Quality Assurance Laboratory Internship
Bedford
Overview:
Position Summary:
Performs a broad range of laboratory work ranging from basic laboratory maintenance to performing specialized studies using scientific methods and techniques applicable to specific studies, and/or other specified assignments within the Product Quality Laboratory.Responsible for carrying out assigned projects independently or with the assistance of additional laboratory personnel. General laboratory tasks include solution preparation, instrument troubleshooting, equipment calibration, instrument quality control, and general housekeeping.
This laboratory internship is geared more towards students pursuing a Biology, Medical Laboratory Science, and other Science Related degrees.
Responsibilities:
Key Accountabilities
Essential Functions:
- Responsible for performing various testing procedures in a laboratory environment
- Performs projects and other assigned activities such as reliability studies, proficiency surveys, validation activities, etc; communicates results, problems and progress in routine or specialized protocols caused by instrument difficulties, or in reagent preparation and/or handling to supervisor and/or applicable teams
- Prepares solutions/samples and performs various laboratory procedures and experiments following established protocols, suggests modifications to protocols/methods as needed
- Understands application of scientific methods to experimental design and problem solving to assist project teams
- Performs other related duties as assigned.
Secondary Functions:
- Compiles and summarizes results of routine maintenance and calibration of laboratory equipment and communicates results
- Maintains accurate, precise records, and writes technical reports as needed
- N/A
- Works with various functional groups throughout the organization
Additional Skills & Capabilities:
- Ability to work compatibly with co-workers and to respond appropriately to instructions or information as required.
- Knowledge of Good Laboratory Practice (GLP).
- Ability to work in a busy biohazardous laboratory environment.
- Able to lift and move materials per current OSHA standards.
Competencies:
- Attention to Detail: Ability to pay close attention to detail is required
- Accuracy: Work is accurate and complete
- Performance Standards: Demonstrated ability to meet department goals
- Communication: Excellent written, verbal and presentation skills
- Discretion:Acts with integrity in all situations and can maintain appropriate confidentiality
- Multi-Tasking: Ability to manage multiple priorities, and support changing business needs
- Collaboration: Ability to work within a team to bring best solutions to the team or customer
- Independence: self-motivated-works under minimal supervision
- Professionalism: Must demonstrate professionalism during all interactions within company, customer and third parties
- Takes Initiative: Serves as a role model for “Quality First” by continuously improving on what matters most to customers
- Problem Solving: Promptly and effectively handles issues and problems
- Decision Making:Makes decisions based on data and risk determination
Qualifications:
Minimum Knowledge & Experience required for the position:
- Currently pursuing B.S. in Engineering, Finance, Business, Marketing with a minimum of 2 college semesters complete.
- Ability to multitask.
RandstadLynnfield, 12 mi from Bedford (MA)
As a quality assurance associate, you will be responsible for inspecting materials and packaging to make sure they meet quality requirements. The job involves the completion of daily QA reports and documentation.
Equal Opportunity Employer: Race...
Boston, 14 mi from Bedford (MA)
Job Description:
The Sr. Quality Specialist – Compliance is recognized as an expert internally in the principles and application of quality assurance and compliance. The Sr. Quality Specialist will coordinate GMP activities in support of clinical...
BioPharma Consulting JAD GroupCambridge, 10 mi from Bedford (MA)
The Manager of Quality Assurance Operations will work within the DP / CMC / Alliance QA Operations team and is responsible for providing support to all GMP aspects of drug product (DP) manufacturing, CMC and alliance management.
This role...