QC Chemist II

Abbott

South Portland (ME)

On-site

USD 55,000 - 75,000

Full time

6 days ago
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Benefits offered by this job

Medical and Prescription Drug Plans
Dental Plan
Vision Plan
Health Savings Account (HSA)
Flexible Spending Accounts
Supplemental Life Insurance
Short Term Disability
Long Term Disability
Critical Illness Insurance
Hospital coverage
Accident Insurance
401(k)

Job summary

Abbott is seeking a QC Chemist II in South Portland, ME for a 3-month, onsite assignment. This role supports raw material, in-process material, and finished product testing, plus stability studies and investigations under GMP guidelines.

The candidate will perform routine analyses, manage workload, maintain training, and ensure compliant documentation while collaborating with the lab team and senior staff.

Qualifications

  • Bachelor's degree or equivalent required.
  • 2-5 years of related work experience.
  • Working knowledge of GMP and quality systems.

Responsibilities

  • Performs routine analysis using approved test methods.
  • Prioritizes workload to meet customer needs.
  • Maintains training records and supports training of other personnel.
  • Follows GMP requirements for laboratory operations, testing, results, and documentation.
  • Performs method development, validation, and transfer per protocols.
  • Prepares protocols and reports under supervision.
  • Maintains a safe work environment.

Skills

Analytical testing
GMP compliance
Documentation
English language

Education

Bachelor's degree

Job description

Job Title: QC Chemist II
Location: South Portland, ME 04106
Duration: 3 months
Work Arrangement: 100% Onsite
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.
Consultants Eligible Benefits Upon Waiting Period:
  • Medical and Prescription Drug Plans
  • Dental Plan
  • Vision Plan
  • Health Savings Account (for High Deductible Health Plans)
  • Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
  • Supplemental Life Insurance
  • Short Term Disability (coverage varies by state)
  • Long Term Disability
  • Critical Illness, Hospital coverage, Accident Insurance
  • MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
  • 401(k)

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.

Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.

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