Position for Service Executive (instrumentation) in Chemistry

Highlights:

1. You will install, demonstrate, maintain and provide after sales service support for the consumables and accessories related to chromatography equipments.
2.  You will also be responsible for growing the AMC business, ensuring payment collection, sales lead generation.
3. Should be self motivated and professional
4. Required: B.E/ Diploma in Electronics
5. Experience: 2-4 years of service experience in the field of Analytical or Life Sciences or similar instrumentation systems.
6. Contact detailsIf your profile suits any of the above requirements email your CV with an image of your recent photograph indicating the job code to hrd@spincotech.com

Position for team leader Quality Assurance

Highlights:

1. Reporting to the Quality Manager, your responsibilities will include ensuring continuous improvement of the quality and compliance systems, internal and external audits, customer complaints and special project work.
2. You will be working autonomously and be required to make technical decisions in a past paced environment.
3. Required SkillsYou will be a proactive quality focused individual with excellent communication skills (verbal and written).
4. QualificationYou will hold a tertiary qualification in Food Technology or similar
5. ExperienceHave previous QA leadership experience within a food / beverage / pharma manufacturing environment.
6. Contact detailsIf you wish to apply for the above position please mail your resume to: alison_tervit@kellyservices.com
   Ref : NZ8534AT000131
   More details:
   http://www.linkedin.com/in/alisontervit

Research Associate position in Clinical research

Highlights:

1. Position for research scientist for clinical trials; perform evaluation of site capability and make recommendation for inclusion in clinical trial.
2. Assume ambassadorial role to facilitate communication between sites and Key Novartis line functions to increase value proposition to investigators.
3. Facilitate preparation and collection of site level documents.
4. Execute site initiation and training activities.
5. Perform monitoring visits according to monitoring plan.
6. Manage site drug supply management.
7. Resolve site level update of technical systems (Clin Admin, EDC).
8. Ensure site activities in line with milestones (i.e. startup, recruitment, closeout, etc).
9. Manage recruitment implementing appropriate contingency plans as needed.
10. Assure continual GCP, ICH and Novartis SOP compliance (Informed consent process, Source data verification, AE and SAE reporting, IN, protocol, drug accountability etc.) Resolve deviations to standard by remedial action and training.

Research Scientist: Senior Computational Biologist

Highlights:

1. Leads Computational Biology projects for Next-Generation sequencing. Plans and conducts novel analyses of Next-Gen sequence data, defines computational tasks needed to make data available, and develops custom software as needed. Collaborates closely with the Bioinformatics Support lead for Next-Gen sequencing, the sequencing lab PIs and research scientists to ensure that the computational needs of next-gen sequencing and analysis are appropriately met. Duties/Responsibilities Works in conjunction with Senior Computational Biologist to establish project goals consistent with Next-Gen sequencing group goals which reflect core lab and research client needs. Provides project oversight in order to maximize effective use of project resources. Facilitates information flow between team members, the project leader and senior management and other parts of the company.
2. 
   

Senior Safety Associate position in Pharmaceutical

Highlights:

1. With at least 3/4 years experience within Drug Safety you will be responsible for the following:
1. Review serious adverse experience (SAE) information received from Investigator sites and adverse experiences (AEs) from post marketing sources for completeness and regulatory compliance
2. Perform quality control review of completed individual and periodic safety reports and ensure compliance with regulatory reporting requirements
3. Prepare safety data reports for submissions to clients
4. Prepare and/or review expedited safety reports for submission to
5. Regulatory Authorities 
   • Represent global safety and pharmacovigilance group at project meetings
   • Assist in compilation of regulatory submissions, i.e., annual reports, periodic safety update reports
   • Be the safety lead for projects; to include set-up, project management, client liaison
   • Maintain current knowledge of all applicable FDA/EU/ICH guidelines and regulations relating to safety and pharmacovigilance reporting
   • Mentor Safety Associates and other members of the global safety and pharmacovigilance group involved in safety data processing