Job Title: Cleaning Validation Analyst
Location: Onsite in Swindon
FTE: Full time
Start date: ASAP
Contract Length: 12 Months with an high chance of extension
Planet Pharma is collaborating with a leading global healthcare company that provides specialized services to the pharmaceutical, biotechnology, and consumer health industries. This organization excels in the development, manufacturing, and delivery of drugs, biologics, and consumer health products.
We are seeking a Cleaning Validation Analyst to join their team. In this role, you will be responsible for swabbing production equipment and analyzing samples in accordance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) procedures.
Full training will be provided, and you will have the opportunity to work closely with an experienced scientist to support you in the execution of tasks.
Key Responsibilities:
* Perform swabbing of production equipment and sample analysis, adhering to GMP and GLP standards.
* Utilize laboratory equipment and techniques, such as balances, pH meters, and HPLC (High-Performance Liquid Chromatography), for analysis.
* Work within an active pharmaceutical manufacturing and laboratory environment, ensuring compliance with relevant GMP standards for each area.
* Handle controlled documentation, including the printing of documents, and understand and implement written instructions accurately.
* Conduct analytical tasks with a high accuracy rate, aiming for "Right First Time" results.
* Manage daily tasks with supervision and guidance, ensuring that the correct specifications and testing methods are followed, including validation protocols.
* Complete assigned tasks within the specified timeframes.
* Maintain clean and organized laboratory spaces following 5S principles.
* Ensure compliance with GMP, including adherence to Standard Operating Procedures (SOPs), archiving, and completing ComplianceWire tasks.
* Follow Environmental, Health, and Safety (EH&S) protocols, ensuring all activities are performed in line with defined risk assessments and COSHH (Control of Substances Hazardous to Health) guidelines.
Requirements:
* Experience with cleaning validation or validation within a GMP/GLP environment.
* Using techniques such as Balances, pH meter, HPLC.
If you would like to discuss this vacancy further or to discuss your career options in confidence, please email me on: folubodun@planet-pharma.co.uk
If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help!
About Planet Pharma
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognized by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency.
We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.