Falkirk
On-site
GBP 40,000 - 60,000
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An established industry player is seeking a Quality Assurance professional to ensure compliance and quality in pharmaceutical processes. In this pivotal role, you will provide QA input on project activities, participate in quality investigations, and ensure adherence to cGMP standards. Your attention to detail and strong communication skills will be essential as you work collaboratively with cross-functional teams to resolve issues and prepare for regulatory audits. This is an exciting opportunity to contribute to the quality assurance of innovative pharmaceutical products in a dynamic environment.
- Experience in QA processes and documentation review.
- Strong analytical skills to identify issues and solutions.
- Provide QA input to project activities and documentation.
- Participate in quality investigations and CAPA development.
- Act as QA representative for new product introductions.
Attention to detail
Good communication skills
Good organisation skills
Ability to work effectively individually and as part of a team
Ability to analyse data
Problem-solving skills
Ability to prioritise workload
Ability to follow instruction accurately
Escalation skills
Key Roles and Responsibilities:- Provide QA input to project activities including review and approval of change requests, specifications, Standard Operating Procedures, Manufacturing Procedures and Analytical Procedures.
- Participate in quality related investigations, assist in the development and approval of effective CAPA in order to resolve production, audit and customer issues.
- Identify and escalate any identified cGMP areas of concern.
- Participate in validation activities including approval of protocols and reports for analytical methods, manufacturing processes, analytical / production / packaging equipment and cleaning procedures.
- Participate in the audits of suppliers, production and support functions as required.
- Be involved in the preparation for MHRA/FDA and other regulatory body audits.
- Review the relevant documentation relating to incoming raw materials and perform the disposition activities as required.
- Review manufacturing, laboratory and associated documentation prior to performing the relevant disposition of final products. Where potential issues exist, these are to be highlighted to the QA manager.
- Act as the QA representative for the introduction of new products, being a key member of the multi-functional team including R&D, QC and manufacturing thus ensuring that all cGMP documents are appropriate and all cGMP requirements are satisfied.
Competencies:- Attention to detail
- Good communication skills, both verbal and written
- Good organisation skills
- Ability to work effectively individually and as part of a team
- Ability to analyse data and information to make considered decisions
- The ability to identify root cause of problems to determine appropriate solutions
- Ability to prioritise workload to ensure timelines are met
- Ability to follow instruction accurately
- Ability to escalate issues as appropriate.