Development Scientist II, Analytical Development and Clinical QC (ADQC)

This is what you will do:

Development Scientist IIwill be a key team member in Alexion’sExternal Analytical Development  and Quality Control group.

This positionisresponsible formaintainingthe highest standard of quality and complianceofexternalquality control testing(GMP) laboratories.

This candidate willbe responsible for initiation and ownership of laboratory investigations (LIRs) through strong liaisonwithexternal contract laboratoriesandchange controls relevant to ADQC biologic programs. The candidate willensuretimely, compliant, and high-quality delivery for LIR closure toenable the generation of final release

CoAs.The role willwork closely with internal Quality Assurance, Compliance, Analytical Development and Stabilityteamsto ensure product to patients.

• Responsible for generating and/or mirroring, reviewing, providing assessments,and driving ownership ofLIRs to close outOut-of-Specification (OOS), Out-of-Trend (OOT), and atypical resultswithstructured root cause analysis, impact assessment,and/or corrective/preventive actions (CAPAs).

• Designinvestigationaltestingplans ensuring compliant closure of all testing related investigations within the quality system.

• Leadand/orfacilitatecross-functional meetings with quality assurance to ensure structured investigation alignment.

• Create plans,track,and present timelines to meet established targets,goals,and objectives.

• Perform review of analytical data to ensure expected assay performance.

• Identify opportunities for improvement in systems and make recommendations for effective changes to ensure compliance withcGMP.

• Strong presentation skills

• A successful candidate will havestrongmentalacuitywith high attention to detail and ability tomaintainaccuracy in documentation and processes.

• Excellent analytical and problem-solving skills with the ability to conduct risk assessments and root cause analysis.

• A broad knowledge of Pharmaceutical Quality Assurance,regulatory compliance,and/or quality control inclusive of cGMP, FDA regulations, familiarity with ICH guidelines and EU regulations.

• Strongproficiencyin quality management systems and effective communication skills for interacting with cross-functional teams.

• Strongproficiencywith MSWord,Excel,PowerPoint.

• Ability tobend, reach and stand,withliftingto
  15poundsandcarryingover short distances.

• Ability to travel up to 10%, if needed.

• Advanced (M.S. or Ph.D.) degree in Biochemistry, Chemistry or related discipline with2-5years (Ph.D.) or10+ (M.S.) hands on biological analytical development experience inpharmaceuticalindustry.

• Working knowledge in validated documentation systems:
  Veeva Vault (EQV), LIMS,Val Genesis,Kneat, etc.

• Knowledge of pharmaceutical/biotechnology manufacturing process

• Database management /statistical analysis(e.g., JMP,Tableau, SAS) withproficiencyin Microsoft Share Pointand /or BOX.

31-Jul-2026

13-Aug-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.