Quality Control Analyst Job at Novitium Pharma (East Windsor)

Quality Control Analyst

We are looking for a detail-oriented Quality Control Analyst who will play a key...

Location

United States , DeLand

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Experience in data analysis, quality assurance, and data validation within business systems or ERP environments
Proficiency in writing SQL queries and using data investigation techniques to identify inconsistencies or root causes
Ability to test system changes, evaluate report accuracy, and verify the impact of updates before release
Familiarity with ERP platforms and related reporting structures used to support operational and financial processes
Strong analytical and problem-solving skills with the ability to interpret findings and recommend corrective actions
Effective communication skills for working with cross-functional teams, trainers, and business stakeholders
Payroll-related experience is strongly preferred
Ability to manage multiple priorities in a fast-paced quality control and validation setting

Job Responsibility

Evaluate upcoming system releases by performing hands-on testing and confirming that existing features continue to function as intended before deployment
Examine new enhancements in depth, investigate unexpected behavior, and identify likely causes of defects or performance issues
Review, revise, and create reports to ensure they meet business needs and produce dependable results
Test reporting outputs for completeness and accuracy prior to release, resolving discrepancies through structured analysis
Query and assess data across multiple databases using SQL and related scripting techniques to support troubleshooting and reporting validation
Confirm that system transactions and workflows generate correct financial and operational outcomes through detailed data checks
Assist with database data-load activities and verify the integrity of records after processing is complete
Communicate findings clearly to trainers and stakeholders, offering practical recommendations that improve user readiness and support quality-focused training
Collaborate with functional partners and technical teams to ensure system behavior remains aligned with established business processes and expected outcomes

What we offer

medical
vision
dental
life and disability insurance
401(k) plan

Fulltime

Quality Control Analyst

We are supporting a growing and forward-thinking API manufacturer within the med...

Location

United Kingdom , Sandwich, Kent

Salary:

28000.00 - 30000.00 GBP / Year

Cranleigh STEM

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensic Science, or related discipline (or equivalent experience)
Proven industrial or commercial laboratory experience using HPLC (assay and impurity analysis)
Experience in QC testing of APIs
Strong understanding of GMP environments
Good working knowledge of Microsoft Office (Word, Excel)
Excellent attention to detail and data accuracy
Ability to prioritise workload and adapt to changing priorities
Effective written and verbal communication skills
Right to work in the UK

Job Responsibility

Perform analytical and physical testing of Active Pharmaceutical Ingredients (API)
Conduct HPLC analysis (assay and impurities) within an industrial/commercial laboratory environment
Support production schedules through timely and accurate testing
Work collaboratively with Production and Quality Assurance teams to ensure GMP compliance
Accurately record, analyse, and report results in line with regulatory requirements
Contribute to maintaining controlled manufacturing processes aligned with international regulatory standards

Fulltime

Quality Control Analyst

SRG is partnering with a global leader in chemical manufacturing to recruit a nu...

Location

United Kingdom , Grangemouth, Falkirk

Salary:

Not provided

SRG

Expiration Date

Until further notice

Requirements

HND or degree in a relevant scientific discipline (or equivalent experience)
Hands-on experience with HPLC and/or GC is essential
Proven track record in HPLC, LC-MS, or GC analysis within an industrial setting preferred
Ability to work independently and as part of a team
Comfortable working in a fast-paced environment

Job Responsibility

Perform high-throughput QC analysis of raw materials, in-process samples, and finished products
Conduct analytical testing using HPLC, GC, FTIR, UV-Vis, and other wet chemistry techniques
Carry out swabbing and hygiene monitoring across the plant
Ensure strict compliance with health and safety standards
Analyse and interpret results accurately
Calibrate and maintain laboratory equipment
Collaborate effectively within a team environment

What we offer

Shift allowance available

Fulltime

Quality Control Analyst

As Quality Control Analyst you will be responsible for ensuring software meets t...

Location

Egypt , Cairo

Salary:

Not provided

Coca-Cola HBC

Expiration Date

Until further notice

Requirements

Bachelor’s degree in computer science, Information Technology, or a related field. Master’s degree preferred
3 years of hands-on experience as a Software Tester or in a similar role, working on high-availability web platforms
Certification in ISTQB Foundation Level Agile Tester (CTFL-AT) is required
Experience with MS D365 CRM is a must
Strong knowledge of testing technologies, tools and techniques
Proficiency with test management and experience with bug tracking tools
Experience in working in Agile software development teams
Excellent problem-solving skills and attention to detail
Strong communication skills and proven ability to work in a multicultural environment
Self-critical mindset and strive for continuous improvement

Job Responsibility

Plan, design and implement test cases for new and existing software features based on the business requirements
Define test suites to enrich the Product test plan in incremental cycles
Prepare and coordinate all related all test activities prior to test execution
Execute the test cases to validate newly developed user stories
Identify automation-candidate scenarios to increase the regression coverage
Report defects, track their status, verify bug fixes, analyze new issues or regressions, and communicate them to the developers
Bug lifecycle management (reporting, tracking, escalation, verification) by using Defect management tool (azureDevOps)
Contribute to update and maintain the documentation on testing practices, environments, and tools
Plan, define, and execute comprehensive Integration, Smoke, and Regression Testing
Design User Acceptance Tests (UAT) to ensure product quality for end-users and provide necessary support to Key Users during the UAT phase

What we offer

Bonus incentives
IT Equipment
Learning programs
Medical Insurance
Free product quota
Work with iconic brands
Supportive team
Work from home

Fulltime

Senior Quality Control Analyst

SRG are delighted to be partnered with a world-leading cell and gene therapy man...

Location

United Kingdom , Edinburgh

Salary:

Not provided

SRG

Expiration Date

Until further notice

Requirements

Demonstrable prior experience in a GMP quality control lab environment
Team leadership experience
Expert level practical knowledge of flow cytometry
Experience in assay validation
Prior experience in a cell and gene therapy manufacturing organisation

Job Responsibility

Lead the analytical quality control team on a shift
Be a go-to person for technical queries related to the workflow and general GMP enquiries
Collaborate closely with manufacturing/production to ensure GMP method transfer and compliance

Fulltime

Analyst, Quality Control, Microbiology

In this essential role, you will serve as the Microbiology Quality Control Analy...

Location

United Kingdom , Oxford

Salary:

Not provided

Moderna

Expiration Date

Until further notice

Requirements

BSc in a relevant scientific discipline with 5 years Quality Control experience in a cGMP organization with a focus on Microbiology
Hands-on experience of various Microbiology testing techniques and analyses (e.g. Vitek, Isolator Technology, Bioburden, BET, Sterility, others)
Working knowledge of relevant and current FDA, EU, ICH guidelines and regulations preferred
Working experience in a GMP environment
Ability to collaborate effectively in a dynamic, cross-functional matrix environment
Ability to efficiently prioritise and complete multiple projects and tasks in a fast-paced environment
Proven ability to conduct investigations

Job Responsibility

Conducting routine environmental monitoring (EM) and sampling of critical utilities such as water systems in a GMP manufacturing facility
Executing microbiological analyses including TOC, Conductivity, Bioburden, Endotoxin, Sterility, and other GMP QC methods
Supporting GMP testing for product release, stability, and validation samples
Preparing, shipping, and receiving contract laboratory samples, including those for microbiological identification
Participating in new microbiological method transfers in collaboration with Analytical Sciences & Technology (AS&T) teams
Supporting development, implementation, and maintenance of laboratory systems in line with cGMP expectations
Performing general laboratory support activities including reagent preparation, equipment maintenance, and housekeeping
Participating in audit readiness activities, including support to internal and external audit teams
Assisting in equipment and method qualifications, and potentially troubleshooting assay methods and instrumentation
Drafting and revising SOPs, protocols, reports, and contributing to quality system documentation (e.g., deviations, CAPAs, EM excursions, and change controls)

What we offer

Best-in-class healthcare, plus voluntary benefit programs
A holistic approach to well-being with access to fitness, mindfulness, and mental health support
Family building benefits, including fertility, adoption, and surrogacy support
Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
Savings and investments to help you plan for the future
Location-specific perks and extras

Fulltime

Analyst, Quality Control, Chemistry & Stability

The Role: Joining Moderna offers the unique opportunity to be part of a pioneeri...

Location

Australia , Melbourne

Salary:

Not provided

Moderna

Expiration Date

Until further notice

Requirements

BSc in a relevant scientific discipline (Chemistry preferred) with 5 years Quality Control experience in a cGMP organization with a focus in Analytical Chemistry
Hands on experience with analytical chemistry techniques including, but not limited to, HPLC, UPLC, particle analysis and plate reader-based assays
Working knowledge of relevant and current FDA, EU, ICH guidelines and regulations preferred
Working experience in a GMP environment
Ability to collaborate effectively in a dynamic, cross-functional matrix environment
Ability to efficiently prioritize and complete multiple projects and tasks in a fast-paced environment
Proven ability to conduct investigations

Job Responsibility

Perform GMP QC Chemistry methods including HPLC, UPLC, UV, and Particle Analysis via Dynamic Light Scattering
Execute HPLC (AEX) and NaOH plate reader-based assays to support process stat testing
Support method transfer projects internally and externally in collaboration with Analytical Sciences & Technology (AS&T) teams
Execute general lab operational tasks aligned with cGMP, including reagent preparation, equipment maintenance, and good documentation practices
Provide audit support for both internal and regulatory inspections
Create, review, and revise SOPs, protocols, and reports aligned with evolving quality standards and compliance frameworks
Support all stability program operations: perform sample set downs, pulls, inventory checks, labeling, and data entry in LIMS and inventory systems
Maintain and trend stability data using statistical analysis
produce stability tables, charts, protocols, and final reports
Troubleshoot assay methods and lab equipment as needed

What we offer

Best-in-class healthcare, plus voluntary benefit programs to support your unique needs
A holistic approach to well-being with access to fitness, mindfulness, and mental health support
Family building benefits, including fertility, adoption, and surrogacy support
Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
Savings and investments to help you plan for the future
Location-specific perks and extras

Fulltime

Senior Quality Control Analyst

We are looking for a highly skilled, hands-on Senior Quality Control Analyst to ...

Location

Canada , Vancouver

Salary:

88000.00 - 110000.00 CAD / Year

AbCellera Biologics

Expiration Date

Until further notice

Requirements

Deep, hands-on Microbiology experience in a regulated (GMP) QC environment
Experience mentoring or leading team members working within microbiology labs or cleanroom/controlled environments
8+ years of hands-on QC microbiology experience in a GMP setting
Bachelor’s degree in Microbiology or a related life sciences field
Clear communication, collaboration, and calm, structured decision-making under pressure
Strong ownership, accountability, and a solutions-focused mindset
Organized, detail-oriented, and committed to inspection readiness and data integrity
Thrives in an environment requiring in-lab leadership, cross-functional coordination, and prioritization of operational needs

Job Responsibility

Leading Microbiology operations, including bioburden, endotoxin, microbial ID, growth promotion, EM sampling, water testing, and trending
Troubleshooting microbiological assays, contamination events, and EM deviations, ensuring timely and compliant resolution
Providing daily in-lab mentorship to the QC team, fostering strong technique, aseptic practices, and microbiological best practices
Ensuring microbiology labs and adjacent QC spaces remain inspection-ready, including GMP housekeeping and equipment readiness
Coordinating stability pulls, sample preparation, testing, and data tracking across QC programs
Overseeing sample receipt, chain-of-custody, aliquoting, storage conditions, and distribution workflows
Supporting routine sampling, testing, and trending of Utilities (WFI, clean steam, compressed gases) with appropriate documentation
Reviewing micro data packages, protocols, reports, and testing documentation for accuracy and adherence to ALCOA++ principles

What we offer

Equity
Annual bonus dependent on team and company performance
6% (non-match) RRSP contribution
CAD $1,500 annual Active Lifestyle Allowance
Annual vacation
Professional development opportunities
Comprehensive health benefits
Scientific and technical mentorship
Strong sense of community and connections through work, clubs, and socials

Fulltime

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