Recipharm är ett ledande CDMO-företag (Contract Development and Manufacturing Organisation) inom läkemedelsindustrin och har cirka 6000 anställda. Recipharm erbjuder tillverkningstjänster av läkemedel i olika former, produktion av material till kliniska prövningar och API:er, samt farmaceutisk produktutveckling.
Recipharm tillverkar flera hundra olika produkter åt såväl stora läkemedelsföretag som mindre utvecklingsbolag. Bolaget omsätter cirka 6 miljarder kronor och har utvecklings- och tillverkningsanläggningar i Frankrike, Indien, Israel, Italien, Portugal, Spanien, Storbritannien, Sverige, Tyskland och USA med huvudkontor i Stockholm, Sverige. Recipharms B-aktie (RECI B) är noterad på Nasdaq Stockholm.
För mer information besök http://www.recipharm.com
Recipharm tillverkar flera hundra olika produkter åt såväl stora läkemedelsföretag som mindre utvecklingsbolag. Bolaget omsätter cirka 6 miljarder kronor och har utvecklings- och tillverkningsanläggningar i Frankrike, Indien, Israel, Italien, Portugal, Spanien, Storbritannien, Sverige, Tyskland och USA med huvudkontor i Stockholm, Sverige. Recipharms B-aktie (RECI B) är noterad på Nasdaq Stockholm.
För mer information besök http://www.recipharm.com
Quality Assurance Manager Recipharm (HQ)
Spännande uppdrag hos ledande kontraktstillverkare i tillväxt med en attraktiv kultur
Company: Recipharm AB (publ)
Global Headquarter: Drottninggatan 29, 101 32 Stockholm, Sweden
Role: Quality Assurance Manager – Auditor within Corporate Quality Management
Reporting to: Director Quality Management (based in Stockholm/HQ)
Place of position: Prio 1: Stockholm area (inclusive Uppsala/Mälardalen) with the opportunity to frequent commuting to the Global Headquarter, Drottninggatan 29, central Stockholm
Prio 2: Skåne or Gothenburg/Västra Götaland (Sweden)
The role as Quality Assurance Manager
Recipharm is a growing company with an increasing demand for our services. Consequently, the company is now looking for a Quality Assurance Manager- Auditor who can strengthen our team for Recipharm Corporate Quality Management Group. The job holder will report to the Director, Quality Management based at the Recipharm Global Headquarters in central Stockholm
The QA Manager will have the responsibility to plan and perform quality audits on suppliers and contract holders to Recipharm globally. In addition to this the QA Manager will have the responsibility to work with global quality agreements for suppliers and global procedures within our responsibilities.
The QA Manager will also further lead GMP training, assist in quality related issues and follow current Good Manufacturing Practice trends and guidelines. All parts of the job are done in near cooperation with Recipharm subsidiaries.
The new QA Manager is a key member of the QA department with 5 QA colleagues who are based in Sweden (3), Europe (2) and India (1). The team has frequent contact for support, updates and best practise sharing. There are regular team meetings and physical team gatherings two times a year.
The job involves travelling both within and outside Europe (mainly in Europe and to USA/Asia).�
Opportunities with the role
If you are a person that is passionate about supplier management and quality and wants to have an independent and flexible role within one of the leading CDMO (Contract Development and Manufacturing Organisation) in the pharmaceutical industry, this is an excellent opportunity for you.
You will have the opportunity to work in a fast growing, entrepreneurial and highly decentralised Swedish company with Headquarters in a modern office facility in central Stockholm.
You will have the opportunity to plan and execute your tasks in an independent and flexible way together with your colleagues from Europe and India (working from the office, home office, affiliates and during travelling).
You will have the opportunity to work internationally with different cultures, profiles and environments
You will join a professional QA team with a pleasant culture and collaboration. This in a growing entrepreneurial company with an informal and personal atmosphere where each employee's contribution is important for the company's development and results.
Profile
Required Qualifications and Skills
• Academic education with alignment towards natural science, e.g. Pharmacy, Chemistry etc.; could also be compensated with documented experience in the relevant field
• Substantial experience from manufacturing (GMP) of pharmaceuticals (for instance QA, QC, Supplier management, Supplier quality, QA logistics or similar positions)
• Earlier work experience of audits is meritorious
• Experience from working with suppliers is an advantage
• IT skills, proficient with Microsoft Office products
• Very good in English, both speaking and writing
Professional and Personal Competences
• Driven and solution-oriented personality with the ability to independently initiate, plan, accomplish and follow up on audits in a structured and effective manner (solid Project Manager)
• Solid communicator, with presentation and intercultural skills
• Ability to analyse data and translate outcome to actions and clear recommendations
• Well-developed interpersonal and relation building skills
• Dynamic and flexible personality who adapts to- and enjoys development and change
Contact
For inquires, applications and more information about the QA Manager position, please contact:
Magnus Klingberg or Jenny Ringh, Recruitment consultants at PeakSearch.
magnus.klingberg@peaksearch.se, +46 (0) 8 545 00 100, +46 (0)70 678 09 92
jenny@peaksearch.se, +46 (0) 8 545 00 100 +46 (0)70 235 81 99
http://www.peaksearch.se
Global Headquarter: Drottninggatan 29, 101 32 Stockholm, Sweden
Role: Quality Assurance Manager – Auditor within Corporate Quality Management
Reporting to: Director Quality Management (based in Stockholm/HQ)
Place of position: Prio 1: Stockholm area (inclusive Uppsala/Mälardalen) with the opportunity to frequent commuting to the Global Headquarter, Drottninggatan 29, central Stockholm
Prio 2: Skåne or Gothenburg/Västra Götaland (Sweden)
The role as Quality Assurance Manager
Recipharm is a growing company with an increasing demand for our services. Consequently, the company is now looking for a Quality Assurance Manager- Auditor who can strengthen our team for Recipharm Corporate Quality Management Group. The job holder will report to the Director, Quality Management based at the Recipharm Global Headquarters in central Stockholm
The QA Manager will have the responsibility to plan and perform quality audits on suppliers and contract holders to Recipharm globally. In addition to this the QA Manager will have the responsibility to work with global quality agreements for suppliers and global procedures within our responsibilities.
The QA Manager will also further lead GMP training, assist in quality related issues and follow current Good Manufacturing Practice trends and guidelines. All parts of the job are done in near cooperation with Recipharm subsidiaries.
The new QA Manager is a key member of the QA department with 5 QA colleagues who are based in Sweden (3), Europe (2) and India (1). The team has frequent contact for support, updates and best practise sharing. There are regular team meetings and physical team gatherings two times a year.
The job involves travelling both within and outside Europe (mainly in Europe and to USA/Asia).�
Opportunities with the role
If you are a person that is passionate about supplier management and quality and wants to have an independent and flexible role within one of the leading CDMO (Contract Development and Manufacturing Organisation) in the pharmaceutical industry, this is an excellent opportunity for you.
You will have the opportunity to work in a fast growing, entrepreneurial and highly decentralised Swedish company with Headquarters in a modern office facility in central Stockholm.
You will have the opportunity to plan and execute your tasks in an independent and flexible way together with your colleagues from Europe and India (working from the office, home office, affiliates and during travelling).
You will have the opportunity to work internationally with different cultures, profiles and environments
You will join a professional QA team with a pleasant culture and collaboration. This in a growing entrepreneurial company with an informal and personal atmosphere where each employee's contribution is important for the company's development and results.
Profile
Required Qualifications and Skills
• Academic education with alignment towards natural science, e.g. Pharmacy, Chemistry etc.; could also be compensated with documented experience in the relevant field
• Substantial experience from manufacturing (GMP) of pharmaceuticals (for instance QA, QC, Supplier management, Supplier quality, QA logistics or similar positions)
• Earlier work experience of audits is meritorious
• Experience from working with suppliers is an advantage
• IT skills, proficient with Microsoft Office products
• Very good in English, both speaking and writing
Professional and Personal Competences
• Driven and solution-oriented personality with the ability to independently initiate, plan, accomplish and follow up on audits in a structured and effective manner (solid Project Manager)
• Solid communicator, with presentation and intercultural skills
• Ability to analyse data and translate outcome to actions and clear recommendations
• Well-developed interpersonal and relation building skills
• Dynamic and flexible personality who adapts to- and enjoys development and change
Contact
For inquires, applications and more information about the QA Manager position, please contact:
Magnus Klingberg or Jenny Ringh, Recruitment consultants at PeakSearch.
magnus.klingberg@peaksearch.se, +46 (0) 8 545 00 100, +46 (0)70 678 09 92
jenny@peaksearch.se, +46 (0) 8 545 00 100 +46 (0)70 235 81 99
http://www.peaksearch.se