Qualified Person

Clinigen is a rapidly growing global specialty pharmaceutical services business with a unique combination of services across the pharmaceutical lifecycle.
We currently have over 1,000 employees headquartered in the UK with global offices in the US, EU (Belgium, Germany, France), Asia Pacific and South Africa.
Clinigen is growing rapidly and is positioned well for an exciting future of continued expansion.
To support our growth, we are seeking a diligent, detail-oriented and experienced Qualified Person on a part-time basis (2 days per week) to join our highly skilled and collaborative Quality team.
You will have oversight of business activities, relating to contract manufacturers, suppliers and technical due diligence activities.
In addition, the role includes the execution of the legal duties of a Qualified Person (QP) as defined under Directives 2001/83/EC and 2001/20/EC, in compliance with EudraLex Vol.
4 Annex 16 and Annex 13, the Rules and Guidance for Pharmaceutical Manufacturers and Distributors (the Orange Guide) as published by the MHRA, and any other applicable laws, guidelines, or regulations required by any group company.
Key responsibilities include:
To ensure that manufacturing activities at assigned CMOs are appropriately managed in accordance with EU GMP under directive 2003/94/EC and in compliance with EudraLex Vol.
4 Annex 16 and EudraLex Vol.
4 Annex 13, the Rules and Guidance for Pharmaceutical Manufacturers and Distributors (The Orange Guide) as published by the MHRA and any other applicable rule, guideline and legislation (or equivalent standards for overseas facilities)
To ensure that manufacturing activities relating to CTS services for IMPs manufactured and packed at overseas partner facilities are conducted in accordance with equivalent standards to those required by EU GMP
To ensure that the operations do not compromise the quality of medicines
To ensure that adequate records are maintained relating to the legal duties of the QP
To participate in the audit of the Clinigen quality system and to carry out independent audits of marketing authorisation holders necessary.
suppliers and partner facilities and processes
To ensure that appropriate standards of GDP and GMP are maintained
To employ due diligence in the discharge of his/her duties and to report to senior management and the MHRA any suspicious events of which he/she becomes aware.
To be named on site MIA licenses (currently MIA(IMP) only) and perform the legal duties of the QP in accordance with directives 2001/83/EC and 2001/20/EC and in compliance with EudraLex Vol.
4 Annex 16 and EudraLex Vol.
4 Annex 13, the Rules and Guidance for Pharmaceutical Manufacturers and Distributors (The Orange Guide) as published by the MHRA and any other applicable rule, guideline and legislation when called upon to do so.
Eligible to act as a QP under directive 2001/83/EC (preferably under the permanent provisions)
Experienced in aseptically produced sterile products and ideally lyophilized dosage form
Ideally, experience of QP certification for release of clinical trial materials under directive 2001/20/EC inclusive of dosage form manufacturing and clinical packing
Demonstrable business and commercial awareness combined with patient focus
Experience of working independently and as part of a team
Experience of working across multiple time zones and in global business cultures (particularly US and Japan)
Must also have knowledge of:
Directive 2001/20/EC as amended on the wholesale distribution of medicinal products for human use
Official Guidelines on GDP of medicinal products for human use
The conditions of the MIA for which he or she is nominated
The products traded under the licence and the conditions necessary for their safe storage and distribution
The categories of persons to whom products may be distributed
Be familiar with any changes that may be introduced into legislation and any variations that may be granted in respect of the licence for which he/she is named as RP
Comply with the expectations of their professional body in relation to CPD
Ideally have experience of the Quality Assurance and regulatory environment for the supply of unlicensed medicines used to support patient needs when a licensed medicine alternative is not available.
This could be in local or overseas countries.
Interested?
We would love to hear from you, please apply today for consideration.
#J-18808-Ljbffr