CrawlJobs Logo
Tucker Parker Smith Group Logo Tucker Parker Smith Group · Quality Control

Qc Lab Assistant

United States, Northridge 22.00 USD / Hour · Job Posted June 14, 2026
Apply Position
Job Link Share

Job Description

We are seeking a motivated and detail-oriented QC Lab Assistant to support Quality Control operations within a pharmaceutical manufacturing environment focused on inhalation and transdermal products. This is an excellent entry-level opportunity for someone interested in gaining hands-on laboratory experience in a regulated manufacturing setting.

Job Responsibility

  • Collect, wash, dry, and properly store laboratory glassware following SOPs and cGMP guidelines
  • Operate automated glassware washers and perform manual washing as needed
  • Use approved cleaning agents and follow laboratory cleaning procedures
  • Maintain cleanliness, organization, and 5S standards throughout the laboratory
  • Perform sporicide cleaning in designated laboratory areas
  • Monitor and maintain inventory of laboratory glassware, chemicals, and reagents
  • Handle laboratory waste according to EHS and safety procedures
  • Wear appropriate PPE and follow all laboratory safety requirements
  • Support additional laboratory activities and assist the QC team as needed
  • Perform other related duties assigned by management

Requirements

  • High school diploma or equivalent required
  • Strong attention to detail and organizational skills
  • Basic math and writing skills
  • Ability to follow safety procedures and work in a laboratory environment
  • Comfortable lifting up to 50 lbs. (glassware, water compounds, and supplies)
  • Ability to work independently and within a team environment
  • Flexible and dependable with a strong work ethic

Nice to have

  • Previous experience working in a laboratory or manufacturing environment
  • Familiarity with cGMP practices and SOP-driven environments
  • Understanding of 5S workplace organization principles
  • Experience handling laboratory cleaning or inventory responsibilities

What we offer

  • Great entry-level opportunity within the pharmaceutical industry
  • Hands-on experience in a Quality Control laboratory environment
  • Opportunity for extension or long-term conversion based on performance
  • Collaborative team environment with training and growth potential
Tucker Parker Smith Group - All Job Offers

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Suggested Tags: Frontend Developer Secretary Talent Manager Salesforce Administrator Data Analyst
Similar Jobs for

Qc Lab Assistant

8 matching positions

Qc & Formulation Assistant

SRG is working with an independent contract manufacturer of personal care / skin...
Location
Location
United Kingdom , Brighouse
Salary
Salary:
28000.00 - 30000.00 GBP / Year
srgtalent.com Logo
SRG
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 2+ years recent experience in QC testing / wet chemistry and formulation within the personal care / skincare industry
  • Willing and able to work stood up in a Fast-paced manufacturing environment on the factory floor
  • Experience of working to cosmetic regulations such as EU Cosmetics Regulation, UK REACH, FDA, BRC etc.
  • Strong communication skills and can relay information accurately
  • Full right to work in the UK - there is no sponsorship available for this role
Job Responsibility
Job Responsibility
  • QC testing of raw materials, in-process samples and finished product to check batches meet specifications
  • Development and implementation of SOP's and QC procedures
  • Lab techniques include PH testing, viscosity, stability testing and packaging compatibility testing
  • Conduct routine microbiological and physical testing on products to ensure batches are compliant against industry regulations
  • Work in harmony with Production and QA to achieve production delivery plans and resolve any quality issues
  • Collaborate with stakeholders to ensure R&D, production and packaging compliance and resolve any inconsistencies to ensure batch consistency
  • Formulation and development of batches to help improve new and existing batches
  • Fulltime
Read More
Arrow Right

Process Scientist I

This position is responsible for material processing, reagent formulation, techn...
Location
Location
United States , Stillwater
Salary
Salary:
61000.00 - 70000.00 USD / Year
int.diasorin.com Logo
Diasorin
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Associates degree in Chemistry, Biology or Medical Technology required or Bachelor's or Master's degree preferred in Chemistry, Biology, Medical Technology or related science field or a 2 year degree (i.e. MLT) with equivalent experience
  • 1+ years of related laboratory experience and/or demonstrated competence within the in-vitro diagnostic industry
  • Basic understanding of immunology and immunoassay techniques
  • Ability to work in a regulated environment
  • Working knowledge of general lab equipment (e.g. pH meter, balances, mixers, etc.)
  • Working knowledge of MS Excel
  • familiarity with Google Suite
  • Basic understanding of statistical analysis
  • Advanced skills in: Math and calculations
  • Writing and documentation
Job Responsibility
Job Responsibility
  • Perform material processing and reagent for formulation bulk intermediates and components
  • Determine reprocessing need for calibrator, controls, and conjugates with assistance
  • Perform Good laboratory practices - maintain clean workspace in QC and Reagent Prep labs
  • Contribute to group Reagent Prep and QC duties, including lab and equipment maintenance
  • Utilize SAP (kitting, ordering to Cost Center, assign expiration dates, etc.) to ensure correct dating, accounting, and flow through facility
  • Participate in inventory accountability - PSA count, cycle counts, accurate kitting, etc.
  • Perform in-process testing and final Quality Control for LIAISON products per established procedures using the LIAISON analyzer family
  • Assign calibrator values to optimize kit performance
  • Assign kit control ranges per established procedures
  • Monitor internal control supplies and manufacture new controls as needed
What we offer
What we offer
  • health benefits
  • retirement and financial wellbeing
  • time off programs
  • wellbeing support and perks
  • annual incentive program
  • Fulltime
Read More
Arrow Right

Student Assistant for Biochemical Laboratory Work

As a student assistant, you will work closely with our team of three scientists ...
Location
Location
Denmark , København
Salary
Salary:
Not provided
life-science-talent-solutions.dk Logo
Life Science Talent
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Have a flair for laboratory work and wet-lab experience
  • Possess a basic understanding of enzyme kinetics
  • Work in a structured, analytical, and reliable manner
  • Are comfortable following detailed protocols
  • Are motivated to learn and contribute to a small, dynamic team
  • Are about to finish their bachelor’s degree and/or have at least two years left of their graduate studies
Job Responsibility
Job Responsibility
  • Production of assay products and substrates
  • Packaging and shipment of finished kits
  • Routine laboratory tasks and maintenance like buffer preparation etc.
  • Enzymatic analyses for quality control (QC)
  • Supporting assay development projects
  • Participation in stability studies and robustness testing
  • Thorough documentation of all work in accordance with our internal standards and our commitment to Good Laboratory Practice (GLP)
  • Parttime
Read More
Arrow Right

Quality Control (Laboratory Assistant)

Summer Opportunity Laboratory Assistant – Quality Control needed in Ledbury with...
Location
Location
United Kingdom , Ledbury
Salary
Salary:
32043.00 GBP / Year ▼
pertemps.co.uk Logo
Pertemps Network Group
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Strong attention to detail and a methodical approach
  • Confident with computers (SAP experience is a bonus)
  • Able to thrive in a fast-paced environment
  • Good communication skills
  • Previous lab or production testing experience (helpful but not essential)
Job Responsibility
Job Responsibility
  • Acting as the key contact for QC lab activities during your shift
  • Carrying out daily equipment checks to keep everything running smoothly
  • Sampling and preparing materials from production lines
  • Performing wet chemistry testing
  • Conducting fruit quality checks (weight, condition, Brix)
  • Comparing results against specifications and flagging any issues
  • Accurately recording data in SAP systems
  • Managing lab stock and chemical inventory
  • Keeping the lab clean, safe, and organised
  • Supporting both Quality and Production teams
What we offer
What we offer
  • Free on-site parking
  • Valuable hands-on lab experience in a real production setting
  • Exposure to quality control processes in the food industry
  • A supportive, team-focused environment
  • A great addition to your CV for future science or manufacturing roles
  • Fulltime
Read More
Arrow Right

Lab Technician

We're looking for a Laboratory Technician to help keep our lab running smoothly ...
Location
Location
Netherlands , Amsterdam
Salary
Salary:
Not provided
cradle.bio Logo
Cradle
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • MBO-3/4, HBO, BSc, or equivalent degree in Biotechnology, Laboratory Science, or a related field
  • Familiarity with aseptic techniques and routine lab operations
  • Organized, precise, and safety-conscious
  • Proactive communicator who keeps colleagues informed
  • Comfortable working independently during quieter lab hours
  • Fluent in English
Job Responsibility
Job Responsibility
  • Maintain a tidy, safe, and well-organized laboratory according to ML-1 and ML-2 standards and 5S principles
  • Restock consumables, reagents, and media
  • update inventory records
  • Perform daily equipment checks and assist with general lab upkeep
  • Handle biological and chemical waste according to safety protocols
  • Set up, clean, and maintain lab instruments such as balances, pipettes, and pH meters
  • Write and update SOPs, protocols, and experiment documentation
  • Provide general administrative support to the Lab Manager as needed
  • Prepare, sterilize, and label media and buffers
  • Record batch details accurately and track expiry dates
What we offer
What we offer
  • Competitive salary
  • Generous equity stake
  • Wide range of benefits
  • Career progression opportunities
  • Fulltime
Read More
Arrow Right

Associate Document Coordinator

Labcorp is seeking a Remote, UK based, Associate Document Coordinator to join ou...
Location
Location
United Kingdom , Ripon
Salary
Salary:
Not provided
themuse.com Logo
The Muse
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in Life Sciences
  • Strong communication, organisation and time management skills
  • Excellent attention to detail
  • Ability to work collaboratively paired with a solution orientated approach
  • Ability to learn / utilise word processing software, database, spreadsheet, and specialised software
Job Responsibility
Job Responsibility
  • Works with Study Coordinators (SCs) and Analytical Coordinators (ACs), as appropriate, to prepare, monitor, maintain, and understand the finalization/archival scheduling mechanism and successfully performs applicable tasks around study archival
  • Notifies necessary personnel of study finalization/archival
  • Assists in gathering required paper/electronic items for archival
  • Prepares and proofs required paperwork in a timely, efficient, and error-free manner
  • Learns to read and understand study protocols, sample analysis outlines, amendments, study schedules, regulatory requirements, and Labcorp SOPs/P&Ps as they pertain to client deliverables (i.e. shipping, archival, data retrieval, and compilation etc.)
  • Learns to prepare and proof required paperwork for document and/or supply shipments in a timely, efficient, and error-free manner
  • Learns client-specific requirements for cover letters, inventories, or additional materials, as appropriate
  • Learns to proof tables and figures prepared by others
  • Learns and successfully performs applicable tasks around table and figure preparation, including proficiency with applicable data collection systems and preparation software
  • Learns and successfully performs report to data QC of at least one study type
What we offer
What we offer
  • Health Insurance
  • Health Reimbursement Account
  • Dental Insurance
  • Vision Insurance
  • Life Insurance
  • Short-Term Disability
  • Long-Term Disability
  • Pet Insurance
  • Mental Health Benefits
  • FSA
  • Fulltime
Read More
Arrow Right

Chemistry Technician I/II

The Quality Control Technician supports the Quality Control department by assist...
Location
Location
United States , Wichita
Salary
Salary:
Not provided
fagron.com Logo
Fagron
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • A bachelor’s degree in a science field and 0-2 years in pharmaceutical quality control or combination of QC and other pharmaceutical quality experience. (graduate school may be considered toward) experience)
  • Previous experience in a pharmaceutical quality control position adhering to cGMP guidelines preferred.
  • Clear and effective communication Skills.
  • Ability to concentrate for extended periods of time and follow established safety and procedures.
  • Computer experience using Microsoft Office.
Job Responsibility
Job Responsibility
  • Collect and prepare samples for chemical analysis as required
  • HPLC testing, UV-vis testing, TOC testing, pH testing, conductivity testing, water content Karl Fischer volumetric and coulometric
  • Participate in method development
  • Help manage sample tracking
  • Help maintain lab organization
  • Lab Waste management
  • Adhere to procedural and regulatory guidelines for controlled substances
  • Assist in the quality process, and ensure the integrity of product quality, manufacturing, certification and release activities.
  • Adhere to the company safety regulations and assist in the training and awareness of safety guidelines to new employees in the department.
  • Maintain a clean, orderly and safe work environment.
What we offer
What we offer
  • Competitive salary
  • Comprehensive benefits
  • Performance package
  • Ability to be part of an international leader in an expanding industry.
  • Fulltime
Read More
Arrow Right

Medical Laboratory Scientist Group Lead

Medical Laboratory Scientist Group Lead - Mount Kisco, NY, Monday to Friday, 8:0...
Location
Location
United States , Mount Kisco
Salary
Salary:
35.59 - 58.75 USD / Hour
questdiagnostics.com Logo
Quest Diagnostics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Three (3) to five (5) years of clinical experience as a Medical Technologist within the designated discipline
  • Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation)
  • United States educated candidates must provide a detailed original transcript
  • Bachelor's Degree Medical Technology, Chemistry or Biology or Previously qualified as a Technologist under 42 CFR 493. 1433 published in March 14, 1990
  • Comprehensive theoretical and operational job knowledge in designated specialty required
  • Knowledge of organizational/departmental policies and procedures
  • Proven leadership and problem-solving skills
  • Must be detail-oriented, have the ability to work independently, establish work priorities for self and others and to handle several tasks simultaneously for maximum department efficiency
  • Ability to schedule and manage resources to meet department goals
  • Interpersonal skills necessary to deal courteously and effectively with supervisors, co-workers and clients
Job Responsibility
Job Responsibility
  • Demonstrate proficiency in all duties of a Medical Technologist I and II
  • Perform and report on assigned analytical tests in accordance with applicable Standard Operating Procedures (SOP) ensuring that applicable quality control requirements are met
  • Actively support and comply with laboratory policies and procedures for specimen handling and processing, test analysis, reporting and maintaining records of patient test results
  • Adhere to analytical schedules to maintain turnaround time of results including STATS or critical results to clients
  • Perform, review and document QC analysis to ensure accuracy of clinical data and proper instrument function
  • Make quality control decisions regarding the disposition of an assay or test
  • Review requests for validity checks and recommend an appropriate course of action taking into account the limitations of specimen requirements and the effects of time and the quality of additional and/or repeat testing
  • Serve as a technical resource for the department by investigating and resolving analytical testing problems, recommending a course of action in instances identified as beyond acceptable limits, and responding to non-routine/complex inquiries and/or requests from clients and sales representatives
  • Assist Lab Supervisor by monitoring workflow to meet testing schedules
  • distributing and reviewing work assignments
What we offer
What we offer
  • Day 1 Medical, supplemental health, dental & vision for FT employees who work 30+ hours
  • Best-in-class well-being programs
  • Annual, no-cost health assessment program Blueprint for Wellness
  • healthyMINDS mental health program
  • Vacation and Health/Flex Time
  • 6 Holidays plus 1 'MyDay' off
  • FinFit financial coaching and services
  • 401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months of service
  • Employee stock purchase plan
  • Life and disability insurance, plus buy-up option
  • Fulltime
Read More
Arrow Right