SOMOS BILINGUES!
859 578-8992 recruiting@peopleplace.com

21-35 of 35 results
Sort By

- Cincinnati, OH

Job Description: Responsibilities include supporting daily compliance and systems activities. Performs audits (internal and vendor audits), supports change control program, complaints and any customer services related to Documentation Center. Also works with manufacturing to identify resolution to events while working with Quality Management. The candidate will perform general QA work, using their ability as a skilled contributor in completing tasks where judgment is required in resolving....


The positions serves as the site’s Oral Solid Dosage (OSD) platform leader and reports directly to the Sr. Director of Process Development. Responsibilities include management and oversight of multiple early and late stage development projects and support personnel. Job Functions: Demonstrates technical expertise in OSD technology and methodologies. Lead site related process development, scale-up, commercialization and tech transfer responsibilities Collaboratively develop project strategies....


Company is seeking a Principal Engineer to lead projects in the Biologics process development and clinical manufacturing projects. The individual will design, develop, scale-up and optimize drug substance and drug product unit operations for protein therapeutics. Experience managing projects from Discovery integration through GMP manufacturing, with both internal and external partners are required. The candidate should have strong technical, communication and interpersonal skills, be able to....

- Buffalo, NY

Provides quality oversight to the Chemistry & microbiology laboratories and product transfer by supporting all work. Work in partnership with the aforementioned groups to produce quality work in compliance with all applicable regulations. - Review/approve deviations, OOS's, OOT's, EE's, and change controls. - Perform audits of the chem & micro labs. - Review/approve protocols, investigative studies, raw data and reports. - Establish and control quality programs to ensure conformance....


Senior Regulatory Affairs Specialist (Medical Device) Newark, DE (Relocation Assistance Provided) Competitive Base Salary, Bonus 10%, 6 401K Match, Full Benefits, 4 weeks PTO We have a newly created opening for a Senior Regulatory Affairs Specialist position with a longstanding client; multi-billion global medical instrumentation company. They have strong revenue growth, a stable environment, very low turnover, and offer the opportunity to work on customized, complex medical products that....


My client is expanding their team and they look to hire a Manager of Business Development to better serve their new and existing clients. This is a great opportunity for a Scientist to go from the bench to the business side. The ideal candidate will take on the following tasks:Work closely with the Director of Business Development and assist with selling services to pharmaceutical and biotechnology clientsUnderstand the drug development needs of the clients and positively position the firm as....


My client is expanding their team and they look to hire a Manager of Business Development to better serve their new and existing clients. This is a great opportunity for a Scientist to go from the bench to the business side. The ideal candidate will take on the following tasks:Work closely with the Director of Business Development and assist with selling services to pharmaceutical and biotechnology clientsUnderstand the drug development needs of the clients and positively position the firm as....

- Danbury, CT

Our client - a growing Pharmaceutical company located in the Danbury, CT area - is looking for a Validation Associate. The Validation Associate will be responsible for supporting all aspects of equipment qualification (IQ/OQ/PQ) as well as supporting process validation programs. The Validation Associate will be involved with creating and implementing various protocols as well as Final Reports. The qualified candidate will have 1-5 years of Pharmaceutical Industry experience - as well as some....


Top tier Pharmaceutical company (one n Boston and one in NJ nd one in Seattle)Required:Has completed management of a study or group of studies from planning through close out (Phase 3)Experience with managing VendorsExperience working on global studies with CROs Nice to Have:Experience supporting writing clinical study reports,Supporting sNDA or NDA submissions, Supporting pre-Inspection preparation,Participating in Sponsor Inspections by Regulatory BodiesExperience managing or leading teams....


Top tier growing Global Pharmaceutical company is looking for a vibrant and sharp Manager of Regulatory Affairs to join their dynamic Team The is company has been named top new Pharma and one of the Best Employers in 2017 The role canbe in EITHER their Seattle, WA HQ or their NEW offices in San Francisco (full relocation package offered- And great benefits too) Must be a self starter with initiative and Regulatory Affairs experience in the Pharma industry- must have Regulatory affairs and CMC....


Position: Gastroenterology Hospitalist Location: Tucson, AZ Our client is seeking a Gastroenterology Hospitalist to join their established practice in beautiful Tucson, Arizona. Physicians can expect to enter a practice with high patient demand and a loyal patient base, in an expanding suburban market. The culture is one that values open communication and feedback from its physicians. Preferred candidate will have three (3) to five (5) years' experience and be BE/BC. Also, will consider new....


Our client - a growing Pharma company - is looking for a Head of Quality for their site located in the Louisville, KY area.The Head of Quality will be responsible for oversight of all QA and QC activities at the site.They will have responsibility for implementing, improving and maintaining Quality Systems (i.e. CAPA, Investigations, Change Control etc.), as well as reviewing and approving all validation and technical reports.Additionally, the Head of Quality will be the primary point of....


ID 1230 R&D Scientist - Pharmaceuticals -- injectables or semisolid exp Location Arlington Heights, IL Summary This role will provide technical expertise for process development to expand manufacturing processes and will aid pilot scale to commercial batches. DutiesConduct pilot scale batchesSupport launch batchesPrepare protocols for verification batchesAssemble proper reports and prepare presentations RequirementsBS Degree, Masters preferred5+ years of industry experienceExperience....


Top Tier Progressive Bio Pharmaceutical company with offices in Seattle and San Francisco is expanding They are looking to hire a Director of Regulatory Advertising and Promo Description Company rates #1 in Northwest! They are a clinical-stage company developing novel cellular immunotherapies based on two distinct and complementary platforms – Chimeric Antigen Receptors (CARs) and T Cell Receptors (TCRs) technologies. Our goal is to revolutionize medicine by re-engaging the body’s immune....

- Somerville, NJ

Our client - a growing Pharmaceutical company in central NJ - is looking for a Clinical Operations Manager. The Clinical Operations Manager will be responsible for the planning and execution of clinical trials. The Clinical Operations Manager will: Lead the study team in order to develop the study planHelp select the CROReview study feasibility assessmentsHelp oversee site selection/site qualificationOversee the management of the logistics of clinical material The qualified candidate will have

21-35 of 35 results