Senior QA Specialist

Oxford Global Resources; Dublin; On-site; EUR 90,000 - 120,000; Full time

Benefits offered by this job

Health insurance

Pension contributions

Paid holidays

Job summary

Oxford Global Resources in Dublin is seeking an experienced QA professional to lead quality assurance activities supporting new products, facilities and process changes in a cGMP environment. The role collaborates with Technical Services, Engineering, Manufacturing and QC to ensure compliant release of materials.

You will review validation, qualification and regulatory documents, manage deviations and CAPAs, and support internal and external audits.

Qualifications

• Minimum 6–8 years in pharma QA/quality environment.
• Strong knowledge of cGMP for manufacturing and/or packaging.
• Experience with sterility assurance and GMP management in pharma/biopharma.
• Excellent accuracy and attention to detail.
• Proficient in QA documentation, audits and regulatory inspections.

Responsibilities

• Provide QA oversight for new product introductions and facility qualifications.
• Review and approve qualification/validation documents for facilities, equipment and processes.
• Support deviations investigations, CAPAs and change controls.
• Coordinate GMP document reviews and finished product release activities.
• Interact with cross-functional teams (Operations, Engineering, QC, QA, Facilities, IT).

Skills

cGMP

QA Oversight

Regulatory liaison

Analytical testing

Documentation

Education

BSc in science/pharmacy

Tools

Delta-V

Veeva Vault

Job description

Are you interested in progressing your career in life sciences? Are you ready to challenge yourself and join a global leader in pharmaceutical manufacturing? Are you an experienced QA professional with a background in analytical / QC environments or NPIs / Tech Transfers? Don't hesitate, this could be the perfect opportunity for you!

Job Description

The position is responsible for delivery of quality assurance activities at the company's Dublin location to ensure new products, facilities, equipment, technologies and other continuous improvements are introduced and manufactured in accordance with cGMP, Corporate and Regulatory requirements.

The successful candidate executes the site QA activities in order to protect the safety, quality and efficacy of our products, thereby ensuring the availability of correct, safe product for our Patients, and assuring the security of the company's business and global markets. This key role must ensure effective interaction with other departments and locations regarding GMP Document review and finished product releases. In particular, this will involve partnering with major stakeholders such as Technical Services, Engineering, Manufacturing, QC, QPs and Planning to optimize patient supply.

Key Responsibilities

• Quality Oversight for new product introduction in Bulk Drug Substance facility
• Quality oversight for new or modified facilities, equipment, technologies, including analytical, as well as other continuous improvements and requalifications
• Site QA responsibility to provide technical expertise for all QA and compliance topics / issues relating to the company's manufacturing Facility
• Review and Approve project documents involving cross-functional, multi-departmental teams including: Operations, Process Engineering, Quality Control, Quality Assurance, Facilities, Equipment and others
• Review and approval of qualification/verification/validation documents for facilities, equipment, processes, analytical methods, suppliers, software and others. (e.g. URS, Facility, Utility, IT Systems, Test Methods, and Equipment validations) to ensure compliance with current regulatory expectations, EU, FDA and Corporate Standards and Internal Procedures
• Quality oversight on operations and technical services to review and approve process descriptions , sampling plans, operational procedures, process validation and cleaning validation documents
• Review and Approve TRA's, MSRs, SAP requests related to new products
• QA review all analytical facility, equipment and method qualifications and validations
• Ensure all Materials are sampled and released as per the approved specifications and procedures
• Investigation and approval of deviations generated encountered during qualification/validation testing
• Participation in the project change control program and deviations for modifications to new and existing systems, processes and equipment
• Provide guidance to project teams on Quality regulations for validation strategy and approach
• Performs timely review of documentation/investigations/reports highlighting and assisting in the resolution of issues commensurate with the level of risk
• Ensures schedules for review and approval of GMP documents are maintained to meet the needs of Commercial Operations groups
• Provide sound QA and Compliance support to manufacturing, engineering, automation, utilities, supply chain, material movement and laboratories
• Provide support for deviation investigations, including root cause analysis, and corrective & preventative action (CAPAs) proposals and initiatives
• Actively support audit readiness activities and regulatory agency and internal audits.

Key Requirements

• A minimum of 6-8 years relevant experience within the pharma industry or a related field
• Strong knowledge of cGMP requirements for pharmaceutical manufacturing and/or packaging required
• Experience of sterility assurance for drug products and in manufacturing processes for pharmaceutical products and processes strongly desirableDirect experience of GMP management within a pharma/biopharma company is essential, and will include exposure to FDA, HPRA/EMA or other authorities of similar standing
• Excellent accuracy and attention to detail
• Good knowledge of relevant computer packages e.g. Delta-V, Veeva Vault or similar
• Planning and organizing skills are required to plan, execute and track commitments of Quality Assurance and to adjust to changing priorities
• High level technical skills including analytical, auditing, pharmaceutical manufacturing and regulatory inspection management. Technical writing skills required. Previous QA experience aligned to Technical Services, Engineering/CQV reviews, operational (batch records, procedures), supplier qualification, packaging lines, warehousing (including temperature mapping of, along with fridges and freezers) and QC analytical qualifications/validations and laboratories of particular interest
• Excellent interpersonal skills are required, as is the ability to communicate well, both verbally and written
• The individual in this position is expected to represent the company's pharmaceutical interests, objectives and policies in a responsible and professional manner
• Third level qualification e.g. B.Sc. in science/pharmacy or equivalent with a minimum of 6-8 years' experience in cGMP Quality environment; or equivalent combination of education and experience.

Benefits

• Competitive and attractive employee compensation package
• Pension contributions
• Health insurance
• Paid holidays

Location

Dublin | Ireland

Desired Skills and Experience

• A minimum of 6-8 years relevant experience within the pharma industry or a related field.
• Strong knowledge of cGMP requirements for pharmaceutical manufacturing and/or packaging required.
• Experience of sterility assurance for drug products and in manufacturing processes for pharmaceutical products and processes strongly desirable.
• Direct experience of GMP management within a pharma/biopharma company is essential, and will include exposure to FDA, HPRA/EMA or other authorities of similar standing.
• Excellent accuracy and attention to detail
• Good knowledge of relevant computer packages e.g. Delta-V, Veeva Vault or similar
• Planning and organizing skills are required to plan, execute and track commitments of Quality Assurance and to adjust to changing priorities.
• High level technical skills including analytical, auditing, pharmaceutical manufacturing and regulatory inspection management. Technical writing skills required. Previous QA experience aligned to Technical Services, Engineering/CQV reviews, operational (batch records, procedures), supplier qualification, packaging lines, warehousing (including temperature mapping of, along with fridges and freezers) and QC analytical qualifications/validations and laboratories of particular interest.
• Excellent interpersonal skills are required, as is the ability to communicate well, both verbally and written.
• The individual in this position is expected to represent the company's pharmaceutical interests, objectives and policies in a responsible and professional manner.
• Third level qualification e.g. B.Sc. in science/pharmacy or equivalent with a minimum of 6-8 years' experience in cGMP Quality environment; or equivalent combination of education and experience.