Top 1 chemist Jobs in norwich ny

Chemist I
Norwich Pharmaceuticals Inc —Norwich, NY
- $62,354 a year
- Full-time
- Bachelor of Science
- Analysis skills
- Bachelor's degree
- Wellness program
- Health savings account
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2d

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Chemist I
Norwich Pharmaceuticals Inc —Norwich, NY
When laboratory management must be notified to determine whether an investigation is warranted. Perform routine sample analysis requiring general laboratory…
$62,354 a year
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2d
Environmental Specialist - Hazardous Waste Profiler
Solvents & Petroleum Service, Inc. —Syracuse, NY
Ensure compliance with RCRA, EPA, DOT, and state regulations. Environmental science, chemistry, or environmental compliance.
$26 - $36 an hour
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QC Chemist
Gfs Chemicals Inc —Powell, OH
Record results for all tests on QC worksheets, data entry to the ERP system, and certificate of analysis generation. Perform basic calibrations on equipment.
$23 - $26 an hour
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2d
Quality Control Analyst I
Belcan —Delaware, OH
Typically requires a bachelor's degree. Performs various scientific analyses to evaluate the quality of raw materials, in-process materials, and finished goods…
$26.50 an hour
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Chemist I

Norwich Pharmaceuticals Inc -
Norwich, NY

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Job Details

Full-time
$62,354 a year
2 days ago

Benefits

Wellness program
Health savings account
Paid holidays
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Paid time off
Vision insurance
Life insurance
Prescription drug insurance

Qualifications

Bachelor's degree

Full Job Description

SUMMARY OF POSITION

The Quality Control Chemist I:

Performs routine testing to assess the conformance of raw materials, finished products, and/or stability samples to predetermined product specifications.
Performs routine testing in conformance with approved procedures, accurately and concisely documents data, and reports results.
Demonstrates a basic knowledge of SOP’s and GMP regulations as related to the pharmaceutical quality control laboratory.

ORGANIZATION STRUCTURE

The Quality Control Chemist I / Microbiologist I reports into the Manager Quality Control or Team Leader Quality Control.

RESPONSIBILITIES

Primary responsibilities of this role include the following:

Safety
- Perform job functions in a safe manner consistent with site safe practices and regulatory (e.g. – OSHA) requirements
- Participate in weekly/monthly safety training, identify potential safety hazards and cooperate with investigations of safety related incidents
Compliance
- Conduct assigned tasks in compliance with cGXP requirements, current industry standards, compendia standards, FDA expectations and internal procedures
- Assist with laboratory investigations to ensure they are conducted in a timely manner and are completed within established target completion dates
- Maintain required level of training needed to perform a GMP task
Productivity
- Perform routine sample analysis requiring general laboratory skills such as weighing, pipetting, titration, and basic operation of laboratory instrumentation
- Comprehend and follow approved test methods accurately in the performance of sample analysis to ensure adherence to “Right-the First Time” philosophy
- Perform analysis with a practical understanding of the test procedure and instrument operation
- Use available software to control instrumentation, collect data, process and calculate results, and report results
- Perform testing to evaluate physical characteristics of raw materials and finished products
- Work under direction provided by supervisor
- Calculate results and assess conformance with specifications
- Notify manager immediately of nonconforming data or unexpected occurrences
- Organize work schedule to complete assigned tasks efficiently and on schedule
- Maintain accurate record of analysis and perform documentation to company standards
- Prepare test solutions, reagents, and samples used in analysis
- Other duties as assigned

QUALIFICATIONS

BS in Chemistry, Biochemistry, Microbiology or Biology or related discipline
0-3 years experience in a pharmaceutical QC laboratory environment
Understanding of cGXP requirements preferred
Organization, communication and interpersonal skills

GMP DECISION-MAKING AUTHORITY

Responsible for decisions related to:

When laboratory management must be notified to determine whether an investigation is warranted
Maintain required level of training needed to perform a GMP task
Suitability of analytical equipment/instruments for use.

The anticipated base salary range for this position is $62,354.00. This position is eligible for Alvogen’s annual discretionary bonus and comprehensive benefits package, consisting of medical and prescription drug coverage (two PPO plans and an HDHP with Health Savings Account and employer contribution), dental, vision, flexible spending accounts. Alvogen’s benefits package also includes a retirement savings program, long-term care coverage, paid time off (176 hours to start) inclusive of sick time, disability benefits, life insurance, a wellness program, and 13 company recognized paid holidays per year. We anticipate this position will be posted on 03/06/2026 and remain open for at least 30 days. To apply, select the apply button and submit your application.

“An Equal Opportunity Employer, including disability/vets.”

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