Associate Scientist, Quality Control (12 months FTC)

at  Jazz Pharmaceuticals

Sittingbourne ME9, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate28 Dec, 2024Not Specified30 Sep, 20241 year(s) or aboveTitration,Interpersonal Skills,Peer Relationships,Concessions,Analytical Instruments,Teams,Ftir,Communication Skills,Shares,Biotechnology,Priority Setting,It,Analytical Techniques,PipettingNoNo
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Description:

IF YOU ARE A CURRENT JAZZ EMPLOYEE PLEASE APPLY VIA THE INTERNAL CAREER SITE.

Jazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global biopharmaceutical company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines and novel product candidates, from early- to late-stage development, in neuroscience and oncology. We actively explore new options for patients including novel compounds, small molecules and biologics, and through cannabinoid science and innovative delivery technologies. Jazz is headquartered in Dublin, Ireland and has employees around the globe, serving patients in nearly 75 countries. For more information, please visit www.jazzpharma.com and follow @JazzPharma on Twitter.

BRIEF DESCRIPTION

To analyse and report on QC test samples (e.g. packaging items, raw materials, intermediates, finished products and stability samples) in accordance with cGMP.

REQUIRED KNOWLEDGE, SKILLS, AND ABILITIES

  • Typically >1 year relevant post degree work experience, ideally in the Pharmaceutical, Biotechnology or a related industry
  • Experience of using routine analytical instruments (e.g. HPLC, GC, TLC, FTIR, UV etc.) and of routine analytical techniques (titration, pipetting, etc)
  • Working knowledge of office IT packages
  • Good level of written and verbal communication skills
  • Excellent attention to detail and ‘concern for quality’
  • Understanding of cGMP

REQUIRED/PREFERRED EDUCATION AND LICENSES

  • Bachelor’s degree in science or related discipline

Responsibilities:

  • Perform analytical testing using HPLC, GC, TLC, FTIR, UV and other required techniques in accordance with written procedures
  • Provide clear and accurate records of all work performed
  • Record data into appropriate records and notify management of any OOS, OOT, OOE or questionable results
  • Ensures that all results are reported and approved in a timely manner
  • Identifies any non-compliances or deviations and notifies management
  • Ensures that all equipment is fully calibrated and serviced prior to testing
  • Applies appropriate SOPs and test methods to all testing to ensure compliance and quality of resulting data
  • Maintains a clean and tidy work environment, including carrying out housekeeping tasks as assigned
  • Maintains stocks of consumables, chemicals, solvents, etc through regular stock checks and re-ordering when required
  • Carries out checking of analytical documentation (where experience and training allows)
  • Assists with sampling of raw material samples as required
  • Actively looks for and implements improvements in productivity and efficiency within own work area
  • Works in accordance with the systems in place with regards to health & safety, security and the environment
  • Undertakes other activities, indirectly related or unrelated to the above listed accountabilities, as assigned by line manager
  • Operates in accordance with the company corporate values of being patient driven, passionate, innovative, collaborative, accountable, having integrity and achieving excellence


REQUIREMENT SUMMARY

Min:1.0Max:6.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

The pharmaceutical biotechnology or a related industry

Proficient

1

Sittingbourne ME9, United Kingdom