QC Chemist II

Experis Austria; South Portland (ME); On-site; USD 45,000 - 48,000; Full time

Job summary

Experis in South Portland, ME is seeking a QC Chemist II to join one of our leading healthcare clients on a 3-month, 100% onsite assignment. This role offers exposure to GMP environments and opportunity to contribute to material release and stability studies.

Responsibilities include performing routine analyses with approved methods, prioritizing workloads to meet timelines, maintaining training status, following GMP documentation, and supporting change controls, OOS/OOT investigations, and

Qualifications

• Bachelor's degree or equivalent required.
• 2-5 years of related work experience with knowledge of GMP
• Proficiency in English required.
• Will perform task in a quality system environment.

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 explanations or justifications to the change.
• Recognizes OOS, OOT, and exception events.
• Initiates and conducts investigations under supervision of senior staff.
• Carries out method development, validation, verification, and transfer following protocols.
• Prepares technical protocols and reports under general supervision.
• Maintains a safe working environment per procedures.

Skills

Routine analysis

GMP compliance

English language

Education

Bachelor's Degree

Tools

Analytical testing methods

Job description

$33.0 - $35.0/hourly Posted 2 days ago Less than 10 applies 2 min average apply

Experis

South Portland, ME 04106

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.

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 in 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.

If you’re interested, please click “Apply” button.

$33.0 - $35.0/hourly Posted 2 days ago Less than 10 applies 2 min average apply