Quality Analyst Salary at Firstconnect Digital BETA

Job Title: Quality Control Consultant Location: New Jersey (Onsite/Hybrid – as required) Industry: Pharmaceutical / Life Sciences Job Overview: Our client is digitizing their laboratory operations, transitioning from paper-based systems to a fully paperless process. They are seeking a Quality Control Consultant with strong laboratory experience to lead and guide the integration of laboratory instruments into their existing LIMS system. Key Responsibilities: Lead and support the integration of lab instruments into the LIMS system Set up and perform LIMS integrations, including configuring hardware/software connections Ensure balances and lab instruments are networked and communicating with LIMS Collaborate with site and global teams to gather requirements and define new procedures Provide expert guidance on best practices for paperless lab operations Required Skills & Experience: Hands-on experience integrating lab instruments with LIMS (any major LIMS platform) Prior experience setting

Work for a Central New Jersey (Somerset County) area company that produces electro-mechanical power connection products. Quality Specialist (Quality Assurance): Summary: The Quality Specialist is responsible for supporting quality improvement initiatives, reducing defects, and ensuring processes meet company standards. This role involves conducting defect analysis, implementing corrective actions, and working with production teams to improve quality and efficiency. Key Responsibilities: * Quality Improvement Projects: o Lead and support initiatives focused on reducing production defects, waste, scraps, and rework. o Work closely with production teams to implement corrective and preventive actions (CAPA). o Track and report progress on assigned quality improvement projects. * Defect Analysis & Troubleshooting: o Investigate recurring quality issues and assist in root cause analysis. o Support data collection and trend analysis on defects and process inefficiencies. o Recommend and help

Job Type Full-time Description The QC Analyst II will be responsible for analytical testing and data verification supporting both late-stage clinical and commercial small molecule and biosimilar products in cGMP-compliant laboratories. A strong background in protein chemistry will be essential to perform and troubleshoot techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays. A demonstrated ability to collaborate across multiple departments to drive timely resolution of projects, laboratory investigations, and process improvements is required. Analytical testing to support product in-process, release, and stability programs. Strong knowledge of cGMP, Quality Systems, and ICH / regulatory guidance. Conduct, compile, and/or review Out of Specification lab investigations, deviations, and corrective and preventative actions plans. Work with cross-functional teams to advance projects, maintain equipment, and author

Quality Control Analyst: Microbiology - Contract - Philadelphia PA Join this team as a Quality Control Analyst and play a key role in maintaining top-tier quality standards! If you have a keen eye for detail and a passion for compliance, this could be your perfect opportunity. Primary Responsibilities: This role will support quality control testing operations, focusing on microbial testing of drug products. This includes tasks such as bioburden, endotoxins, mycoplasma, gram stain, environmental monitoring, and sterility techniques. We are looking for someone who can efficiently manage multiple priorities and demonstrate a strong sense of urgency. Skills & Requirements: Bachelor's degree in biological sciences or equivalent. Ability to work effectively with multi-disciplined teams. Strong attention to detail and technical skills. Proficient in managing multiple priorities with tight deadlines. High level of ownership and accountability. Proficiency in Microsoft Office applications (Outl

Quality Control Analyst II - Contract - Philadelphia, PA We are on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world. Proclinical is seeking a Quality Control Analyst II specializing in Microbiology to join our client's team in Philadelphia. Primary Responsibilities: The successful candidate will support quality control testing operations, focusing on microbial testing for drug products. This includes tasks such as bioburden, endotoxins, mycoplasma, gram stain, environmental monitoring, and sterility techniques. Skills & Requirements: Bachelor's degree in biological sciences or a related field. Experience in the pharmaceutical industry within a Quality Control role. Ability to work effectively with multi-disciplined teams. Strong attention to detail and technical skills. Capability to manage multiple priorities with tight deadlines. High level of ownership and accountability. Familiarity with GDP, GLP

Job Type Full-time Description Position Summary Specialist III QA is a regular employee in a full-time exempt position at Kashiv Biosciences. The responsibility for document management lies with this role, including issuance and retrieval of logbooks, laboratory notebooks, issuance of protocol and report numbers, and management of documentation. The employee will support the activities of the QA department in review of QC data and reports, and other reports such as SOPs, CAPAs, Deviations, Change Controls and OOS as needed. Requirements Essential Duties & Responsibilities •Writes, revises, and reviews standard operating procedures (SOPs). •Conduct reviews of release testing, stability testing, raw material testing, method validations, equipment qualifications and calibrations, technical protocols and reports to ensure compliance with internal procedures and policies, good documentation practices (GDPs), current good manufacturing practices (cGMP), ICH, and other applicable regulations.

The Quality Assurance Analyst is responsible to ensure the generation and completion of investigation reports (i.e Nonconformance and Root Cause investigations for Corrective and Preventative Actions (CAPA)). Functional responsibilities include support and execution of root cause analysis and the determination of appropriate corrective/preventative actions as a result of investigation findings. This includes, but is not limited to, providing quality, compliance, and technical feedback/review/approval regarding quality and manufacturing investigations. The incumbent will also support the trending associated with quality and manufacturing investigations, Key Performance Indicators (KPIs) and / or other Quality Metrics, support and compile reporting regarding COQ (Cost of Quality), APR Annual Product Review, support internal Validation (IQ/OQ/PQ) protocol completion, support regulatory and customer audits and interact with the customer to resolve concerns regarding quality and manufacturi

Role name: Quality Lead/MANAGER Role Description: API XP Lead Test Analyst, Selenium, TOSC Competencies: Selenium Experience (Years): 10 & Above Essential Skills: API XP Lead Test Analyst, Selenium, TOSC Desirable Skills: API XP Lead Test Analyst, Selenium, TOSC Country: United States Branch | City | Location: MOUNT LAUREL, NJ Diverse Lynx LLC is an Equal Employment Opportunity employer. All qualified applicants will receive due consideration for employment without any discrimination. All applicants will be evaluated solely on the basis of their ability, competence and their proven capability to perform the functions outlined in the corresponding role. We promote and support a diverse workforce across all levels in the company.