*Quality Control Analyst - Dartford - Top CDMO globally*
Location:
Onsite in Dartford
Start date:
ASAP
Work Arrangement:
Site-based (no remote work)
Type of position:
Freelance. Minimum 6 month contract with the view to extend
Job Description
Planet Pharma are
global contract development and manufacturing organization (CDMO)
that works with pharmaceutical, biotech, and consumer health companies to help develop, manufacture, and supply medicines. They're one of the biggest players in the industry and are heavily involved in
clinical packaging, commercial manufacturing, drug delivery technologies, and supply‑chain services
.
Job responsibilities:
Quality Control Analyst responsible for performing analytical testing to support smooth and compliant production operations. This role involves conducting in‑process and composite sample analysis, reviewing and approving QC data for release, and ensuring all work aligns with GMP and EHS standards. The position requires strong analytical capability, accurate documentation, method development support, and the preparation of technical reports for internal and external stakeholders.
Key Responsibilities
* Conduct Quality Control testing on in‑process and composite samples using defined analytical methods and Standard Operating Procedures.
* Perform analytical work within agreed timelines while ensuring full compliance with GMP and Environmental Health and Safety (EHS) requirements.
* Review, approve, and report QC data to support product release, ensuring accuracy, efficiency, and adherence to cGMP standards.
* Carry out a range of analytical techniques including particle size analysis, cleaning verification, FTIR, DSC, surface area analysis, and identification testing.
* Support method development and validation activities, including cleanability assessments, troubleshooting, optimisation, and technology transfer.
* Ensure all documentation is accurate, legible, and clearly presented in accordance with cGMP expectations.
* Prepare test methods for particle size and cleaning verification analysis.
* Generate analytical test reports such as Statements of Results, Certificates of Analysis, and Cleaning Certificates for internal teams or external clients.
Requirements:
* Completed training in PTA, CTA, PCA, MFA or equivalent pharmaceutical administrative/technical roles
* Practical hands‑on experience in quality control for pharmaceuticals and packaging materials
* Strong command of English, both written and verbal
* Highly detail‑oriented with the ability to work independently and accurately
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.