AMD Physicochemical Laboratory Technician
3PBIOVIAN, Noáin, Chartered Community of Navarre, Spain
Are you looking for an opportunity to develop your professional career in a CDMO Analytical Methods Development Department?
Responsibilities
Coordinate the developments, implementation, qualification and transfer of physicochemical analytical methods, including the design of experiments, review of documentation and generation of protocols, reports and presentations as required.
Supervise execution of sample analyses, review and communicate results.
Develop standard operating procedures related to analytical methods and the operation of the area.
Prepare protocols, reports and final reports of stability studies, forced degradation studies, reference material characterisation, re‐testing of reference materials, investigations and other non‐GMP studies.
Manage stability studies, sample and sample location control, analysis times and execution of analytical runs.
Participate in technical meetings and maintain fluid communication with involved departments.
Propose operational improvements oriented to quality and efficiency.
Write transfer protocols of physical‐chemical methods.
Provide technical responsibility for activities within assigned projects.
Qualifications
Between 3 and 4 years of experience in:
Pharmaceutical, biopharmaceutical, biotechnological sector or research centres.
Analytical techniques: HPLC, UPLC, fluorescence, DAD, UV‐VIS, PDA, ELSD/CAD/MS.
Experience with recombinant proteins, mAbs, biosimilars, ADCs.
Method validations (valuable).
Handling of Agilent equipment with Empower 3.
Supervision and coordination of personnel.
Participation in technical meetings with customers.
Knowledge in GMP regulations and qualification/validation of analytical methods.
Permanent stable position in a competitive growing company.
Competitive time‐off package with 39 paid days of vacation and an extra day off on 26 December.
Flexibility to work in shifts.
Advanced English (C1 / Advanced).
University degree in Biochemistry, Biology, Biotechnology, Chemistry or related area.
Master's degree (valuable) or PhD (valuable) in the related area.
Valuable knowledge in GMP regulations and in the qualification/validation of analytical methods.
Benefits
Competitive time‐off package: 39 paid days of vacation plus an extra day off on 26 December.
Flexible compensation plan: up to 30 % of the gross annual salary can be allocated to tax‐free daily services (childcare, health insurance, academic training, etc.).
Company benefits club: exclusive prices and discounts on a variety of products and services (Booking, FNAC, Rituals, El Corte Íngles, etc.).
Relocation assistance for hires residing outside Navarra.
...And so much more!
Senior level
Mid‐Senior level
Employment type
Full‐time
Job function
Manufacturing and Research
Industries
Pharmaceutical Manufacturing and Biotechnology Research
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