Sales Analyst for Pharmaceutical Company – 1yr Contract Our large pharma client in Irvine, CA is in need of a Sales Analyst on a temp to hire basis. We are one of the few agencies that pays 65% of health insurance costs. MINIMUM REQUIREMENTS: • Bachelor’s degree in Business, Computer Science, or Information Technology, Healthcare […]
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IRB Regulatory Coordinator Temp Needed in West Los Angeles Growing Oncology Clinical Trial site needs a temporary IRB Regulatory Coordinator in the west side of Los Angeles. This is a temp to hire position. Responsibilities: Will provide support for clinical research protocols, informed consents, etc. Will assist with all aspects of clinical research regulatory to ensure compliance to […]
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Regulatory Affairs Manager Drug Device Combo, 12 months in Pleasanton,CA Our large drug/device combo client in Pleasanton, CA needs a temp-to-hire Regulatory Affairs Manager Drug Device Combo. This contract is estimated to last 12 months with the possibility of being hired directly. This person will coordinate most aspects of company regulatory activities and may interface with domestic […]
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Quality Engineers – Quality Improvement Project in Orange County Are you a fix-it person? Do you have significant medical device experience? We have a medical device Quality Improvement Project expected to last 9 months in Orange County. The project is to improve operations process and manufacturing. A team of engineers is to be deployed to […]
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HR Generalist Needed, Glendale, CA We are in need of an HR Generalist to manage on boarding (and off boarding) of staff and temps placed with our clients. This is an internal position working directly for MEIRxRS family of companies at our office on 100 N Brand Blvd, Glendale, CA (check your commute). Qualifications 3 or […]
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[itemscope name=”JobPosting”] Cancer Research Nurse A Cancer Research Nurse is needed by our client in Santa Monica, CA. Candidate should have experience in Oncology and wants to grow by serving patients enrolled in clinical trials.
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Director of Clinical Research Operations – Monrovia, CA Oncology clinic needs someone to ensure federally-funded projects are completed on time, in scope and on budget. This person will work with Principal Investigators, Project Directors, CRCs, Clinical Data Analysts and report to the head of operations. The Director of Clinical Research Operations will serve as the primary […]
read more Regulatory Affairs Associate Drug Device Combo, 12 weeks in Pleasanton,CA Our large drug/device combo client in Pleasanton, CA needs a temporary Regulatory Affairs Associate. This contract is estimated to last 12 weeks. This person will coordinate most aspects of company regulatory activities and may interface with domestic and international health authorities. Qualifications: • BS or BA […]
read more Product Development Compliance Manager – Tulsa OK Relocation assistance to Tulsa, OK approved for this position. Required Minimum of 5 years’ experience in a Quality Systems / Regulatory Compliance environment 3-5 years’ experience in medical device industry preferably in Endodontics Irrigation and Obturation BS in Bio Sciences, Engineering or related field Solid understanding of medical […]
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Medical Affairs Manager – Houston, TX Our client needs a full time Medical Affairs Manager experienced in investigator initiated research. Relocation assistance is available. Requirements Advanced degree in a scientific field. 8 or more years experience as a Medical Affairs Manager, in medical device industry Management of investigator initiated research Experience developing and managing project […]
read more R&D Project Reporting Specialist – temporary in Irvine CA This is estimated to be a one year temporary R&D Project Reporting Specialist position in Irvine CA. We cover 65% of health insurance. Requirements Bachelor’s degree with 6 years relevant work experience or 4 years relevant work experience with a Master’s degree. 2 years relevant experience […]
read moreSupplier Quality Specialist Needed in Branchburg, NJ A major pharma client is in need of a temporary Supplier Quality Specialist. This position is estimated to last 6 months. Required knowledge and Skills: B.S. degree Microsoft Words, Excel, and Power-point Presentation Computer Excellent interpersonal and communication skills Preferred Knowledge and Skills: General knowledge about GMP & GDP […]
read moreContracts Administrator Temp in Irvine, CA Our pharma client in Irvine needs a temporary Contracts Administrator for one year. Qualifications Preferred 2-3 years in corporate office setting Great attention to detail. Great multitasking ability Bachelor’s degree Job Summary: Working with lead paralegal in preparing, examining, analyzing, negotiating, and revising contracts for commercial consulting in the […]
read moreFormulations Product Development Lab Tech Contract in Irvine, CA Our client needs a Contractor to work as Product Development Professional. Contract is estimated for 12 months at their facility in Irvine, CA. Possibility for conversion to full-time after a year. We offer benefits including employer contribution to healthcare for this position. You must have authorization […]
read moreSr. Clinical Operations Associate – Contract Position, Pharma in Irvine Our pharma client needs two Sr. Clinical Operations Associates for a one-year contract. They will work with the Clinical Trial Manager and Operations Study Lead in the operational execution of assigned clinical studies. Requirements Science degree preferably in science or health-related field Previous experience of working on […]
read moreProject Planner III R&D – Contract Position, Pharma in Irvine A Project Planner is needed by our pharmaceutical client in Irvine, CA. This is a one-year on-site position. Requirements: Life science and/or business degree with at least 5 years of experience in the industry, preferably with a sponsor or CRO. MS degree and PMP certification […]
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Medical Science Liaison – Dermatology Work From Home Near San Francisco Our client needs a Medical Science Liaison with Dermatology experience who lives in the San Francisco, CA area to cover the Northwest geography. Education and Experience • Advanced degree with health science background (Pharm.D, M.D., Ph.D, preferred) • Preferred minimum 3 year total specific industry […]
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Medical Communications Jobs We have multiple Medical Communications Jobs at our large pharma clients in Irvine, CA and Los Angeles on a contract basis. Most urgent need is for a Medical Communications Specialist to work with team of medical information professionals to capture unsolicited medical inquiries from health care professionals, consumers, and
read moreRegulatory Affairs Project Manager Job – Medical Device Our client needs a Regulatory Affairs Project Manager to support Asia Pacific (Japan, China, South Korea and Taiwan) regulatory approvals for implantables. Comfort and experience working hands on with design and validation reports and other technical files is needed. Requirements Previous experience authoring or approving design and validation […]
read moreMedical Monitor Oncology Job (US-Based Remote) We have a medical monitor oncology job for a doctor with experience in clinical drug development. The doctor will help our foreign-based client with their US clinical trials. Work is estimated to take 20 hours per month to start. Requirements Medical Doctorate (MD) or equivalent 5 years clinical drug […]
read moreGlobal Pharmaceutical Labeling Manager – Contract position in Irvine CA Our client needs a Contractor to work as Manager of Global Pharmaceutical Labeling. Contract is estimated for 12 months at their facility in Irvine, CA. Possibility for conversion to full-time after a year. We offer benefits including employer contribution to healthcare for this position. You […]
read moreHuman Resource Accounting Assistant job openings Boutique search agency in Glendale, CA seeks hiring for the first of multiple Human Resource Accounting Assistant job openings. We need someone part time who can become full time as we fulfill the needs of new clients. Requirements Both: 1-2 years experience in Human Resources and 1-2 years experience […]
read moreGVP Pharmacovigilance Audits – Senior GVP Audit/Project Manager Needed Our client needs a full-time Senior GVP Audit/Project Manager to handle their GVP Pharmacovigilance Audits. This person will plan and perform domestic and international GVP audits to assess the company’s compliance to local and international government regulations. They will also assess internal SOPs as they relate […]
read moreClinical Operation Manager Needed, Remote / Work from Home Clinical Operation Manager needed by our client to co-ordinate clinical study design and implementation at a program and functional level according to Good clinical practice (GCP). Clinical Operation Manager Qualifications Position requires a minimum of a Bachelor of Science degree and at least 5 years of clinical […]
read moreOncology Medical Writer Needed, Remote Work Our client is in need of an experienced oncology medical writer. The medical writer will translate the scientific hypotheses of clinical trials into lay terms for patient population and patient navigators. Ideally, you have experience in consumer-facing communication. The client is developing software to better match stage
read moreQA Engineer – Medical Devices & IVD Manufacturer, Los Angeles, CA QA Engineer needed to manage the selection, qualification, and monitoring of suppliers including finished device, OEM, and contract manufacturers. This person will play a key role in working with suppliers to resolve quality issues (SCAPAs), resolving internal non-conforming product issues, addressing incoming inspection challenges, including […]
read moreSenior Regulatory Affairs Associate (Chicago Area, IL) Summary: This position is ideal for Ideal for someone looking to lead Regulatory strategy at the company’s facility located in the Chicago area. This Regulatory Affairs Professional will be responsible for: Development/Revision of
read moreLaboratory Assistant – Medical Devices & IVD Manufacturer, Los Angeles, CA Laboratory Assistant needed to perform routine equipment maintenance, assure adequate stock and labeling of laboratory reagents and consumables, manage chemical and biological waste, sanitize lab surfaces, and monitor environmental controls. Requirements B.S. in Chemistry, molecular biology or biological sciences 1-4 years hands-on experience in a regulated, […]
read moreVP Clinical Development – Rare and Orphan Diseases VP Clinical Development for a small clinical-stage pharma company in Los Angeles San Fernando Valley. Candidate needs to have a MD, be experienced in rare and orphan disease studies and have significant experience clinical trials. Requirements M.D. or D.O. with specialty training, preferably CNS diseases 10 -15 years […]
read moreProduct Development Engineer- Medical Devices & IVD Manufacturer, Los Angeles, CA Product Development Engineer needed to oversee the development and manufacture of low cost, plastic devices including disposable blood collection devices. Requirements At least 5 years of experience in the development of medical devices Bachelor’s degree in an engineering discipline preferred. Mechanical and/or electrical engineering background […]
read moreVP Genomic Research, Los Angeles CA VP Genomic Research needed to manage operational and logistical tasks of genomic test development to ensure efficient execution of studies for molecular diagnostic products within established budgets and timelines, ensuring all activities occur in compliance with the appropriate regulations. The candidate will be responsible for designing the test development process, directing […]
read moreDirector of IVD Manufacturing and Supply Chain Director of IVD Manufacturing and Supply Chain needed for an in-vitro diagnostics (IVD) client in Los Angeles, CA. The role is responsible for working with Product Development to select and manage key suppliers. Work alongside management and sales to establish forecasts and delivery schedules for key materials. This role will also […]
read moreVP Regulatory and Clinical Affairs needed in Los Angeles, CA VP Clinical Affairs needed to develop and implement clinical studies and molecular diagnostics validation strategy. The VP will coordinate the efforts of internal and external resources to ensure fast patient recruitment, trial site selection, trial plan optimization, and execution of trials with a focus on data quality. […]
read more[itemscope name=”JobPosting”] Oncology Research Nurse An Oncology Research Nurse is needed by our client in Santa Monica, CA. Candidate should have experience in Oncology and wants grow by serving patients enrolled in clinical trials.
read more[itemscope name=”JobPosting”] Business Development / Sales -Cardio Medical Devices In the ever-evolving world of business and real estate, professionals seeking growth and new opportunities must stay informed and equipped with the right skill set. If you are an experienced sales manager or account manager looking to make a significant impact in the cardiovascular medical device […]
read moreBiotechnology Jobs vs Biotechnology Careers Biotechnology jobs are for short-term goals. Biotechnology careers include your long-term goals. You can manage this journey through a combination of education, certifications and experience. Only then can you arrive at the destination you are most interested in. Biotechnology jobs includeClinical Trials, Clinical Research, Quality, Regulatory, and Medical Affairs, Engineering and […]
read moreCommercial Development Director / Sales (East Coast, West Coast, Europe) The Commercial Development Director will set a road map for the sales team. The client is a Contract Manufacturer that provides bulk drug formulation and manufacturing. They also provide primary and secondary packaging capabilities for solid dose drugs. Their technologies include granulation, coating, blending, encapsulation, […]
read moreDirector Account Management – Southern California The Director Account Management will help establish pharmacies in clinics.
read moreClinical Project Manager (Part-Time Contract ) – Philadelphia, PA A Clinical Project Manager (part time contract) is needed for a Contract Research Organization (CRO) to work in their office in the Philadelphia area. This position will report directly to the Chief Medical Officer and includes responsibility for coordinating and managing all aspects of clinical study […]
read moreClinical Affairs Director – TX or Upper Midwest Clinical Affairs Director will lead and manage the Clinical Affairs Department globally, reporting to
read moreClinical Studies Manager – Austin, TX Clinical Studies Manager plays a major role in coordinating clinical studies, from qualification of clinical study sites through monitoring of clinical study activities and completion of
read moreClinical Pharmacist, Los Angeles Requirements Oncology experience 2 years experience after boards
read moreVP Clinical Operations in San Diego, CA Education & Experience: Oncology experience MS/PhD degree or similar
read moreVP Medical Affairs in San Diego Education & Experience: MD required Oncology experience required.
read moreMedical Device Compliance Auditor for Boston or Minneapolis Area Medical Device Quality and Regulatory Compliance professionals needed for two opportunities to assess non-active medical devices and their manufacturers per the European Medical Devices Directives, other applicable Regulatory Systems and International standards, including related client and project management 50% Audit Perform regulatory audits of clients per European […]
read moreGMP Regulations for Friday the 13th Happy Friday the 13th! Remember, if you need a GMP or Quality specialist who knows the regulations below then don’t be scared. Call MEIRxRS.
read moreQuality Apprenticeship Program Featured on CA.gov The State of California, Department of Industrial Relations has listed our two Quality Apprenticeships: Chemistry Quality Control Technician and Microbiology Quality Control Technician. These represent two out of the three apprenticeships available in the Health Services category. The Division of Apprenticeship Standards (DAS) creates
read moreFSMA Half Day Workshop Attendees Give 4.6 Stars Did you make the QLN FSMA half day workshop in Irvine? The 97 attendees seemed extremely satisfied with the Sept 24th, 2015 event, giving it an overall rating of 4.6 (scale 1-5). Easy FSMA Launched EasyFSMA website www.easyfsma.com was launched by the Quality Leadership Network (QLN) members, […]
read moreDirector of Quality GCP in San Diego, CA We are searching for a Director of Quality GCP in San Diego, CA for a client in Phase III Trials. Candidates must have at least 4 years of experience in GCP to be considered.
read moreSr. Clinical Planning Manager Large Pharma Client Needs Your Clinical Trial Expertise! A Clinical Planning Manager, capable of handling 12 teams with 25 members each of both internal and external members, is urgently needed by our client. You will use your 8 + years of industry experience to proactively identify potential pitfalls and steer the team around them. […]
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Providing staffing, executive search, GxP auditing and recruiting for life sciences & bio-science companies.
100 N. Brand Blvd, Suite 306
Glendale, CA 91203
info@meirxrs.com
sales@meirxrs.com
