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job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!   location: Whippany, New Jersey job type: Contract salary: $36.39 - 42.81 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Job Summary Purpose: The Medical Affairs Writer supports the department in coordinating medical training and compliance-related tasks, provide group support in medical writing and administration of research, partnerships, and HCPs (healthcare providers) contracts. Reporting to the VP of US Medical Affairs, the Medical Writer will be supporting needs arise within the US Medical Affairs team, including the medical directors. Key Tasks: Perform medical writing to support scientific publications, medical training programs, and conduct internal publication clearance for the US medical affairs departmentSupport the VP of US Med Aff on local medical governance-related activities such as compliance tracking, local standard operating procedure updates and roll out to meet compliance requirementsSupport the coordination of medical inquires, medical or product research, and fellowship programsHelp set agenda and scheduling with goals to build capabilities and performance excellence and efficiency of the teamOversee and administer all department contracts and purchase orders including those with scientific thought leaders, healthcare providers, vendors, clinical study sites, and advisory boardsFacilitate fair market value assessment and ensure contractual compliance by interfacing with procurement and legal departmentsOther administrative tasks to support the collective team   qualifications: Qualification & Competencies: B.Sc in a biomedical science discipline (e.g. pharmacology, biology, biochemistry, pharmacy, medical sciences), preferably with one or more years of work experience in a biomedical settingAbility to see and comprehend the big picture of a project team, yet thorough and attentive to the intricate details of the scientific workBeing resourceful and possessing good problem-solving skills to resolve issues, reach project objectives and milestones on timeAbility to work in a multi-stakeholder, multidisciplinary setting with Medical Directors, Compliance, Procurement, and other business functionsSelf-motivated person focused on delivering team/project outcomesExcellent verbal and written communication skills, with the willingness to learn new tools and approachesDemonstrated proficiency in using and agility in learning business applications such as Word, Excel, PowerPoint, MS TEAMS, MS AI copilot  skills: MS-WORD, MS-EXCEL, MS-Powerpoint Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). This posting is open for thirty (30) days.

job summary: The Laboratory Assistant I (Scientific); (Temp Analyst) is dedicated to the Microbiology Laboratory. The role of the Laboratory Assistant I (Scientific) will be that of various Microbial testing, data entry, EM Sample receipt, ordering and stocking supplies.   location: Ridgefield, New Jersey job type: Contract salary: $25.00 - 28.17 per hour work hours: 8 to 4 education: Bachelors   responsibilities: This role is responsible for providing the day-to-day operation, Lab support and testing for the Micro team.  qualifications: - The candidate must have basic quality control microbiology experience. Such as bioburden testing, membrane filtration, conductivity and total organic carbon is preferred.   skills: Quality control, Microbiology Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). This posting is open for thirty (30) days.

job summary: Performs routine lab tests under the guidance of Medical Technologists and Laboratory Supervisor. Sets up and monitors automated test procedures. Performs manual procedures requiring judgment. Uses pre-calibrated and/or automated devices.   location: Clifton, New Jersey job type: Contract salary: $35.00 - 38.88 per hour work hours: 11 to 7 education: Bachelors   responsibilities: Duties and Responsibilities: Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result; Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens; Analyze specimens using approved testing procedures (see department SOPs). Review and release test results. Follow CLIA, HIPAA, OSHA, and safety guidelines as described in their respective guidelines. Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and all maintenance performed; Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance. Identify problems that may adversely affect test performance or reporting of test results, correct the problems encountered or immediately notify the senior technologist or supervisor. Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications. Follow department procedure in reporting critical results to clients. If applicable, answer questions from customers or other lab personnel. Maintain complete records of all testing performed on-site. Maintain general appearance of the department. Make sure reagents/test kits have received dates, expiration dates, and if applicable opened dates. Review/train on new procedures. Attend monthly department and any additional training/educational meetings. Participate in all applicable safety training sessions. Know the location and contents of the safety manual. Know the location/use of all applicable safety equipment. May perform some moderate-complexity testing with specific on-site training provided. Perform other duties as directed by supervisor. This is not an exhaustive list of all duties and responsibilities, but rather a general description of the work performed by this position.  qualifications: Qualifications: Education Preferred: BS/BA in Chemistry or Biology, or Associates degree in a Laboratory Science or Medical Technology or Work Experience: 1 - 3 year Clinical experience preferred. Other: Must have the ability to establish work priorities and handle several procedures simultaneously. Must interact with other departments. Contact with clients may be required, good customer service skills are important. Must protect patient confidentiality at all times. Role is located within Northern Lights Hospital - verify additional requirements needed for any placements at this location before you submit candidates. Items listed will be required for any placement at this hospital site State of Credentials Licenses Required: MLS / MST certification   skills: Molecular Biology, Biology, Chemistry, GLP (Good Laboratory Practice), Sample Preparation, Sample Testing Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). This posting is open for thirty (30) days.