Qc Analyst Job at SRG (Worthing)

Qc Analyst

Lead the development, validation, and transfer of analytical methods, including ...

Location

Ireland , Wicklow

Salary:

Not provided

Randstad

Expiration Date

July 02, 2026

Requirements

Bachelor's degree in Science or related field
Experience in a regulated laboratory environment.

Job Responsibility

Lead the development, validation, and transfer of analytical methods, including troubleshooting cleaning validation challenges
Provide technical oversight during tech transfers, process validation, and commercial manufacturing phases to monitor production and analytical outcomes
Author and review critical laboratory documentation, including method protocols, SOPs, calibration procedures, and analytical test records
Execute raw material, intermediate, and stability testing while overseeing sampling protocols for utility systems like water, nitrogen, and steam
Lead laboratory investigations, troubleshoot equipment issues, and champion continuous improvement via Lean Six Sigma initiatives
Manage laboratory instrument calibration and maintenance to ensure full regulatory and operational compliance.

Fulltime

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Qc Analyst

Are you ready to play a vital role in ensuring strong product quality in a pharm...

Location

United Kingdom , Hatfield

Salary:

Not provided

Proclinical

Expiration Date

Until further notice

Requirements

Strong knowledge of Quality Control, Quality Assurance, GMP, and regulatory compliance
Ability to interpret complex data and present findings effectively
Proficiency in computer applications such as Word, Excel, and PowerPoint
Familiarity with GMP guidelines and regulations
Excellent problem-solving, decision-making, and time management skills
Effective communication and teamwork abilities
Professional behavior and self-awareness

Job Responsibility

Test all materials in accordance with agreed specifications and procedures
Qualify laboratory equipment, including URS, IQ, OQ, and PQ processes
Maintain and calibrate laboratory equipment following approved procedures
Manage laboratory Quality Systems and Quality Management Systems
Draft Standard Operating Procedures (SOPs) under supervision
Support internal and external audit processes and schedules
Assist in preparing for and hosting competent authority inspections
Investigate deviations and implement corrective and preventive actions (CAPAs)
Contribute to technology transfer projects, particularly QC aspects
Implement and manage change control activities

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

New

Qc Analyst (Cosmetics & Medical Devices)

Randstad Inhouse, Specialty Pharma, for a multinational company in consumer heal...

Location

Italy , Pomezia

Salary:

28000.00 - 34000.00 EUR / Year

Randstad

Expiration Date

August 14, 2026

Requirements

Bachelor's or Master's degree
Good knowledge of English
Knowledge of the following analytical techniques and instruments: HPLC (High-Performance Liquid Chromatography)
GC (Gas Chromatography)
Ion Chromatography (IC)
UV Spectrophotometry
Atomic Absorption
Robotic Titrator
pH meter
Viscometer

Job Responsibility

Perform analytical and chemical-physical testing on finished products in compliance with GMP standards and internal procedures
Execute stability studies and analytical validation activities on cosmetic products and medical devices
Perform routine and non-routine analyses on finished products and raw materials
Support complaint management activities and related investigations
Conduct investigations on finished products (e.g. deviations, OOS/OOT results)
Ensure proper use, maintenance, and calibration of laboratory equipment
Collaborate with cross-functional teams (QA, Production, Regulatory Affairs)

Quality Control (QC) Analyst

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

Location

United Kingdom , Grangemouth

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

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

Senior Analyst, QC Chemistry

This is where you make a difference in our patients’ safety. As a member of the ...

Location

United Kingdom , Thetford

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Science based degree (preferably in Chemistry, BioChemistry Biology OR Microbiology)
Experience working in a laboratory essential
Demonstrates strong leadership skills
Excellent understanding of Microsoft Office Packages
Previous experience in a GMP environment/ pharmaceutical QC laboratory

Job Responsibility

Manage and develop direct reports through performance reviews (ACE Check-In) and identify training or development needs
Conduct testing, stability studies, reporting, and checking/reviewing of results in accordance with relevant local and global procedures, testing methods, protocols, and/or pharmacopeial requirements
Ensure direct reports meet safety, quality, and performance standards, and escalate any issues to the QC Manager
Initiate, conduct, and manage quality records, such as deviations, CAPAs, effectiveness checks, and laboratory investigations
Initiate and coordinate document updates, change controls, and successfully manage timelines for implementation of changes
Perform the batch release activities
Participate in internal, customer, and regulatory audits
complete any assigned action items in a timely manner
Perform if required and coordinate general laboratory support activities including housekeeping, equipment maintenance, and inventory of supplies and reagents/ standards
Perform and coordinate calibration checks in accordance with written procedures

What we offer

25 days annual leave + bank holidays
Employee discount scheme
Blue light card
Progression opportunities
Subsided canteen
Westfield healthcare
Up to 8% pension contribution
Employee assistance programme
Support for Parents
Continuing Education/ Professional Development

Fulltime

QC Analyst (API)

ABOUT THE JOB: Conduct analytical testing and ensure accurate documentation for ...

Location

Singapore

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

Requirements

1 to 3 years of experience in a pharmaceutical laboratory environment (Quality Control, Quality Assurance, or Production preferred)
Experience with aseptic techniques is considered an advantage
Completed apprenticeship as a laboratory assistant or equivalent qualification
Strong teamwork skills and a results-driven mindset
Knowledge of GMP, GxP standards, TQM principles, and laboratory best practices
Familiarity with QC testing, sampling procedures, and laboratory equipment
Structured, rigorous, and able to work efficiently in a regulated environment
Analytical, resilient, and committed to operational excellence
Comfortable working in a shift-based organization

Job Responsibility

Conduct analytical testing and ensure accurate documentation for: API / drug substance / drug product / finished product samples
Complaint samples
Stability samples
Packaging material samples
Handle sample storage and laboratory documentation in accordance with cGxP standards
Guarantee compliance with data integrity principles
Perform maintenance, calibration, and qualification of analytical equipment
Support stability activities, including testing and documentation (when not centralized)
Strictly adhere to HSE guidelines and proactively identify and report risks
Maintain a constant state of inspection readiness

What we offer

Global Diversity: Be part of an international team of 110+ nationalities
Trust and Growth: 70% of our leaders starting at entry-level
Continuous Learning: internal Academy and over 250 training modules
Vibrant Culture: afterworks, networking events
Meaningful Impact: CSR initiatives, including the WeCare Together program

Fulltime

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Qc Analyst

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