Home › Companies › Bostonanalytical › Chemist II
Chemist II
Bostonanalytical · Salem, New Hampshire, 03079, United States · Active · BambooHR
Job facts
| Field | Value |
|---|---|
| Company | Bostonanalytical |
| Title | Chemist II |
| Normalized title | - |
| Department / team | 415 - Chemistry |
| Location | Salem, United States |
| Work model | - |
| Employment type | Full Time |
| Salary | - |
| Status | active |
| ATS provider | BambooHR |
| Posted / first seen | 2026-06-02 / 2026-06-03 |
| Changed / last seen | 2026-06-03 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Bostonanalytical. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through BambooHR. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Salem. | Open |
| Department jobs | Active postings in 415 - Chemistry. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Bostonanalytical |
| Source | 9bf143cb-7c0a-49c9-96e6-04c61ed8d038 |
| ATS provider | BambooHR |
Description
JOB SUMMARY
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and BA Sciences Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development.
PRIMARY DUTIES AND RESPONSIBILITIES
Prepares and analyzes products to determine chemical and physical properties.
Will perform work under partial supervision and will provide over site to projects and assist other chemists as needed.
Works under partial supervision with chemists and other client personnel regarding research, procedures performed, related results and prepares reports.
Is a subject matter expert in some techniques and will mentor others. Work to learn and improve on others techniques and tasks.
Performs data generation, analysis and more complicated problem solving with a minimal rework.
Reviews and assesses deviations; includes performing risk assessments, participating in root cause analysis investigations, tracking, follow-up and reporting.
Works under partial supervision to ensure all work performed is performed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.
Ensures all work performed strictly adheres to company, client and pharmacopeial methodologies.
Performs system maintenance and calibrations to ensure equipment is operating with specified requirements.
Proper handling of hazardous waste in compliance with the company and DES hazardous waste rules.
Documents work in a clear and organized manner.
Follows all safety rules and regulations and conducts periodic safety audits.
Follows all cGMP rules and regulations.
REQUIREMENTS AND QUALIFICATIONS
Qualification include a bachelor’s degree in chemistry or a related discipline is required with 1+ years of related experience. Knowledge of cGMPs and related compliance regulations and guidances required.
MINIMUM SKILLS REQUIREMENTS
Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently.
A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.
Must have excellent organizational, verbal communication and technical documentation skills.
Solid computer skills.
Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.
Must be a team player with integrity and concern for the quality of company products, services and staff members.
Full job record
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| Source ID | 9bf143cb-7c0a-49c9-96e6-04c61ed8d038 |
| Board ID | 9bf143cb-7c0a-49c9-96e6-04c61ed8d038 |
| Provider | bamboohr |
| Provider Job Key | 157 |
| Title | Chemist II |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Salem, New Hampshire, 03079, United States |
| Department | 415 - Chemistry |
| Team | — |
| Employment Type | full_time |
| Workplace Type | — |
| Remote Policy | — |
| Country | United States |
| Region | — |
| City | Salem |
| Salary Raw | — |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://bostonanalytical.bamboohr.com/careers/157 |
| Apply URL | https://bostonanalytical.bamboohr.com/careers/157 |
| First Seen At | 2026-06-03 10:33:52Z |
| Last Seen At | 2026-06-06 10:24:02Z |
| Last Checked At | 2026-06-06 10:24:02Z |
| Last Changed At | 2026-06-03 10:33:52Z |
| Inactive At | — |
| Source Posted At | 2026-06-02 00:00:00Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=bamboohr/board=bostonanalytical/date=2026-06-06/2026-06-06T10-24-01-447Z-e4a4eadb9a14c740be17322d9b891394ef297fb85bdf8c536a9f3d135984ff63.json |
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"description": "<p><span style=\"font-weight: bold\">JOB SUMMARY</span></p>\n<p>The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and BA Sciences Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. </p>\n<p><br></p>\n<p><span style=\"font-weight: bold\">PRIMARY DUTIES AND RESPONSIBILITIES</span></p>\n<ul>\n<li>Prepares and analyzes products to determine chemical and physical properties.</li>\n<li>Will perform work under partial supervision and will provide over site to projects and assist other chemists as needed.</li>\n<li>Works under partial supervision with chemists and other client personnel regarding research, procedures performed, related results and prepares reports.</li>\n<li>Is a subject matter expert in some techniques and will mentor others. Work to learn and improve on others techniques and tasks.</li>\n<li>Performs data generation, analysis and more complicated problem solving with a minimal rework.</li>\n<li>Reviews and assesses deviations; includes performing risk assessments, participating in root cause analysis investigations, tracking, follow-up and reporting.</li>\n<li>Works under partial supervision to ensure all work performed is performed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.</li>\n<li>Ensures all work performed strictly adheres to company, client and pharmacopeial methodologies.</li>\n<li>Performs system maintenance and calibrations to ensure equipment is operating with specified requirements.</li>\n<li>Proper handling of hazardous waste in compliance with the company and DES hazardous waste rules.</li>\n<li>Documents work in a clear and organized manner.</li>\n<li>Follows all safety rules and regulations and conducts periodic safety audits.</li>\n<li>Follows all cGMP rules and regulations.</li>\n</ul>\n<p> </p>\n<p><span style=\"font-weight: bold\">REQUIREMENTS AND QUALIFICATIONS</span></p>\n<p>Qualification include a bachelor’s degree in chemistry or a related discipline is required with 1+ years of related experience. Knowledge of cGMPs and related compliance regulations and guidances required.</p>\n<p><br></p>\n<p><span style=\"font-weight: bold\">MINIMUM SKILLS REQUIREMENTS</span></p>\n<ul>\n<li>Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently.</li>\n<li>A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.</li>\n<li>Must have excellent organizational, verbal communication and technical documentation skills.</li>\n<li>Solid computer skills.</li>\n<li>Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.</li>\n<li>Must be a team player with integrity and concern for the quality of company products, services and staff members.</li>\n</ul>",
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