FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in analytical chemistry and quality control processes, including proficiency in HPLC, Spectrophotometry, and various immunochemistry techniques. Ensures compliance with cGMP standards and effectively participates in method validation and technical transfer.
Highest-signal resume keywords
HPLCSpectrophotometryImmuno-ElectrophoresisCGMP ComplianceOut of Specification Investigation
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Analytical ChemistryProtein AnalysisExcipient AnalysisKarl-Fischer TechniqueFT-IR TechniqueNIR TechniqueGCAAFlame-PhotometryMethod Validation
Soft Skills
Excellent CommunicationStrong Interpersonal SkillsOrganizational SkillsAnalytical SkillsProblem-Solving Skills
Industry Keywords
Quality ControlLaboratory ComplianceTechnical TransferCAPARegulatory Inspections
About the role
Key responsibilities & impact- Carry out raw material, in-process and finished product chemistry and immunochemistry analysis
- Perform in-process and finished product QC, including protein and excipient analysis using Spectrophotometry, Immuno-electrophoresis, HPLC, GC, AA and Flame-photometry
- Conduct raw material QC using Karl-Fischer, FT-IR and NIR techniques
- Ensure laboratory processes, equipment and services are appropriately installed, qualified and maintained
- Participate in verification, validation and technical transfer of analytical testing procedures
- Ensure compliance with cGMP, company specifications and procedures
- Investigate Out of Specification (OOS) and Out of Trend (OOT) results
- Participate in and take responsibility for QC-related CAPAs
- Adhere to the QC documentation system and prepare document change requests
- Develop, improve and implement QC procedures, processes and systems
- Support Quality department and cross-functional projects and continuous improvement initiatives
- Participate in international QC and wider quality project teams; travel may be required
- Maintain safety, cleanliness and compliance of the laboratory and work area
- Prepare for and support regulatory and internal inspections and audits
- Provide hands-on guidance and training when needed
- Work shifts when required
Requirements
What you’ll need- Bachelor’s degree in Chemistry, Biochemistry or closely related scientific field
- Requires a minimum of 2 years of related experience.
- Knowledge of a wide array of analytical techniques/instruments including HPLC, Spectrophotometry and Electrophoresis.
- Knowledge of specific product analysis (e.g. IC, AA, GC, Flame-photometry and Kjeldahl techniques) desirable
- Knowledge of raw material analysis (e.g. Karl-Fischer, FT-IR and NIR techniques) desirable
- Experience with investigating Out of Specification and Out of Trends.
- Experience in method transfer and verification/validation desirable.
- Knowledge of analytical techniques for biologics or protein-based therapeutics desirable.
- Excellent verbal and written communication.
- Strong interpersonal skills with ability to interact with all levels of personnel in a professional manner.
- Strong organizational, analytical and problem-solving skills.
Benefits
Comp & perks- A highly competitive salary package
- Group pension scheme - Contribution rates are (3%/ 5%/ 7%) and company will match
- Private medical insurance for the employee
- Ongoing career development opportunities within a rapidly growing organisation
- Strong focus on succession planning and internal promotion
- Dedicated education and professional development allowance
- Wellness and social initiatives, including activities such as padel and summer events
