Laboratory Manager
Top Quality Recruitment (TQR)
Laboratory Manager The Laboratory manager will oversee customer projects and internal initiatives, ensuring timely delivery and quality standards. Responsibilities include managing workflow, monitoring progress, and holding the team accountable for departmental objectives. Key Activities Lead a team of 3–5 technical R&D staff, overseeing daily activities and ensuring the timely completion of both customer-driven and internal projects. Actively participate in quality control and research & development efforts within the Essential Oils Division, supporting the formulation of customized citrus and spice essential oil blends and specialty products. Provide regular feedback, mentorship, and training to team members to uphold organizational performance and quality standards. Collaborate closely with cross-functional teams—including Production, Quality Assurance, and Sales—to align processes, troubleshoot challenges, and ensure both short-term deliverables and long-term strategic goals are met. Ensure strict adherence to standard operating procedures (SOPs), as well as safety, environmental, and regulatory compliance across all laboratory activities. Perform additional duties as assigned by management to support the ongoing growth and success of the division. Preferred Skills Excellent leadership, communication, and organizational skills. Demonstrated ability to manage multiple projects and meet deadlines in a fast-paced environment. Working knowledge of laboratory safety standards and regulatory compliance. Education & Experience Bachelor’s degree in Chemistry, Chemical Engineering, or a related field. Minimum of 5 years of experience in a laboratory or manufacturing environment, with at least 2 years in a supervisory or management role. Finding a great opportunity that fosters growth, a great culture, and leadership opportunities can be difficult. Top Quality Recruitment (TQR) connects professionals with leadership opportunities across the Packaging, Food and Beverage, Medical Devices, and Biotechnology industries. With 50+ years of experience, we believe in one-to-one communication and finding the best candidate/employer match possible. TQR is an equal-opportunity employer that encourages diversity. We will consider all applications. Accommodation for applicants with disabilities is available upon request. We thank all applicants for their interest and appreciate the time and effort involved; however, due to the large volume of resumes received only those candidates selected for an interview will be contacted. Please attach your resume to your application. Job ID: 7781 #J-18808-Ljbffr
- ...the customer. Interprets data on project issues and makes good business decisions with support from experienced team members or line manager. Works to ensure that all clinical deliverables meet the customer's time/quality/cost expectations. Maintains profitability by...SuggestedContract workLocal area
$65k - $80k
...requires a proactive, self-starting individual who can effectively manage patient-facing responsibilities while ensuring strict adherence... ..., storage, and shipment in compliance with protocol and laboratory requirements. Collaborate with investigators, site staff, cardiac...SuggestedFull timeTemporary workWork at officeLocal areaMonday to Friday$65k - $80k
...experience, a strong attention to detail, and the ability to work independently. The role includes coordinating trial activities, managing patient interactions, and ensuring regulatory compliance. Benefits include 20 PTO days, holidays, and comprehensive healthcare options...Suggested- ...highly collaborative team? We're partnering with an exciting clinical research organization that is continuing to expand its project management team. This is an opportunity for an experienced Clinical Project Manager to join a warm, welcoming group of professionals who are...Suggested
- ...local prosperity, Still Bright is leveraging its proprietary processing technology to change the industry. Position Summary The Laboratory Manager owns the day-to-day operations of Still Bright’s headquarters lab — keeping it running, stocked, calibrated, compliant, and...SuggestedFull timeLocal areaRemote workRelocation
- ...experience through our 12-week fellowship program. - The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full portfolio of clinical trials. GCS supports more than 300 Phase I...Part timeFor contractorsLocal area
- ...Hims & Hers is seeking a Laboratory Supervisor to oversee the daily operations of the clinical/core laboratory. The role emphasizes accurate... .... You will supervise scheduling, training, and performance management, and assist with SOP development and process improvements. A...
- EPM Scientific is seeking a Clinical Project Manager to join a collaborative CRO team in New Jersey. You will drive clinical study delivery across Phase I-III, coordinating with sponsors and internal stakeholders to ensure high-quality trials. The ideal candidate has 3+...
$60k - $70k
...Responsibilities: Under the direct supervision of the Nurse Manager of Clinical Research Center (CRC), you will be responsible for... ...all team members (i.e., physicians, nurses, hospital, and laboratory staff) to ensure that services are coordinated and delivered to...Temporary work- Get AI-powered advice on this job and more exclusive features. The Clinical Research Coordinator will oversee the day-to-day operations of clinical trials, ensuring they are conducted ethically and according to protocol. Key Activities Protocol Familiarization : Understanding...Full timeContract work
$70k - $80k
...of the research team (i.e., physicians, nurses, hospital, and laboratory staff), and the research sponsors – to ensure that services are... ...consenting/retention; activation; regulatory compliance, data management, and ensuring Serious Adverse Events (SAEs) are completed and...Full timeTemporary workWork at officeRemote work- Vitalief is seeking an experienced Clinical Research Coordinator to join our team as a full-time employee supporting Phase II-IV oncology interventional trials at a community hospital site in Newark, NJ. This role is ideal for someone with 6–12 months of coordination experience...Full time
$55k - $60k
...pharmaceutical-sponsored, ECOG, and investigator-initiated studies.Manage trials across multiple oncology disease groups, including GYN,... ..., infusion teams, nursing staff, radiology, pathology, laboratories, and other clinical departments.Monitor patient safety, document...Full timeTemporary workWork at officeRemote workMonday to Friday1 day per week- ...Coordinator is responsible for the overall coordination, organization, management, and efficient implementation of clinical trials. The CRC... ...medical terminology to communicate with physician office and laboratory staff. Demonstrate the initiative to act independently,...Work at office
- ...Clinical Research Coordinator The Clinical Research Coordinator is responsible for the oversight of data management activities, protocol management activities and regulatory compliance with federal and local regulations as they relate to the conduct of clinical trials...Local area
- ...Clinical Research Coordinator to support clinical trials, particularly in Oncology. The role involves patient interaction, data management, and ensuring regulatory compliance. Candidates must have a Bachelor’s Degree and at least 2 years of clinical research experience...Full time
- ...Bayer is seeking a Learning Experience & AI Enablement Manager to shape innovative learning across US Pharmaceuticals. You’ll blend instructional design, AI-enabled learning, and technology to deliver scalable, measurable solutions that improve performance across the organization...
$173.2k - $272.6k
...development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical development and studies... ...job posting end date. SummaryLocation: USA - New Jersey - Rahway; USA - Massachusetts - Boston (MA Parcel B Laboratory)Type: Full timeFull timeFor contractorsLocal areaFlexible hours$282.2k
...-clinical to post-licensure). The Senior Clinical Director may manage the entire cycle of clinical development for their assigned studies... ...: USA - New Jersey - Rahway; USA - Massachusetts - Boston (MA Parcel B Laboratory); USA - Pennsylvania - Upper GwyneddType: Full timeFull timeFor contractorsLocal areaVisa sponsorshipFlexible hours$65k - $78k
...The CRC will collaborate closely with the Principal Investigator and research leadership to support the successful execution, management, and ongoing operations of the vascular medical device observational registry. WHY VITALIEF? Impactful Work: Contribute to...Full timeTemporary workWork at officeRemote work2 days per week3 days per week$65k - $78k
...offers a hybrid work setup with 2-3 days onsite and a salary range between $65,000 and $78,000 based on experience. The role includes managing study activities, ensuring compliance, and collaborating with the research team. Ideal candidates must hold a relevant Bachelor's...$22 - $23 per hour
...data entry, test material preparation and data collection. This position may coordinate and execute projects assigned by the Clinic Manager while abiding by Good Clinical Practice (GCP) guidelines. Job Functions Performs station and instrumentation duties on other...Hourly payWork experience placementImmediate start- Vitalief is seeking a Clinical Research Coordinator in New Brunswick, NJ, to manage Oncology-related trials. Responsibilities include patient screening, consent, and managing patient care, while collaborating with healthcare teams. A Bachelor's degree and 1-2 years of...
$75k - $85k
...pharmaceutical‑sponsored, ECOG, and investigator‑initiated studies. Manage trials across multiple oncology disease groups, including GYN,... ..., infusion teams, nursing staff, radiology, pathology, laboratories, and other clinical departments. Monitor patient safety, document...Full timeTemporary workWork at officeRemote workMonday to Friday1 day per week- Vitalief is seeking an experienced Clinical Research Coordinator to join our team as a full-time employee supporting Phase II-IV oncology interventional trials at a community hospital site in Newark, NJ. This role focuses on coordinating multiple trials with a collaborative...Full time
$173.2k - $272.6k
...Atherosclerosis & Metaboslim medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical development and studies, including development strategy, study design, initiation,...For contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$110k - $140k
...breakthroughs for patients. POSITION OVERVIEW Vitalief is seeking an experienced Pre & Post-Award Clinical Research Grants Project Manager to support a major statewide clinical research initiative for a leading academic medical center in New Jersey. The Project...Full timeTemporary workWork at officeRemote work$32 - $50.73 per hour
Medical Laboratory Scientist II - Edison, NJ, On-Call 2:00PM- 10:30PM - Every other weekend as needed Quest Diagnostics is hiring a Medical... ...controls and/or (c) work practice controls as directed by management.Answer questions from clients or other lab personnel, if applicable...Full timeWork experience placementWork at officeLocal areaShift workWeekend workAfternoon shift$310.9k
...marketed medicines in the Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. The Executive Director will manage and oversee the entire cycle of late stage clinical development from Phase 2 to Phase V, including development of program strategy...Full timeFor contractorsLocal areaFlexible hours$190.8k - $300.3k
...assessments, systematic reviews and meta-analyses, and economic modelling. Key responsibilities also include development of American Managed Care Pharmacy (AMCP) dossiers for U.S. payers and Global Value Dossiers for use by local subsidiaries in their HTA submissions.The...Full timeFor contractorsLocal areaWorldwideFlexible hours
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