2017 Abbott Laboratories jobs in Hackettstown,NJ

Medical Laboratory Scientist, Per Diem, HMC

Atlantic Health System

Hackettstown, NJ 07840

ABB

Hackettstown, NJ 07840

Must understand and perform all job requirements in compliance with ISO 9001
High School Diploma or equivalent, plus at least 2 years of experience in Quality Control or Manufacturing
Must have valid work authorization to work for ABB in the United States
Physically capable of lifting up to 40 lbs, performing repetitive tasks, and standing for 8-hour shifts
Comfortable working with heavy equipment and navigating non-climate controlled environments
Strong communication, computer, and analytical skills; able to collaborate across teams

Thorlabs

Newton, NJ 07860

Must be able to wear appropriate clothing and personal protective equipment such as but not limited to masks, glasses, gloves, and specialty garments.
High School Diploma or equivalent work experience.
Must have the ability to cross train in all areas of the department, including but not limited to visual and dimensional inspection, data entry.
The employee may lift or move objects up to 20 pounds.
Capable of reading mechanical drawings and interpret dimensional tolerances.

Marvin

Wharton, NJ 07885

Have a smartphone
Have reliable transportation - you'll be traveling to retail locations and events in your area.
Are comfortable on your feet - you'll be standing and moving around during your shift.
Flexibility to work a minimum of 15 hours per week
18 years of age or older
Can lift up to 40 lbs

Johnson and Johnson

Raritan, NJ 08869

Proficient in performing technical writing (e.g., test methods, SOP's, protocols, etc.)
Minimum of a Bachelor's or equivalent University Degree required
Experience with aseptic processing in biosafety cabinets and/or ISO 5 clean room
Demonstrated experience successfully working in an analyst role/level and proficiency using analytical methodologies within a functional laboratory
Requires up to 5% domestic travel to other sites/locations
Experience within Biopharmaceutical or Pharmaceutical industry
Advanced degree (MSc., Ph.D.) or focused degree in Biology, Biochemistry, Chemistry, or related scientific field is preferred
Excellent written and verbal communication skills
Experience performing one or more of the following cellular and/or molecular based techniques: qPCR, Flow Cytometry, ELISA, Cell Culture, and/or Potency assays
Minimum of two (2) years of relevant work experience
Experience with Quality Control document reviews and regulatory inspection processes
Requires the ability to meet the physical demands (lift up to 20 lbs, stand or sit for extended periods of time in a laboratory setting), to perform visual inspections of materials (color, appearance, particles, etc.), and to document observations during laboratory testing
Knowledge of cGMP regulations and Good Documentation Practices (GDP)
Requires ability and flexibility to work 10-hour shifts between the operational hours of 4:00pm - 2:00am (Sunday - Wednesday), and provide occasional support on the weekends or other shifts