Laboratory Manager — cGMP Methods & QA Lead
Experic
Experic in Cranbury, NJ seeks a senior analytical leader to manage laboratory activities from raw material testing through finished product release. You will lead a small team of analysts, ensuring regulatory compliance and timely product delivery. You will develop, validate, and troubleshoot analytical methods (HPLC, GC, UV-Vis, FTIR, dissolution) with cross-functional teams, review data per GDP, and mentor staff while supporting regulatory inspections and CAPA resolutions. #J-18808-Ljbffr Experic
$125k - $155k
...responsible for the hands-on management of all laboratory activities, from raw... ...in compliance with cGMP, FDA, and ICH... ...while also overseeing the method development, validation... ...fast-paced role, you’ll lead a small but dedicated... ...teams (Manufacturing, QA, PDE, BD) to ensure seamless...SuggestedContract workWork at office$63k - $93k
Innophos is seeking a Quality Assurance Documentation Specialist for their Cranbury, NJ location. This role involves managing supplier quality documentation while ensuring compliance with regulatory standards. The ideal candidate has a degree in Food Science or a related...SuggestedWork at officeRemote work$80k - $100k
...responsibilities, this role provides day-to-day leadership to QA Associates, including work planning, performance management, and oversight of team deliverables in partnership... ...in a GMP or Quality Assurance environment (lead or senior experience preferred). Demonstrated...SuggestedShift work- ...QA Manager A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-... ...as well as the review of SOPs, investigations, specifications, methods, validation reports, cleaning verification reports, analytical...Suggested
$130.72k - $196.08k
...therapeutics to improve the lives of patients. As a Senior Clinical Trial Manager (CTM), you will play a pivotal role in driving the success of... ...environment where you will be empowered to take ownership and lead with autonomy. Key Responsibilities Lead the operational...SuggestedFull timeFixed term contract$119.12k - $178.68k
...support site feasibility, selection, activation, and ongoing site management. Drive in the oversight of service providers, tracking... ...work to connect employees while being immersed in our powerful laboratories. Whether you're in one of our office spaces or working remotely...Full timeFixed term contractWork at officeRemote work- ...seeking a dedicated and detail-oriented QA Manager to support the organization's commitment... ...and organizational skills. ● Ability to lead quality improvement initiatives and support... ...operational systems, and quality management methods. ● Ability to collaborate effectively...Work at officeLocal area
$73k - $128k
...title Quality Control Manager, PCT Work location... ...5 days a week). Laboratory and office-based role... ...QC Physiochemistry Lead is responsible for... ...This role oversees method execution, data integrity... ...to Manufacturing, QA, Regulatory, and... ...in compliance with cGMP, GLP, CFR, and...Work at officeAfternoon shift$166.75k - $228.85k
...Quality Microbiology, is responsible for leading Integra LifeSciences operational microbiology... ...monitoring• Bacterial endotoxin test method validation and monitoring• Bioburden test... ...long-term strategies and advise a team of managers and scientists across the Quality...Full timeTemporary work- Sun Pharma is seeking a qualified leader to oversee QA and QC operations in New Brunswick, New Jersey. The position requires ensuring compliance with cGMP standards and managing quality goals aligned with global objectives. Applicants should have a Bachelor's degree in...
$99.6k - $184.2k
...accounting, upholding workplace safety, managing our supply chain and sampling, supporting... ...investor relations documentServe as a key lead with legal & compliance on various workgroupsDevelops... ...in the development of tools and methods that will result in more accurate...Local areaFlexible hoursNight shift$119.12k - $178.68k
...support site feasibility, selection, activation, and ongoing site management.Drive in the oversight of service providers, tracking... ...work to connect employees while being immersed in our powerful laboratories. Whether you’re in one of our office spaces or working remotely...Full timeFixed term contractWork at officeRemote work$110.8k - $150.8k
...General Description: Manages all Quality Control (QC) Chemistry Laboratory - Capillary... ...Functions of the Job: Lead the QC Chemistry (CE) laboratory... ...analytical methods such as reduced and non-... ...Knowledgeable with USP/EP and cGMP/EU GMP regulations. Familiar...Hourly payFull timeLocal area$235k - $275k
...artificial intelligence. This position leads the development, prioritization, and execution... ...opportunities.2) Research & Innovation Management- Lead the design and implementation of... ...design and statistical/quantitative methods, including measurement science and/or psychometrics...Full timeWorldwide- ...ensuring products meet quality standards. The ideal candidate will have at least 10 years of relevant experience, be familiar with cGMP regulations, and possess strong leadership and analytical skills. Competitive salary and benefits offered, including 401(k) matching...
$140k - $182k
...cardiovascular disease preventable, curable and no longer the leading cause of death in the world. It is Kardigan's mission to develop... ...difference, every day. Kardigan is seeking a Clinical Trial Manager to contribute to the planning, oversight and delivery of its...Full timeContract workRemote work- ...Job Description Job Description Clinical Laboratory Director & Vice President, Translational & Computational Pathology Location:... ...& Vice President - Translational & Computational Pathology to lead pathology strategy, assay development, and clinical laboratory...Full timeRelocation packageMonday to FridayDay shift
$54.02k - $86.45k
...The Clinical Research Coordinator will: 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...Full timeWork experience placementWork at officeLocal areaShift work$138k - $160k
...forward. Role Overview As a Clinical Trial Manager, you will leverage extensive experience... ...startup to closeout. You will coordinate and lead cross‑functional teams, CROs, and vendors... ...sciences, nursing, pharmacy, medical laboratory technology, or related field (preferred)....- ...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
- ...Research Coordinator (CRC), you will be an integral part of studies at Astera Cancer Care by recruiting participants, collecting and managing the study data for the successful management of clinical trials. This is a full-time position.Responsibilities Include:Provide...Full timeWork experience placementLocal areaImmediate start
$60k - $70k
...Under the direct supervision of the Nurse Manager of Clinical Research Center (CRC), you... ...(i.e., physicians, nurses, hospital, and laboratory staff) to ensure that services are coordinated... ...(SAEs) are completed and reported to the QA Manager and sponsor, if necessary, within...Temporary work- ...of the research team (i.e., physicians, nurses, hospital, and laboratory staff), and the research sponsors – to ensure that services are... .../retention ; activation; regulatory compliance, data management, and ensuring Serious Adverse Events (SAEs) are completed and...Full timeTemporary workWork at officeRemote work
$170k - $200k
...Brunswick, NJ is seeking a Quality Assurance Leader to oversee compliance with cGMP regulations. The ideal candidate will have a Bachelor's degree and at least ten years of experience in QA leadership within a pharmaceutical environment, ensuring successful regulatory...$175k - $245k
...success. The OpportunityAs Head of Pharma Solutions R&D, you will lead a globally focused innovation organization that transforms... ...innovation into commercial outcomes and business growth. Experience managing innovation portfolios, strategic investments, and cross-functional...Temporary workImmediate start- ...and follow Guerbet on Linkedin, Twitter, Instagram and YoutubeWHAT WE ARE LOOKING FORGuerbet is looking for a qualified, dynamic QA Manager to enhance our quality management system through comprehensive SOP development, review, and revision, ensuring compliance with FDA...For contractorsLocal area
- A Clinical Trial Manager with 3-8 years of experience in the planning, execution, oversight, and delivery of clinical trials in accordance... ...study budgets, forecasts, and review of vendor contracts. Lead study team meetings and provide regular updates to senior management...
- 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...
- Position Title: Clinical Laboratory Director & VP, Translational & Computational Pathology Location: North Brunswick, NJ (On-Site) Reports... ...leadership and direct scientific contributions as needed. Lead laboratory accreditation, inspections, audits, and regulatory interactions...Relocation package
- Aya Healthcare in East Brunswick, NJ, seeks a Clinical Research Coordinator for an immediate 13-week assignment in an outpatient clinic. The days shift (08:00-17:00), 5 x 8-hour schedule, with weekly pay ranging from $1,729.80 to $1,959.80, starts on 08/24/2026, and 1 opening...Weekly payImmediate startDay shift
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Laboratory Manager — cGMP Methods & QA Lead. Be the first to apply!


