Offer summary

Qualifications:

1-2 years of regulatory CMC experience, Experience in pharmaceuticals or biotech, Understanding of pharmaceutical product lifecycle, Experience preparing regulatory documentation, Organized and self-motivated individual.

Key responsabilities:

Write regulatory CMC documentation for quality

Ensure accuracy and regulatory compliance of documents

Act as client liaison and represent ProPharma

Manage multiple projects and meet deadlines

Collaborate with cross-functional teams for success

Job description

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 worlds 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 RD 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.

The Regulatory Sciences Officer, Lifecycle Management has responsibilities and inputs into the following core areas:
Client Experience
Regulatory Affairs Activities (strategic operational)
Contracts and Time Management
Finance Invoicing
Quality Team performance metrics
Training

Responsibilities:

Regulatory CMC writing of pharmaceutical quality documentation (CTD-Modules 2.3 3, IMPD, ASMF).
Ensure all regulatory documents are accurate and comply with relevant regulations.
Act as a client liaison and represent ProPharma in a professional and effective manner.
Coordinate and manage multiple projects simultaneously while ensuring deadlines are met.
Collaborate with cross-functional teams and stakeholders to ensure project success.

Requirements:

1-2 years of regulatory CMC experience working in the biotech or pharmaceutical industry.
Experience working across different projects concurrently.
Understanding of the pharmaceutical product life cycle.
Experience in preparing documentation for regulatory authorities.
Organised, proactive and self-motivated individual with a keen eye for detail, ability to prioritise tasks effectively and ability to delegate to team members.

Lifelancer ( https://lifelancer.com ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech, data science and IT domains.

Please use the below Lifelancer link for job application and quicker response.

https://lifelancer.com/jobs/view/19a1489d71aa73fad47d59c9521b6cc5

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