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***50% onsite*** The Associate Scientist – Virus/Viral Vector Downstream Development will be responsible for downstream process and analytical development. The position will be part of ...
Mon - Fri 6:00a.m-3:00p.m; rot Saturdays Minimum of 6 months experience.Under the direction of the area supervisor, perform daily activities of the Patient Service Center /Mobile Phlebotomy ...
Description: Medical Writer Clinical II (QC Position) Education/Experience Requirements: Years of experience/education and/or certifications required: 2 – 4 years exp, BA required, ...
Description: Job Title: Product Complaint Analyst I Candidates with Product Quality Complaint experience preferred and especially Device Complaint related experience. Individual will work in ...
Purpose and Scope of Position The Specialist, QA is responsible for reviewing GMP documentation, and ensuring that commercial products and materials meet required quality characteristics. The ...
Required Competencies: Knowledge, Skills, and Abilities Basic knowledge of cGMP, OSHA, USP and EP Ability to multi-task and be flexible Strong teamwork skills Ability to complete routine tasks ...
Bachelors Degree in Science (preferrably Biology, Chemistry, Biochemistry). Focus in a discipline 2+ years experience. Good Computer Skills, including Microsoft Excel, Word and ...
Willing to work on a weekend shift as needed. Description: Provides clerical and administrative support related to documentation processes and systems. Pre-approves and routes documents for ...
Description: Responsibilities include, but are not limited to: Perform all tasks associated with the manufacture of clinical and commercial product following batch records and SOPs Work as part ...
M-F 8:30am-3:30pm 30 Hours a weekpotential for temp to hire all ages at least 4-5 years experienceThe Patient Services Representative I (PSR I) represents the face of the company to patients who ...
In a team setting and cGMP environment, perform routine analytical testing in support of release and raw material samples. Conducts routine and non-routine testing of materials and product using a ...
The QA Product Release Associate is responsible for ensuring the safety, efficacy, purity, and quality of manufactured products through compliance with relevant quality standards, regulations and ...
Mon-Fri,8am-4:30pmThe Laboratory Associate I may perform any of the following activities under the direct and constant supervision of Clinical Laboratory Scientist (CLS) as described in the ...
As a Pharmacovigilance Scientist you will participate in the triage process for incoming documents to insure timely and effective medical and scientific evaluation of adverse event information. You ...
Description R&D Scientist will work independently and as part of cross-functional teams supporting the development of diagnostic products. This position will work a minimum of 80% at a ...
Consultant, (senior) data analyst, Disease Stratification, Translational Bioinformatics Job Description Candidate will have to work onsite once site reopens We seek a talented, collaborative ...
Mon - Fri 7:00 - 15:30Perform the daily activities as described below. Basic Purpose: Perform various routine laboratory functions in a precise and accurate fashion to assist the laboratory ...
The hours are 7:00am -4:00pm M-F and every other Sat temp replacementTemp to Hire.The Patient Services Representative I (PSR I) represents the face of the company to patients who come in, both as ...
Monday- Friday 7am-11am, Saturday rotation. 20 Hours a weekCould have potential for temp to hire. Flexibility with schedules and working at other locations is always a plus. Top requirements: ...
Qualifications: Bachelor’s Degree in Microbiology, Biology or related scientific discipline. Minimum of 1 - 2 years of experience in biopharmaceutical industry, preferably working in a ...
