QA Lab Technician

Full Time
Fall River, MA
Posted
Job description
Adecco is working with a pharmaceutical manufacturer in Fall River, MA. This role is Full time, Direct hire and onsite.

Duties and Responsibilities:
Quality Control (QC) Lab Technician's job duties and tasks include but are not limited to the following:
  • Perform sample management for all incoming raw materials, in-process, finished products and stability
  • samples including but not limited to receipt, logging distribution and destruction and update the status in ILMS (Laboratory Management System).
  • Coordinate chemical and reference standard inventory in the lab, verifying the expired chemicals and
  • standards and discarding as per company procedures and update all inventories in ILMS.
  • Update the stability summary reports after the completion of analytical testing.
  • Oversee temperature and humidity monitoring for stability chambers
  • Assist in sample loading in stability chambers and submitting stability samples as per schedule.
  • Assist in the shipment of the samples to contract labs as required
  • Provide general housekeeping in the QC Lab and any other functional activities as assigned by management.

Education and Experience
  • Minimum of High School Diploma or equivalent education (ex. GED) and three (3) years of relevant experience.
  • Must have good computer skills and proficient user of Microsoft Office Tools to include Word, Excel, Outlook, PowerPoint, and other lab-related systems.
  • Must have excellent communication skills.
  • Must be able to clearly communicate in English (verbally and written).
  • Must possess a positive, professional attitude toward work and willingness to cooperate with co-workers and
  • supervisors.
  • Metered Dose Inhalation (MDI) pharmaceutical industry experience is preferred.

Physical Requirements
  • Work standing or walking unassisted for 75% or greater of an 8-hour period.
  • Able to wear appropriate personal protective equipment, when required.
  • Sitting at a desk and/or working at a computer or other "screen" 75% or greater of an 8-hour period.
  • Able to lift 35 pounds with or without assistance.

Working Conditions, and Work Schedule
  • This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc.
  • Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required.
  • Typical work schedule is Monday through Friday. Must be willing and able to work any assigned shift ranging from first or second shift.
  • May be assigned to work on an alternate work-shift basis, where required (Day, Evening, Night). Weekend or Holiday work may also be requested and/or required.
  • No remote work available.
  • No employment sponsorship or work visas

Equal Opportunity Employer/Veterans/Disabled. To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit http://www.adeccousa.com/candidate-privacy/. The Company will consider qualified applicants with arrest and conviction records.


About Adecco Life Sciences:

Leveraging the power of relationship building and the Adecco brand, we work to align candidates with permanent positions based on skillset and job requirements. Our personal and tailored approach assures that our candidates are placed into positions that align with their long-term goals. We specialize in recruiting for permanent positions within the Life Sciences industry. Here are just some of the roles we specialize in: - Biotechnology - Pharmaceutical - Clinical Research/Trials - Medical Devices - Quality Assurance - Engineering

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