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

Lead BIS Operations - Site Manager

Job Description

Job Title Lead BIS Operations – Site Manager Role Summary Lead and manage day‑to‑day IT operational activities across multiple campus sites, ensuring high‑quality desktop, infrastructure, and base‑building support. Oversee on‑site support teams, coordinate with external vendors, and drive continuous improvement in service delivery within a regulated life‑sciences environment. Expectations - Maintain operational reliability during rapid campus expansion. - Deliver fast, effective user support and uphold service level targets. - Implement and enforce ITIL/ITSM best practices. - Foster strong relationships with users, vendors, and internal stakeholders. Key Responsibilities - Supervise on‑site support staff and external contractors across all buildings. - Manage desktop technology, base‑building IT systems, and related infrastructure. - Resolve incidents, implement proactive maintenance, and ensure system stability. - Coordinate equipment procurement, installation, and upgrades with vendors. - Develop and refine scalable support processes and documentation. - Ensure compliance with regulated industry standards (e.g., GMP, GLP). - Monitor and report on key performance metrics and improvement initiatives. Required Skills - 10+ years of hands‑on IT operations and support experience, including leadership. - Proven experience in a highly regulated life‑sciences or biotech setting. - Deep knowledge of desktop environments, infrastructure support, and multi‑site management. - Expertise in ServiceNow, ITIL, ITSM processes, and change management. - Strong leadership, mentorship, and team‑building capabilities. - Excellent stakeholder engagement and communication skills. - Energetic, proactive, and solution‑orientated mindset. - Dutch language proficiency preferred (French acceptable). Required Education & Certifications - Bachelor’s degree in Computer Science, Information Technology, or related field (or equivalent practical experience). - ITIL Foundation or equivalent ITSM certification. - ServiceNow Certified Administrator or similar platform certification.

Ghent, Belgium

On site

Senior

06-11-2025

Company Name

Planet Pharma

Job Title

Consumer Engagement Strategist

Job Description

Job Title: Consumer Engagement Strategist Role Summary: Lead strategy, content, and optimisation of regional consumer websites across Northern Europe to deliver compliant, engaging, and data‑driven digital experiences. Expactations: Deliver cross‑market web projects on schedule, collaborate with creative agencies and internal teams, and turn consumer insights and analytics into continuous performance improvements. Key Responsibilities: - Define and execute the regional website strategy and roadmap, aligning global objectives with local market needs. - Plan, create, and optimise content, including global templates and localized campaigns. - Coordinate with creative agencies to localise marketing assets and develop consumer‑first content. - Drive SEO, web analytics, and performance monitoring to increase visibility and engagement. - Ensure compliance with legal, medical, IT, and regulatory requirements in partnership with cross‑functional stakeholders. - Oversee content governance, quality assurance, and innovation initiatives. - Use data insights to identify opportunities for UX improvements and new digital initiatives. Required Skills: - 3+ years in digital marketing, website management, or consumer engagement roles. - Proven expertise in website content strategy, SEO, and UX optimisation. - Strong project management and cross‑market delivery experience. - Ability to collaborate effectively with agencies, marketing, medical, legal, IT, and compliance teams. - Data‑driven mindset with experience analysing web metrics and consumer behaviour. - Excellent communication and stakeholder management skills. Required Education & Certifications: - Bachelor’s degree in Marketing, Communications, Digital Media, or related field (or equivalent experience). - Certifications in web analytics, SEO, or digital project management preferred.

Hampshire, United kingdom

Hybrid

13-11-2025

Company Name

Planet Pharma

Job Title

Contract CMC Statistician

Job Description

**Job title** Contract CMC Statistician **Role Summary** Provide statistical expertise for continuous process verification, method, and equipment development in pharma CMC. Plan, design, analyze experiments, interpret results, and support decision‑making through evidence‑based statistics. **Expectations** * Deliver statistically sound analysis plans and reports within deadlines. * Communicate findings clearly to scientists and stakeholders. * Champion Quality by Design and Design Space concepts in statistical practice. **Key Responsibilities** 1. Prepare statistical analysis and modeling plans for CMC studies. 2. Design and execute experiments (DoE) for process, method, and equipment development. 3. Conduct statistical analyses using R, including generalized linear models, linear mixed models, and other appropriate methods. 4. Interpret analysis results and author concise reports. 5. Advise scientists on statistical design and interpretation, ensuring robust study outcomes. 6. Propose and implement statistical tools and solutions for recurring data needs. 7. Train and disseminate statistical best practices across the organization. **Required Skills** * Proficiency in R programming. * Strong knowledge of experimental data analysis, generalized linear models, and linear mixed models. * Experience with Design of Experiments (DoE). * Excellent written and verbal communication in English. * Analytical, critical, and independent thinking; strong problem‑solving and prioritization. **Desirable / Additional Skills** * Bayesian statistics. * Machine learning methods. * Understanding of biotechnology industry processes. * Knowledge of French or Dutch. **Required Education & Certifications** * Master’s or PhD in Statistics, Data Science, or life sciences/engineering with a statistical focus.

Brussels, Belgium

Hybrid

13-11-2025

Company Name

Planet Pharma

Job Title

Associate Scientist- Analytical Development and Quality Control

Job Description

**Job title:** Associate Scientist – Analytical Development and Quality Control **Role summary:** 12‑month contract supporting external analytical development and QC. Responsible for capturing, verifying, and standardizing assay performance data across platforms for early to late‑stage clinical programs. Provides data trending, dashboards, and reporting for stakeholders, supports SOP updates, and participates in method evaluation and analytical transfer/validation within a cGMP environment. **Expectations:** - Deliver precise, validated assay data for global testing network. - Communicate clear reports, dashboards, and summaries to stakeholders. - Enhance data pipelines, metadata standards, and trending workflows. - Ensure compliance with cGMP regulations and safe handling of biological/hazardous materials. **Key responsibilities:** - Capture, verify, and standardize assay performance data across platforms. - Interface with laboratory teams to refine data pipelines and improve metadata standards. - Produce dashboards and periodic reports for stakeholders; support SOP updates. - Verify analytical data for assay performance and assist with transfer/validation reports. - Contribute to analytical method evaluation as needed. - Maintain cGMP compliance and lab safety protocols. **Required skills:** - Hands‑on experience developing and executing analytical methods for biological products in a cGMP environment. - Critical evaluation of scientific documentation and testing data. - Proficiency in JMP, electronic documentation, and quality management systems. - Strong written and verbal communication; collaborative cross‑functional teamwork. - Excellent organization, attention to detail, creative and complex problem‑solving. - Ability to work safely with biological, infectious, and hazardous materials (PPE). - Proficiency in MS Office (Word, Excel, Outlook, Visio, PowerPoint). **Required education & certifications:** - Bachelor’s or Master’s degree in Chemistry, Biochemistry, Molecular & Cell Biology or related discipline. - 3–6+ years experience in an analytical laboratory setting, preferably in pharma/biotech (less required for advanced degree). - Knowledge of cGMP regulations for analytical testing, validation, and transfer. - Certifications in GMP or related quality systems preferred.

New haven, United states

On site

Junior

20-11-2025