Planet Pharma

About the Company

Founded in 2012, Planet Pharma has a dedicated team of seasoned professionals with extensive experience supporting the Life Sciences industry, specifically:
- Medical Device
- Pharmaceuticals
- Diagnostics
- Biotechnology
- CRO
- CMO
- Specialty Providers
- Labs/ Healthcare

Our goal is to create an organization that strengthens the employer-employee dynamic by connecting clients with talent — ultimately making staffing more personal and creating enduring, valuable relationships. We achieve this by leveraging cutting-edge technology and flexible service delivery models that enable us to provide personalized solutions for your business.

Planet Pharma has offices throughout North America, Europe, and APAC. All locations operate with shared attributes at the heart of everything we do!

We provide the following solutions:
- Contract Staffing
- Direct Hire
- SOW projects
- Retained Search
- Executive Search

Listed Jobs

Company Name

Planet Pharma

Job Title

Process Development Associate

Job Description

**Job Title:** Process Development Associate **Role Summary:** Supports the development, characterization, scale‑up, and manufacturing of upstream (cell culture) and downstream (purification) processes for early‑stage drug substance programs. Works within an integrated bioprocess team handling antibodies, BiTEs, oncolytic viruses, bispecifics, and siRNAs, applying platform methods and innovative solutions to advance clinical candidates. **Expactations:** - Collaborative team player with strong problem‑solving aptitude. - Ability to manage multiple projects and meet timelines. - Proactive in learning and applying both cell‑culture and purification techniques. - Attention to detail in data recording, analysis, and regulatory documentation. **Key Responsibilities:** - Design and execute bench‑scale experiments covering the full drug substance workflow (shake‑flask, bioreactor, filtration, chromatography). - Perform mammalian cell culture at various scales and purification runs at bench/pilot level. - Document experimental procedures and results in lab notebooks and electronic systems. - Analyze data, generate reports, and present findings to the development team. - Contribute to technical reports and regulatory filing support. - Participate in technology‑development initiatives aimed at process automation and continuous improvement. - Develop competency in both upstream and downstream processes to become a well‑rounded process development scientist. **Required Skills:** - Hands‑on experience with mammalian cell culture (shake flasks, bioreactors). - Familiarity with purification techniques (filtration, chromatography) at bench scale. - Strong analytical skills; ability to interpret data and troubleshoot experiments. - Excellent written and verbal communication for reporting and presentations. - Proficiency in laboratory documentation and basic data‑analysis software. - Ability to work independently and within cross‑functional teams. **Required Education & Certifications:** - Bachelor’s degree in Biochemistry, Chemical Engineering, Biotechnology, Molecular Biology, or a related scientific discipline (required). - Master’s degree or PhD in a relevant field is preferred. - Knowledge of GMP and regulatory documentation standards is advantageous. - No specific certifications required; however, relevant training in bioprocessing or cell‑culture techniques is a plus.

Thousand oaks, United states

On site

12-09-2025

Company Name

Planet Pharma

Job Title

QC Analyst - Chemistry & Stability

Job Description

**Job Title:** QC Analyst – Chemistry & Stability **Role Summary:** Perform analytical and stability testing in a GMP‑compliant Quality Control laboratory supporting the development and manufacturing of mRNA and biologic products. Generate high‑quality data for regulatory submissions and operate within a digital LIMS/AI‑enhanced environment. **Expectations:** - Hold a degree in Chemistry, Biology, or related science. - Demonstrate prior QC laboratory experience in pharma/biotech. - Apply strong knowledge of GMP, data integrity, and regulatory standards. - Exhibit proficient use of modern analytical instrumentation and digital lab systems. - Communicate effectively, solve problems, and support continuous improvement initiatives. **Key Responsibilities:** - Conduct hands‑on analytical testing using HPLC, UPLC, GC, UV, KF, DLS, etc. - Execute and manage stability studies, including sample pulls, data trending, and reporting. - Support material and product testing throughout the development lifecycle. - Prepare technical reports and contribute data to regulatory submissions. - Operate within LIMS and AI‑enabled QC platforms, ensuring data integrity. - Collaborate with cross‑functional teams, assist with lab operations, training, and process improvement. **Required Skills:** - Proficiency with HPLC/UPLC, GC, UV spectroscopy, KF, DLS, and related instruments. - Experience with LIMS and digital QC tools. - Strong analytical and problem‑solving abilities. - Excellent written and verbal communication. - Organizational skills and attention to detail. **Required Education & Certifications:** - Bachelor’s degree in Chemistry, Biology, or a related scientific discipline. - Knowledge of GMP; any relevant QC or analytical certifications is advantageous.

Oxford, United kingdom

On site

17-09-2025

Company Name

Planet Pharma

Job Title

Quality Control Associate

Job Description

**Job Title:** Quality Control Associate **Role Summary:** Focus on stability programme management, analytical chemistry, advanced instrumentation use, and regulatory submissions. Emphasis on GMP compliance, data integrity, and team mentoring. **Expectations:** - 5-7 years QC lab experience in pharma/biotech. - Proficiency in GMP, regulatory standards, and analytical techniques. - Ability to manage stability programs and support audits. **Key Responsibilities:** - Execute analytical testing (HPLC, UPLC, GC, KF, UV, DLS) for raw materials, in-process samples, and drug substances. - Oversee stability program execution, including sample pulls, data trending, reporting, and documentation. - Support regulatory submissions (FDA, EMA, ICH) and ensure GMP/GxP compliance. - Serve as subject matter expert during audits and inspections. - Mentor junior staff and optimize lab operations. **Required Skills:** - Advanced knowledge of analytical instruments (HPLC, UPLC, GC, etc.). - Regulatory compliance and electronic documentation expertise. - Problem-solving, organization, and technical writing for reports/submissions. - Fluent English (written and verbal). **Required Education & Certifications:** - Bachelor’s degree in Chemistry, Biology, or related scientific field. - Demonstrated understanding of GMP and ICH guidelines.

Oxford, United kingdom

On site

Mid level

18-09-2025

Company Name

Planet Pharma

Job Title

Cell Based Assay Scientist

Job Description

**Job Title:** Cell Based Assay Scientist **Role Summary** Conduct hands-on research to develop and execute immune cell-based assays for therapeutic discovery, focusing on immunological mechanisms and pathway analysis in a fast-paced, collaborative lab environment. **Expectations** Deliver rigorous scientific outcomes through translational assay design, data analysis, and project execution while adhering to regulatory standards and fostering scientific innovation. **Key Responsibilities** - Design, optimize, and execute immune cell assays (e.g., cytotoxicity, proliferation, MLR, antigen recall) for functional screening and mechanistic studies. - Analyze complex datasets using bioinformatics tools and troubleshoot experimental challenges. - Collaborate across interdisciplinary teams and present findings in cross-functional meetings. - Maintain detailed documentation and ensure compliance with HTA regulatory guidelines. - Uphold laboratory safety and contribute to a culture of scientific excellence. **Required Skills** - Expertise in immunology/cell biology and experience with Fc-mediated depletion techniques (ADCC, ADCP, CDC). - Proficiency in immune cell subset isolation (FACS/MACS) and multi-parameter flow cytometry. - Strong data analysis capabilities in tools like FlowJo, GraphPad Prism, Excel, or R. - Demonstrated project management skills to handle multiple priorities in a dynamic research setting. - Experience with primary human cells and HTA-compliant practices. **Required Education & Certifications** Bachelor’s/Master’s degree in Immunology, Cell Biology, or a related field; relevant postgraduate or industry research experience preferred. No specific certifications required.

London, United kingdom

On site

18-09-2025