JOB DESCRIPTION

• Collect and review lab analytical data, send results to client and assemble hard copy deliverable
• Conduct internal audit
• Assist external audit

QUALIFICATIONS

• Bachelor Degree with Chemistry, Biology or Environmental Science related major; or Associated Degree with Chemistry major
• Proficient in spoken and written English
• Proficient in Excel

JOB DESCRIPTION

We are looking for a qualified GC Lab Analyst to undertake a variety of laboratory techniques for EPA Methods. You will be handling sensitive equipment to analyze samples and conduct tests reporting findings to a laboratory manager and clients. Ideal candidate has a record of GC troubleshooting and maintenance. familiarity with Chem Station EnviroQuant is plus. The individual will be passionate for diligence and accuracy in making things move forward and will promote a positive work environment.

The incumbent will be responsible for QA oversight of laboratory compliance, including but not limited to review and approval of testing and documentation, investigations, method validations/transfers, change controls, stability management.

RESPONSIBILITIES

• Operate testing instrumentation.
• Maintain and perform troubleshooting on GC?s.
• Organize and store all chemicals substances, fluids and compressed gases according to safety instructions
• Record all data and results in specified forms (paper and electronic) with accuracy and responsibility
• Maintain and assist in ordering laboratory supplies

QUALIFICATIONS

• Must have a 4 yr Science degree.
• Bachelor's (Required
• Laboratory Experience: 1 year (Preferred)
• English (Required)
• Maintain and assist in ordering laboratory supplies

A Quality Assurance professional at a cGMP facility is responsible for quality review and approval of protocols, reports, change controls, investigations, CAPAs, and other compliance activities related to the quality control/quality assurance of a testing laboratory. The incumbent will be responsible for QA oversight of laboratory compliance, including but not limited to review and approval of testing and documentation, investigations, method validations/transfers, change controls, stability management.

REQUIREMENTS

• A Quality Assurance professional at a cGMP facility is responsible for quality review and approval of protocols, reports, change controls, investigations, CAPAs, and other compliance activities related to the quality control/quality assurance of a testing laboratory. The incumbent will be responsible for QA oversight of laboratory compliance, including but not limited to review and approval of testing and documentation, investigations, method validations/transfers, change controls, stability management.
• Experience in Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements applicable.
• Experience in Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements applicable.

Work Remotely: No
Job Types: Full-time, Part-time

RESPONSIBILITIES

• Performs analysis as per current methodologie
• Performs analysis as per current methodologie
• MUST be able to cover, if needed, in Extractions
• Help to keep lab Organized and Clean
• Help to keep lab Organized and Clean
• Dump samples, Wash glassware, Keep chemicals and supplies in an organized manner, Keep hoods free from garbage and debris

QUALIFICATIONS

• BS Required
• Meticulous and have a high attention to detail
• Able to handle a high volume of work and ability to prioritize
• Willing to change job task quickly for last minute requests
• Able to work independently
• Proficient spoken and written English

Job Type: Full-time

A Laboratory Project Coordinator at a cGMP facility is responsible for tracking and managing sample receipt, work in progress, testing status, and reports for a contract testing laboratory.

The incumbent will be responsible for organization and tracking of samples, testing and documentation related to cGMP testing.

REQUIREMENTS

• Bachelor’s degree in Project Management, Chemistry or related field from an accredited college or university and a minimum 2 years of related experience in a Pharmaceutical cGMP environment.
• Proficiency in MS Office programs (Word, Excel, etc)
• Excellent communication and organizational skills
• Understanding of Analytical Laboratory testing preferred

Employment Requirement

• Oversight of 2 analysts running soil and water environmental samples for Metals by ICP/MS
• Ensure the metals department is following all required QA/QC requirements set forth in TNI (ISO/IEC 17025), SW-846, 40 CFR 136, 40 CFR 141, and NJDEP rules
• Hold departmental training, as necessary
• Work with IT to keep systems up to date
• Continuous improvement

Required Qualifications

• Bachelor’s degree or above from an accredited college in a Science Field, minimum 24 credit hours in chemistry. Transcripts will be required upon offer.
• Minimum one year of laboratory experience and MUST have minimum six months experience operating ICP/MS Agilent 7900/Masshunter 4.6. Ideal candidate will have 5+ years experience
• Experience with AA FIMS 100/WinLab32
• Familiar with analytical procedures and EPA methods 200.8, 6020B, 245.1, 7470A and 7471B
• Familiar with metals digestion EPA methods 3005A, 3050B, 3010A and 200.8
• Proficient spoken and written English
• Punctual, meticulous and reliableStrong computer skills, especially with Microsoft Excel

Responsibilities

• Method and Instrument Proficiency
• Employee Training
• Data Review
• Hire and Terminate
• Oversee metals digestion and evaluate all analytical parameters performed in the department
• Continually improve department and documentation
• Perform troubleshooting and repair instruments as needed
• In coordination with IT Department, prepare and/or install and maintain instrument software to keep current with changing requirements
• Archive and store all analytical raw data in computer backup files for historical revival as needed

IAL is an EOE/Affirmative Action Employer and welcomes applications from all qualified individuals, including minorities, females, individuals with disabilities, and veterans.

Job Type: Full-time
Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off

Schedule:

• Monday to Friday

Ability to commute/relocate:

• Township of Randolph, NJ 07869: Reliably commute or planning to relocate before starting work (Required)

Education:

• Bachelor's (Required)

Experience:

• ICPMS: 1 year (Required)

Work Location:

• In person