Scientist I (LC-MS)

Boston Analytical

Salem (NH)

On-site

USD 70,000 - 90,000

Full time

14 days+

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Job summary

Boston Analytical in Salem, NH is seeking a Scientist II to conduct Extractables & Leachables studies. Responsibilities include preparing and analyzing samples using various analytical techniques like LC-MS, GC-MS, and ICP-MS, as well as maintaining compliance with FDA and cGMP regulations.

The ideal candidate has a B.S. in Chemistry or related field with at least 3 years of experience in a cGMP lab. Strong organizational, communication, and teamwork skills are essential. Join a dynamic team that values integrity and quality in its work.

Qualifications

  • 3+ years' experience performing GC-MS analysis or a master's with 1-3 years' experience.
  • Knowledge of cGMPs and related compliance regulations.
  • Experience working in a cGMP laboratory.

Responsibilities

  • Prepares and analyzes samples and extracts to detect extractables from packaging.
  • Coordinates findings with team members.
  • Maintains and calibrates analytical equipment.
  • Authors detailed cGMP report sections.
  • Develops and validates leachables methods.
  • Trains team members on E&L lab techniques.
  • Writes and edits Standard Operating Procedures.

Skills

GC-MS analysis
LC-MS
ICP-MS
cGMP regulations
interpersonal skills
organizational skills
verbal communication
technical documentation

Education

B.S. in Chemistry or related discipline
Master's degree in a related field

Job description

JOB SUMMARY

The Scientist II sets up Extractables & Leachables studies and conducts quantitative and qualitative analyses according to FDA, cGMP, and Boston Analytical Inc. Standard Operating Procedures. Duties include analysis of extract and pharmaceutical product samples using LC-MS, GC-MS, and/or ICP-MS. A Scientist II will also develop and validate leachables methods for these techniques.

PRIMARY DUTIES AND RESPONISIBITIES
  • Prepares and analyzes samples and sample extracts to detect and identify extractables from pharmaceutical packaging and leachables from drug product samples.
  • Coordinate findings with team members.
  • Maintain and calibrate analytical equipment following established procedures.
  • Author detailed cGMP report sections for work performed.
  • Develop and validate leachables methods for LC-MS, GC-MS, and/or ICP-MS.
  • Train other team members on the various techniques performed in the E&L lab.
  • Write, maintain, and edit departmental Standard Operating Procedures.
  • Perform peer review of work from other team members.
  • Perform assigned tasks and duties independently with minimal supervision.
  • Prepares samples for analysis by GC‑MS.
  • Analysis of sample solutions by liquid injection and headspace GC‑MS to adequately resolve and identify all compounds.
  • With the help of the NIST library, identify detected extractables.
  • Incorporate data into detailed, concise analytical report along with data from other techniques.
  • Develop GC‑MS methods for drug product stability testing.
  • Performs system maintenance and calibrations to ensure equipment is operating within specified requirements. Ensures all work performed strictly adheres to Company, client and Pharmacopial requirements.
  • Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules.
REQUIREMENTS & QUALIFICATIONS

B.S. in Chemistry or related discipline with 3+ years’ experience performing GC‑MS analysis or a master's with 1-3 years of experience. Knowledge of cGMPs and related compliance regulations and guidance required. Experience working in a cGMP laboratory.

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.
  • Must be a team player with integrity and concern for the quality of Company products, services and staff members.
  • Demonstrated ability to perform analysis using GC‑MS.
  • Strong drive to learn and improve current skill set.
  • Documented success managing multiple tasks and deadlines to successful completion that is within customer expectations.
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