Title: Preproduction Coordinator
Start date: ASAP
Duration: 12 months- With an high chance of extension or going permanent
FTE: Full time 5 Days/week
Location: Bathgate, Scotland
Company Summary
Our client is a global provider of advanced delivery technologies, development, and manufacturing solutions for drugs, biologics, and consumer health products. They operate across a wide range of sectors, including pharmaceuticals, biologics, over-the-counter (OTC) products, and dietary supplements. You will be part of a company that emphasizes innovation. Their focus on cutting-edge technologies and solutions in drug delivery and manufacturing can be exciting for those interested in working on the forefront of the industry. In addition they operate on a global scale, which can offer the chance to work with diverse teams and on international projects. This global presence can provide valuable exposure and experience in different markets and cultures.
Role Summary
This is a full time 12 months contract with a high chance of extension. We have several contractors in this team already and they love it there. Our contractors average 5 years with this client or they take them permanent.
In this role As the Preproduction Coordinator you will ensure the integrity of clinical trial supplies packaged on site. clinical trial packaging documentation to meet, Client, Study and Regulatory requirements. You will also complete documentation in accordance to relevant SOPs and to comply with GMP high quality standards ensuring all deviations are documented as required. Lastly you will participate in the implementation of any new systems or upgrades to systems pertaining to Preproduction department.
Essential Responsibilities
- Complete documentation in accordance to relevant SOPs and to comply with GMP.
- Maintain high quality standards ensuring all deviations are documented as required.
- Report to your Line Manager any issues which may impact on the quality or timelines specified for the packaging of supplies.
- Competently perform tasks as detailed by the Preproduction skills matrix.
- Participate in the implementation of any new systems or upgrades to systems pertaining to Preproduction department.
Key Requirements
- Pharma experience or education highly advantageous.
- Experience in GMP or GDP environment is essential
- Happy to be 100% onsite
- Can start within 2-4 weeks
If you would like to discuss this vacancy further or to discuss your career options in confidence, please contact Femi Olubodun via telephone on +44 (0) 2039288387 or email on: [email protected]
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.