Ich Q10 Jobs in Others

html headhead body span idspandescpThis is a remote positionp div span classfont stylefontfamily arial helvetica sansserif sansserifspan classsize stylefontsize pxPSC Biotech provides the life sciences with essential services to ensure that health care products are developed manufactu More...

html headhead body span idspandescpThis is a remote positionp div span classfont stylefontfamily arial helvetica sansserif sansserifspan classsize stylefontsize pxPSC Biotech provides the life sciences with essential services to ensure that health care products are developed manufactu More...

- Must have 2 years in the med surg or nephrology unit. We can look for people with 1 year experience only if they are from a really big hospital -Willing to endorse a WA license if they do not have one (as soon as they get an offer) -BLS certificate required -Can consider Travel N More...

3rd shift role - 10pm - 8am Could be any of the following shift but will be set once they start working 3rd shift. MUST train on 1st for the first couple weeks. Sun-Wed, Mon-Thurs, Tues-Fri, or Wed - Sat - flexible to work OT on weekends 1. Can it extend - Yes2. Is this role 100% onsi More...

Job Title: Registered Dietitian/Nutrition Scientist Location: Columbus, OH - On-site Contract Duration: 3-month assignment Work Hours: Monday to Friday, 8:30 AM to 5:00 PM RD Dietitian/Nutrition Scientist - Pediatrics Nutrition Science Our location in Columbus, OH, currently More...

Job Title: - Case Management Assistant Job Location: - 3330 Lomita Boulevard Torrance, CA 90505 Job Duration: 3+ months (High Possibility of Extension) Pay Rate: $28.00/hour on W2 Shift: Day 5x8-Hour (08:00 - 16:30) Schedule is 5x8 with one weekend day Job Description: Required Qualif More...

Responsibilities: Education : BS/BA degree in Scientific Discipline (Masters or higher preferred) with 5-7 years in the pharmaceutical industry, preferably with 1-3 years CMC regulatory experience Participate in the development of the CMC regulatory strategy for post-approval small m More...

Responsibilities: Serves as functional lead, providing support and sharing technical expertise with other functions, especially the clinical/research scientists engaged in the scientific aspects of the clinical development study/project(s). Serves as lead study programmer on one or m More...

Description: 3rd shift role - 10pm - 8am Could be any of the following shift but will be set once they start working 3rd shift. MUST train on 1st for the first couple weeks. Sun-Wed, Mon-Thurs, Tues-Fri, or Wed - Sat - flexible to work OT on weekends 1. Can it extend - Yes 2. Is th More...

Responsibilities: Responsible to communicate new regulatory guidelines. Lead the strategic efforts in the interpretation of relevant and new quality guidelines to ensure that the current and phase appropriate requirements and standards are properly and timely implemented Provide su More...

Responsibilities: Support strategic initiatives by leading projects to design and deploy process and technology related improvements and monitoring of R&D vendor issues for trends across the operational areas Develop and write vendor issue procedures Support in developing establish More...

Responsibilities: Represent the Quality function on product and process development project teams. Actively support and engage in design reviews. Lead or support design activities including design verification, validation, specification setting and justification, test method develo More...

Position: Pricing and Contract Strategy Manager/Study Contract Manager (SCM) Location: Wilmington DE HYBRID (3 days onsite/2 days remote) Duration: Long Term Description: Study Contract Manager (SCM) play an important role in driving the costings and contracts being responsible for More...

Wilmington, DE Contract Duration: 10-36 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Specialist Study Management in the Wilmington, DE area. Must be local to Wilmington, DE, non-remote position Own and maintain quality for the study file as the loc More...

Requirements Minimum education: Master Years of work experience: 8 year(s) Responsibilities A biotechnology leader on the east coast needs multiple Senior Statistical Programming consultants to support their team on a long-term basis. This is an exciting opportunity to be part of More...

Wilmington, DE Contract Duration: 12-36 months Possibility for FTE Conversion Rate: Negotiable Responsibilities: Excellent employment opportunity for a Pricing and Contract Strategy Manager in the Wilmington, DE area. Local to Wilmington: HYBRID (3 days onsite/2 days remote) Study More...

Description: LOCATION: Local to Wilmington: HYBRID (3 days onsite/2 days remote) *Possibility for FTE Conversion* Study Contract Manager (SCM) play an important role in driving the costings and contracts being responsible for negotiation and budgeting in clinical trials and for dev More...

DescriptionKnowledge of analytical laboratory techniquesExperience with analytical instrumentation, particularly HPLCAbility to learn new laboratory equipment and techniquesExcellent verbal and written communication skillsKnowledge of cGMPs, USP/EU regulations, and ICH guidelinesAnal More...

Role: Clinical Research Associate Location: NewHaven, CT Duration: 12+ months Responsibilties: Member of the clinical team responsible for conducting multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior staff in planning study co More...

Provide leadership and expert oversight of clinical studies including project planning, budget, resource management and contract research organization negotiation and management Contributes to clinical development plans and ensures alignment to business and regulatory strategies Act More...