Vice- President, Global Regulatory Affairs - NC Pharma |
| I am working on behalf of a North Carolina pharmaceutical firm to retain a top-notch candidate to ... |
|
Associate Director- Clinical Quality Assurance (Specialty Pharma) |
| Our client, a specialty pharmaceutical company with headquarters in Research Triangle Park, NC, is ... |
|
Clinical Data Manager II |
| Job Category: Biotech/R&D/Science Career Level: Experienced (Non-Manager) ... |
|
SR. QUALITY ASSOCIATES |
| As a member of the Quality Operations Analytical Support group, the incumbent will assist in the ... |
|
QUALITY ASSOCIATE III |
| The responsibility of the position is to support quality systems site wide for Engineering/U... |
|
PHYSICIST - UNIQUE OPPORTUNITY! |
| Our client, an extremely established company in RTP, is currently looking for a Physicist in R... |
|
SAS Programmer |
|
Statworks, Inc is a high quality specialty provider of biostatistical analysis and ... |
|
Senior Scientist - Molecular Biology / Drug Transport |
| Qualyst, Inc. is a biotechnology company dedicated to the development of novel ADMET (absorption, ... |
|
Biostatistician - Direct-Hire Opportunity |
| Company: Yoh Clinical Location: US-NC-Raleigh/Durham-RTP Status: Full Time, Employee Job C... |
|
Pharmacovigilance Technology Manager |
| LocationResearch Triangle Park, NC
Provides project management and technical oversight for ... |
|
|
QA DEVIATION SPECIALISTS
| Details |
Country: USA
Location: North Carolina-Raleigh/Durham-RTP Research Triangle Park, NC
Total applied: 35 |
|
QA DEVIATION SPECIALISTS
As one of the world's foremost providers of premium protein therapies, Talecris not only saves lives, but we also improve the quality of life for people everywhere. If you are a professional who shares our passion for making a difference, let us make a positive difference in your career. Our innovative organization, one of Research Triangle Park's 50 fastest-growing privately held companies, has the following opportunity at our RTP, NC facility:QA DEVIATION SPECIALISTS TALECRIS PLASMA RESOURCESWe now have two openings in our QA & Regulatory Department for individual contributors to:-Bridge cGMPs and the FDA/TPR Quality Plan-Facilitate Donor Center compliance-Ensure proper reporting and handling of product incidents and customer complaints-Evaluate adequacy of documentation and completeness of incident reports (PIRs and MIRs)-Evaluate corrective actions-Monitor customer complaints, nonconformance, and incidents relating to BPDRs-Develop system-wide CAPAs -Conduct new hire training on investigation and incident reportingTo qualify, we require:-Bachelor's degree in Chemistry, Biology, or Medical Technology-2 years' experience in biologics/drug manufacturing or in an FDA-regulated facility-Expertise in cGMPs and FDA regulations-Knowledge of quality control principlesInterested persons may apply by emailing their resume as a word or text document to kathleen.fleming@talecris.com . No online applications, agencies or phone calls please. Talecris Biotherapeutics offers a competitive compensation & benefits package including immediate 401(k) vesting and profit sharing. Relocation available for the right candidate who brings high energy and top talent to the position. All benefits take effect day one of employment. Talecris is proud of its work/life/balance initiatives & its generous tuition reimbursement program. We have the expertise, resources & established business infrastructure to develop, manufacture & market biotechnology products internationally. An Equal Opportunity Employer M/F/D/V, Talecris Biotherapeutics is committed to enhancing & maintaining cultural diversity within our work environment.
|
| Related jobs |
|
|
Molecular Biologist
RTI is an independent organization dedicated to conducting innovative, multidisciplinary research that improves the human condition. With a worldwide staff of more than 4...
|
|
|
Regulatory Document Management Associate - Pharma (top dollar/contract to start)
Our client, a specialty pharmaceutical firm headquartered in the RTP area, is actively recruiting for a sharp and capable document control ...
|
|
|
Director of Product Service and Support
Job Description
As a Director of Product Service and Support at Centice, you will be responsible for the overall pre and post implementation customer experience for all ...
|
|
|
Quality Control Chemical Technician (Temporary)
Chemical Technician (Temporary) will work with Quality Control performing assays accurately and reliably using automated and manual methods. Use of laboratory ...
|
|
|
Business Analyst
Responsibilities include developing proposals including scope of work and budgets; negotiating with clients for financial and contractual aspects of proposals, contracts ...
|
|
|
Regional Pharmaceutical Sales Rep - Direct Hire
Our client, a rapidly expanding pharmaceutical firm headquartered in RTP, North Carolina, is actively recruiting for a sharp, self-motivated, persuasive, persistent ...
|
|
|
Sr. Process Controls Engineer
Client – Growing Pharma Co. - WW sales of $1B+ & 3.5K people need a Sr. Process controls engineer for their plant with DELTA V DCS exp in pharmaceuticals. Excellent R...
|
|
|
Scientist III
LOCATION US-NC-Research Triangle Park JOB TYPE Full Time, Employee ...
|
|
|
Production Associate II Molecular Biology
PRODUCTION ASSOCIATE, MOLECULAR BIOLOGY
Argos Therapeutics, Inc. is a venture capital-backed pioneer in immunotherapy. The Company’s focus is bringing ...
|
|
|
Clinical Operations Manager OR CRA II
Job ID: RDS08-02 Position Title: Clinical Operations Manager OR CRA IIWorking Location: NC, CaryEmployment Status: Full-TimeRequired Experience: 3 yearsRequired E...
|
|
|