For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
We are currently looking to collaborate with an experienced Freelance Technology Transfer Project Manager to support us on an exciting challenge with a key client within the Pharmaceutical sector (small molecules) which can be remotely performed from Germany. For this position, we require the successful applicant to be able to offer approx. 4 hours per week availability; work on the project for at least 3 months in duration and ideally have immediately availability.
Key responsibilities include:
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Managing our client’s Technology Transfer process/program for small molecules.
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Write, review analytical and process validation protocols.
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Write and review regulatory documents.
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Support the project management in EU.
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Preparing and executing validation documents.
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Understanding the hours budgeted for completion of each task on a specific.
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Individuals must represent the company and division at client sites and interact confidently with clients, contractors, management, and peers.
Qualifications
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Qualified candidates will possess a Bachelor’s degree in a related field or above
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Must have demonstrated exposure working on Technology transfers with small molecules
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Fluency in English and German is a must
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Have the ability to fulfil the requirements set out in the job spec
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Candidates must have excellent verbal communication and technical writing skills.
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Familiarity with many aspects of validation is expected.
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Proficient in Microsoft Word, Excel, PowerPoint.
Additional information
All candidates must be legally eligible to work Germany and ideally based there already.
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***