QUALITY CONTROL ASSOCIATE ANALYST and SUPPORT (Long term Temporary position)

at  Wapt

2108 Couvet, ne, Switzerland -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate01 Sep, 2024Not Specified02 Jun, 2024N/AGmp,Team Spirit,EnglishNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

Overview:
This position is responsible to perform all type of analytical testing that is required for release of packaging materials and all the environmental sampling. The position is responsible for the documentation management for the QC Laboratory, the sample management and the management of the consumable (Reagent & others) by purchasing, receptioning and providing the Couvet Laboratory in time with materials. The management of the standards for the analytical testing is under the responsibility of this position. Additional responsibilities can be the support of the analytical testing, handling of deviations and change controls likewise the follow up and performs of complaints.
As a QC team member, the person filling this position supports all activities to continuously maintain the GMP status of the QC Laboratory.
Long Term Temporary Position*

Responsibilities:

  • This position is responsible to ensure all EHS requirements in laboratory:
  • Respect EHS procedure and rules
  • Report immediately all incidents and near-misses to the management and/or to the EHS representative people
  • Performs visual inspection and analytical testing according to Packaging material and release specifications
  • Performs visual inspection of materials, AQL sampling and testing
  • Manage the samples for the QC Laboratory like raw material & Bulk reception/destruction, stabilities reception/destruction etc..
  • Performs review of analytical data
  • Performs basic laboratory work (buffer preparation, waste disposal management, washing of lab dishes, cleaning of the labs etc.)
  • Performs management supply of consumables
  • Performs sampling of environmental monitoring for the Site (set up, sampling, coordination)
  • Writes specific standard operations procedures (e.g. operation and maintenance of equipment)
  • Performs general activities for the QC Laboratory (documents archives, labelling and documentation scanning)
  • Participate to the visual management and the 5S of the QC Laboratory
  • Can be assigned special tasks and project work

Qualifications:

KNOWLEDGE / SKILLS / ABILITIES:

  • Basic knowledge in laboratory activities in quality control and analytical testing
  • Basic knowledge in GDP and GMP
  • Conscientious, responsible and engagement, flexible, logical and very good organized
  • Excellent team spirit
  • Good knowledge in English and French
  • Knowledge of most common office software

Responsibilities:

  • This position is responsible to ensure all EHS requirements in laboratory:
  • Respect EHS procedure and rules
  • Report immediately all incidents and near-misses to the management and/or to the EHS representative people
  • Performs visual inspection and analytical testing according to Packaging material and release specifications
  • Performs visual inspection of materials, AQL sampling and testing
  • Manage the samples for the QC Laboratory like raw material & Bulk reception/destruction, stabilities reception/destruction etc..
  • Performs review of analytical data
  • Performs basic laboratory work (buffer preparation, waste disposal management, washing of lab dishes, cleaning of the labs etc.)
  • Performs management supply of consumables
  • Performs sampling of environmental monitoring for the Site (set up, sampling, coordination)
  • Writes specific standard operations procedures (e.g. operation and maintenance of equipment)
  • Performs general activities for the QC Laboratory (documents archives, labelling and documentation scanning)
  • Participate to the visual management and the 5S of the QC Laboratory
  • Can be assigned special tasks and project wor


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

2108 Couvet, NE, Switzerland