QC Analyst Job at SRG (Falkirk)

Qc Analyst Ii

Performs analyses of Clinical Chemistry, Critical Care, Coagulation and/or Micro...

Location

United States , Orangeburg

Salary:

24.00 - 29.00 USD / Hour

werfen

Expiration Date

Until further notice

Requirements

B.S./B.A. Degree in Science or Medical Technology or equivalent required
2 years clinical laboratory experience with a basic knowledge of quality control principles

Job Responsibility

Performs automated and manual assays as detailed in departmental/plant SOPs and QC Monographs including raw material, in-process and finished product
Interprets test results against specifications and decides if assays pass or fail
Maintains documentation of all work performed in accordance with GMP requirements
Evaluates product complaints upon Team Leader or Team Champion's request
Performs product stability, proficiency, environmental testing and water system testing
Responsible for routine preventive maintenance, general trouble shooting, general cleanliness and calibration of Lab equipment
Updates departmental SOP's and QC Monographs as directed by Team Leader or Senior QC Analyst
Performs microbial testing per SOP's and QC Monographs
Orders required laboratory supplies, reagents and other consumables
Monitors proper storage conditions and expiration dates

Fulltime

QC Analyst II

Performs analyses of Clinical Chemistry, Critical Care, Coagulation and/or Micro...

Location

United States , Orangeburg

Salary:

24.00 - 29.00 USD / Hour

werfen

Expiration Date

Until further notice

Requirements

B.S./B.A. Degree in Science or Medical Technology or equivalent required
2 years clinical laboratory experience with a basic knowledge of quality control principles
Ability to lift and move materials per current OSHA standards

Job Responsibility

Performs automated and manual assays as detailed in departmental/plant SOPs and QC Monographs including raw material, in-process and finished product
Interprets test results against specifications and decides if assays pass or fail
Maintains documentation of all work performed in accordance with GMP requirements
Evaluates product complaints upon Team Leader or Team Champion's request
Performs product stability, proficiency, environmental testing and water system testing
Responsible for routine preventive maintenance, general trouble shooting, general cleanliness and calibration of Lab equipment
Updates departmental SOP's and QC Monographs as directed by Team Leader or Senior QC Analyst
Performs microbial testing per SOP's and QC Monographs
Orders required laboratory supplies, reagents and other consumables
Monitors proper storage conditions and expiration dates

Fulltime

QC Analyst

Are you a QC Analyst/Analytical Chemist based in Central Belt of Scotland lookin...

Location

United Kingdom , Falkirk

Salary:

Not provided

SRG

Expiration Date

Until further notice

Requirements

Degree or equivalent in a relevant scientific discipline
Experience in QC Analytical techniques such as UV, HPLC, FTIR
Previous effective experience in a similar environment is essential
Prior experience working in a regulated GxP environment

Job Responsibility

Use a range of analytical chemistry techniques- predominantly HPLC
Ensuring all analysis and documentation are conducted and recorded in compliance with GMP standards
Working to set protocols within a busy environment
Preparation and update of SOPs, instructions and protocols and other Quality Control documentation
Checking and reviewing of data in compliance with Data Integrity requirements
Assist in investigation of quality incidents and other problem solving forums and complete QMS documentation in a timely manner
Perform stability study programme activities, storage of in process, and final products samples and retention sample management
Supporting the team leader where required

What we offer

bonus scheme
healthcare
flexi-time
additional shift bonus

Fulltime

Senior QC Analyst

At Target Healthcare Group, we are pioneers in the pharmaceutical industry, comm...

Location

Salary:

Not provided

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Bachelor’s or Master’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field
Minimum 5–8 years of QC laboratory experience in the pharmaceutical or biopharmaceutical industry
Strong working knowledge of analytical techniques such as HPLC, GC, UV-Vis, FTIR, TOC and dissolution
Proven experience in method validation, instrument troubleshooting, and data integrity compliance
Excellent understanding of cGMP, GLP, and regulatory requirements
Strong attention to detail and analytical thinking
Proficiency in laboratory software including Chromeleon
Strong communication, leadership, and mentoring skills
Ability to work independently and manage multiple priorities under tight timelines

Job Responsibility

Perform qualitative and quantitative chemical and microbiological analyses of raw materials, in-process samples, finished products, and stability samples using validated methods (e.g., HPLC, GC, UV, FTIR, Dissolution)
Review and verify analytical data, ensuring accuracy, completeness, and compliance with cGMP and SOPs
Lead out-of-specification (OOS), out-of-trend (OOT), and deviation investigations, including root cause analysis and CAPA development
Support release testing and timely completion of batch records to ensure uninterrupted product supply
Participate in method validation, method transfer, and equipment qualification activities
Develop and optimise analytical methods as required to support new product development or process changes
Troubleshoot complex analytical and instrumentation issues independently and provide guidance to peers
Ensure all activities comply with cGMP and ICH, and other applicable regulatory guidelines
Prepare, review, and maintain laboratory documentation including test records, logbooks, and SOPs
Support internal and external audits and respond to audit findings

What we offer

Active Social and charity committee
Cycle to Work Scheme
Electric Vehicle Scheme
Eye Care Vouchers

Qc Analyst

SRG are currently working with a global pharmaceutical manufacturer based in Liv...

Location

United Kingdom , Speke, Liverpool

Salary:

15.25 GBP / Hour

SRG

Expiration Date

Until further notice

Requirements

Degree qualified in Chemistry, Biochemistry, Biomedical Science or a related scientific discipline
Demonstrated practical experience
Prior industrial experience in a GMP regulated environment is highly desirable
Knowledge of pharmacopoeias
Skills performing raw materials testing highly desired
Strong verbal & written communication skills

Job Responsibility

Perform analytical, biosafety & cell science testing on raw materials, intermediates and finished products
Complete laboratory documentation accurately and in accordance with industry regulatory standards
Utilise technical expertise to troubleshoot various assays as required

Fulltime

Qc Analyst Ii, Microbiology

We are looking for an enthusiastic Microbiology Analyst to support the cGMP Qual...

Location

Canada , Vancouver

Salary:

78200.00 - 92000.00 CAD / Year

AbCellera Biologics

Expiration Date

Until further notice

Requirements

5+ years of QC experience in addition to a Bachelor’s degree
Master’s degree in a relevant scientific discipline and 3+ years of QC experience
Strong knowledge and experience in Good Manufacturing Practices (GMPs), QC microbiological testing and method qualification requirements
Experience with using Milliflex Oasis, Charles River Endosafe nexgen-MCS, LIMS, as well as basic benchtop techniques such as Gram staining, plate reading, vacuum filtration and LAL gel-clot
Excellent interpersonal skills, ability to work independently and in a team environment, detail oriented, organized and methodical in execution of tasks
Ability to problem solve with sound analytical thinking

Job Responsibility

Providing microbial support for aseptic product manufacturing in a cGMP regulated environment
Performing site support activities such as environmental monitoring, compressed gas and water system sampling within the graded manufacturing area
Planning, scheduling, and coordinating microbiological sampling and testing activities to support manufacturing operations, including routine monitoring, batch-related testing, and time-critical samples, ensuring alignment with production schedules and testing timelines
Carrying out a variety of routine microbiological techniques on utilities including but not limited to bioburden, endotoxin, TOC, conductivity and growth promotion testing on incoming microbial media
Responsible for micro release testing on raw materials, in-process drug substance and final product samples
Evaluating and reviewing test results for conformance to appropriate specifications and highlighting any suspect results to the QC Lab Manager
Participating in identification, investigation (deviations/out of specifications) and resolution of problems in the microbiology lab
Authoring method verification protocols, SOPs, WIs and TMs based on industry standard compendial methods

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
Teams and social groups to build community and connections

Fulltime

New

Senior Scientist I, Quality Control

This position is within the Quality Control structure, under the Quality Organiz...

Location

United States , Verona

Salary:

90000.00 - 108000.00 USD / Year

Arrowhead Pharmaceuticals, Inc

Expiration Date

Until further notice

Requirements

M.S. in Chemistry (or related field) with 7+ years relevant laboratory experience
B.S. in Chemistry (or related field) with 9+ years of relevant laboratory experience
Fully knowledgeable of cGMP and ICH laboratory requirements and operations
Proficient and demonstrated experience with analytical instrumentation, test methodology/validations/transfers, data acquisition systems, and typical cGMP policies/practices

Job Responsibility

Fully knowledgeable of cGMP requirements and ICH guidelines
Works independently to meet project timelines and deliverables with minimal supervision to no supervision
Collaborates routinely with Analytical Development on procedural method transfers and may participate in the execution of method validation protocols
Performs routine analytical testing of pharmaceutical raw materials, in-process samples, finished products and stability samples using established test methods and procedures
Proficient with various analytical instrumentation theory and practice
Executes training requirements for assigned SOPs and participates in department specific training modules
Independently completes complex instrumentation for testing according to written test methods and procedural documents to analyze samples
Demonstrates proficiency with a variety of instrumentation (e.g., HPLC, GC, LC-MS, KF, FTIR, Endotoxin plate readers, and/or Raman spectroscopy) and will assist in training on instrumentation
Is a subject matter expert in technical aspects of both instrumentation and workflow management and prioritization
Performs analyses in a timely and efficient manner to support ongoing prioritized studies

What we offer

competitive salaries and an excellent benefit package

Fulltime

QC Analyst

QC Analyst required on a temporary 6-month contract, based in Cheshire. Requirin...

Location

United Kingdom , Cheshire

Salary:

27000.00 - 33000.00 GBP / Year

SRG

Expiration Date

Until further notice

Requirements

Recent Degree in Chemistry (or similar)
Knowledge and/or recent, proven industrial experience of wet chemistry analysis, HPLC and/or GC
Willingness to learn and develop
Work well within a small team with good time management and organisational skills

Job Responsibility

Performing wet chemistry techniques to analyse raw materials and finished products (including titrations, pH testing, density testing and others)
Using analytical instrumentation for analysis including HPLC, GC and IC through following methodology provided
Recording and reporting data within the quality system- completing documents and spreadsheets accurately
Reporting results in a timely fashion under direction and priority
Performing analytical investigations and tests to meet research and customer needs
Having responsibility for maintenance and upkeep of analytical equipment
Approving and rejecting raw materials

What we offer

An opportunity to gain great experience within a highly respected, multi-national company, with significant intellectual property potential and commercial impact
37.5 hours, Mon-Fri, 8:30-4:30 (with flexibility)
Full training can be provided

Fulltime

QC Analyst

SRG

Location:
United Kingdom , Falkirk

Category:
Quality Control

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
December 25, 2025

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