Spezialisierte Personalberater für Ihre Branche

Our client is a Global leader in the pharmaceutical/ biotech industry. Currently hiring an Empower Analyst. Ideally we seek someone with a strong background in lab systems, who would like to work in an exciting start up environment.

The company is now at a pivotal point in their growth stage, where they are hiring more specialized skills to build on their current success.

The successful Empower Analyst will be the subject matter expert on Empower, working in a LACE boxes and a Citrix environment. This is a GxP manufacturing site for our client so a GMP/GDP background is ideal but an Lab systems background with demonstrable performance is key.

Empower Analyst Provide end to end Empower support and administration, including:

• Validation Support
• Change Control and Test Plan
• System Data Integrity Maintenance Support
• System Compliance Support
• Project Coordination
• Lab Administration Oversight
• Investigation Support
• Audit Response/Support
• Technical SME on Empower software
• System Repair
• Continuous Improvement
• Data Integration
• Advanced End-User Support/Training on Software
• Training
• Data Backup Configuration
• Configuration Specification
• SOP Authoring for Client approval
• Programing/Scripting

For further information please call Funmi Gbadamosi at NonStop Consulting INC on +1 617 420 4128 OR Send a copy of your Resume to [email protected]

My client is one of the fastest growing Biotech companies in Europe, they design and develop their own drugs and are know as one of the top employers in Ireland. They are currently looking for a Senior QA Validation Specialist in Cleaning.

Requirements:

My client is looking for outstanding people who are excited by a start-up environment, and recognise the opportunities that this offers and wants to be challenged, they offer great progression and development opportunities. If you have 5+ years of Cleaning validation experience within the Biotech/Pharmaceutical industry please do get in touch!

Job Tasks and Responsibilities

Responsible for all aspects of the Cleaning Validation programs on-site for a large scale Bio-pharmaceutical Drug Substance production facility.

• Generate, execute and/or review master and completed qualification and validation protocols, produce summary reports and associated data for conformance to regulations, SOPs, specifications and other applicable acceptance criteria.
• Analyse testing results
• Review, edit and approve deviation notifications, deviation investigations, and corrective actions.
• Review, edit and approve change controls, SOPs, reports and other documentation.
• Collaborate with other departments to resolve issues.
• Trains/advise other less experienced Specialists.
• Supervise, provide direction and assign work to Validations Specialists to meet goals and deadlines.
• Manage and drive projects
• Stay current with industry trends, regulatory requirement updates, and communicate updates to rest of team
• May manage full time employees

Skills and experience

• BS/BA in Engineering, Chemistry, or Life Sciences
• 5+ years of related experience within the field of Cleaning Validation in Bio-pharmaceutical, Aseptic Fill/Finish or API manufacturing
• Line-management experience
• Willingness to travel

What's in it for you?

Not only do you get the opportunity to work for one of the top rated employers in Ireland, who are leading the way in the Pharmaceutical/Biotech industry. My client is also offering fantastic progression and development opportunities.

To hear more about this opportunity simply click the apply now button now!

My client; one of the leading consultancies in Germany is currently recruiting for a Head of Eco-Toxicology. They offer exposure to an international network and great career opportunities. As well as the opportunity to work on a wide range of projects, allowing you to increase your knowledge and expertise within the field.

Your main responsibilities will include:

• Disciplinary and scientific leadership of the eco-toxicology section
• Prepare dossiers independently for the authorisation of agro-chemicals, biocides and other chemicals within the European Union according to current regulations
• Conduct first and higher tier risk assessments for active substances and related products with particular focus on eco-toxicological effects according to internationally agreed guidance and regulations
• Monitor contracted standard and higher tier eco-toxicological studies
• Review and evaluate eco-toxicological data, including published literature
• Prepare expert statements and position papers
• Manage projects and interact with international clients
• Participate in international conferences and workshops

Experience required:

• Degree (M.Sc., Dr.rer.nat. or Ph.D.) in biology, ecology, agricultural sciences or related disciplines
• At least 6 years of experience in regulatory eco-toxicology of agro-chemicals
• Excellent communication skills
• Group leadership experience would be expected
• Fluency speaking in English; German, French or another additional European language would be beneficial
• Careful, reliable and swift working style
• Self-motivated, flexible, open and well organised personality; able to work under pressure
• Eager to learn and establish a good working relationship with colleagues, clients and regulatory authorities

Next to excellent professional development opportunities, our client offers you competitive salary

For a confidential discussion about this role and to take a positive step in your career simply click the apply now button!

Job Summary:

My client is one of the largest CRO's and Consultancies in the world, they work with both small and large companies both within Europe as well as Internationally, they are looking to recruit a regulatory Eco-Toxicologist to their team. The role can be based at any of their offices across Europe and will offer a lot of variety as well as interesting projects to work on.

Requirements:

Job Tasks and Responsibilities

You will be responsible for managing a small Toxicology team, where you will be mentoring junior members of the team, this role also gives you the opportunity to work on a numerous interesting projects giving you a lot of variety while still keeping thinks challenging. There is a further possibility of stepping into management. This role will not just include a mixture of technical and management, but full business running from the recruitment of staff to growing the business.

Skills and experience

• Regulatory Eco-toxicologist
• Around 5 years of experience
• Strong Risk Assessment and Study Monitoring Experience
• Willingness to travel

What's in it for you?

Not only do you get the opportunity to work for one of the top rated employers in Ireland, who are leading the way in the Pharmaceutical/Biotech industry. My client are also offering fantastic progression and development opportunities.

To hear more about this opportunity simply click the apply now button now!

Regulatory Officer - REACH & (M)SDS

My client is dynamic privately owned chemical company that has grown from a one man operation to an international company with over 330 members of staff in 11 locations around the world. They specialise in Chemicals, additives & Silicone with a strong focus on customer led R&D.

Key Responsibilities:

• Maintaining (M)SDS, REACH compliance and registrations.
• Anticipate regulatory changes to ensure products are compliant
• Advise clients on regulatory product compliance

My client also offers the opportunity to work with and be fully trained in cosmetic registrations and food contact regulations, allowing you to diversify your knowledge and skills.

To Be Successful:

• A PHD in Chemistry
• 2+ years of experience in similar function
• Knowledge and experience within REACH compliance and/or SDS compliance is essential.
• Experience and knowledge of cosmetics and/or food a plus!

For more information on this position, please click the apply now button!