Quality Control (QC) Analyst Job at SRG (Grangemouth)

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

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

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

Quality Control Analyst II

Quality Control Analyst II - Contract - Norton, MA. Are you passionate about qua...

Location

United States , Norton

Salary:

40.00 - 45.00 USD / Hour

Proclinical

Expiration Date

Until further notice

Requirements

Degree in biology, biochemistry, chemistry, or a related scientific field (Associate degree or Biotech Certificate considered)
Experience in GMP quality control within the pharmaceutical or biotechnology industry
Knowledge of microbiology testing and environmental monitoring/critical utility sampling
Familiarity with quality events such as investigations, deviations, CAPAs, and change controls

Job Responsibility

Conduct routine and non-routine analytical HPLC/UPLC or microbiological assays for various samples
Support weekend laboratory operations and maintain accurate training records
Adhere to testing schedules and ensure timely completion of assignments to meet project timelines and quality metrics
Assist in maintaining laboratory equipment and inventory for smooth operations
Submit data promptly and review data as needed to ensure efficiency
Perform operational tasks such as critical utility sampling, environmental monitoring, and product testing
Contribute to updating controlled documents, including SOPs, work instructions, and test methods
Ensure compliance with internal standards, policies, and regulatory guidelines (e.g., GMP, GLP, ICH)
Collaborate with QC and cross-functional teams to support quality control operations
Participate in inspection readiness activities and support audits and inspections

Fulltime

New

Quality Control Validation Analyst

Join our team as QC Validation Analyst and start a new adventure in an internati...

Location

Italy , Latina

Salary:

26000.00 - 50000.00 EUR / Year

Amaris Consulting

Expiration Date

Until further notice

Requirements

2-3 years of experience with HPLC analysis using Empower3 software
Knowledge of cGMP and QC laboratory procedures in the pharmaceutical industry
Academic background: Degree in Chemistry, Pharmaceutical Chemistry and Technology or related field
Experience in analytical method validation in a GMP-regulated chemistry laboratory
Fluent Italian and good command of English
You have an ability to work precisely and efficiently in a regulated environment

Job Responsibility

Perform chemical analysis using HPLC with Empower3 software
Execute and document QC testing activities in compliance with GMP guidelines
Design and execute validation protocols for analytical methods (e.g., HPLC, GC, UV-Vis) in compliance with ICH and GMP guidelines
Perform validation experiments to assess accuracy, precision, specificity, linearity, range, detection and quantitation limits, robustness, and system suitability
Prepare and review validation documentation, including protocols, reports, and risk assessments
Support method transfer and verification activities between laboratories or from R&D to QC
Collaborate with cross-functional teams to ensure product quality compliance

What we offer

An international community bringing together 110+ different nationalities
An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities
A robust training system with our internal Academy and 250+ available modules
A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.)
Strong commitments to CSR, notably through participation in our WeCare Together program

Fulltime

Analyst II, Quality Control Microbiology

The incumbent will support the implementation and execution of core microbiology...

Location

United States , Durham

Salary:

70000.00 - 115000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Bachelor's or Master's degree in a scientific discipline
2+ years' relevant experience in the pharmaceutical/biotech industry
Excellent verbal and written communication skills
Strong writing skills
Strong team player that has a customer service approach and is solution oriented
Attention to detail and the ability to work equally well individually as within a multi-disciplinary team
Excellent time management skills
Consistent delivery of high-quality work at all times

Job Responsibility

Draft documentation for the microbiology programs (SOPs, WIs, Protocols, reports etc.)
Conduct and draft investigations for the microbiology programs (EM excursions, lab deviations, product OOS's, etc.)
Support the implementation and execution of microbiology laboratory programs, including bioburden, endotoxin, and rapid sterility testing, method verifications, media growth promotion and gram staining
Support the implementation and execution of the environmental monitoring (EM) program
Review and approve laboratory data for the microbiology programs
Support the incoming testing and management of raw materials
Assist with the data analysis and trending program for EM data
Support the implementation of the disinfectant efficacy qualification program
Partner with CQV representative to support the implementation of QC lab equipment by providing technical assistance during the development and execution of IQ/OQ/PQ protocols
Provide assistance for the implementation of the site LIMS

Fulltime

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Quality Control (QC) Analyst

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