Experience

Bachelor’s or Master’s degree in a scientific discipline (e.g., Pharmaceutical Sciences, Chemistry, Biology, or related field) or equivalent industry experience desirable but not essential.
Minimum 2 years’ experience in a GMP-regulated pharmaceutical or biotechnology environment, preferably supporting IMP manufacturing or clinical trial supply.
Demonstrated experience working within a Quality Management System (QMS) including deviations, CAPAs, change controls, investigations and audit responses..
Experience reviewing batch manufacturing records (BMRs), manufacturing documentation and quality data to support batch release and QP certification.
Experience supporting regulatory inspections, client audits and internal audits in a GMP environment.

Knowledge, Skills, and Abilities

Strong working knowledge of GMP, GCP and GLP regulations, with good understanding of EU GMP requirements and clinical trial manufacturing expectations.
In-depth understanding of Quality Management Systems, including deviation investigations, CAPA management, change control and risk management processes.
Strong experience reviewing manufacturing and quality documentation, including batch records, specifications, protocols and reports.
Demonstrated ability to lead or support complex deviation investigations and root cause analysis activities.
Good understanding of data integrity principles (ALCOA+) and regulatory expectations for documentation and electronic systems.
Experience supporting audit readiness and inspection preparation within regulated pharmaceutical environments.
Ability to provide technical QA oversight and guidance to cross-functional teams including Production, QC and R&D.
Familiarity with electronic Quality Management Systems (eQMS) such as Master Control or similar platforms.
Strong written and verbal communication skills with the ability to communicate quality requirements across departments.
Ability to prioritise multiple quality activities and work effectively in a fast-paced regulated environment
Demonstrated ability to mentor and support the development of junior QA personnel.

Personal Attributes

Highly organised
Effective communicator able to translate technical concepts to non-technical users.
Strong project management and change control skills.
Able to influence and drive adoption of new systems across multidisciplinary teams

Physical Demands and Work Environment
While performing the duties of this job, there may be certain physical demands required for the position.

Regularly required to sit at a desk and use a computer
May occasionally be required to stand, walk, bend, or reach
Occasionally required to lift items up to 10kg, such as document boxes or computer equipment
Work is typically performed in a standard office environment

Other Duties
This job description describes the principal duties of the position but is not intended to be an exhaustive list of all responsibilities. Employees may be required to undertake additional duties appropriate to the role and level of responsibility.

Limitations and Disclaimer
The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. The Company is committed to making reasonable adjustments to the workplace to ensure the role is accessible to all candidates, including those with disabilities. To perform the job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently.

About the Company

MedPharm

Topical and transdermal drug delivery CDMO

MedPharm is a contract development and manufacturing organization focused on topical, transdermal, and mucosal drug delivery. It provides end-to-end services from formulation development through clinical and commercial manufacturing, including analytical testing and regulatory support, and operates proprietary delivery platforms such as MedSpray, MedTherm, and AquaRMed to enable multiple administration routes. The company combines contract research with a patent portfolio and offers lifecycle support across development and manufacturing, differentiating itself from competitors. A July 2024 merger with Tergus Pharma expanded capabilities to include hormone-based and highly potent drugs, enhancing scale and scope with the aim of helping pharma and biotech move products from early formulation to scalable manufacturing.

Company size: Not listed
Company stage: Grant
Total funding: $390K
Headquarters: Guildford, United Kingdom
Founded: 1999

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