QC Chemist II

Experis (Austria)

South Portland (ME)

Presencial

USD 45.000 - 48.000

Jornada completa

Hace 2 días
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Descripción de la vacante

Experis (Austria) is seeking a QC Chemist II to join a leading healthcare client in South Portland, ME. This 3‑month contract is 100% onsite with a pay range of $33–$35 per hour (W2).

Responsibilities include routine analytical testing under GMP, material/product release support, investigations, and documentation. Requirements: a Bachelor’s degree and 2–5 years of experience; strong English; GMP environment proficiency.

Formación

  • 2–5 years of related work experience.
  • Working knowledge of GMP and laboratory documentation.
  • Ability to perform analytical testing per approved methods.

Responsabilidades

  • Performs routine analysis using approved test methods in a timely manner.
  • Supports material and product release testing under GMP.
  • Maintains training status and supports training of other lab personnel.
  • Follows GMP requirements for testing, results, and documentation.
  • Initiates investigations under supervision and assists with change controls.

Conocimientos

English proficiency
GMP knowledge

Educación

Bachelor's degree or equivalent

Descripción del empleo

Job Title: QC Chemist II

Location: South Portland, ME 04106

Duration: 3 months

Work Arrangement: 100% Onsite

Pay Range: $33 - $35 per hour (W2)

We are seeking a “QC Chemist II” to join one of our leading healthcare clients.

Description
Main Purpose of the Role

Support raw material, in-process material, and finished product lot release, stability studies, engineering evaluations, and any relevant investigation by performing required analytical testing under the GMP environment.

Main Responsibilities
  • Performs routine analysis using approved test methods in a timely manner.
  • Prioritizes assigned workload to meet the customer’s needs.
  • Maintains current status on all training requirements and supports training activities for other laboratory personnel.
  • Understands and follows GMP requirements with respect to laboratory operation, testing, results generation, and documentation.
  • Carries out change requests/change controls as needed and be able to provide necessary explanations or justifications to the change.
  • Recognizes OOS, OOT, and exception events.
  • Initiates and conducts investigation under the supervision of senior laboratory staff.
  • Carries out method development, validation, verification, and transfer by following established protocols whenever required.
  • Prepares technical protocols and reports as needed under general supervision.
  • Maintains a safe working environment in accordance with established procedures and requirements.
  • Cultivates a wide range of internal networks and begins to develop an extensive external network of resources to facilitate completion of tasks.
  • Plans, organizes, and prioritizes own daily work routine to meet established schedule.
  • Exercises authority and judgment within defined limits to determine appropriate action.
  • Proficient in English Language
Education

Bachelors Degree or an equivalent combination of education and work experience.

Experience
  • 2-5 years of related work experience with a good understanding of specified functional area.
  • Working technical knowledge and application of concepts, practices and procedures.
  • General understanding of business unit/group function.
  • Will perform this job in a quality system environment.
  • Failure to adequately perform tasks can result noncompliance with governmental regulations.
  • Works on problems of moderate scope where analysis of situations or data requires a review of identifiable factors.
  • Exercises judgment within defined procedures and practices to determine appropriate action.
  • Has a broad knowledge of technical alternatives and an understanding of their impact on the systems environment.

We are looking for the candidate who are eligible to work with any employers without sponsorship.

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